Stephen Chanock
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American physician and geneticist
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Stephen Chanock's Degrees
- Masters Medicine University of California, San Francisco
- Bachelors Biology University of California, Santa Cruz
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Why Is Stephen Chanock Influential?
(Suggest an Edit or Addition)According to Wikipedia, Stephen Jacob Chanock is an American physician and geneticist. He currently serves as Director of the Division of Cancer Epidemiology and Genetics at the U.S. National Cancer Institute . Biography Stephen Chanock is the son of NIH scientist Robert M. Chanock, discoverer of human respiratory syncytial virus.
Stephen Chanock's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
- Genome-wide association study identifies novel breast cancer susceptibility loci (2007) (2351)
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (2010) (1961)
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
- Genome-Wide Association Study reveals genetic risk underlying Parkinson’s disease (2009) (1770)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2009) (1735)
- Chronic Granulomatous Disease: Report on a National Registry of 368 Patients (2000) (1583)
- A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer (2007) (1520)
- Replicating genotype–phenotype associations (2007) (1367)
- LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants (2015) (1191)
- Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
- Assessing the probability that a positive report is false: an approach for molecular epidemiology studies. (2004) (1172)
- Genome-wide association study of prostate cancer identifies a second risk locus at 8q24 (2007) (1156)
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) (1107)
- Large-scale genotyping identifies 41 new loci associated with breast cancer risk (2013) (1063)
- Multiple loci identified in a genome-wide association study of prostate cancer (2008) (970)
- Association analysis identifies 65 new breast cancer risk loci (2017) (922)
- Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24 (2007) (757)
- Genome-wide association study of circulating vitamin D levels (2010) (722)
- Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia. (2005) (693)
- Estimation of effect size distribution from genome-wide association studies and implications for future discoveries (2010) (651)
- Assessing the Probability That a Positive Report is False: An Approach for Molecular Epidemiology Studies (2004) (629)
- Identification of ten loci associated with height highlights new biological pathways in human growth (2008) (626)
- Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer (2009) (618)
- A common coding variant in CASP8 is associated with breast cancer risk (2007) (591)
- Hematotoxicity in Workers Exposed to Low Levels of Benzene (2004) (588)
- A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) (2009) (578)
- Powerful SNP-set analysis for case-control genome-wide association studies. (2010) (576)
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
- Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes (2018) (559)
- MicroRNA Related Polymorphisms and Breast Cancer Risk (2014) (557)
- Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array (2012) (550)
- Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer. (2012) (544)
- A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33 (2010) (542)
- Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies. (2011) (536)
- Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer (2013) (534)
- A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. (2009) (532)
- The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
- Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (516)
- Detectable clonal mosaicism from birth to old age and its relationship to cancer (2012) (514)
- Detectable clonal mosaicism and its relationship to aging and cancer (2012) (512)
- Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche (2014) (511)
- Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (2018) (509)
- Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer (2015) (502)
- Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2 (2009) (502)
- Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies (2010) (477)
- Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants (2015) (471)
- A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation (2008) (471)
- A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma (2010) (469)
- NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses (2005) (468)
- Performance of common genetic variants in breast-cancer risk models. (2010) (430)
- A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci (2010) (423)
- A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer (2014) (416)
- Genome-wide association studies identify four ER negative–specific breast cancer risk loci (2013) (411)
- FTO genotype is associated with phenotypic variability of body mass index (2012) (407)
- Heterogeneity of Breast Cancer Associations with Five Susceptibility Loci by Clinical and Pathological Characteristics (2008) (390)
- Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium. (2006) (390)
- A double-blind comparison of empirical oral and intravenous antibiotic therapy for low-risk febrile patients with neutropenia during cancer chemotherapy. (1999) (389)
- Patterns of somatic structural variation in human cancer genomes (2020) (377)
- ABO blood group and the risk of pancreatic cancer. (2009) (375)
- A mutational signature reveals alterations underlying deficient homologous recombination repair in breast cancer (2017) (365)
- Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits (2013) (365)
- Genome-wide association studies identify novel loci associated with age at menarche and age at natural menopause (2009) (363)
- Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk (2017) (359)
- Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes (2017) (353)
- Anthropometric measures, body mass index, and pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan). (2010) (332)
- Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita. (2007) (326)
- Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies (2013) (325)
- Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women. (2020) (322)
- Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2014) (322)
- The landscape of recombination in African Americans (2011) (312)
- Large-scale genomic analyses link reproductive ageing to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair (2015) (308)
- A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor–negative breast cancer (2011) (306)
- Fusariosis associated with pathogenic fusarium species colonization of a hospital water system: a new paradigm for the epidemiology of opportunistic mold infections. (2001) (305)
- A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2 (2009) (305)
- Cancer survivorship--genetic susceptibility and second primary cancers: research strategies and recommendations. (2006) (301)
- Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. (2013) (300)
- Cigarette smoking and pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium. (2009) (300)
- Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
- Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome. (2003) (298)
- Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study (2011) (295)
- Genome-wide association analysis identifies three new breast cancer susceptibility loci (2012) (291)
- Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models. (2009) (281)
- Discovery of common and rare genetic risk variants for colorectal cancer (2018) (279)
- Mutation of GATA3 in human breast tumors (2004) (279)
- Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia (2012) (277)
- SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes (2005) (277)
- Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma (2014) (275)
- Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer (2014) (273)
- The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers (2016) (267)
- Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. (2011) (263)
- Genome-Wide and Candidate Gene Association Study of Cigarette Smoking Behaviors (2009) (262)
- Common variants at 19p13 are associated with susceptibility to ovarian cancer (2010) (262)
- Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease. (1998) (253)
- Loci associated with skin pigmentation identified in African populations (2017) (253)
- Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants (2011) (252)
- Breast Cancer Risk From Modifiable and Nonmodifiable Risk Factors Among White Women in the United States. (2016) (250)
- Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3 (2011) (246)
- Identification of a new prostate cancer susceptibility locus on chromosome 8q24 (2009) (245)
- Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer (2017) (244)
- A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry (2013) (244)
- Pancreatic cancer risk and ABO blood group alleles: results from the pancreatic cancer cohort consortium. (2010) (237)
- Angiotensin II induces p67phox mRNA expression and NADPH oxidase superoxide generation in rabbit aortic adventitial fibroblasts. (1998) (236)
- Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy (2013) (235)
- Genomic DNA hypomethylation as a biomarker for bladder cancer susceptibility in the Spanish Bladder Cancer Study: a case-control study. (2008) (229)
- Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions (2012) (227)
- SNPs in cancer research and treatment (2004) (226)
- Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers. (2013) (225)
- Genome-wide association study of glioma and meta-analysis (2012) (225)
- Gene targeting of X chromosome-linked chronic granulomatous disease locus in a human myeloid leukemia cell line and rescue by expression of recombinant gp91phox. (1993) (222)
- Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk (2014) (218)
- A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone–Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation (2012) (216)
- A subset-based approach improves power and interpretation for the combined analysis of genetic association studies of heterogeneous traits. (2012) (213)
- Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors (2017) (213)
- A Spectrum of Severe Familial Liver Disorders Associate with Telomerase Mutations (2009) (211)
- The 5p15.33 Locus Is Associated with Risk of Lung Adenocarcinoma in Never-Smoking Females in Asia (2010) (210)
- Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer (2015) (210)
- Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21 (2011) (210)
- Genome-Wide Meta-Analysis Identifies Regions on 7p21 (AHR) and 15q24 (CYP1A2) As Determinants of Habitual Caffeine Consumption (2011) (204)
- Genetic evidence of assortative mating in humans (2017) (199)
- Meta-analysis of new genome-wide association studies of colorectal cancer risk (2012) (197)
- Comprehensive molecular characterization of mitochondrial genomes in human cancers (2017) (197)
- The Scientific Foundation for Personal Genomics: Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention Multidisciplinary Workshop (2009) (196)
- GWASdb: a database for human genetic variants identified by genome-wide association studies (2011) (194)
- Polymorphisms in GSTT1, GSTZ1, and CYP2E1, Disinfection By-products, and Risk of Bladder Cancer in Spain (2010) (192)
- Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium. (2011) (192)
- SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes (2004) (190)
- Genome-wide Association Study Identifies Multiple Risk Loci for Chronic Lymphocytic Leukemia (2013) (190)
- Von Hippel-Lindau (VHL) Inactivation in Sporadic Clear Cell Renal Cancer: Associations with Germline VHL Polymorphisms and Etiologic Risk Factors (2011) (189)
- C-reactive protein and risk of lung cancer. (2010) (186)
- Cytokine polymorphisms in the Th1/Th2 pathway and susceptibility to non-Hodgkin lymphoma. (2006) (186)
- Identification of Novel Genetic Markers of Breast Cancer Survival (2015) (185)
- Genome-wide association study identifies new prostate cancer susceptibility loci. (2011) (183)
- A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. (2012) (182)
- Genome-wide Association Study Identifies Two Susceptibility Loci for Osteosarcoma (2013) (181)
- Cortisolemic indices predict severe infections in Cushing syndrome due to ectopic production of adrenocorticotropin. (2000) (180)
- A Genome-Wide Association Study Identifies New Susceptibility Loci for Esophageal Adenocarcinoma and Barrett’s Esophagus (2013) (179)
- Risk of Spontaneous Preterm Birth is Associated With Common Proinflammatory Cytokine Polymorphisms (2005) (178)
- A common haplotype of interleukin-4 gene IL4 is associated with severe respiratory syncytial virus disease in Korean children. (2002) (178)
- A federated ecosystem for sharing genomic, clinical data (2016) (177)
- Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia (2009) (176)
- Oxidative damage-related genes AKR1C3 and OGG1 modulate risks for lung cancer due to exposure to PAH-rich coal combustion emissions. (2004) (174)
- PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS (2016) (174)
- The phosphorylation targets of p47phox, a subunit of the respiratory burst oxidase. Functions of the individual target serines as evaluated by site-directed mutagenesis. (1995) (174)
- Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32 (2010) (171)
- Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium. (2011) (167)
- Etiologic heterogeneity among non-Hodgkin lymphoma subtypes. (2008) (166)
- Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway. (2009) (166)
- Safety, Tolerance, and Pharmacokinetics of a Small Unilamellar Liposomal Formulation of Amphotericin B (AmBisome) in Neutropenic Patients (1998) (165)
- Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction (2021) (163)
- Current status of genome-wide association studies in cancer (2011) (163)
- Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses (2006) (162)
- Immunogenetic Risk and Protective Factors for the Idiopathic Inflammatory Myopathies: Distinct HLA-A, -B, -Cw, -DRB1, and -DQA1 Allelic Profiles Distinguish European American Patients With Different Myositis Autoantibodies (2006) (162)
- Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma (2012) (159)
- Vitamin D-related genes, serum vitamin D concentrations and prostate cancer risk. (2009) (159)
- Evidence of Gene–Environment Interactions between Common Breast Cancer Susceptibility Loci and Established Environmental Risk Factors (2013) (159)
- Association of breast cancer outcome with status of p53 and MDM2 SNP309. (2006) (158)
- Common variants of FUT2 are associated with plasma vitamin B12 levels (2008) (156)
- Genetic Variation in the Nucleotide Excision Repair Pathway and Bladder Cancer Risk (2006) (155)
- Meta-analysis identifies four new loci associated with testicular germ cell tumor (2013) (155)
- Genetic variation at the CYP19A1 locus predicts circulating estrogen levels but not breast cancer risk in postmenopausal women. (2007) (155)
- Functional Variant of Manganese Superoxide Dismutase (SOD2 V16A) Polymorphism Is Associated with Prostate Cancer Risk in the Prostate, Lung, Colorectal, and Ovarian Cancer Study (2007) (152)
- High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays (2009) (152)
- Constitutional telomerase mutations are genetic risk factors for cirrhosis (2011) (151)
- A common 8q24 variant in prostate and breast cancer from a large nested case-control study. (2007) (151)
- Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite (2015) (151)
- Genetic Polymorphisms in Base-Excision Repair Pathway Genes and Risk of Breast Cancer (2006) (150)
- Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways (2012) (150)
- Inflammation-Related Gene Polymorphisms and Colorectal Adenoma (2006) (149)
- Meta-analyses identify 13 novel loci associated with age at menopause and highlights DNA repair and immune pathways (2011) (149)
- Characterization of gene-environment interactions for colorectal cancer susceptibility loci. (2012) (149)
- Beyond odds ratios — communicating disease risk based on genetic profiles (2009) (149)
- DNA fingerprinting of the NCI-60 cell line panel (2009) (148)
- Characterizing Associations and SNP-Environment Interactions for GWAS-Identified Prostate Cancer Risk Markers—Results from BPC3 (2011) (146)
- Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer (2018) (146)
- Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types. (2016) (146)
- PCR and single-strand conformational polymorphism for recognition of medically important opportunistic fungi (1995) (146)
- Tumor necrosis factor (TNF) and lymphotoxin-alpha (LTA) polymorphisms and risk of non-Hodgkin lymphoma in the InterLymph Consortium. (2010) (145)
- Using genetic variation to study human disease. (2001) (145)
- An IL6 promoter polymorphism is associated with a lifetime risk of development of Kaposi sarcoma in men infected with human immunodeficiency virus. (2000) (144)
- Genome-Wide Association Studies, Field Synopses, and the Development of the Knowledge Base on Genetic Variation and Human Diseases (2009) (144)
- Directional dominance on stature and cognition in diverse human populations (2015) (144)
- GWASdb v2: an update database for human genetic variants identified by genome-wide association studies (2015) (144)
- Obesity and risk of esophageal adenocarcinoma and Barrett's esophagus: a Mendelian randomization study. (2014) (142)
- Genome-wide association study identifies a common variant associated with risk of endometrial cancer (2011) (142)
- A candidate gene approach to searching for low-penetrance breast and prostate cancer genes (2005) (140)
- Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma (2020) (140)
- Genome-wide association study identifies multiple susceptibility loci for diffuse large B-cell lymphoma (2014) (140)
- Genetic Susceptibility Loci for Breast Cancer by Estrogen Receptor Status (2008) (139)
- Genome-wide association study of colorectal cancer identifies six new susceptibility loci (2015) (138)
- Common genetic variants in proinflammatory and other immunoregulatory genes and risk for non-Hodgkin lymphoma. (2006) (136)
- Genome-wide association study identifies multiple loci associated with bladder cancer risk. (2014) (136)
- Selected Genetic Polymorphisms in MGMT, XRCC1, XPD, and XRCC3 and Risk of Head and Neck Cancer: A Pooled Analysis (2005) (135)
- Rapid Extraction of Genomic DNA from Medically Important Yeasts and Filamentous Fungi by High-Speed Cell Disruption (1998) (134)
- Amphotericin B lipid complex in pediatric patients with invasive fungal infections. (1999) (134)
- A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. (2009) (133)
- Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors (2016) (133)
- Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types. (2015) (133)
- Population Substructure and Control Selection in Genome-Wide Association Studies (2008) (133)
- Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations (2014) (133)
- Common variants in immune and DNA repair genes and risk for human papillomavirus persistence and progression to cervical cancer. (2009) (133)
- Polymorphisms in immune function genes and risk of non-Hodgkin lymphoma: findings from the New South Wales non-Hodgkin Lymphoma Study. (2007) (132)
- Genome-wide association study of tanning phenotype in a population of European ancestry. (2009) (132)
- BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2 (2018) (131)
- Therapy‐Induced Alterations in Host Defense in Children Receiving Therapy for Cancer (1997) (131)
- Genetic predisposition to mosaic Y chromosome loss in blood (2019) (131)
- A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease. (2013) (131)
- A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease. (1997) (130)
- Large-Scale Evaluation of Candidate Genes Identifies Associations between VEGF Polymorphisms and Bladder Cancer Risk (2007) (130)
- A large-scale candidate gene association study of age at menarche and age at natural menopause (2010) (129)
- Polymorphisms in the DNA nucleotide excision repair genes and lung cancer risk in Xuan Wei, China (2005) (128)
- Discovery of Novel Biomarkers by Microarray Analysis of Peripheral Blood Mononuclear Cell Gene Expression in Benzene-Exposed Workers (2005) (128)
- Diabetes and risk of pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium (2013) (127)
- Cardiovascular manifestations of human immunodeficiency virus infection in infants and children. (1989) (127)
- Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure. (2006) (126)
- International cancer seminars: a focus on esophageal squamous cell carcinoma (2017) (126)
- Family history of cancer and risk of pancreatic cancer: A pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan) (2010) (126)
- Burden of Nonsynonymous Mutations among TCGA Cancers and Candidate Immune Checkpoint Inhibitor Responses. (2016) (125)
- Common Genetic Variants and Risk for HPV Persistence and Progression to Cervical Cancer (2010) (124)
- Characterizing Genetic Risk at Known Prostate Cancer Susceptibility Loci in African Americans (2011) (123)
- Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome. (2010) (123)
- IGF-1, IGFBP-1, and IGFBP-3 Polymorphisms Predict Circulating IGF Levels but Not Breast Cancer Risk: Findings from the Breast and Prostate Cancer Cohort Consortium (BPC3) (2008) (123)
- Genetic polymorphisms in the one‐carbon metabolism pathway and breast cancer risk: A population‐based case–control study and meta‐analyses (2007) (123)
- Identification of nine new susceptibility loci for endometrial cancer (2018) (122)
- A genome-wide association study identifies alleles in FGFR 2 associated with risk of sporadic postmenopausal breast cancer (2012) (122)
- Genetic variation in the base excision repair pathway and bladder cancer risk (2007) (121)
- Genome-wide association study of circulating retinol levels (2011) (120)
- Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course. (2013) (120)
- NAT 2 slow acetylation , GSTM 1 null genotype , and risk of bladder cancer : results from the Spanish Bladder Cancer Study and meta-analyses (2005) (120)
- Genome-wide association studies in cancer--current and future directions. (2010) (120)
- LDlinkR: An R Package for Rapidly Calculating Linkage Disequilibrium Statistics in Diverse Populations (2020) (120)
- Somatic Genomics and Clinical Features of Lung Adenocarcinoma: A Retrospective Study (2016) (120)
- Pathway analysis of breast cancer genome-wide association study highlights three pathways and one canonical signaling cascade. (2010) (119)
- Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue (2014) (119)
- Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study (2015) (119)
- Widespread purifying selection at polymorphic sites in human protein-coding loci (2003) (119)
- Phase I Metabolic Genes and Risk of Lung Cancer: Multiple Polymorphisms and mRNA Expression (2009) (117)
- Polymorphisms in oxidative stress genes and risk for non-Hodgkin lymphoma. (2006) (117)
- Enhanced Statistical Tests for GWAS in Admixed Populations: Assessment using African Americans from CARe and a Breast Cancer Consortium (2011) (117)
- Transforming Epidemiology for 21st Century Medicine and Public Health (2013) (116)
- An Absolute Risk Model to Identify Individuals at Elevated Risk for Pancreatic Cancer in the General Population (2013) (116)
- Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042. (2009) (116)
- Prognostic significance of host immune gene polymorphisms in follicular lymphoma survival. (2007) (116)
- A prospective study of mitochondrial DNA copy number and risk of non-Hodgkin lymphoma. (2008) (116)
- GWAS of Follicular Lymphoma Reveals Allelic Heterogeneity at 6p21.32 and Suggests Shared Genetic Susceptibility with Diffuse Large B-cell Lymphoma (2011) (114)
- Common variants in ZNF365 are associated with both mammographic density and breast cancer risk (2011) (114)
- Mosaic loss of chromosome Y is associated with common variation near TCL1A (2016) (114)
- A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences. (2015) (113)
- Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease. (2000) (113)
- Polymorphisms in DNA repair genes, smoking, and bladder cancer risk: findings from the international consortium of bladder cancer. (2009) (113)
- Role of oxygen radicals generated by NADPH oxidase in apoptosis induced in human leukemia cells. (1998) (113)
- Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (2014) (112)
- Ascorbate recycling in human neutrophils: induction by bacteria. (1997) (112)
- Variation in the Selenoenzyme Genes and Risk of Advanced Distal Colorectal Adenoma (2008) (112)
- Single nucleotide polymorphic discrimination by an electronic dot blot assay on semiconductor microchips (1999) (111)
- Pathway analysis of genome-wide association study data highlights pancreatic development genes as susceptibility factors for pancreatic cancer. (2012) (111)
- GSTM1 null and NAT2 slow acetylation genotypes, smoking intensity and bladder cancer risk: results from the New England bladder cancer study and NAT2 meta-analysis. (2011) (111)
- Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses (2019) (110)
- Genome-wide association study identifies common variants associated with circulating vitamin E levels (2011) (110)
- Longer Telomere Length in Peripheral White Blood Cells Is Associated with Risk of Lung Cancer and the rs2736100 (CLPTM1L-TERT) Polymorphism in a Prospective Cohort Study among Women in China (2013) (110)
- Common Gene Variants in the Tumor Necrosis Factor (TNF) and TNF Receptor Superfamilies and NF-kB Transcription Factors and Non-Hodgkin Lymphoma Risk (2009) (110)
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31 (2013) (110)
- Occupational trichloroethylene exposure and renal carcinoma risk: evidence of genetic susceptibility by reductive metabolism gene variants. (2010) (109)
- Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1. (2013) (109)
- Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers (2008) (107)
- Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia (2016) (107)
- Estimating the heritability of colorectal cancer. (2014) (107)
- Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility (2009) (107)
- Vitamin D Receptor Polymorphisms and Breast Cancer Risk: Results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (2009) (106)
- Genome-wide meta-analyses of smoking behaviors in African Americans (2012) (106)
- Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease. (2002) (106)
- Immunogenetic Risk and Protective Factors for the Idiopathic Inflammatory Myopathies: Distinct HLA-A, -B, -Cw, -DRB1 and -DQA1 Allelic Profiles and Motifs Define Clinicopathologic Groups in Caucasians (2005) (105)
- Bladder cancer risk and genetic variation in AKR1C3 and other metabolizing genes. (2008) (105)
- Candidate Genes and Single Nucleotide Polymorphisms (SNPs) in the Study of Human Disease (2002) (105)
- Performance of high-throughput DNA quantification methods (2003) (104)
- Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Yeager M, Orr N, Hayes RB, Jacobs KB, Kraft (2007) (104)
- Validation of Genome-Wide Prostate Cancer Associations in Men of African Descent (2010) (104)
- Common genetic polymorphisms modify the effect of smoking on absolute risk of bladder cancer. (2013) (104)
- Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia (2014) (103)
- Variants of the IL8 and IL8RB genes and risk for gastric cardia adenocarcinoma and esophageal squamous cell carcinoma. (2004) (102)
- Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript (2011) (102)
- Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium (2017) (102)
- Novel Common Genetic Susceptibility Loci for Colorectal Cancer (2018) (102)
- Polymorphisms in inflammatory cytokines and Fcγ receptors in childhood chronic immune thrombocytopenic purpura: a pilot study (2001) (101)
- Genome-Wide Association Study of Relative Telomere Length (2011) (101)
- Polymorphisms in Th1-type cell-mediated response genes and risk of gastric cancer. (2007) (101)
- Alcohol intake and pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium (PanScan) (2010) (101)
- Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region. (2014) (101)
- Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma. (2020) (101)
- Safety, tolerance, and pharmacokinetics of amphotericin B lipid complex in children with hepatosplenic candidiasis (1997) (100)
- Kathleen Cuningham Foundation Consortium For Research Into Familial Breast Cancer (2008) (100)
- Polymorphisms in Apoptosis and Cell Cycle Control Genes and Risk of Brain Tumors in Adults (2007) (100)
- Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression (2013) (100)
- A genome-wide association study of early menopause and the combined impact of identified variants (2013) (99)
- Nucleotide Excision Repair Gene Polymorphisms and Risk of Advanced Colorectal Adenoma: XPC Polymorphisms Modify Smoking-Related Risk (2006) (99)
- Genetic variation at the SLC23A1 locus is associated with circulating concentrations of L-ascorbic acid (vitamin C): evidence from 5 independent studies with >15,000 participants. (2010) (98)
- Exploring SNP‐SNP interactions and colon cancer risk using polymorphism interaction analysis (2006) (98)
- Influence of Cytotoxic T Lymphocyte-associated Antigen 4 (CTLA4) Common Polymorphisms on Outcome in Treatment of Melanoma Patients With CTLA-4 Blockade (2008) (98)
- A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23. (2012) (97)
- A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3. (2011) (97)
- Evidence for single-dose protection by the bivalent HPV vaccine—Review of the Costa Rica HPV vaccine trial and future research studies (2018) (97)
- The UBC-40 Urothelial Bladder Cancer cell line index: a genomic resource for functional studies (2015) (96)
- Assessment of measuring circulating levels of interleukin-6, interleukin-8, C-reactive protein, soluble Fc gamma receptor type III, and mannose-binding protein in febrile children with cancer and neutropenia. (1999) (96)
- Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer (2016) (95)
- Prevalence in the United States of Selected Candidate Gene Variants (2008) (95)
- Arachidonate lipoxygenase (ALOX) and cyclooxygenase (COX) polymorphisms and colon cancer risk. (2004) (95)
- Germline TP53 variants and susceptibility to osteosarcoma. (2015) (95)
- Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor (2017) (94)
- Sequence analysis of the mannose-binding lectin (MBL2) gene reveals a high degree of heterozygosity with evidence of selection (2004) (94)
- Systems biology of human benzene exposure. (2010) (94)
- Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma among women in Connecticut (2006) (93)
- Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk. (2007) (93)
- Gene-nutrient interactions among determinants of folate and one-carbon metabolism on the risk of non-Hodgkin lymphoma: NCI-SEER case-control study. (2007) (93)
- Prostate Cancer Susceptibility in Men of African Ancestry at 8q24. (2016) (93)
- LDassoc: an online tool for interactively exploring genome-wide association study results and prioritizing variants for functional investigation (2018) (92)
- Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours (2015) (91)
- Consortium analysis of 7 candidate SNPs for ovarian cancer (2008) (91)
- Telomere length in white blood cell DNA and lung cancer: a pooled analysis of three prospective cohorts. (2014) (91)
- Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants. (2015) (91)
- Characterization of large structural genetic mosaicism in human autosomes. (2015) (91)
- Isolation of a complex of respiratory burst oxidase components from resting neutrophil cytosol. (1994) (90)
- Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium. (2011) (90)
- A pooled investigation of Toll-like receptor gene variants and risk of non-Hodgkin lymphoma. (2009) (89)
- Analysis of the 10q11 Cancer Risk Locus Implicates MSMB and NCOA4 in Human Prostate Tumorigenesis (2010) (89)
- Genome-Wide Diet-Gene Interaction Analyses for Risk of Colorectal Cancer (2014) (89)
- Variation in KLK genes, prostate-specific antigen and risk of prostate cancer (2008) (88)
- ESR1/SYNE1 Polymorphism and Invasive Epithelial Ovarian Cancer Risk: An Ovarian Cancer Association Consortium Study (2010) (88)
- Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33. (2014) (88)
- Two Susceptibility Loci Identified for Prostate Cancer Aggressiveness (2015) (88)
- Variant in Sex Hormone-Binding Globulin Gene and the Risk of Prostate Cancer (2007) (87)
- Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility (2020) (87)
- Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. (2016) (87)
- Invasive fungal infections in children: recent advances in diagnosis and treatment. (1996) (86)
- Interleukin-15 Augments Superoxide Production and Microbicidal Activity of Human Monocytes against Candida albicans (1998) (86)
- Genome-wide association study identifies multiple risk loci for renal cell carcinoma (2017) (86)
- Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1. (2015) (86)
- A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma. (2015) (85)
- Effects of macrophage colony-stimulating factor on antifungal activity of mononuclear phagocytes against Aspergillus fumigatus. (1995) (84)
- Estimation of absolute risk for prostate cancer using genetic markers and family history (2009) (84)
- Polymorphisms in the DNA base excision repair genes APEX1 and XRCC1 and lung cancer risk in Xuan Wei, China. (2005) (84)
- Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21 (2016) (83)
- Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry (2011) (83)
- Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes. (2006) (83)
- Effects of DNA mass on multiple displacement whole genome amplification and genotyping performance (2005) (83)
- Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants (2018) (83)
- Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data (2016) (83)
- Serum selenium and risk of prostate cancer-a nested case-control study. (2007) (82)
- LIN28B polymorphisms influence susceptibility to epithelial ovarian cancer. (2011) (82)
- Expression of Genes Encoding Innate Host Defense Molecules in Normal Human Monocytes in Response to Candida albicans (2005) (82)
- Evaluation of polygenic risk scores for predicting breast and prostate cancer risk (2011) (82)
- Evolving risk factors for infectious complications of cancer therapy. (1993) (82)
- Genomewide meta‐analysis identifies loci associated with IGF‐I and IGFBP‐3 levels with impact on age‐related traits (2016) (82)
- Variant ABO Blood Group Alleles, Secretor Status, and Risk of Pancreatic Cancer: Results from the Pancreatic Cancer Cohort Consortium (2010) (81)
- PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3). (2010) (81)
- Common genetic variants in the PSCA gene influence gene expression and bladder cancer risk (2012) (81)
- HLA polymorphisms in African Americans with idiopathic inflammatory myopathy: allelic profiles distinguish patients with different clinical phenotypes and myositis autoantibodies. (2006) (81)
- Genetic variation in five genes important in telomere biology and risk for breast cancer (2007) (80)
- Analysis of Genes Critical for Growth Regulation Identifies Insulin-like Growth Factor 2 Receptor Variations with Possible Functional Significance as Risk Factors for Osteosarcoma (2007) (80)
- Genomic structure, chromosomal localization, start of transcription, and tissue expression of the human p40-phox, a new component of the nicotinamide adenine dinucleotide phosphate-oxidase complex. (1996) (80)
- Pooled analysis of genetic variation at chromosome 8q24 and colorectal neoplasia risk. (2008) (79)
- Genetic variation in the sodium-dependent vitamin C transporters, SLC23A1, and SLC23A2 and risk for preterm delivery. (2006) (79)
- Variants in interferon‐alpha pathway genes and response to pegylated interferon‐Alpha2a plus ribavirin for treatment of chronic hepatitis C virus infection in the hepatitis C antiviral long‐term treatment against cirrhosis trial (2009) (79)
- Common genetic variation and human disease. (2008) (78)
- A comprehensive analysis of common genetic variation in MUC1, MUC5AC, MUC6 genes and risk of stomach cancer (2010) (78)
- Polymorphisms in folate metabolic genes and lung cancer risk in Xuan Wei, China. (2005) (78)
- Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank (2018) (78)
- Cumulative Burden of Colorectal Cancer-Associated Genetic Variants is More Strongly Associated With Early-onset vs Late-onset Cancer. (2019) (78)
- The new sequencer on the block: comparison of Life Technology’s Proton sequencer to an Illumina HiSeq for whole-exome sequencing (2013) (78)
- Genetic variation in telomere maintenance genes, telomere length, and lung cancer susceptibility. (2009) (77)
- Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia (2017) (77)
- Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers. (2010) (77)
- Variants in inflammation genes and the risk of biliary tract cancers and stones: a population-based study in China. (2008) (77)
- A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any Age (2014) (77)
- Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2017) (77)
- Prostate cancer (PCa) risk variants and risk of fatal PCa in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium. (2014) (76)
- Genetic and Non-genetic Predictors of LINE-1 Methylation in Leukocyte DNA (2013) (75)
- Polymorphisms in Angiogenesis-Related Genes and Prostate Cancer (2008) (75)
- Genetic variants in DNA repair pathway genes and risk of esophageal squamous cell carcinoma and gastric adenocarcinoma in a Chinese population. (2013) (75)
- Genetic basis for adverse events after smallpox vaccination. (2008) (75)
- Genetic variants in caspase genes and susceptibility to non-Hodgkin lymphoma. (2006) (75)
- Single nucleotide polymorphisms in the TP53 region and susceptibility to invasive epithelial ovarian cancer. (2009) (75)
- Challenges of SNP genotyping and genetic variation: its future role in diagnosis and treatment of cancer (2006) (74)
- A genome-wide association study of breast cancer in women of African ancestry (2012) (74)
- Polymorphisms in one‐carbon metabolism and trans‐sulfuration pathway genes and susceptibility to bladder cancer (2007) (74)
- Association of type 2 diabetes susceptibility variants with advanced prostate cancer risk in the Breast and Prostate Cancer Cohort Consortium. (2012) (73)
- Comparison of yield and genotyping performance of multiple displacement amplification and OmniPlex™ whole genome amplified DNA generated from multiple DNA sources (2005) (73)
- Nitric oxide synthase gene polymorphisms and prostate cancer risk. (2009) (73)
- Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome (2016) (72)
- Genetic variation in tumor necrosis factor and lymphotoxin-alpha (TNF–LTA) and breast cancer risk (2007) (72)
- Host immune gene polymorphisms in combination with clinical and demographic factors predict late survival in diffuse large B-cell lymphoma patients in the pre-rituximab era. (2008) (71)
- CYP17 Genetic Variation and Risk of Breast and Prostate Cancer from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3) (2007) (71)
- Common Genetic Variation in TP53 Is Associated with Lung Cancer Risk and Prognosis in African Americans and Somatic Mutations in Lung Tumors (2007) (70)
- Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer (2017) (70)
- Polymorphisms in folate metabolizing genes and risk for spontaneous preterm and small-for-gestational age birth. (2006) (70)
- Polymorphisms in interleukin -2, -6, and -10 are not associated with gastric cardia or esophageal cancer in a high-risk chinese population. (2004) (70)
- Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters, SLC23A1 and SLC23A2 (2004) (70)
- Polymorphisms in immunoregulatory genes, smoky coal exposure and lung cancer risk in Xuan Wei, China. (2007) (70)
- Genetic Variation in the HSD17B1 Gene and Risk of Prostate Cancer (2005) (69)
- A Genome-Wide Association Study of Prognosis in Breast Cancer (2010) (69)
- Assessment of Interactions between PAH Exposure and Genetic Polymorphisms on PAH-DNA Adducts in African American, Dominican, and Caucasian Mothers and Newborns (2008) (69)
- Five Polymorphisms and Breast Cancer Risk: Results from the Breast Cancer Association Consortium (2009) (69)
- Genetic polymorphisms in the oxidative stress pathway and susceptibility to non-Hodgkin lymphoma (2007) (69)
- Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers. (2014) (69)
- Associations of autozygosity with a broad range of human phenotypes (2019) (68)
- Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer. (2012) (68)
- The ATM missense mutation p.Ser49Cys (c.146C>G) and the risk of breast cancer (2006) (68)
- Renal cell carcinoma, occupational pesticide exposure and modification by glutathione S-transferase polymorphisms. (2008) (68)
- Polymorphisms in cytokine and cellular adhesion molecule genes and susceptibility to hematotoxicity among workers exposed to benzene. (2005) (67)
- Common genetic variants in the interleukin-6 and chitotriosidase genes are associated with the risk for serious infection in children undergoing therapy for acute myeloid leukemia (2005) (67)
- Shared heritability and functional enrichment across six solid cancers (2018) (67)
- Genetic polymorphisms and benzene metabolism in humans exposed to a wide Range of air concentrations (2007) (67)
- Genetic susceptibility to distinct bladder cancer subphenotypes. (2010) (67)
- Common genetic variants in the 9p21 region and their associations with multiple tumours (2013) (67)
- Prostaglandin-endoperoxide synthase 2 (PTGS2) gene polymorphisms and risk of biliary tract cancer and gallstones: a population-based study in Shanghai, China. (2006) (66)
- Landscape of Combination Immunotherapy and Targeted Therapy to Improve Cancer Management. (2017) (66)
- Eighteen Insulin-like Growth Factor Pathway Genes, Circulating Levels of IGF-I and Its Binding Protein, and Risk of Prostate and Breast Cancer (2010) (66)
- Haplotype analysis of the HSD17B1 gene and risk of breast cancer: a comprehensive approach to multicenter analyses of prospective cohort studies. (2006) (66)
- Genetic variation in the bioactivation pathway for polycyclic hydrocarbons and heterocyclic amines in relation to risk of colorectal neoplasia. (2011) (66)
- Polymorphisms in XPD and TP53 and mutation in human lung cancer. (2004) (66)
- Polymorphism analysis of six selenoprotein genes: support for a selective sweep at the glutathione peroxidase 1 locus (3p21) in Asian populations (2006) (66)
- Dietary quercetin, quercetin-gene interaction, metabolic gene expression in lung tissue and lung cancer risk. (2010) (66)
- Risk of Non–Hodgkin Lymphoma Associated with Germline Variation in Genes that Regulate the Cell Cycle, Apoptosis, and Lymphocyte Development (2009) (66)
- Genomics: When the smoke clears ... (2008) (65)
- Mutations in the SBDS gene in acquired aplastic anemia. (2007) (65)
- Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies (2015) (65)
- Mendelian Randomization Study of Body Mass Index and Colorectal Cancer Risk (2015) (65)
- Immune mechanisms in non-Hodgkin lymphoma: joint effects of the TNF G308A and IL10 T3575A polymorphisms with non-Hodgkin lymphoma risk factors. (2007) (65)
- Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African Americans. (2011) (65)
- A saturated map of common genetic variants associated with human height (2022) (65)
- 3'-UTR and functional secretor haplotypes in mannose-binding lectin 2 are associated with increased colon cancer risk in African Americans. (2012) (65)
- Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never‐smoking women in Asia: a report from the female lung cancer consortium in Asia (2015) (64)
- Assessment of copy number variation using the Illumina Infinium 1M SNP‐array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study (2011) (64)
- Glutathione S-transferase polymorphisms, cruciferous vegetable intake and cancer risk in the Central and Eastern European Kidney Cancer Study. (2007) (64)
- Evaluation of Candidate Stromal Epithelial Cross-Talk Genes Identifies Association between Risk of Serous Ovarian Cancer and TERT, a Cancer Susceptibility “Hot-Spot” (2010) (64)
- Associations of Classic Kaposi Sarcoma with Common Variants in Genes that Modulate Host Immunity (2006) (63)
- A genome-wide association study of prostate cancer in West African men (2014) (63)
- Colorectal cancer susceptibility loci as predictive markers of rectal cancer prognosis after surgery (2017) (63)
- Common genetic variation in TP53 and its flanking genes, WDR79 and ATP1B2, and susceptibility to breast cancer (2007) (62)
- Single-nucleotide polymorphisms in selected cytokine genes and risk of adult glioma. (2007) (62)
- Polymorphism Interaction Analysis (PIA): a method for investigating complex gene-gene interactions (2008) (62)
- Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium (2014) (62)
- Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses (2016) (62)
- Common Variation in Genes Related to Innate Immunity and Risk of Adult Glioma (2009) (62)
- Variant genotypes of FcγRIIIA influence the development of Kaposi's sarcoma in HIV-infected men (2000) (61)
- Genome-wide association study of survival in patients with pancreatic adenocarcinoma (2012) (61)
- Polymorphisms in DNA repair genes and risk of non-Hodgkin’s lymphoma in New South Wales, Australia (2007) (61)
- Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma. (2007) (61)
- Testicular germ cell tumor susceptibility associated with the UCK2 locus on chromosome 1q23. (2013) (60)
- A single nucleotide polymorphism tags variation in the arylamine N-acetyltransferase 2 phenotype in populations of European background (2010) (60)
- Genome-wide scan of 29,141 African Americans finds no evidence of directional selection since admixture. (2014) (60)
- Generalizability of established prostate cancer risk variants in men of African ancestry (2015) (60)
- Genetic variation in sodium-dependent ascorbic acid transporters and risk of gastric cancer in Poland. (2009) (60)
- Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies. (2012) (60)
- Interleukin-8 Polymorphisms Are Not Associated with Gastric Cancer Risk in a Polish Population (2006) (60)
- CYP1A1 Val462 and NQO1 Ser187 polymorphisms, cigarette use, and risk for colorectal adenoma. (2005) (60)
- An Analysis of Growth, Differentiation and Apoptosis Genes with Risk of Renal Cancer (2009) (60)
- Infectious complications of patients undergoing therapy for acute leukemia: current status and future prospects. (1997) (59)
- Population structure of human gut bacteria in a diverse cohort from rural Tanzania and Botswana (2019) (59)
- Genome-Wide Association Study of Circulating Estradiol, Testosterone, and Sex Hormone-Binding Globulin in Postmenopausal Women (2012) (59)
- Prediction of breast cancer risk by genetic risk factors, overall and by hormone receptor status (2012) (59)
- Candidate gene approach evaluates association between innate immunity genes and breast cancer risk in Korean women. (2009) (59)
- Comprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortium. (2010) (59)
- Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the ovarian cancer association consortium pooled analysis (2008) (59)
- A new statistic and its power to infer membership and phenotype in a genome-wide association study using genotype frequencies (2009) (59)
- Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer. (2013) (59)
- Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway. (2008) (59)
- Metabolic Gene Variants and Risk of Non-Hodgkin's Lymphoma (2006) (58)
- Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer (2017) (58)
- Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity. (2009) (58)
- SNPs, haplotypes, and cancer: applications in molecular epidemiology. (2004) (58)
- Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell disease (2008) (58)
- Genetic variation in N-acetyltransferase 1 (NAT1) and 2 (NAT2) and risk of non-Hodgkin lymphoma (2006) (57)
- A large study of androgen receptor germline variants and their relation to sex hormone levels and prostate cancer risk. Results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium. (2010) (57)
- Integration Analysis of Three Omics Data Using Penalized Regression Methods: An Application to Bladder Cancer (2015) (57)
- MDM2 SNP309 and SNP354 Are Not Associated with Lung Cancer Risk (2006) (57)
- Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer. (2015) (57)
- GSTM1, GSTT1, and GSTP1 Polymorphisms and Risk of Advanced Colorectal Adenoma (2005) (57)
- Caspase polymorphisms and genetic susceptibility to multiple myeloma (2008) (56)
- Polymorphisms in genes involved in DNA double-strand break repair pathway and susceptibility to benzene-induced hematotoxicity. (2006) (56)
- A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data (2011) (56)
- Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma. (2012) (56)
- Analysis of nucleotide diversity of NAT2 coding region reveals homogeneity across Native American populations and high intra-population diversity (2007) (56)
- Common Genetic Variants in Prostate Cancer Risk Prediction—Results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3) (2012) (56)
- Detection of Somatic Mutations by High-Resolution DNA Melting (HRM) Analysis in Multiple Cancers (2011) (56)
- Genetic variation in base excision repair genes and the prevalence of advanced colorectal adenoma. (2007) (56)
- Common genetic variation and risk of gallbladder cancer in India: a case-control genome-wide association study. (2017) (55)
- A genome-wide association study of marginal zone lymphoma shows association to the HLA region (2015) (55)
- Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels (2011) (55)
- The respiratory burst oxidase. (1994) (55)
- Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers (2019) (55)
- Hair dye use is not associated with risk for bladder cancer: evidence from a case-control study in Spain. (2006) (55)
- Genetic variation in TP53 and risk of breast cancer in a population-based case control study. (2007) (54)
- DRD2 genetic variation in relation to smoking and obesity in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (2006) (54)
- TERT gene harbors multiple variants associated with pancreatic cancer susceptibility (2015) (54)
- Efficient study design for next generation sequencing (2011) (54)
- Childhood Exposure to Secondhand Smoke and Functional Mannose Binding Lectin Polymorphisms Are Associated with Increased Lung Cancer Risk (2009) (54)
- Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer. (2016) (54)
- Green tea consumption, genetic susceptibility, PAH-rich smoky coal, and the risk of lung cancer. (2005) (54)
- Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies. (2009) (54)
- Radiation-related genomic profile of papillary thyroid carcinoma after the Chernobyl accident (2021) (54)
- Evaluation of durability of a single-dose of the bivalent HPV vaccine: the CVT Trial. (2020) (54)
- Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations (2016) (53)
- Genetic Polymorphisms in Folate Metabolism and the Risk of Stomach Cancer (2007) (53)
- Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study. (2009) (53)
- Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer (2019) (53)
- Genetic variation, nucleotide diversity, and linkage disequilibrium in seven telomere stability genes suggest that these genes may be under constraint (2005) (53)
- Genetic Variations in the Sonic Hedgehog Pathway Affect Clinical Outcomes in Non–Muscle-Invasive Bladder Cancer (2010) (53)
- Microsomal epoxide hydrolase polymorphisms and risk for advanced colorectal adenoma. (2005) (52)
- Mannose‐binding lectin‐2 genetic variation and stomach cancer risk (2006) (52)
- Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk (2018) (51)
- High level of functional polymorphism indicates a unique role of natural selection at human immune system loci (2005) (51)
- Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk. (2015) (51)
- Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer. (2011) (51)
- Candidate Gene Polymorphisms for Ischemic Stroke (2009) (51)
- The influence of obesity-related factors in the etiology of renal cell carcinoma—A mendelian randomization study (2019) (51)
- Associations of non-Hodgkin Lymphoma (NHL) risk with autoimmune conditions according to putative NHL loci. (2015) (51)
- Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma (2014) (51)
- Association between chronic disseminated candidiasis in adult acute leukemia and common IL4 promoter haplotypes. (2003) (50)
- Vascular endothelial growth factor gene haplotypes in Kawasaki disease. (2006) (50)
- Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2 (2015) (50)
- Perforin gene mutations in patients with acquired aplastic anemia. (2006) (50)
- GSTM 1 null and NAT 2 slow acetylation genotypes , smoking intensity and bladder cancer risk : results from the New England bladder cancer study and NAT 2 meta-analysis (2011) (50)
- Association of MTHFR gene polymorphisms with breast cancer survival (2006) (50)
- Selected base excision repair gene polymorphisms and susceptibility to biliary tract cancer and biliary stones: a population-based case-control study in China. (2007) (50)
- A Genome-Wide Association Study Identifies A New Ovarian Cancer Susceptibility Locus On 9 p 22 . 2 (2010) (50)
- Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN2A Mutations (2013) (50)
- Germ‐line genetic variation of TP53 in osteosarcoma (2007) (49)
- Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast (2014) (49)
- Tobacco smoking, NAT2 acetylation genotype and breast cancer risk (2006) (48)
- Increased serum concentrations of interleukin-10 in patients with hepatosplenic candidiasis. (1998) (48)
- Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer (2017) (48)
- TGFB1 and TGFBR1 polymorphic variants in relationship to bladder cancer risk and prognosis (2009) (48)
- Using principal components of genetic variation for robust and powerful detection of gene-gene interactions in case-control and case-only studies. (2010) (48)
- One-carbon metabolism gene polymorphisms and risk of non-Hodgkin lymphoma in Australia (2007) (48)
- Genetic reassortment of mammalian reoviruses in mice (1985) (48)
- Changes in host defence induced by malignancies and antineoplastic treatment: implication for immunotherapeutic strategies. (2008) (48)
- Use of 'Omic' technologies to study humans exposed to benzene. (2005) (48)
- Genome-wide association study of age at menarche in African-American women. (2013) (48)
- Genetic variation in telomeric repeat binding factors 1 and 2 in aplastic anemia. (2006) (47)
- Risk of Small-for-Gestational Age is Associated With Common Anti-Inflammatory Cytokine Polymorphisms (2005) (47)
- Ovarian cancer risk and common variation in the sex hormone-binding globulin gene: a population-based case-control study (2007) (47)
- PTEN identified as important risk factor of chronic obstructive pulmonary disease. (2009) (47)
- TNF polymorphisms and prostate cancer risk (2008) (47)
- Genome-wide interaction study of smoking and bladder cancer risk. (2014) (46)
- Genome-wide association study of circulating vitamin D-binding protein. (2014) (46)
- Prostate Cancer Predisposition Loci and Risk of Metastatic Disease and Prostate Cancer Recurrence (2011) (46)
- Quantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium (BPC3). (2009) (46)
- A mechanistic basis for amplification differences between samples and between genome regions (2012) (46)
- A comprehensive analysis of the androgen receptor gene and risk of breast cancer: results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3) (2006) (46)
- Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility (2018) (46)
- Organochlorine exposure, immune gene variation, and risk of non-Hodgkin lymphoma. (2009) (46)
- Lung cancer survival and functional polymorphisms in MBL2, an innate-immunity gene. (2007) (46)
- Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases (2015) (46)
- An analysis of genetic variation across the MBL2 locus in Dutch Caucasians indicates that 3′ haplotypes could modify circulating levels of mannose-binding lectin (2005) (45)
- Identification of modifier genes for cutaneous malignant melanoma in melanoma‐prone families with and without CDKN2A mutations (2009) (45)
- Common genetic variation in the sex hormone metabolic pathway and endometrial cancer risk: pathway-based evaluation of candidate genes. (2010) (45)
- TET2 binds the androgen receptor and loss is associated with prostate cancer (2016) (45)
- All the World's a Stage: Facilitating Discovery Science and Improved Cancer Care through the Global Alliance for Genomics and Health. (2015) (45)
- A Transcriptome-Wide Association Study (TWAS) Identifies Novel Candidate Susceptibility Genes for Pancreatic Cancer. (2020) (45)
- Association of genetic variants in the calcium-sensing receptor with risk of colorectal adenoma. (2004) (44)
- Insulin-like growth factor pathway genetic polymorphisms, circulating IGF1 and IGFBP3, and prostate cancer survival. (2014) (44)
- Phred-Phrap package to analyses tools: a pipeline to facilitate population genetics re-sequencing studies (2011) (44)
- Gene–Environment Interaction Involving Recently Identified Colorectal Cancer Susceptibility Loci (2014) (44)
- Genome-wide association study of germline variants and breast cancer-specific mortality (2019) (44)
- Risk of Meningioma and Common Variation in Genes Related to Innate Immunity (2010) (44)
- Haplotypes of the estrogen receptor beta gene and breast cancer risk (2008) (43)
- Pooled analysis of phosphatidylinositol 3-kinase pathway variants and risk of prostate cancer. (2010) (43)
- Improved imputation of common and uncommon SNPs with a new reference set (2011) (43)
- Genomic and evolutionary classification of lung cancer in never smokers (2021) (43)
- Ex vivo effects of macrophage colony-stimulating factor on human monocyte activity against fungal and bacterial pathogens. (1996) (43)
- Sun exposure, vitamin D receptor gene polymorphisms and risk of non-Hodgkin lymphoma (2007) (43)
- Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes. (2016) (42)
- Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations (2010) (42)
- Large-Scale Pathway-Based Analysis of Bladder Cancer Genome-Wide Association Data from Five Studies of European Background (2012) (42)
- Transforming growth factor beta 1 (TGFB1) gene polymorphisms and risk of advanced colorectal adenoma. (2007) (42)
- Common genetic variants related to genomic integrity and risk of papillary thyroid cancer. (2011) (42)
- Integration of multiethnic fine-mapping and genomic annotation to prioritize candidate functional SNPs at prostate cancer susceptibility regions. (2015) (41)
- Socioeconomic and Nutritional Factors Account for the Association of Gastric Cancer with Amerindian Ancestry in a Latin American Admixed Population (2012) (41)
- Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21 (2018) (41)
- Smoky coal exposure, NBS1 polymorphisms, p53 protein accumulation, and lung cancer risk in Xuan Wei, China. (2005) (41)
- Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium. (2014) (41)
- Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women. (2014) (41)
- Sex differences in oncogenic mutational processes (2019) (41)
- Common genetic variants in candidate genes and risk of familial lymphoid malignancies (2009) (41)
- Division of Cancer Epidemiology and Genetics (2020) (40)
- New evidence that Candida albicans possesses additional ATP-binding cassette MDR-like genes: implications for antifungal azole resistance. (1997) (40)
- A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium. (2014) (40)
- Investigation of the Relationship Between Radiation Dose and Gene Mutations and Fusions in Post-Chernobyl Thyroid Cancer. (2018) (40)
- Apolipoprotein E/C1 locus variants modify renal cell carcinoma risk. (2009) (40)
- Genome-wide association study of endometrial cancer in E2C2 (2013) (40)
- Factors associated with oxidative stress and cancer risk in the Breast and Prostate Cancer Cohort Consortium (2014) (40)
- Common Genetic Variants in miR-1206 (8q24.2) and miR-612 (11q13.3) Affect Biogenesis of Mature miRNA Forms (2012) (40)
- Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes. (2001) (40)
- Immune gene expression profiling reveals heterogeneity in luminal breast tumors (2019) (40)
- Origins, admixture dynamics and homogenization of the African gene pool in the Americas (2019) (40)
- Cross-reactivity between Stomatococcus mucilaginosus and latex agglutination for cryptococcal antigen (1993) (39)
- Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (39)
- A putative exonic splicing polymorphism in the BCL6 gene and the risk of non-Hodgkin lymphoma. (2005) (39)
- Folate metabolism genes, vegetable intake and renal cancer risk in central Europe (2007) (39)
- Single Nucleotide Polymorphisms in the PRDX3 and RPS19 and Risk of HPV Persistence and Cervical Precancer/Cancer (2012) (39)
- Leveraging population admixture to explain missing heritability of complex traits (2014) (39)
- Vitamin D Receptor Polymorphisms and Renal Cancer Risk in Central and Eastern Europe (2008) (39)
- Effect modification of endocrine disruptors and testicular germ cell tumour risk by hormone-metabolizing genes. (2009) (39)
- Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma (2018) (39)
- O2- production by B lymphocytes lacking the respiratory burst oxidase subunit p47phox after transfection with an expression vector containing a p47phox cDNA. (1992) (38)
- Selected single-nucleotide polymorphisms in FOXE1, SERPINA5, FTO, EVPL, TICAM1 and SCARB1 are associated with papillary and follicular thyroid cancer risk: replication study in a German population. (2016) (38)
- COX1 and COX2 polymorphisms and gastric cancer risk in a Polish population. (2007) (38)
- Body mass index and breast cancer survival: a Mendelian randomization analysis (2017) (38)
- Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women. (2016) (38)
- Polymorphisms of Genes in the Lipid Metabolism Pathway and Risk of Biliary Tract Cancers and Stones: A Population-Based Case-Control Study in Shanghai, China (2008) (38)
- Fine-Mapping the HOXB Region Detects Common Variants Tagging a Rare Coding Allele: Evidence for Synthetic Association in Prostate Cancer (2014) (38)
- Likelihood ratio test for detecting gene (G)-environment (E) interactions under an additive risk model exploiting G-E independence for case-control data. (2012) (38)
- 11q13 is a susceptibility locus for hormone receptor positive breast cancer (2012) (38)
- Genetic polymorphisms in alcohol metabolism, alcohol intake and the risk of stomach cancer in Warsaw, Poland (2007) (38)
- Common Genetic Variants and Central Adiposity Among Asian‐Indians (2012) (38)
- ABO blood group and risk of epithelial ovarian cancer within the Ovarian Cancer Association Consortium (2012) (38)
- Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population. (2016) (38)
- Genetic variation in Th1/Th2 pathway genes and risk of non‐Hodgkin lymphoma: a pooled analysis of three population‐based case‐control studies (2011) (38)
- Genetic Variation in Sodium-Dependent Vitamin C Transporters SLC23A1 and SLC23A2 and Risk of Advanced Colorectal Adenoma (2008) (38)
- Missense Variants in ATM in 26,101 Breast Cancer Cases and 29,842 Controls (2010) (38)
- Genome-Wide Search for Gene-Gene Interactions in Colorectal Cancer (2012) (38)
- Comprehensive analysis of hormone and genetic variation in 36 genes related to steroid hormone metabolism in pre- and postmenopausal women from the breast and prostate cancer cohort consortium (BPC3). (2011) (37)
- Cytokine polymorphisms in Th1/Th2 pathway genes, body mass index, and risk of non-Hodgkin lymphoma. (2011) (37)
- Applying new biotechnologies to the study of occupational cancer--a workshop summary. (2004) (37)
- Combining common genetic variants and non‐genetic risk factors to predict risk of cutaneous melanoma (2018) (37)
- Evaluation of Association of HNF1B Variants with Diverse Cancers: Collaborative Analysis of Data from 19 Genome-Wide Association Studies (2010) (37)
- Sharing Clinical and Genomic Data on Cancer - The Need for Global Solutions. (2017) (37)
- Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148 (2017) (37)
- CYP19A1 Genetic Variation in Relation to Prostate Cancer Risk and Circulating Sex Hormone Concentrations in Men from the Breast and Prostate Cancer Cohort Consortium (2009) (37)
- PTGS 2 and IL 6 genetic variation and risk of breast and prostate cancer : results from the Breast and Prostate Cancer Cohort Consortium ( BPC 3 ) (2010) (37)
- Large-scale exploration of gene-gene interactions in prostate cancer using a multistage genome-wide association study. (2011) (37)
- Genetic Variation in the Vitamin D Pathway in Relation to Risk of Prostate Cancer—Results from the Breast and Prostate Cancer Cohort Consortium (2013) (37)
- The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma. (2012) (37)
- Human Pharmacogenomic Variations and Their Implications for Antifungal Efficacy (2006) (37)
- Germline variation at 8q24 and prostate cancer risk in men of European ancestry (2018) (37)
- Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
- Novel Breast Cancer Risk Alleles and Interaction with Ionizing Radiation among U.S. Radiologic Technologists (2010) (36)
- Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia (2013) (36)
- Personal History of Diabetes, Genetic Susceptibility to Diabetes, and Risk of Brain Glioma: A Pooled Analysis of Observational Studies (2013) (36)
- A Mitochondrial Target Sequence Polymorphism in Manganese Superoxide Dismutase Predicts Inferior Survival in Breast Cancer Patients Treated with Cyclophosphamide (2009) (36)
- Analysis of SNPs and Haplotypes in Vitamin D Pathway Genes and Renal Cancer Risk (2009) (36)
- Sequence Variants in the TLR4 and TLR6-1-10 Genes and Prostate Cancer Risk. Results Based on Pooled Analysis from Three Independent Studies (2010) (36)
- Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia (2012) (36)
- A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6 q 14 and 20 q 11 (2012) (36)
- Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong (2010) (36)
- Mosaic Y Loss Is Moderately Associated with Solid Tumor Risk. (2018) (36)
- Sequence Variants of Estrogen Receptor β and Risk of Prostate Cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (2007) (35)
- A pooled analysis of three studies evaluating genetic variation in innate immunity genes and non‐Hodgkin lymphoma risk (2011) (35)
- Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study in multiple populations. (2019) (35)
- Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma. (2017) (35)
- Investigation of gene‐environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors (2015) (35)
- Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk (2020) (35)
- Polymorphic variants in PTGS2 and prostate cancer risk: results from two large nested case-control studies. (2007) (34)
- Polymorphisms in innate immunity genes and risk of childhood leukemia. (2010) (34)
- Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men. (2012) (34)
- Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident (2021) (34)
- A Second Look at Anorectal Infections in Cancer Patients in a Large Cancer Institute: The Success of Early Intervention with Antibiotics and Surgery (2002) (34)
- Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis. (2016) (34)
- Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA) (2015) (34)
- A comprehensive examination of breast cancer risk loci in African American women. (2014) (34)
- Modification of Occupational Exposures on Bladder Cancer Risk by Common Genetic Polymorphisms. (2015) (34)
- Histopathological features of papillary thyroid carcinomas detected during four screening examinations of a Ukrainian-American cohort (2015) (34)
- Common variants in genes that mediate immunity and risk of multiple myeloma (2007) (34)
- Telomere structure and maintenance gene variants and risk of five cancer types (2016) (34)
- Germline determinants of the somatic mutation landscape in 2,642 cancer genomes (2017) (33)
- Large-scale fine mapping of the HNF1B locus and prostate cancer risk. (2011) (33)
- Genetic variation in metabolic genes, occupational solvent exposure, and risk of non-hodgkin lymphoma. (2011) (33)
- Evolution of multiple cell clones over a 29-year period of a CLL patient (2016) (33)
- Granulocyte transfusions. Time for a second look. (1996) (33)
- Human leukocyte antigen (HLA) A1-B8-DR3 (8.1) haplotype, tumor necrosis factor (TNF) G-308A, and risk of non-Hodgkin lymphoma (2010) (33)
- Genetic variants in sex hormone metabolic pathway genes and risk of esophageal squamous cell carcinoma. (2013) (33)
- Variants in blood pressure genes and the risk of renal cell carcinoma. (2010) (33)
- Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysis (2007) (33)
- Identification of New Genetic Susceptibility Loci for Breast Cancer Through Consideration of Gene‐Environment Interactions (2014) (33)
- DNA repair gene polymorphisms and tobacco smoking in the risk for colorectal adenomas. (2011) (33)
- Invasive Candidiasis Stimulates Hepatocyte and Monocyte Production of Active Transforming Growth Factor β (2001) (33)
- Pathway-based analysis of GWAs data identifies association of sex determination genes with susceptibility to testicular germ cell tumors. (2014) (33)
- Guanine nucleotide binding properties of Rac2 mutant proteins and analysis of the responsiveness to guanine nucleotide dissociation stimulator. (1997) (33)
- Successful Genome-Wide Scan in Paired Blood and Buccal Samples (2007) (33)
- Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry. (2016) (33)
- Confirmation of 5p12 As a Susceptibility Locus for Progesterone-Receptor–Positive, Lower Grade Breast Cancer (2011) (33)
- Genomic structure of the human p47-phox (NCF1) gene. (2000) (33)
- Mutation of GATA 3 in human breast tumors (2004) (33)
- The MBL2 ‘LYQA Secretor’ Haplotype Is an Independent Predictor of Postoperative Myocardial Infarction in Whites Undergoing Coronary Artery Bypass Graft Surgery (2007) (33)
- Association of breast cancer risk loci with breast cancer survival (2015) (33)
- Variant genotypes of FcgammaRIIIA influence the development of Kaposi's sarcoma in HIV-infected men. (2000) (33)
- Host immunogenetics and control of human herpesvirus-8 infection. (2006) (33)
- One gene and one outcome? No way. (2002) (32)
- Human rotaviruses and genome RNA. (1983) (32)
- Cyclin D1 splice variant and risk for non-Hodgkin lymphoma (2006) (32)
- Analysis of chemotherapeutic response in ovarian cancers using publicly available high-throughput data. (2014) (32)
- A comprehensive resequence analysis of the KLK15–KLK3–KLK2 locus on chromosome 19q13.33 (2009) (32)
- Immunomodulation of invasive fungal infections. (2003) (32)
- Variants in hormone-related genes and the risk of biliary tract cancers and stones: a population-based study in China. (2009) (32)
- Rare germline variants in known melanoma susceptibility genes in familial melanoma (2017) (32)
- Polymorphism of genes related to insulin sensitivity and the risk of biliary tract cancer and biliary stone: a population-based case–control study in Shanghai, China (2008) (32)
- An IL 6 promoter polymorphism is associated with a lifetime risk of development of Kaposi sarcoma in men infected with human immunodeficiency virus (2000) (32)
- Genetic variation in innate immunity and inflammation pathways associated with lung cancer risk (2012) (32)
- Functional characterization of the 12p12.1 renal cancer-susceptibility locus implicates BHLHE41 (2016) (31)
- Medical issues related to caring for human immunodeficiency virus‐infected children in and out of the home (1993) (31)
- Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study (2014) (31)
- Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene (2016) (31)
- The mannose-binding lectin (MBL2) haplotype and breast cancer: an association study in African-American and Caucasian women. (2006) (31)
- Study of common functional genetic polymorphisms of FCGR2A, 3A and 3B genes and the risk for cryptococcosis in HIV-uninfected patients. (2007) (31)
- Somatic sequence alterations in twenty-one genes selected by expression profile analysis of breast carcinomas (2007) (31)
- PRRC2A and BCL2L11 gene variants influence risk of non-Hodgkin lymphoma: results from the InterLymph consortium. (2012) (31)
- Constituents of Household Air Pollution and Risk of Lung Cancer among Never-Smoking Women in Xuanwei and Fuyuan, China (2019) (31)
- Detectable clonal mosaicism in the human genome. (2013) (31)
- Genetic variation in hormone metabolizing genes and risk of testicular germ cell tumors (2008) (31)
- Common germline polymorphisms associated with breast cancer-specific survival (2015) (31)
- Germline sequencing DNA repair genes in 5,545 men with aggressive and non-aggressive prostate cancer. (2020) (31)
- Genetic susceptibility to diffuse large B‐cell lymphoma in a pooled study of three Eastern Asian populations (2015) (30)
- Joint associations between genetic variants and reproductive factors in glioma risk among women. (2011) (30)
- Genotypes and haplotypes in the insulin-like growth factors, their receptors and binding proteins in relation to plasma metabolic levels and mammographic density (2008) (30)
- Genetic determinants of serum lipid levels in Chinese subjects: a population-based study in Shanghai, China (2009) (30)
- HLA Class I and II Diversity Contributes to the Etiologic Heterogeneity of Non-Hodgkin Lymphoma Subtypes. (2018) (30)
- Polymorphisms in DNA Repair and One-Carbon Metabolism Genes and Overall Survival in Diffuse Large B-Cell Lymphoma (DLBCL) and Follicular Lymphoma (2008) (30)
- Genome-Wide Association Study of Prostate Cancer–Specific Survival (2015) (30)
- Effects of Natural Selection on Interpopulation Divergence at Polymorphic Sites in Human Protein-Coding Loci (2005) (30)
- Genetic variants reflecting higher vitamin e status in men are associated with reduced risk of prostate cancer. (2014) (30)
- Genetic Predictors of Circulating 25-Hydroxyvitamin D and Risk of Colorectal Cancer (2013) (30)
- Mosaic chromosome Y loss and testicular germ cell tumor risk (2017) (30)
- Impact of atopy on risk of glioma: a Mendelian randomisation study (2018) (30)
- Life-threatening reaction to trimethoprim/sulfamethoxazole in pediatric human immunodeficiency virus infection. (1994) (30)
- Seventh international meeting on single nucleotide polymorphism and complex genome analysis: ‘ever bigger scans and an increasingly variable genome’ (2006) (29)
- Cytokine signaling pathway polymorphisms and AIDS-related non-Hodgkin lymphoma risk in the multicenter AIDS cohort study (2010) (29)
- Genetic variants in fas signaling pathway genes and risk of gastric cancer (2014) (29)
- Polymorphisms of estrogen receptors and risk of biliary tract cancers and gallstones: a population-based study in Shanghai, China. (2010) (29)
- Genetic variation in CYP17 and endometrial cancer risk (2008) (29)
- Effect of Gene‐environment Interactions on Mental Development in African American, Dominican, and Caucasian Mothers and Newborns (2010) (28)
- No Association between FTO or HHEX and Endometrial Cancer Risk (2010) (28)
- Common Genetic Variation in TP53 and Risk of Human Papillomavirus Persistence and Progression to CIN3/Cancer Revisited (2009) (28)
- Association of Common Haplotypes of Surfactant Protein A1 and A2 (SFTPA1 and SFTPA2) Genes with Severity of Lung Disease in Cystic Fibrosis (2006) (28)
- Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer. (2009) (28)
- Maternal EPHX1 polymorphisms and risk of phenytoin-induced congenital malformations (2010) (28)
- Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer. (2015) (28)
- The long and short of telomeres and cancer association studies. (2013) (28)
- IL10 and TNF variants and risk of non-Hodgkin lymphoma among three Asian populations (2013) (28)
- Known glioma risk loci are associated with glioma with a family history of brain tumours—A case–control gene association study (2013) (27)
- Association between adult height, genetic susceptibility and risk of glioma. (2012) (27)
- Diagnosis of invasive fungal infections: advances in nonculture systems. (1998) (27)
- Genetic variation of Cytochrome P450 1B1 (CYP1B1) and risk of breast cancer among Polish women (2006) (27)
- Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes (2022) (27)
- Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk. (2020) (27)
- Genotype frequency and FST analysis of polymorphisms in immunoregulatory genes in Chinese and Caucasian populations (2007) (27)
- A network analysis to identify mediators of germline-driven differences in breast cancer prognosis (2020) (27)
- Outdoor air pollution and mosaic loss of chromosome Y in older men from the Cardiovascular Health Study. (2018) (27)
- Genewindow: an interactive tool for visualization of genomic variation (2005) (27)
- Comprehensive Analysis of 5-Aminolevulinic Acid Dehydrogenase (ALAD) Variants and Renal Cell Carcinoma Risk among Individuals Exposed to Lead (2011) (27)
- A Case-Control Investigation of Immune Function Gene Polymorphisms and Risk of Testicular Germ Cell Tumors (2007) (27)
- Promoter variants in the MSMB gene associated with prostate cancer regulate MSMB/NCOA4 fusion transcripts (2012) (27)
- Sex-specific gene and pathway modeling of inherited glioma risk (2017) (27)
- High marks for GWAS (2009) (27)
- Replication of Five Prostate Cancer Loci Identified in an Asian Population—Results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3) (2011) (26)
- Circulating bilirubin levels and risk of colorectal cancer: serological and Mendelian randomization analyses (2020) (26)
- GWASdb v 2 : an update database for human genetic variants identified by genome-wide association studies (2015) (26)
- Vitamin D Pathway Genes, Diet, and Risk of Renal Cell Carcinoma (2009) (26)
- Corroboration of a familial chordoma locus on chromosome 7q and evidence of genetic heterogeneity using single nucleotide polymorphisms (SNPs) (2005) (26)
- A Germline Variant at 8q24 Contributes to Familial Clustering of Prostate Cancer in Men of African Ancestry. (2020) (26)
- Endometrial cancer and genetic variation in PTEN, PIK3CA, AKT1, MLH1, and MSH2 within a population-based case-control study. (2011) (26)
- Variation in innate immunity genes and risk of multiple myeloma (2011) (26)
- Genetic risk variants associated with in situ breast cancer (2015) (26)
- The ageing genome, clonal mosaicism and chronic disease. (2017) (26)
- Influence of obesity-related risk factors in the aetiology of glioma (2018) (26)
- Fever in the neutropenic host. (1996) (25)
- Association of Common Susceptibility Variants of Pancreatic Cancer in Higher-Risk Patients: A PACGENE Study (2016) (25)
- A Genome-Wide Scan for Breast Cancer Risk Haplotypes among African American Women (2013) (25)
- Laboratory diagnosis of invasive candidiasis: A rationale for complementary use of culture- and nonculture-based detection systems (1997) (25)
- Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma risk (2013) (25)
- Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer (2020) (25)
- Genome‐wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients (2018) (25)
- Genetic variation in SIPA1 in relation to breast cancer risk and survival after breast cancer diagnosis (2009) (25)
- Summary from an international cancer seminar focused on human papillomavirus (HPV)-positive oropharynx cancer, convened by scientists at IARC and NCI. (2020) (25)
- Characterization of the genomic structure of the human vitamin C transporter SVCT1 (SLC23A2). (2001) (25)
- An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk (2020) (25)
- Transmission of an Azole-Resistant Isogenic Strain of Candida albicans among Human Immunodeficiency Virus-Infected Family Members with Oropharyngeal Candidiasis (1999) (25)
- Polymorphism in the GALNT1 Gene and Epithelial Ovarian Cancer in Non-Hispanic White Women: The Ovarian Cancer Association Consortium (2010) (25)
- Common polymorphisms in critical genes of innate immunity do not contribute to the risk for chronic disseminated candidiasis in adult leukemia patients. (2005) (25)
- Variants of DNA Repair Genes and the Risk of Biliary Tract Cancers and Stones: A Population-Based Study in China (2008) (24)
- Genetic background comparison using distance‐based regression, with applications in population stratification evaluation and adjustment (2009) (24)
- Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types (2015) (24)
- Genome-wide SNP typing reveals signatures of population history. (2008) (24)
- Identifying novel susceptibility genes for colorectal cancer risk from a transcriptome-wide association study of 125,478 subjects. (2020) (24)
- Refining the Prostate Cancer Genetic Association within the JAZF1 Gene on Chromosome 7p15.2 (2010) (24)
- Variations in Chromosomes 9 and 6p21.3 with Risk of Non–Hodgkin Lymphoma (2010) (24)
- Characterising cis-regulatory variation in the transcriptome of histologically normal and tumour-derived pancreatic tissues (2017) (24)
- Circulating levels and promoter polymorphisms of interleukins-6 and 8 in pediatric cancer patients with fever and neutropenia. (2004) (24)
- Correction: Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry (2011) (24)
- Genetic overlap between autoimmune diseases and non‐Hodgkin lymphoma subtypes (2019) (24)
- Insulin‐like growth factor pathway genes and blood concentrations, dietary protein and risk of prostate cancer in the NCI Breast and Prostate Cancer Cohort Consortium (BPC3) (2013) (24)
- Common Obesity-Related Genetic Variants and Papillary Thyroid Cancer Risk (2012) (24)
- A genome-wide pleiotropy scan for prostate cancer risk. (2015) (23)
- Racial Disparities in Lung Cancer Survival: The Contribution of Stage, Treatment, and Ancestry (2018) (23)
- Meeting report from the joint IARC–NCI international cancer seminar series: a focus on colorectal cancer (2019) (23)
- A comprehensive resequence‐analysis of 250 kb region of 8q24.21 in men of African ancestry (2014) (23)
- Limited evidence that cancer susceptibility regions are preferential targets for somatic mutation (2015) (23)
- Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis. (2018) (23)
- Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study. (2013) (23)
- Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations (2016) (23)
- Defining targets for investigating the pharmacogenomics of adverse drug reactions to antifungal agents. (2008) (23)
- Comprehensive assessment of genetic variation of catechol-O-methyltransferase and breast cancer risk. (2006) (23)
- Genetic Variants in Epidermal Growth Factor Receptor Pathway Genes and Risk of Esophageal Squamous Cell Carcinoma and Gastric Cancer in a Chinese Population (2013) (23)
- Genetic variation in PRL and PRLR, and relationships with serum prolactin levels and breast cancer risk: results from a population-based case-control study in Poland (2011) (23)
- A Mixed-Effects Model for Powerful Association Tests in Integrative Functional Genomics. (2018) (23)
- Nonsteroidal anti‐inflammatory drugs and other analgesic use and bladder cancer in northern New England (2013) (23)
- Genetic variants in DNA repair genes and the risk of cutaneous malignant melanoma in melanoma‐prone families with/without CDKN2A mutations (2012) (22)
- A Common 8 q 24 Variant in Prostate and Breast Cancer from a Large Nested Case-Control Study (2007) (22)
- Human genetics and respiratory syncytial virus disease: current findings and future approaches. (2013) (22)
- Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (22)
- Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China (2009) (22)
- FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium (2014) (22)
- Occupational solvent exposure, genetic variation of DNA repair genes, and the risk of non-Hodgkin’s lymphoma (2012) (22)
- The NADPH Oxidase of Leukocytes: The Respiratory Burst Oxidase (1997) (22)
- Comprehensive screen of genetic variation in DNA repair pathway genes and postmenopausal breast cancer risk (2010) (22)
- Pancreatic cancer risk is modulated by inflammatory potential of diet and ABO genotype: a consortia-based evaluation and replication study (2018) (22)
- Common Single Nucleotide Polymorphisms in Genes Related to Immune Function and Risk of Papillary Thyroid Cancer (2013) (22)
- Common Variation at 1q24.1 (ALDH9A1) Is a Potential Risk Factor for Renal Cancer (2015) (22)
- Common Genetic Variation in GATA-Binding Protein 3 and Differential Susceptibility to Breast Cancer by Estrogen Receptor α Tumor Status (2007) (22)
- Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut (2010) (22)
- Evaluating Polygenic Risk Scores for Breast Cancer in Women of African Ancestry. (2021) (22)
- Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer (2009) (22)
- Common genetic variants in sex hormone pathway genes and papillary thyroid cancer risk. (2012) (22)
- Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men (2020) (21)
- Associations of common variants in genes involved in metabolism and response to exogenous chemicals with risk of multiple myeloma. (2009) (21)
- Scanning the horizon: What is the future of genome-wide association studies in accelerating discoveries in cancer etiology and prevention? (2007) (21)
- NAT2 slow acetylation and GSTM1 null genotypes increase bladder cancer risk: results from the Spanish Bladder Cancer Study and meta-analyses (2008) (21)
- The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive disease. (2014) (21)
- Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma (2012) (21)
- Genetic Effects and Modifiers of Radiotherapy and Chemotherapy on Survival in Pancreatic Cancer (2011) (21)
- Breast cancer susceptibility risk associations and heterogeneity by E-cadherin tumor tissue expression (2013) (21)
- Lack of Association of Transforming Growth Factor-β1 Polymorphisms and Haplotypes with Prostate Cancer Risk in the Prostate, Lung, Colorectal, and Ovarian Trial (2007) (21)
- Polymorphisms in genes involved in innate immunity and susceptibility to benzene-induced hematotoxicity (2011) (21)
- Genetic variation in immune function and susceptibility to human filariasis (2003) (21)
- Genetic architectures of proximal and distal colorectal cancer are partly distinct (2020) (21)
- GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer. (2016) (21)
- A Meta-analysis of Multiple Myeloma Risk Regions in African and European Ancestry Populations Identifies Putatively Functional Loci (2016) (20)
- The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer (2019) (20)
- The paradox of mutations and cancer (2018) (20)
- A Genome-Wide Association Study of Renal Cell Carcinoma among African Americans (2013) (20)
- Polymorphisms in DNA repair genes and risk of non‐Hodgkin lymphoma in a pooled analysis of three studies (2010) (20)
- Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls (2018) (20)
- Mining variations in genes of innate and phagocytic immunity: current status and future prospects (2000) (20)
- Relationship between interferon regulatory factor 4 genetic polymorphisms, measures of sun sensitivity and risk for non-Hodgkin lymphoma (2009) (20)
- Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy (2015) (20)
- Elevated Platelet Count Appears to Be Causally Associated with Increased Risk of Lung Cancer: A Mendelian Randomization Analysis (2019) (20)
- Functional profiling of uncommon VCAM1 promoter polymorphisms prevalent in African American populations (2007) (20)
- Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity (2009) (20)
- A report of cytokine polymorphisms and COPD risk in Xuan Wei, China. (2008) (19)
- CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk (2016) (19)
- Role of one-carbon metabolizing pathway genes and gene–nutrient interaction in the risk of non-Hodgkin lymphoma (2013) (19)
- Polymorphisms in pattern‐recognition genes in the innate immunity system and risk of non‐Hodgkin lymphoma (2013) (19)
- MicroRNA Processing and Binding Site Polymorphisms Are Not Replicated in the Ovarian Cancer Association Consortium (2011) (19)
- Genetic signatures of gene flow and malaria-driven natural selection in sub-Saharan populations of the "endemic Burkitt Lymphoma belt" (2019) (19)
- Next generation modeling in GWAS: comparing different genetic architectures (2014) (19)
- Polymorphisms of an Innate Immune Gene, Toll-Like Receptor 4, and Aggressive Prostate Cancer Risk: A Systematic Review and Meta-Analysis (2014) (19)
- Circulating adipokine concentrations and risk of five obesity‐related cancers: A Mendelian randomization study (2020) (19)
- Sex specific associations in genome wide association analysis of renal cell carcinoma (2019) (19)
- Reproductive aging-associated common genetic variants and the risk of breast cancer (2012) (19)
- LINE-1 methylation in leukocyte DNA, interaction with phosphatidylethanolamine N-methyltransferase variants and bladder cancer risk (2014) (19)
- The devil is in the DNA (2007) (19)
- Interactions between genome-wide significant genetic variants and circulating concentrations of insulin-like growth factor 1, sex hormones, and binding proteins in relation to prostate cancer risk in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium. (2012) (19)
- Evolving concepts of prevention and treatment of invasive fungal infections in pediatric bone marrow transplant recipients. (1996) (19)
- Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphoma (2017) (19)
- No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer. (2016) (18)
- Lack of association between modifiable exposures and glioma risk: a Mendelian randomization analysis (2019) (18)
- Comprehensive Evaluation of One-Carbon Metabolism Pathway Gene Variants and Renal Cell Cancer Risk (2011) (18)
- Effects of Electron-Beam Irradiation on Whole Genome Amplification (2005) (18)
- Genetic Admixture and Population Substructure in Guanacaste Costa Rica (2010) (18)
- Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan (2020) (18)
- Evolutionary dynamics of the human NADPH oxidase genes CYBB, CYBA, NCF2, and NCF4: functional implications. (2013) (18)
- Application of Multi-SNP Approaches Bayesian LASSO and AUC-RF to Detect Main Effects of Inflammatory-Gene Variants Associated with Bladder Cancer Risk (2013) (18)
- Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility. (2016) (18)
- A Common Genetic Variant in FCGR3A-V158F and Risk of Kaposi Sarcoma Herpesvirus Infection and Classic Kaposi Sarcoma (2005) (18)
- Characterizing Genetic Susceptibility to Breast Cancer in Women of African Ancestry (2017) (18)
- Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia. (2014) (18)
- Genetic Variation in the TP53 Pathway and Bladder Cancer Risk. A Comprehensive Analysis (2014) (18)
- Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer. (2018) (18)
- Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries (2022) (17)
- Protein-altering germline mutations implicate novel genes related to lung cancer development (2020) (17)
- Polymorphisms in JAK/STAT signaling pathway genes and risk of non-Hodgkin lymphoma. (2013) (17)
- Genetic variation in catechol-O-methyltransferase (COMT) and obesity in the prostate, lung, colorectal, and ovarian (PLCO) cancer screening trial (2007) (17)
- SNPing away at innate immunity. (1999) (17)
- Mosaic chromosome 20q deletions are more frequent in the aging population. (2017) (17)
- Transcriptome-Wide Association Study Identifies New Candidate Susceptibility Genes for Glioma. (2019) (17)
- Genetic Modifiers of Progression‐Free Survival in Never‐Smoking Lung Adenocarcinoma Patients Treated with First‐Line Tyrosine Kinase Inhibitors (2017) (17)
- Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathways. (2019) (17)
- Association of COMT haplotypes and breast cancer risk in caucasian women. (2010) (17)
- Age‐specific genome‐wide association study in glioblastoma identifies increased proportion of ‘lower grade glioma’‐like features associated with younger age (2018) (17)
- RAD51B Activity and Cell Cycle Regulation in Response to DNA Damage in Breast Cancer Cell Lines (2014) (16)
- Genetic variation in the inhibin pathway and risk of testicular germ cell tumors. (2008) (16)
- Inflammatory gene variants and the risk of biliary tract cancers and stones: a population-based study in China (2012) (16)
- Genetic variation in cell cycle and apoptosis related genes and multiple myeloma risk. (2009) (16)
- LIN 28 B Polymorphisms Influence Susceptibility to Epithelial Ovarian Cancer (2011) (16)
- Common genetic variation in GATA-binding protein 3 and differential susceptibility to breast cancer by estrogen receptor alpha tumor status. (2007) (16)
- Circulating Metabolic Biomarkers of Screen-Detected Prostate Cancer in the ProtecT Study (2018) (16)
- Transcriptional networks inferred from molecular signatures of breast cancer. (2008) (16)
- Genome-wide association study of susceptibility loci for breast cancer in Sardinian population (2015) (16)
- Genetic variation in POT1 and risk of thyroid subsequent malignant neoplasm: A report from the Childhood Cancer Survivor Study (2020) (16)
- Transcriptome-wide association study of breast cancer risk by estrogen-receptor status (2020) (16)
- Xenobiotic metabolizing genes, meat-related exposures, and risk of advanced colorectal adenoma. (2010) (16)
- Cholesterol auxotrophy as a targetable vulnerability in clear cell renal cell carcinoma. (2021) (16)
- Plasma Carotenoid- and Retinol-Weighted Multi-SNP Scores and Risk of Breast Cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (2013) (16)
- International cancer seminars: a focus on kidney cancer. (2016) (16)
- Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits (2020) (15)
- Hemochromatosis gene mutations and distal adenomatous colorectal polyps. (2005) (15)
- Genetic contributions to the association between adult height and testicular germ cell tumors. (2011) (15)
- Genetic variation and hematology: single-nucleotide polymorphisms, haplotypes, and complex disease. (2003) (15)
- Significant interactions between maternal PAH exposure and haplotypes in candidate genes on B[a]P-DNA adducts in a NYC cohort of non-smoking African-American and Dominican mothers and newborns. (2014) (15)
- CHEK2, MGMT, SULT1E1 and SULT1A1 Polymorphisms and Endometrial Cancer Risk (2011) (15)
- Variation in the SLC23A1 gene does not influence cardiometabolic outcomes to the extent expected given its association with l-ascorbic acid1234 (2014) (15)
- Further Confirmation of Germline Glioma Risk Variant rs78378222 in TP53 and Its Implication in Tumor Tissues via Integrative Analysis of TCGA Data (2015) (15)
- Predicting Lung Cancer Occurrence in Never-Smoking Females in Asia: TNSF-SQ, a Prediction Model (2019) (15)
- Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP (2014) (15)
- A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC 14 A 1 , a urea transporter gene on chromosome 18 q 12 . 3 (2011) (15)
- Large-Scale Evaluation of Genetic Variants in Candidate Genes for Colorectal Cancer Risk in the Nurses' Health Study and the Health Professionals' Follow-up Study (2008) (15)
- Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data (2012) (15)
- Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women. (2019) (15)
- Toward mapping the biology of the genome (2012) (15)
- A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (2021) (15)
- CYBB, an NADPH‐oxidase gene: restricted diversity in humans and evidence for differential long‐term purifying selection on transmembrane and cytosolic domains (2008) (14)
- Polymorphisms in DNA repair pathway genes, body mass index, and risk of non‐Hodgkin lymphoma (2013) (14)
- Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association Consortium (2021) (14)
- Genetic Variation in the Androgen Receptor Gene and Endometrial Cancer Risk (2009) (14)
- An investigation of the association of genetic susceptibility risk with somatic mutation burden in breast cancer (2016) (14)
- Mendelian randomisation study of the relationship between vitamin D and risk of glioma (2018) (14)
- Genetic Variation on 9p22 Is Associated with Abnormal Ovarian Ultrasound Results in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (2011) (14)
- Genetic association studies in cancer: Good, bad or no longer ugly? (2006) (14)
- Variants of the IL 8 and IL 8 RB Genes and Risk for Gastric Cardia Adenocarcinoma and Esophageal Squamous Cell Carcinoma (2004) (14)
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17 q 21 . 31 (2013) (14)
- Risk of Testicular Germ Cell Tumors and Polymorphisms in the Insulin-Like Growth Factor Genes (2008) (14)
- Genomic and functional analysis of the sodium-dependent vitamin C transporter SLC23A1–SVCT1 (2007) (14)
- Common genetic variants and risk for non‐Hodgkin lymphoma and adult T‐cell lymphoma/leukemia in Jamaica (2009) (14)
- Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade. (2014) (14)
- A Two‐Platform Design for Next Generation Genome‐Wide Association Studies (2012) (14)
- The population genetics of Quechuas, the largest native South American group: autosomal sequences, SNPs, and microsatellites evidence high level of diversity. (2012) (14)
- Genome-wide association study of endometrial cancer in E 2 C 2 (2014) (14)
- A High-risk Haplotype for Premature Menopause in Childhood Cancer Survivors Exposed to Gonadotoxic Therapy (2018) (14)
- Polymorphisms in complement system genes and risk of non‐Hodgkin lymphoma (2012) (14)
- Vegetables- and antioxidant-related nutrients, genetic susceptibility, and non-Hodgkin lymphoma risk (2008) (14)
- A meta-analysis of genome-wide association studies of multiple myeloma among men and women of African ancestry. (2020) (14)
- Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus (2016) (14)
- Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer. (2015) (14)
- Human Leukocyte Antigen Class I and II Alleles and Overall Survival in Diffuse Large B-Cell Lymphoma and Follicular Lymphoma (2011) (14)
- Effects of electron-beam irradiation on buccal-cell DNA. (2003) (13)
- The MBL 2 ‘ LYQA Secretor ’ Haplotype Is an Independent Predictor of Postoperative Myocardial Infarction in Whites Undergoing Coronary Artery Bypass Graft Surgery (2007) (13)
- Identification of 22 susceptibility loci associated with testicular germ cell tumors (2021) (13)
- Comparative Histopathologic Analysis of "Radiogenic" and "Sporadic" Papillary Thyroid Carcinoma: Patients Born Before and After the Chernobyl Accident. (2018) (13)
- HSD17B1 Genetic Variants and Hormone Receptor–Defined Breast Cancer (2008) (13)
- Patterns of low‐affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell disease (2002) (13)
- The Potential for Enhancing the Power of Genetic Association Studies in African Americans through the Reuse of Existing Genotype Data (2010) (13)
- Integrative molecular characterization of gallbladder cancer reveals microenvironment-associated subtypes. (2020) (13)
- Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer (2018) (13)
- Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia. (2020) (13)
- Genetic variation and the assessment of risk in septic patients (2006) (13)
- Inherited genetic variation and overall survival following follicular lymphoma (2012) (13)
- Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data. (2016) (13)
- Treatment of fungal infections in neutropenic children. (1999) (13)
- Common genetic variants in the 8q24 region and risk of papillary thyroid cancer (2012) (13)
- Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance. (2020) (13)
- Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays (2018) (13)
- Cross-Cancer Pleiotropic Associations with Lung Cancer Risk in African Americans (2018) (12)
- Bladder Cancer, Disinfection Byproducts, and Markers of Genetic Susceptibility in a Case-control Study from Spain (2006) (12)
- Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma. (2016) (12)
- Significant interactions between maternal PAH exposure and single nucleotide polymorphisms in candidate genes on B[ a ]P-DNA adducts in a cohort of non-smoking Polish mothers and newborns. (2016) (12)
- The expression of NA antigens in people withunusual Fcγ receptor III genotypes (2001) (12)
- Association of CYP1B1 Haplotypes and Breast Cancer Risk in Caucasian Women (2009) (12)
- Association between Genetic Variants in the 8q24 Cancer Risk Regions and Circulating Levels of Androgens and Sex Hormone–Binding Globulin (2010) (12)
- Common genetic variants in metabolism and detoxification pathways and the risk of papillary thyroid cancer. (2012) (12)
- Meeting report from the joint IARC-NCI international cancer seminar series: a focus on colorectal cancer. (2019) (12)
- The Etiology of Childhood Immune Thrombocytopenic Purpura: How Complex Is It? (2003) (12)
- Genetic variations in CC chemokine receptors and hypertension. (2006) (12)
- The genomic and epigenomic evolutionary history of papillary renal cell carcinomas (2018) (12)
- Genetic variation in N-acetyltransferases 1 and 2, cigarette smoking, and risk of non-Hodgkin lymphoma (2009) (12)
- A Rare Germline HOXB13 Variant Contributes to Risk of Prostate Cancer in Men of African Ancestry (2022) (12)
- Exome-Wide Association Study of Endometrial Cancer in a Multiethnic Population (2014) (11)
- Prostate cancer meta-analysis from more than 143,000 men identifies 57 novel prostate cancer susceptibility loci (2016) (11)
- Mosaic 13q14 deletions in peripheral leukocytes of non-hematologic cancer cases and healthy controls (2015) (11)
- Subphenotype meta-analysis of testicular cancer genome-wide association study data suggests a role for RBFOX family genes in cryptorchidism susceptibility (2018) (11)
- Pathway analysis of bladder cancer genome-wide association study identifies novel pathways involved in bladder cancer development (2016) (11)
- SLC6A3 and body mass index in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial (2009) (11)
- Using genetic variation to study immunomodulation. (2002) (11)
- A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma. (2011) (11)
- Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (11)
- National Cancer Institute Prostate Cancer Genetics Workshop. (2011) (11)
- Variation in Effects of Non-Hodgkin Lymphoma Risk Factors According to the Human Leukocyte Antigen (HLA)-DRB1*01:01 Allele and Ancestral Haplotype 8.1 (2011) (11)
- Single Nucleotide Polymorphisms in the TP 53 Region and Susceptibility to Invasive Epithelial Ovarian Cancer (2009) (11)
- Genome-wide association studies and "the art of the soluble". (2010) (11)
- A step toward slaying the hydra of second cancers (2011) (11)
- Correlation between prostate volume and single nucleotide polymorphisms implicated in the steroid pathway (2017) (11)
- Risk of therapy-related myelodysplastic syndrome/acute myeloid leukemia after childhood cancer: a population-based study (2019) (11)
- Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (2019) (11)
- Diversity in the Glucose Transporter-4 Gene (SLC2A4) in Humans Reflects the Action of Natural Selection along the Old-World Primates Evolution (2010) (11)
- Association between Chronic Disseminated Candidiasis in Adult Acute Leukemia and Common IL 4 Promoter Haplotypes (2003) (11)
- Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes (2016) (11)
- Genome-Wide Association Study in Irradiated Childhood Cancer Survivors Identifies HTR2A for Subsequent Basal Cell Carcinoma. (2019) (11)
- Genetic variants in the 8q24 locus and risk of testicular germ cell tumors (2008) (11)
- Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia (2018) (11)
- CYP 1 A 1 Val 462 and NQO 1 Ser 187 polymorphisms , cigarette use , and risk for colorectal adenoma (2005) (11)
- Genome-Wide Association Study of Serum Selenium Concentrations (2013) (10)
- Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families (2013) (10)
- Inflammatory-Related Genetic Variants in Non–Muscle-Invasive Bladder Cancer Prognosis: A Multimarker Bayesian Assessment (2016) (10)
- Genetic Variation in a4GnT in Relation to Helicobacter pylori Serology and Gastric Cancer Risk (2009) (10)
- GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer (2017) (10)
- Chromosomal Aberrations and Survival after Unrelated Donor Hematopoietic Stem Cell Transplant in Patients with Fanconi Anemia. (2018) (10)
- Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche DTU Orbit (05/11/2017) (2014) (10)
- Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. (2021) (10)
- Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women (2021) (10)
- White Blood Cell Count and Risk of Incident Lung Cancer in the UK Biobank. (2019) (10)
- Infection prevention strategies for children with cancer and AIDS: contrasting dilemmas. (1995) (10)
- The association between inflammation‐related genes and serum androgen levels in men: The prostate, lung, colorectal, and ovarian study (2012) (10)
- cis sequence effects on gene expression (2007) (10)
- Body Mass Index Genetic Risk Score and Endometrial Cancer Risk (2015) (10)
- Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection (2006) (10)
- GWAS is going to the dogs (2014) (10)
- Common genetic variants in epigenetic machinery genes and risk of upper gastrointestinal cancers. (2015) (10)
- Haplotype Analysis of the HSD 17 B 1 Gene and Risk of Breast Cancer : A Comprehensive Approach to Multicenter Analyses of Prospective Cohort Studies (2006) (10)
- Polymorphisms in genes involved in Th1-type cell-mediated response and the risk of gastric cancer (2005) (10)
- Telomere stability genes are not mutated in osteosarcoma cell lines. (2005) (10)
- A custom 148 gene‐based resequencing chip and the SNP explorer software: new tools to study antibody deficiency (2010) (10)
- Prediction of non-muscle invasive bladder cancer outcomes assessed by innovative multimarker prognostic models (2016) (10)
- Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data (2017) (10)
- Innate immunity gene polymorphisms and the risk of colorectal neoplasia. (2013) (10)
- Association between breast cancer genetic susceptibility variants and terminal duct lobular unit involution of the breast (2017) (9)
- The renal lineage factor PAX8 controls oncogenic signalling in kidney cancer (2022) (9)
- Single-Nucleotide Polymorphisms in Genes Encoding for CC Chemokines were Not Associated with the Risk of Non-Hodgkin Lymphoma (2013) (9)
- Controversies in the treatment of neutropenia in cancer patients (1998) (9)
- MBL2 and Hepatitis C Virus Infection among Injection Drug Users (2008) (9)
- Genetically predicted telomere length is associated with clonal somatic copy number alterations in peripheral leukocytes (2020) (9)
- Genetic variants in frizzled-related protein (FRZB) and the risk of colorectal neoplasia (2009) (9)
- Pediatric infection with the human immunodeficiency virus: issues for the otorhinolaryngologist. (1989) (9)
- Genetic Polymorphisms in Oxidative Stress Pathway Genes and Modification of BMI and Risk of Non-Hodgkin Lymphoma (2012) (9)
- Whole genome amplification of buccal cytobrush DNA collected for molecular epidemiology studies (2007) (9)
- Co-incidence of RCC-susceptibility polymorphisms with HIF cis-acting sequences supports a pathway tuning model of cancer (2019) (9)
- Altered regulation of DPF3, a member of the SWI/SNF complexes, underlies the 14q24 renal cancer susceptibility locus (2021) (9)
- A multilayered post-GWAS assessment on genetic susceptibility to pancreatic cancer (2020) (8)
- Reply to ‘Mosaic loss of chromosome Y in leukocytes matters’ (2018) (8)
- Field Study of the Possible Effect of Parental Irradiation on the Germline of Children Born to Cleanup Workers and Evacuees of the Chornobyl Accident. (2020) (8)
- Corrigendum: The genomic landscape of juvenile myelomonocytic leukemia (2015) (8)
- Genetic Variation in the HSD 17 B 1 Gene and Risk of Prostate Cancer (2005) (8)
- Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (2022) (8)
- Prostate cancer meta-analysis from more than 145,000 men to identify 65 novel prostate cancer susceptibility loci. (2017) (8)
- Detectable chromosome X mosaicism in males is rarely tolerated in peripheral leukocytes (2021) (8)
- Genetic polymorphisms in IL10RA and TNF modify the association between blood transfusion and risk of non‐Hodgkin lymphoma (2012) (8)
- Toxicological considerations in the application and interpretation of susceptibility biomarkers in epidemiological studies. (2004) (8)
- Tracing Lung Cancer Risk Factors Through Mutational Signatures in Never-Smokers. (2020) (8)
- Corrigendum to Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression [Human Molecular Genetics, 22, (2013), 2520-2528] doi: 10.1093/hmg/ddt086 (2013) (8)
- Using germ-line genetic variation to investigate and treat cancer. (2004) (8)
- A Genome-Wide “Pleiotropy Scan” Does Not Identify New Susceptibility Loci for Estrogen Receptor Negative Breast Cancer (2014) (8)
- Initial reporting from the prospective National Cancer Institute (NCI) COVID-19 in Cancer Patients Study (NCCAPS). (2021) (8)
- Searching for causal relationships of glioma: a phenome-wide Mendelian randomisation study (2020) (8)
- One thousand genomes imputation in the national cancer institute breast and prostate cancer cohort consortium aggressive prostate cancer genome‐wide association study (2013) (8)
- Abstract 2931: Inherited variation at chromosome 12p13.33 includingRAD52influences squamous cell lung carcinoma risk (2012) (7)
- Methods for detecting interactions between genetic polymorphisms and prenatal environment exposure with a mother‐child design (2010) (7)
- Immune-Related Adverse Events After Immune Checkpoint Inhibitors for Melanoma Among Older Adults (2022) (7)
- Testicular germ cell tumor susceptibility associated with the UCK 2 locus on chromosome 1 q 23 (2013) (7)
- The chromosome 2 p 21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma (2012) (7)
- Subsequent Neoplasm Risk Associated With Rare Variants in DNA Damage Response and Clinical Radiation Sensitivity Syndrome Genes in the Childhood Cancer Survivor Study. (2020) (7)
- Occupational solvent exposure, genetic variation in immune genes, and the risk for non-Hodgkin lymphoma (2013) (7)
- A 584 bp deletion in CTRB2 inhibits chymotrypsin B2 activity and secretion and confers risk of pancreatic cancer. (2021) (7)
- Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma (2020) (7)
- Granulocyte Transfusions: Time for a Second Look (1997) (7)
- Correction: Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci (2015) (7)
- A Resequence Analysis of Genomic Loci on Chromosomes 1q32.1, 5p15.33, and 13q22.1 Associated With Pancreatic Cancer Risk (2013) (7)
- Assessing Disease Risk in Genome-wide Association Studies Using Family History (2012) (7)
- Genome-Wide Association Study Data Reveal Genetic Susceptibility to Chronic Inflammatory Intestinal Diseases and Pancreatic Ductal Adenocarcinoma Risk (2020) (6)
- Lipid Trait Variants and the Risk of Non-Hodgkin Lymphoma Subtypes: A Mendelian Randomization Study (2020) (6)
- Smoking Modifies Pancreatic Cancer Risk Loci on 2q21.3 (2021) (6)
- Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer (2022) (6)
- Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (2018) (6)
- Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element (2021) (6)
- Sub-multiplicative interaction between polygenic risk score and household coal use in relation to lung adenocarcinoma among never-smoking women in Asia. (2020) (6)
- Ages at menarche- and menopause-related genetic variants in relation to terminal duct lobular unit involution in normal breast tissue (2016) (6)
- Application of a Novel Score Test for Genetic Association Incorporating Gene-Gene Interaction Suggests Functionality for Prostate Cancer Susceptibility Regions (2011) (6)
- 7q21-rs6964587 and breast cancer risk: an extended case–control study by the Breast Cancer Association Consortium (2011) (6)
- Comprehensive resequence analysis of a 123‐kb region of chromosome 11q13 associated with prostate cancer (2012) (6)
- Polymorphisms in Th1/Th2 Cytokine Genes, Hormone Replacement Therapy, and Risk of Non-Hodgkin Lymphoma (2011) (6)
- Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk (2011) (6)
- Breast cancer risks associated with missense variants in breast cancer susceptibility genes (2021) (6)
- SNPs Meet CNVs in Genome-Wide Association Studies: HGV2007 Meeting Report (2008) (6)
- Polymorphisms in integrin genes and lymphoma risk. (2011) (6)
- Combining genome-wide studies of breast, prostate, ovarian and endometrial cancers maps cross-cancer susceptibility loci and identifies new genetic associations (2020) (6)
- Hepcidin-regulating Iron-metabolism Genes and Pancreatic Ductal Adenocarcinoma: A Pathway Analysis of Genome-wide Association Studies (2020) (6)
- Common breast cancer risk loci predispose to distinct tumor subtypes (2019) (6)
- Abstract LB-23: Meta-analysis of genome-wide association studies identifies multiple loci associated with chronic lymphocytic leukemia. (2013) (6)
- Detectible mosaic truncating PPM1D mutations, age and breast cancer risk (2019) (6)
- Genetic polymorphisms of the GNRH1 and GNRHR genes and risk of breast cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3) (2009) (6)
- Constitutional Loss-of-Function Mutations in Telomerase Are Genetic Risk Factors for Acute Myeloid Leukemia. (2007) (6)
- Breast cancer susceptibility polymorphisms and endometrial cancer risk: a Collaborative Endometrial Cancer Study. (2011) (6)
- Discovery of common and rare genetic risk variants for colorectal cancer (2018) (6)
- Common variants in breast cancer risk loci predispose to distinct tumor subtypes (2022) (6)
- LIM domain only 2 protein expression, LMO2 germline genetic variation, and overall survival in diffuse large B-cell lymphoma in the pre-rituximab era (2012) (6)
- A twist on admixture mapping (2011) (6)
- Molecular characterization of the mouse p47-phox (Ncf1) gene and comparative analysis of the mouse p47-phox (Ncf1) gene to the human NCF1 gene. (2000) (6)
- Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study. (2021) (6)
- Incident disease associations with mosaic chromosomal alterations on autosomes, X and Y chromosomes: insights from a phenome-wide association study in the UK Biobank (2021) (6)
- Genetic variation at the 8q24 locus confers risk to multiple myeloma (2012) (5)
- Rationale and design of a double-blind randomized non-inferiority clinical trial to evaluate one or two doses of vaccine against human papillomavirus including an epidemiologic survey to estimate vaccine efficacy: The Costa Rica ESCUDDO trial (2021) (5)
- Genome-Wide Gene–Diabetes and Gene–Obesity Interaction Scan in 8,255 Cases and 11,900 Controls from PanScan and PanC4 Consortia (2020) (5)
- CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers (2021) (5)
- Sex-related effect on immunotherapy response: implications and opportunities. (2019) (5)
- Reflections on events surrounding the time of diagnosis in pediatric oncology. (2001) (5)
- Genome-wide scan of 29,141 African Americans finds no evidence of selection since admixture (2013) (5)
- Large-scale cross-cancer fine-mapping of the 5p15.33 region reveals multiple independent signals (2021) (5)
- Joint IARC/NCI International Cancer Seminar Series Report: Expert consensus on future directions for ovarian carcinoma research. (2021) (5)
- Differences in risk factors for molecular subtypes of clear cell renal cell carcinoma (2021) (5)
- Pathway Analysis of Renal Cell Carcinoma Genome-Wide Association Studies Identifies Novel Associations (2020) (5)
- Telomere Length-Associated Genetic Variants and the Risk of Thyroid Cancer in Survivors of Childhood Cancer: A Report from the Childhood Cancer Survivor Study (CCSS) (2018) (5)
- Advantage of Using Allele-Specific Copy Numbers When Testing for Association in Regions with Common Copy Number Variants (2013) (5)
- Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility (2020) (5)
- Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer (2011) (5)
- The case for increasing diversity in tissue-based functional genomics datasets to understand human disease susceptibility (2022) (5)
- Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk (2007) (5)
- Estimation of radiation gonadal doses for the American–Ukrainian trio study of parental irradiation in Chornobyl cleanup workers and evacuees and germline mutations in their offspring (2021) (5)
- Improved Imputation of Common and Uncommon Single Nucleotide Polymorphisms (SNPs) with a New Reference Set (2011) (5)
- Germline Genetic Variants and Lung Cancer Survival in African Americans (2017) (5)
- Leveraging Family History in Population‐Based Case‐Control Association Studies (2014) (5)
- Massively parallel reporter assays combined with cell-type specific eQTL informed multiple melanoma loci and identified a pleiotropic function of HIV-1 restriction gene, MX2, in melanoma promotion (2019) (5)
- HLA-A, -B, -Cw, -DQA1 and -DRB1 alleles in a Caucasian population from Bethesda, USA (2004) (5)
- Genetically Determined Height and Risk of Non-hodgkin Lymphoma (2020) (4)
- Long-term follow-up and infectious complications of therapy for acute lymphoblastic leukemia in children (2000) (4)
- Publisher Correction: Shared heritability and functional enrichment across six solid cancers (2019) (4)
- Cloning and chromosomal localization of Ncf4, the mouse homologue of p40-phox (1997) (4)
- Stomaching multigene panel testing: what to do about CDH1? (2019) (4)
- A p 47-phox Pseudogene Carries the Most Common Mutation Causing p 47-phox – deficient Chronic Granulomatous Disease (2013) (4)
- Common variants in ZNF 365 are associated with both mammographic density and breast cancer risk (2019) (4)
- Erratum to: The UBC-40 Urothelial Bladder Cancer cell line index: a genomic resource for functional studies (2016) (4)
- Mendelian Randomization Analysis of n-6 Polyunsaturated Fatty Acid Levels and Pancreatic Cancer Risk (2020) (4)
- Validation of the performance of a comprehensive genotyping assay panel of single nucleotide polymorphisms in drug metabolism enzyme genes (2008) (4)
- Fine mapping of 14q24.1 breast cancer susceptibility locus (2012) (4)
- Genetics and geography of leukocyte telomere length in sub-Saharan Africans (2020) (4)
- Pre-HCT mosaicism increases relapse risk and lowers survival in acute lymphoblastic leukemia patients post-unrelated HCT. (2021) (4)
- Cytokines in the management of infectious complications in children with cancer (1995) (4)
- Polymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4 (2013) (4)
- Genetic association studies: marking them well. (2006) (4)
- Genetic variants in XRRC5 may predict development of venous thrombotic events in myeloma patients on thalidomide. (2009) (4)
- Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility (2021) (4)
- Abstract 942: Imputation from The 1000 Genomes Project identifies rare large effect variants of BRCA2-K3326X and CHEK2-I157T as risk factors for lung cancer; a study from the TRICL consortium (2014) (4)
- Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2017) (4)
- Genome‐wide association studies in melanoma: off to a good start (2012) (4)
- Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN 2 A Mutations (2013) (4)
- Abstract LB-272: Genome-wide association study identifies multiple susceptibility loci for diffuse large B-cell lymphoma (2014) (4)
- Meta- and Pooled Analyses Tumor Necrosis Factor ( TNF ) and Lymphotoxin- a ( LTA ) Polymorphisms and Risk of Non-Hodgkin Lymphoma in the InterLymph Consortium (2010) (4)
- Future perspectives on molecular epidemiology. (2011) (4)
- Genetic variation at CYP 3 A is associated with age at menarche and breast cancer risk : a case-control study (2014) (4)
- Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2019) (4)
- Correction: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer (2016) (4)
- Abstract 5574: High prevalence of germline TP53 mutations in young osteosarcoma cases (2015) (4)
- Supplementary Material 5 (2014) (3)
- Polygenic Risk Score Improves Risk Stratification and Prediction of Subsequent Thyroid Cancer after Childhood Cancer (2021) (3)
- Genome-wide association studies in women of African ancestry identified 3 q 26 . 21 as a novel susceptibility locus for oestrogen receptor negative breast cancer (2017) (3)
- How the germline informs the somatic landscape (2021) (3)
- Abstract 4596: Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never-smoking women in Asia: A report from the Female Lung Cancer Consortium in Asia (2015) (3)
- The road ahead: less travelled and more arduous than initially envisioned (2011) (3)
- Viral coinfection analysis using a MinHash toolkit (2019) (3)
- Eighteen Insulin-like Growth Factor (IGF) pathway genes, circulating levels of IGF-1 and its binding protein (IGFBP-3), and risk of prostate and breast cancer (2010) (3)
- Prognostic impact of pre-transplant chromosomal aberrations in peripheral blood of patients undergoing unrelated donor hematopoietic cell transplant for acute myeloid leukemia (2021) (3)
- Shared and distinct genetic etiologies for different types of clonal hematopoiesis (2022) (3)
- Supplementary Material 3 (2015) (3)
- Polygenic risk score for the prediction of breast cancer is related to lesser terminal duct lobular unit involution of the breast (2020) (3)
- Genetic variation in the body mass index of adult survivors of childhood acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort (2020) (3)
- Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility (2020) (3)
- Supplementary Material 6 (2014) (3)
- Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults (2015) (3)
- Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction (2021) (3)
- Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment (2021) (3)
- Comparison of somatic mutation landscapes in Chinese versus European breast cancer patients (2021) (3)
- Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk (2020) (3)
- Population Genetics and Comparative Genetics of CLDN1, a Gene Involved in Hepatitis C Virus Entry (2008) (3)
- Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (2019) (3)
- Erratum to: The UBC-40 Urothelial Bladder Cancer Cell Line Index: a genomic resource for functional studies (2015) (3)
- Supplementary Material 7 (2014) (3)
- Mendelian randomisation study of smoking exposure in relation to breast cancer risk (2021) (3)
- Comment on: Assessing the probability that a positive report is false: An approach for molecular epidemiology studies. Authors' reply (2004) (3)
- Comparison of Radiation Dose Reconstruction Methods to Investigate Late Adverse Effects of Radiotherapy for Childhood Cancer: A Report from the Childhood Cancer Survivor Study (2019) (3)
- Empiric Antifungal Therapy for the Neutropenic Patient (2001) (3)
- Abstract 1591: Large-scale transcriptome-wide association study (TWAS) identifies novel candidate susceptibility genes for pancreatic cancer (2019) (3)
- Genome-wide association study meta-analysis identifies the SOAT1/AXDND1 locus to be associated with hip and forearm fracture risk (2013) (2)
- Book Review The Innate Immune Response to Infection Edited by Stefan H.E. Kaufmann, Ruslan Medzhitov, and Siamon Gordon. 465 pp., illustrated. Washington, D.C., ASM Press, 2004. $115.95. 1-55581-291-0 (2005) (2)
- Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study (2022) (2)
- When the Smoke Clears (2018) (2)
- Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2019) (2)
- Genomic variation in a global village: Report of the 10th annual Human Genome Variation Meeting 2008 (2009) (2)
- Host Genetic Variation in the Cell Cycle and NF-κB Pathways and Overall Survival in Mantle Cell Lymphoma. (2007) (2)
- Fatal esophageal aspergilloma in a leukemic adolescent. (1992) (2)
- Abstract PO-146: Multiethnic GWAS meta-analysis identifies novel variants and informs genetic risk prediction for prostate cancer across populations (2020) (2)
- Investigating the genetic relationship between Alzheimer’s disease and cancer using GWAS summary statistics (2017) (2)
- Sex-specific genome-wide association study in glioma identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21 (2017) (2)
- Abstract 5071: A genome-wide association study suggests evidence of variants at 6p21.32 associated with marginal zone lymphoma (2014) (2)
- Detection of common cytokine and colony stimulating factor gene polymorphisms. (2003) (2)
- Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes (2022) (2)
- Abstract PL01-02: The heritable component of cancer: Insights from genome-wide association studies and beyond (2011) (2)
- Breast Cancer Risk FromModifiable and Nonmodifiable Risk Factors AmongWhiteWomen in the United States (2016) (2)
- Characterization of breakpoint regions of large structural autosomal mosaic events (2017) (2)
- Abstract 2565: Prostate cancer GWAS from more than 89,000 men identifies more than 30 novel prostate cancer susceptibility loci (2016) (2)
- Germline-somatic JAK2 interactions are associated with clonal expansion in myelofibrosis (2022) (2)
- Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA) (2015) (2)
- Risk of Non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair genes (2005) (2)
- Gene editing reveals the effect of thousands of variants in a key cancer gene (2018) (2)
- Abstract 2201: Pathway analysis of breast cancer genome wide association study highlights three pathways and one canonical signaling cascade (2010) (2)
- Abstract 2691: Genome-wide association study identifies two susceptibility loci that modify radiation-related risk for breast cancer after childhood cancer: A report from the Childhood Cancer Survivor Study and St. Jude Lifetime Cohort (2016) (2)
- Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility (2016) (2)
- A UVB-responsive common variant at chromosome band 7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor, AHR. (2021) (2)
- Correction: Vitamin D Metabolic Pathway Genes and Pancreatic Cancer Risk (2015) (2)
- HLA-A, -B, -Cw, -DQA1 and DRB1 in an African American population from Bethesda, USA (2004) (2)
- Stem cells: Subclone wars (2017) (2)
- Polymorphisms in One-Carbon Metabolism Genes and Overall Survival in Diffuse Large B-Cell Lymphoma (DLBCL). (2007) (2)
- Association study between polymorphisms in DNA methylation-related genes and testicular germ cell tumor risk. (2022) (2)
- ImmunoTyper-SR: A Novel Computational Approach for Genotyping Immunoglobulin Heavy Chain Variable Genes using Short Read Data (2022) (2)
- The relationship between blood pressure and risk of renal cell carcinoma (2022) (2)
- Author Correction: Large-scale transcriptome-wide association study identifies new prostate cancer risk regions (2019) (2)
- Body Size at Different Ages and Risk of 6 Cancers: A Mendelian Randomization and Prospective Cohort Study (2022) (2)
- Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction (2021) (2)
- Two truncating variants in FANCC and breast cancer risk (2019) (2)
- Abstract 2789: C-reactive protein and risk of lung cancer (2010) (2)
- Thyroid Cancer Risk in Ukraine Following the Chernobyl Accident (The Ukrainian–American Cohort Thyroid Study) (2017) (2)
- Early foscarnet failure in herpes simplex virus infection in a patient with AIDS. (1997) (2)
- Corrigendum: Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions (2014) (2)
- MBL 2 and Hepatitis C Virus Infection among Injection Drug Users (2016) (2)
- Association between zidovudine-containing antiretroviral therapy exposure in utero and leukocyte telomere length at birth. (2019) (2)
- Does a Multiple Myeloma Polygenic Risk Score Predict Overall Survival of Myeloma Patients? (2022) (2)
- In utero exposure to zidovudine-containing antiretroviral therapy and clonal hematopoiesis in HIV-exposed uninfected newborns. (2021) (2)
- Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (2019) (1)
- A Multi-media Strategy to Integrate Introductory Broad-Based Radiation Science Education in U.S. Medical Schools. (2022) (1)
- Opportunities-and hard work-ahead. (2014) (1)
- Subsequent neoplasm risk associated with rare variants in DNA repair and clinical radiation sensitivity syndrome genes: A report from the Childhood Cancer Survivor Study. (2019) (1)
- Abstract 2643: Interactions between polycyclic aromatic hydrocarbon exposure and genetic polymorphisms on benzo(a)pyrene-DNA adducts in a Polish cohort of mothers and newborns (2012) (1)
- A novel functional variant in 8q24 is associated with regulation of prostate stem cell antigen (PSCA) gene expression and bladder cancer risk (2011) (1)
- The ATM missense mutation Ser49Cys and risk of breast cancer (2008) (1)
- Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma risk (2013) (1)
- Selected issues in children with human immunodeficiency virus infection (1991) (1)
- Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer (2018) (1)
- Telomere Length Measurement by Flow-FISH Distinguishes Dyskeratosis Congenita from Other Bone Marrow Failure Syndromes. (2006) (1)
- Gene–Environment Interactions on Growth Trajectories (2012) (1)
- identifies patients with dyskeratosis congenita Very short telomere length by flow fluorescence in situ hybridization (2011) (1)
- Abstract P3-08-02: Common variants at 10p14 and 1p11.2 display heterogeneity in breast cancer associations by E-cadherin tumor tissue expression in two independent datasets (2012) (1)
- Lead Exposure and Glioma Among Rural Residents: The Upper Midwest Health Study (2006) (1)
- GWAS Explorer: an open-source tool to explore, visualize, and access GWAS summary statistics in the PLCO Atlas (2023) (1)
- Large-scale evaluation of candidate genes for cancer identifies common genetic variants in vascular endothelial growth factor associated with bladder cancer risk (2005) (1)
- Moving towards FAIR practices in epidemiological research. (2022) (1)
- Principles of analysis of germline genetics (2010) (1)
- Abstract 1300: Exploration of rare variants from exome sequencing in families with Waldenstrom macroglobulinemia (WM) (2014) (1)
- A multi-locus genetic association test for a dichotomous trait and its secondary phenotype (2018) (1)
- Identification of nine new susceptibility loci for endometrial cancer (2018) (1)
- Abstract ED3-1: Genome-wide association studies in cancer: Insights in cancer etiology (2010) (1)
- Management of Febrile Episodes in Neutropenic Patients Defining the Role of Meropenem (1999) (1)
- Utilizing Fluidigm's Access Array Long-Range Capability and Roche 454 s Titanium Chemistry to Capture and Sequence the Epstein-Barr Virus (EBV) for Variant Detection. (2010) (1)
- Potential Susceptibility Loci Identified for Renal Cell Carcinoma by Targeting Obesity-Related Genes (2017) (1)
- Leveraging Genetic Determinants of Prostate-Specific Antigen Levels Towards Improving Prostate Cancer Screening (2022) (1)
- Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21 (2018) (1)
- Basic principles and laboratory analysis of genetic variation. (2011) (1)
- A mechanistic basis for amplification differences between samples and between genome regions (2012) (1)
- Multilevel-analysis identify a cis-expression quantitative trait locus associated with risk of renal cell carcinoma (2015) (1)
- Genetic variation in nucleotide excision repair (NER) and bladder cancer risk in the Spanish Bladder Cancer Study (2005) (1)
- Supplementary Material 4 (2015) (1)
- Erratum: Insulin-like growth factor pathway genetic polymorphisms, circulating IGF1 and IGFBP3, and prostate cancer survival (Journal of Experimental Botany (2014) 106:6 (dju085) DOI: 10.1093/jnci/dju085) (2014) (1)
- Large-scale evaluation of candidate genes for urinary bladder cancer susceptibility using Illumina® in the Spanish Bladder Cancer Study (2006) (1)
- GWAS is going to the dogs (2014) (1)
- Polymorphism in the trifunctional enzyme coding gene MTHFD1 and the risk of stomach cancer (2006) (1)
- The genetic and evolutionary basis of gene expression variation in East Africans (2022) (1)
- Cancer Sequencing Gets a Little More Personal (2010) (1)
- Clinical management of HIV infection in infants and children (1990) (1)
- Variation in the SLC 23 A 1 genedoesnot influencecardiometabolicoutcomes to the extent expected given its association with L-ascorbic acid 1 – 4 (2014) (1)
- Prevention and Epidemiology 3 0-UTR and Functional Secretor Haplotypes in Mannose-Binding Lectin 2 Are Associated with Increased Colon Cancer Risk in African Americans (2012) (1)
- Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants (2018) (1)
- International cancer seminars:a focus on colorectal cancer (2019) (1)
- Abstract 242: Large pathway and gene set analysis of GWAS data identifies novel associations for pancreatic cancer (2018) (1)
- Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (1)
- HGV2011: Personalized genomic medicine meets the incidentalome (2012) (1)
- Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2018) (1)
- Immune mechanisms in non-Hodgkin lymphoma: Joint effects of the tumor necrosis factor (TNF) G308A and interleukin 10 (IL10) T3575A polymorphisms with environmental exposures (2007) (1)
- Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma (2022) (1)
- Abstract 401: Functional characterization of the 14q24 renal cancer susceptibility locus implicates SWI/SNF complex member DPF3 via inhibition of apoptosis (2018) (1)
- Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility (2020) (1)
- Polygenic Risk Modelling for Prediction of Epithelial Ovarian Cancer Risk (2020) (1)
- Abstract 4609: Risk loci in telomere structure and maintenance genes across five cancer types: GAME-ON Consortium (2015) (1)
- PLCOjs, a FAIR GWAS web SDK for the NCI Prostate, Lung, Colorectal and Ovarian Cancer Genetic Atlas project (2022) (1)
- Combined somatic mutation and copy number analysis in the survival of familial CLL (2018) (1)
- Author Correction: Pan-cancer analysis of whole genomes (2023) (1)
- Mosaic loss of chromosome Y is associated with common variation near TCL 1 A 1 2 (2016) (1)
- Abstract 2204: Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations reveals new susceptibility loci (2014) (1)
- Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (2018) (1)
- Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers (2020) (1)
- Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study (2014) (1)
- Null Results in Brief MDM 2 SNP 309 and SNP 354 Are Not Associated with Lung Cancer Risk (2006) (1)
- Selected issues in human immunodeficiency virus infection in adolescents (1992) (1)
- Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity. (2022) (1)
- The future of pediatric cancer and complex diseases: Aren't they all? (2007) (1)
- Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk (2007) (1)
- Prediction of non-muscle invasive bladder cancer outcomes assessed by innovative multimarker prognostic models (2016) (1)
- European Mathematical Genetics Meeting, Munich, Germany, 14th–15th May 2009 (2009) (1)
- Corrigendum re "Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma" [Eur Urol 2017;72:747-54]. (2018) (1)
- Discovery and Characterization of Cancer Genetic Susceptibility Alleles (2020) (1)
- Mutations in TERT, the Gene Encoding Telomerase Reverse Transcriptase, in “Acquired” Aplastic Anemia Inhibit Enzymatic Function by a Dominant Negative Mechanism of Action. (2004) (1)
- Polygenic risk score for the prediction of breast cancer is related to lesser terminal duct lobular unit involution of the breast (2020) (1)
- Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy (2015) (1)
- Inflammatory gene variants and the risk of biliary tract cancers and stones: a population-based study in China (2012) (1)
- The DARC side of GWAS. (2010) (1)
- A multilayered post-GWAS assessment on genetic susceptibility to pancreatic cancer (2021) (1)
- Abstract 4349: Identifying causal risk factors of metabolic syndrome for renal cell carcinoma. A Mendelian randomization approach (2016) (1)
- Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry. (2023) (1)
- B-cell non-Hodgkin lymphoma (NHL) subtype risk associated with autoimmune conditions and polygenic risk scores (PRS). (2022) (1)
- A comprehensive analysis of polymorphic variants in steroid hormone and insulin‐like growth factor‐1 metabolism and risk of in situ breast cancer: Results from the Breast and Prostate Cancer Cohort Consortium (2017) (1)
- Interactions between breast cancer susceptibility loci and menopausal hormone therapy in relationship to breast cancer in the Breast and Prostate Cancer Cohort Consortium (2016) (1)
- Polymorphisms In IRS1 and IL6R and Susceptibility To Multiple Myeloma (2013) (1)
- Abstract A78: Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut (2008) (1)
- Abstract SY26-02: Sherlock-Lung: Tracing lung cancer mutational processes in never smokers (2019) (1)
- Supplementary Material 9 (2013) (1)
- Population structure of human gut bacteria in a diverse cohort from rural Tanzania and Botswana (2019) (1)
- Abstract #LB-139: A comprehensive genome-wide association study of lung cancer (2009) (1)
- A network analysis to identify mediators of germline-driven differences in breast cancer prognosis (2020) (1)
- Clonal hematopoiesis and risk of prostate cancer in large samples of European ancestry men. (2022) (1)
- Inflated expectations: Rare-variant association analysis using public controls (2023) (1)
- Hard Work Ahead: Fine Mapping and Functional Follow-up of Susceptibility Alleles in Cancer GWAS (2015) (1)
- Supplementary Material 15 (2013) (1)
- Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer (2018) (1)
- Prevalence of Genetic Variants in the United States: Results from the Third National Health and Nutrition Examination Survey (NHANES III), 1991-1994 (1994) (1)
- Abstract 2634: Polymorphisms in DNA repair genes and risk of multiple myeloma (2012) (1)
- Abstract 843: Imputation and meta-analysis of five genome-wide association studies identify multiple new loci associated with testicular germ cell tumor (2015) (0)
- Polygenic Risk Scores for Prediction of Breast Cancer Risk in Women of African Ancestry: a Cross-Ancestry Approach (2021) (0)
- Abstract 228: Association analysis across different populations identifies 26 new cutaneous melanoma risk loci (2018) (0)
- Abstract LB-330: Genetic variants in the 9p21 region in relation to the risk of multiple tumors (2012) (0)
- Author Correction: Large-scale transcriptome-wide association study identifies new prostate cancer risk regions (2019) (0)
- Genomewide meta-analysis identifies loci associated with IGF-I and IGEBP-3 levels with impact on age-related traits (vol 15, pg 811, 2016) (2017) (0)
- Difference in the Transcriptional Activity of the Interleukin-4 Promoter Haplotypes (2005) (0)
- Abstract 1638: Whole-exome sequencing and protein interaction networks to prioritize candidate genes for cutaneous melanoma susceptibility (2019) (0)
- Mendelian randomisation study of the relationship between vitamin D and risk of glioma (2018) (0)
- Cancer esearch ention and Epidemiology upational Trichloroethylene Exposure and Renal cinoma Risk : Evidence of Genetic Susceptibility by R uctive Metabolism Gene Variants (2010) (0)
- Cytokine Gene Polymorphisms and Overall Survival in Follicular Lymphoma: Results from a Large Population-Based Study. (2006) (0)
- Abstract 2185: Multiple region whole-genome sequencing reveals intratumor heterogeneity and branching clonal architecture of non-clear-cell renal cell carcinoma (2018) (0)
- Large-scale transcriptome-wide association study identifies new prostate cancer risk regions (2018) (0)
- Abstract 4668: Genetic effects and modifiers of radiotherapy and chemotherapy on survival in pancreatic cancer (2011) (0)
- Genome wide association studies for breast and prostate cancer susceptibility loci in the CGEMS initiative (2008) (0)
- Transcriptional Signaling Centers Govern Human Erythropoiesis and Harbor Genetic Variations of Red Blood Cell Traits (2018) (0)
- OP-JNCI200057 329..337 (2021) (0)
- Reproductive aging-associated common genetic variants and the risk of breast cancer (2012) (0)
- Abstract 2641: Polymorphisms in pattern recognition genes in the innate immunity system and risk of non-Hodgkin lymphoma (2012) (0)
- Genes Encoding Telomere-Binding Proteins TERF1, TERF2 and TIN2 Are mutated in Patients with Acquired Aplastic Anemia. (2004) (0)
- An unusual suspect: an uncommon human-specific synonymous coding variant within the UGT1A6 gene explains a GWAS signal and protects against bladder cancer (2011) (0)
- Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia (2012) (0)
- Benzene Hematotoxicity in Workers Exposed to Low Levels (2008) (0)
- A novel functional variant in 8q24 is associated with regulation of prostate stem cell antigen (PSCA) gene expression and bladder cancer risk (2011) (0)
- Abstract 1895: Genetic polymorphisms of an innate immune gene, Toll-Like Receptor 4, and aggressive prostate cancer risk: A systematic review and meta-analysis (2011) (0)
- CHEK 2 , MGMT , SULT 1 E 1 and SULT 1 A 1 Polymorphisms and Endometrial Cancer Risk (2011) (0)
- CIS Sequence Effects on Gene Expression The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters (2007) (0)
- Abstract SY26-02:Sherlock-Lung: Tracing lung cancer mutational processes in never smokers (2019) (0)
- Genome-wide association study of germline variants and breast cancer-specific mortality (2019) (0)
- Abstract 3570: Germline structural variant detection with variation graphs (2017) (0)
- TheUBC-40UrothelialBladderCancercellline index:agenomicresourceforfunctionalstudies (2015) (0)
- The UBC-40 Urothelial Bladder Cancer cell line index: a genomic resource for functional studies (2015) (0)
- Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan (2020) (0)
- Abstract 287: Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue (2014) (0)
- inefficient for lncRNAs predominantly co-transcriptional in the human genome but Deep sequencing of subcellular RNA fractions shows splicing to be (2013) (0)
- Prognostic Impact of Pre-Transplant Chromosomal Aberrations Detected By SNP-Array in Patients Undergoing Unrelated Donor Hematopoietic Cell Transplant for Acute Myeloid Leukemia (2020) (0)
- Genetic Variation in Host Defenses and Viral Infections (2005) (0)
- Abstract PO-055: Molecular characterization of papillary thyroid cancer in relation to ionizing radiation dose following the Chernobyl accident (2021) (0)
- Emmanuel albicans Candida Monocytes in Response to Defense Molecules in Normal Human Expression of Genes Encoding Innate Host (2005) (0)
- Abstract IA22: A comprehensive and integrated approach to identify factors associated with aggressive prostate cancer in African-Americans: The RESPOND Study (2020) (0)
- Acknowledgement to Reveiwers (2011) (0)
- Abstract 4732: Association between genetic variants in the 8q24 cancer risk regions and circulating levels of androgens and sex-hormone binding globulin (2010) (0)
- Abstract IA12: A prospective cohort study embedded into integrated health care systems in the US to study cancer etiology, prevention, and early detection (2020) (0)
- Introduction: sifting through the characterization of hematologic malignancies. (2013) (0)
- The renal lineage factor PAX8 controls oncogenic signalling in kidney cancer (2022) (0)
- Abstract 221: Inherited variants at 3q13.33 and 3p24.1 influences risk of diffuse large B-cell lymphoma (2018) (0)
- Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (2018) (0)
- Abstract 5072: Meta-analysis of genome-wide association studies identifies novel susceptibility loci for follicular lymphoma (2014) (0)
- Genetic variants associated with PDAC also contribute to chronic pancreatitis susceptibility (2015) (0)
- Abstract 2553: Characterization of rare germline variants in somatically mutated melanoma genes in melanoma-prone families. (2013) (0)
- Abstract 935: Genetic variants in chromosome 6p21.3 and risk of non-Hodgkin lymphoma (2010) (0)
- Mendelian randomization study of age at menarche and age at 1 menopause and the risk of colorectal cancer (2018) (0)
- Abstract LB-404: Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin levels in postmenopausal women (2010) (0)
- Abstract 1441: Genetic determinants of PSA levels improve prostate cancer screening (2022) (0)
- Abstract P3-12-05: Genetic Variation in Prolactin and Prolactin Receptor, and Relationships with Serum Prolactin Levels and Breast Cancer Risk (2010) (0)
- Textbook of Pediatric HIV Care: Medical issues related to the care for HIV-infected children in the home, day care, school, and community (2006) (0)
- Pre-Transplant Clonal Mosaicism Is Associated with Increased Relapse and Lower Survival in Acute Lymphoblastic Leukemia Patients Undergoing Allogeneic Hematopoietic Cell Transplant (2020) (0)
- HGV2012: Leveraging Next‐Generation Technology and Large Datasets to Advance Disease Research (2013) (0)
- Genome-wide association study of germline variants and breast cancer-speci fi c mortality (2019) (0)
- Original Contribution Genetic Variation in the Sodium-dependent Vitamin C Transporters, SLC23A1, and SLC23A2 and Risk for Preterm Delivery (2006) (0)
- Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (2017) (0)
- Genome-wide association study confirms lung cancer susceptibility loci on chromosome 5p15 and 15q25 in an African-American population (2016) (0)
- Abstract 223: A meta-analysis of genome-wide association studies of multiple myeloma among African Americans (2018) (0)
- Abstract 2753: Interactions between PAH exposure and genetic polymorphisms on BaP-DNA adducts in a NYC cohort of African American and Dominican mothers and newborns (2011) (0)
- Abstract NG03: Multiethnic prostate cancer GWAS meta-analysis identifies novel variants, improves genetic risk prediction across populations, and informs biological mechanisms of prostate cancer (2021) (0)
- Abstract 1587: Integrated renal cancer post-GWAS functional studies implicates the SWI/SNF DPF3 gene on 14q24 risk locus (2019) (0)
- Abstract #5613: Functional analysis of the promoter of the beta-microseminoprotein gene MSMB demonstrates the importance of a single nucleotide polymorphism in prostate cancer susceptibility (2009) (0)
- Abstract 4626: Genetic susceptibility to diffuse large B-cell lymphoma in a pooled study of three Eastern Asian populations (2015) (0)
- Null Results in Brief Polymorphisms in Interleukin -2, -6, and -10 Are Not Associated with Gastric Cardia or Esophageal Cancer in a High-Risk Chinese Population (2004) (0)
- Genome-wide homozygosity and risk of four non-Hodgkin lymphoma subtypes (2021) (0)
- Genome-wide association study of meningioma as a subsequent neoplasm: A report from the Childhood Cancer Survivor Study (CCSS) and St. Jude Lifetime Cohort (SJLIFE). (2016) (0)
- PLOS ONE Polymorphisms of an Innate Immune Gene, Toll-Like Receptor 4, and Aggressive Prostate Cancer Risk: A Systematic Review and Meta-analysis (2014) (0)
- The new sequencer on the block: comparison of Life Technology’s Proton sequencer to an Illumina HiSeq for whole-exome sequencing (2013) (0)
- Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma (2014) (0)
- Common germline polymorphisms associated with breast cancer-specific survival (2015) (0)
- the Breast Cancer Association Consortium Five Polymorphisms and Breast Cancer Risk : Results from Updated (2009) (0)
- Incident disease associations with mosaic chromosomal alterations on autosomes, X and Y chromosomes: insights from a phenome-wide association study in the UK Biobank (2021) (0)
- ION TORRENT LIBRARY PREPARATION PROCESS USING KAPABIOSYSTEMS LIBRARY QUANTIFICATION KIT SIGNIFICANTLY INCREASES QUANTITATIVE SENSITIVITY AND IMPROVES SAMPLE POOLING FOR MULTIPLEXED SEQUENCING (2011) (0)
- Erratum to: The UBC-40 Urothelial Bladder Cancer Cell Line Index: a genomic resource for functional studies (2015) (0)
- Abstract 2966: A genome-wide scan identifies a new locus associated with pediatric rhabdomyosarcoma (2018) (0)
- Gene-environment interactions in CRC risk loci 1 Title: Characterization of gene-environment interactions for colorectal cancer susceptibility loci Authors and Affiliations: (2012) (0)
- The transition from discovery by genome-wide association studies to validation of clinical risk models: Where are we, what will it take, and when can we expect to be there? (2010) (0)
- Genetic predisposition to mosaic Y chromosome loss in blood (2019) (0)
- Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis (2021) (0)
- The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer (2019) (0)
- Newborns American, Dominican, and Caucasian Mothers and Genetic Polymorphisms on PAH-DNA Adducts in African Assessment of Interactions between PAH Exposure and Updated Version (2008) (0)
- Erratum to: A genome-wide association study of prostate cancer in West African men (2013) (0)
- Detectable chromosome X mosaicism in males is rarely tolerated in peripheral leukocytes (2021) (0)
- Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (0)
- A common 8q24 variant and prostate cancer in a large nested case-control study. (2006) (0)
- Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (0)
- Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility (2018) (0)
- Abstract 1182: Association of prostate cancer candidate genes with overall and aggressive prostate cancer in men of African ancestry (2023) (0)
- Diabetes and risk of pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium (2012) (0)
- Germ-Line Genetic Variations in TP53 and Risk for Pediatric Acute Lymphoblastic Leukemia. (2004) (0)
- Abstract 943: A comprehensive examination of breast cancer risk loci in African American women (2014) (0)
- Abstract 1170: MicroRNA gene polymorphisms in cancer susceptibility loci 5p12, 8q24 and 11q13 (2011) (0)
- Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations (2016) (0)
- MP23-04 POST-GWAS FUNCTIONAL CHARACTERIZATION OF THE 12P11.23 RENAL CANCER SUSCEPTIBILITY LOCUS (2014) (0)
- GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer (2017) (0)
- Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases (2015) (0)
- Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma (2012) (0)
- Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (2019) (0)
- 2015 Reviewer Acknowledgments (2016) (0)
- Abstract 2568: Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women (2016) (0)
- C-107 Towards an Understanding of the Underlying Architecture of Genetic Susceptibility to Cancer (2014) (0)
- Abstract PR06: Research on prostate cancer in men of African ancestry: Defining the roles of genetics, tumor markers, and social stress (2020) (0)
- Abstract PL04-01: The promise of GWAS studies to assess cancer prevention (2012) (0)
- Oncogenic CDK13 mutations impede nuclear RNA surveillance (2023) (0)
- Increased Frequency of Mosaic Chromosomal Alterations in Peripheral Blood Samples of Sub-Saharan African Children with Endemic Burkitt Lymphoma (2022) (0)
- Author Correction: Inferring structural variant cancer cell fraction (2022) (0)
- Shared heritability and functional enrichment across six solid cancers (2019) (0)
- Title: Sex Specific Associations in Genome Wide Association Analysis of Renal Cell Carcinoma (2019) (0)
- Erratum to: A genome-wide association study of prostate cancer in West African men (2014) (0)
- Abstract 683: Identification of common germline variants associated with pediatric rhabdomyosarcoma survival: A report from the Children's Oncology Group (COG) (2022) (0)
- Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction (2021) (0)
- cell disease gene and risk for symptomatic stroke in sickle VCAM1 Variants in the (2011) (0)
- #643 Mannose binding protein variant alleles are associated with rheumatic disorders in patients with chronic granulomatous disease (1998) (0)
- Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (0)
- Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (0)
- Functional Consequences of Genetic Variation across the Entire MBL2 Locus: Possible Identification of 3′ SNPs That Could Modify Circulating Levels of MBL. (2004) (0)
- EstimationofAbsolute Risk for ProstateCancer UsingGeneticMarkers and FamilyHistory (2009) (0)
- Identification and characterisation of novel associations in the CASP 8 / ALS 2 CR 12 region 1 on chromosome 2 with breast cancer risk 2 3 (2014) (0)
- Gene editing reveals the effect of thousands of variants in a key cancer gene (2018) (0)
- Next generation modeling in GWAS: comparing different genetic architectures (2014) (0)
- Germline Genetic and Treatment-Related Risk Factors for Diabetes Mellitus in Survivors of Childhood Cancer: A Report From the Childhood Cancer Survivor Study and St Jude Lifetime Cohorts. (2022) (0)
- Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women (2021) (0)
- Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk (2018) (0)
- Scanning for clues to better use selective estrogen receptor modulators. (2013) (0)
- Gene-environment interactions on mental development in African American, Dominican, and Caucasian Mothers and Newborns (2011) (0)
- Abstract 5066: Generalizability of established prostate cancer risk variants in men of African ancestry (2014) (0)
- Abstract 5061: Post-GWAS functional characterization of the 12p11.23 renal cancer susceptibility locus implicates BHLHE41 (2014) (0)
- 1 LIN 28 B polymorphisms influence susceptibility to epithelial ovarian cancer (2011) (0)
- Fine-mapping identifies two additional susceptibility 9q31.2. (2015) (0)
- Proceedings of the fifth international Molecular Pathological Epidemiology (MPE) meeting (2022) (0)
- 1042 Association between PDL1 variants and muscle invasive bladder cancer prognosis (2016) (0)
- EP4 Advanced Educational Session: Whole Genome Genotyping. (2007) (0)
- Genome-Wide a ssociation Studies and " t he a rt of the Soluble" (2010) (0)
- SeqPlus sequencing methodology enables robust whole-genome sequencing, true variant detection, and novel genomic insights from archival esophageal carcinoma FFPE samples. (2019) (0)
- Fine mapping of 14q24.1 breast cancer susceptibility locus (2011) (0)
- Abstract 688: Multi-stage exome sequencing study of 17,546 aggressive and non-aggressive prostate cancer cases (2022) (0)
- 163 Variants in Interferon-α Pathway Genes and Response to Treatment of Chronic Hepatitis C (2008) (0)
- Host immunogenetics and control of human herpesvims-8 infection. Commentary (2006) (0)
- Pklr Variants Associated with Acute Pain in Sickle Cell Disease Influence ATP Concentrations in Red Blood Cells (2022) (0)
- Abstract 2927: MicroRNA binding site polymorphisms influence ovarian cancer risk in the collaborative oncological gene-environment study (2012) (0)
- Polymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4 (2013) (0)
- Meta-analysis of new genome-wide association studies of colorectal cancer risk (2011) (0)
- Abstract 607: Clonal hematopoiesis alters blood cell counts in the UK Biobank (2019) (0)
- Genetic Susceptibility Markers of Multiple Myeloma in African-Americans (2014) (0)
- Abstract 1297: Genetic reclassification of prostate-specific antigen levels for personalized prostate cancer screening (2017) (0)
- Abstract 1867: DNA repair gene polymorphisms and tobacco smoking and the risk of colorectal adenoma (2010) (0)
- Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis (2023) (0)
- Abstract 3974: A comprehensive resequence-analysis of 250kb region of 8q24 in Africans (2012) (0)
- Illumina® - based multiplexed genotyping indicates a role for altered DNA repair and genomic maintenance in susceptibility to benzene toxicity (2006) (0)
- Abstract 1658: Post-GWAS genetic and functional studies for bladder cancer: An uncommon protective synonymous coding variant within the UGT1A6 gene explains the GWAS signal and affects cellular detoxification (2012) (0)
- Abstract 3369: Mosaic chromosome X copy-number aberrations in leukocytes of never-smoking lung cancer patients: The Female Lung Cancer Consortium in Asia (FLCCA) (2018) (0)
- Study Case-Control metabolism on the risk of non-Hodgkin lymphoma: NCI-SEER Gene-nutrient interactions among determinants of folate and one-carbon (2013) (0)
- Erratum to: The UBC-40 Urothelial Bladder Cancer cell line index: a genomic resource for functional studies (2016) (0)
- Body mass index and breast cancer survival (2017) (0)
- Abstract 4871: Whole-exome sequencing identifies a high frequency of germline deleterious variants in cancer predisposition genes in individuals with osteosarcoma (2017) (0)
- Germline variation at 8q24 and prostate cancer risk in men of European ancestry (2018) (0)
- Role of one-carbon metabolizing pathway genes and gene–nutrient interaction in the risk of non-Hodgkin lymphoma (2013) (0)
- Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays (2018) (0)
- Association analyses identify 31 new risk loci for colorectal cancer susceptibility (2019) (0)
- Genome-Wide Association Study in Irradiated Childhood Cancer Survivors Identifies HTR2A for Subsequent Basal Cell Carcinoma (2019) (0)
- Abstract PL02-05: Genome-wide association studies in cancer: What have we found and what next (2010) (0)
- Abstract 3122: A functionalPOT1variant and risk of thyroid subsequent malignant neoplasm: A report from the Childhood Cancer Survivor Study (2019) (0)
- Host Immunogenetic Single Nucleotide Polymorphisms (SNPs) Predict Overall Survival in Small Lymphocytic Lymphoma. (2006) (0)
- Fine-mapping identifies multiple prostate cancer risk loci on 5p15 some associating with TERT expression (2013) (0)
- The scope of possible combination therapy with immunotherapy and targeted therapy. (2017) (0)
- Inappropriate Citation of Vaccine Article. (2020) (0)
- Abstract 14: Body mass index and type 2 diabetes genetic risk scores and endometrial cancer risk among women of European ancestry. (2012) (0)
- Reply to ‘Mosaic loss of chromosome Y in leukocytes matters’ (2018) (0)
- Abstract 3863: Fine mapping and comprehensive resequencing analysis of a region of chromosome 11q13 reveals multiple independent loci associated with prostate cancer (2010) (0)
- Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in CDKN2A and Pancreatic Cancer. (2022) (0)
- Xenobiotic Metabolizing Genes, Meat-Related Exposures, and Risk of Advanced Colorectal Adenoma (2011) (0)
- Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (2019) (0)
- Common variants in breast cancer risk loci predispose to distinct tumor subtypes (2022) (0)
- Publisher Correction: Mendelian randomisation study of the relationship between vitamin D and risk of glioma (2019) (0)
- Adenovirus and Marrow Transplantation in Children (2000) (0)
- Limited evidence that cancer susceptibility regions are preferential targets for somatic mutation (2015) (0)
- JAK2 V617F Mutation and Associated Chromosomal Alterations Involving JAK2 in Pre-HCT Blood Samples and Transplant Outcomes in Myelofibrosis Subtypes (2022) (0)
- Abstract A105: Dietary quercetin, quercetin‐gene interaction, metabolic gene expression in lung tissue, and lung cancer risk (2010) (0)
- Abstract SY34-01: Genome-wide association studies in cancer: A step in the right direction (2012) (0)
- Abstract 4613: Cross-ancestry genome-wide association study identifies six new loci for breast cancer in women of African and european ancestry (2020) (0)
- Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia (2018) (0)
- Genome-wide association study of circulating vitamin D – binding protein 1 – 4 (2014) (0)
- Abstract 4733: Gene-set analysis of colon cancer genome-wide association data: Identification of the TGF-beta pathway (2010) (0)
- Abstract LB-337: Synergistic effects of twelve common genetic polymorphisms and smoking habits on absolute risk of bladder cancer (2012) (0)
- A comprehensive database for GWAS¬identified human genetic variants: an update of GWASdb (2015) (0)
- Abstract 3508: Association between clonal hematopoiesis and risk of prostate cancer in a large sample of African ancestry men (2023) (0)
- A pleiotropic variant in DNAJB4 is associated with multiple myeloma risk (2022) (0)
- Diagnosis of invasive fungal infections in transplant recipients (1998) (0)
- Time to first cigarette and its impact on lung tumorigenesis (2022) (0)
- #644 Immunologic parameters as predictors for specific infections in children with cancer (1998) (0)
- Contents Vol 3, 2010 (2011) (0)
- Abstract 2682: Analysis of polygenic risk score interaction with coal use and risk of lung adenocarcinoma among never-smoking women in Asia (2019) (0)
- Function and Aggressive Disease The 19 q 12 Bladder Cancer GWAS Signal : Association with Cyclin E Updated (2014) (0)
- Subject Index Vol 3, 2010 (2011) (0)
- Null Results in Brief Cancer Epidemiology , Biomarkers & Prevention A Genome-Wide Association Study of Prognosis in Breast Cancer (2010) (0)
- Environmental and genetic risk factors for t(14;18) subtypes of diffuse large B-cell lymphoma in a population-based, case-control study (2007) (0)
- Abstract 941: Exome sequencing identifiedPOT1, a telomere shelterin gene, as a major susceptibility gene for familial cutaneous malignant melanoma (2014) (0)
- Genetic Variation in TERF1 but Not TERF2 Is Associated with Aplastic Anemia Risk. (2005) (0)
- Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selection (2023) (0)
- Breast Cancer Risk in Women from Ghana Carrying Rare Germline Pathogenic Mutations: A Resource for Genetic Counseling of West African Women (2021) (0)
- Mutations and Polymorphisms Influencing Hemolysis in Hemoglobin Genes and Risk of Pulmonary Hypertension in Sickle Cell Disease: Effect of Hemoglobin SC. (2006) (0)
- Abstract B129: Xenobiotic metabolizing genes, meat intake and risk of advanced colorectal adenoma (2008) (0)
- Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data (2012) (0)
- From copy number alterations to structural variants: the evolutionary cascade of papillary renal cell carcinomas (2018) (0)
- Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer. (2016) (0)
- Abstract 924: Possible joint effects between single nucleotide polymorphisms in inflammation genes and serum androgen levels on risk of prostate cancer (2010) (0)
- Immunoglobulin receptor polymorphisms in stroke and sickle cell disease (2000) (0)
- Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility (2021) (0)
- Selenoproteins and bladder cancer risk: A case-control study (2010) (0)
- Abstract 2783: A novel functional variant is associated with regulation of the prostate stem cell antigen (PSCA) gene and bladder cancer risk in males (2011) (0)
- Influence of obesity-related risk factors in the aetiology of glioma (2018) (0)
- Viral coinfection analysis using a MinHash toolkit (2019) (0)
- Abstract IA-11: An exception to the rule: A coding functional variant at a pancreatic cancer GWAS locus (2020) (0)
- Abstract 2320: Evaluating a polygenic risk score for breast cancer in women of African ancestry (2020) (0)
- Low predictive ability of low penetrance genetic variants for bladder cancer risk among non-smokers (2012) (0)
- Abstract 1443: Identification of enhancer elements at kidney cancer susceptibility loci using MPRA (2017) (0)
- Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (2021) (0)
- Abstract 4729: A genome-wide association study of ovarian cancer prognosis identifies a novel locus for aggressive serous cancer on 19p13 (2010) (0)
- Abstract 2970: Multiple new susceptibility loci identified in genome-wide association study of Ewing sarcoma (2018) (0)
- Abstract 925: Common variants in genes related to immune response and childhood leukemia risk (2010) (0)
- Modifiers of risk for infectious complications of cancer therapy in children: The long road ahead (2007) (0)
- A high-risk genetic profile for premature menopause (PM) in childhood cancer survivors (CCS) exposed to gonadotoxic therapy: A report from the St. Jude Lifetime Cohort (SJLIFE) and Childhood Cancer Survivor Study (CCSS). (2017) (0)
- Abstract 1166: APOBEC deaminases compete with tobacco smoking mutagenesis and affect age at onset of lung cancer (2023) (0)
- Genome-wide association study of endometrial cancer in E2C2 (2013) (0)
- ImageBox3: No-Server Tile Serving to Traverse Whole Slide Images on the Web (2022) (0)
- De Novo and Therapy-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome: Similarities and Differences in SNP-Array Detected Chromosomal Aberrations in Pre-Transplant Blood Samples (2019) (0)
- The riddle of intergenic disease-associated loci (2012) (0)
- Germline Genetic Variants and Pediatric Rhabdomyosarcoma Outcomes: A Report from the Children's Oncology Group. (2023) (0)
- Abstract 1270: Vitamin E related genetic variants and prostate cancer risk: A Mendelian randomization analysis (2017) (0)
- Title : Powerful SNP Set Analysis for Case-Control Genome Wide Association Studies Running Title : Powerful SNP Set Analysis (2010) (0)
- Abstract 4831: Additive and multiplicative gene-environment interactions for colorectal cancer risk. (2013) (0)
- Abstract 4629: Multiple myeloma susceptibility loci examined in African and European ancestry populations (2015) (0)
- Genome-wide association study of endometrial cancer in E2C2 access benefits you. Your story matters (2014) (0)
- A genome-wide association study of breast cancer in women of African ancestry (2012) (0)
- HOST GENETIC VARIATION IN THE TNF AND NF‐ĸB PATHWAYS AND PROGNOSIS IN MANTLE CELL LYMPHOMA: AN ANALYSIS OF 2 STUDIES (2017) (0)
- Nucleotide excision repair polymorphisms and risk of colorectal adenoma (2004) (0)
- Short Communication Variants of the IL8 and IL8RB Genes and Risk for Gastric Cardia Adenocarcinoma and Esophageal Squamous Cell Carcinoma (2004) (0)
- GASTROINTESTINAL MANIFESTATIONS OF CONGENITAL ACQUIRED IMMUNODEFICIENCY SYNDROME IN CHEIDREN (1987) (0)
- Abstract 3118: The MBL2 “LYQA Secretor” Haplotype is an Independent Predictor of Postoperative Myocardial Infarction (MI) in Caucasians Undergoing Coronary Artery Bypass Graft (CABG) Surgery (2006) (0)
- Genetic risk variants associated with in situ breast cancer (2015) (0)
- COVID-19 SeroHub, an online repository of SARS-CoV-2 seroprevalence studies in the United States (2022) (0)
- 289 Post-GWAS functional characterization of the 12p11.23 renal cancer susceptibility locus (2014) (0)
- B-Cell NHL Subtype Risk Associated with Autoimmune Conditions and PRS (2022) (0)
- Abstract B42: A comprehensive resequence-analysis of 250kb region of 8q24 in Africans (2011) (0)
- Abstract LB-336: Association of variant rs2046210 at 6q25.1 (ESR1) with breast cancer risk suggests heterogeneity by E-cadherin tumor tissue expression (2012) (0)
- Genetic Variation of Tumor Necrosis Factor-alpha (TNF) and Risk of Breast Cancer (2006) (0)
- Sex specific associations in genome wide association analysis of renal cell carcinoma (2019) (0)
- An unusual suspect: an uncommon human-specific synonymous coding variant within the UGT1A6 gene explains a GWAS signal and protects against bladder cancer (2011) (0)
- Practice of Epidemiology Likelihood Ratio Test for Detecting Gene ( G )-Environment ( E ) Interactions Under an Additive Risk Model Exploiting G - E Independence for Case-Control Data (2012) (0)
- Linkage disequlibrium (LD) representation of the SERPINA5 gene. (2013) (0)
- Severe reactions to trimethoprim sulfamethoxazole in children infected with the human immunodeficiency virus (1989) (0)
- LAB-MOLECULAR EPIDEMIOLOGY (2012) (0)
- Joint effects of general population polygenic risk scores (PRS) and radiation treatment on subsequent neoplasm risk among childhood cancer survivors: A report from the Childhood Cancer Survivor Study (CCSS). (2022) (0)
- Observational and genetic associations between cardiorespiratory fitness and cancer: a UK Biobank and international consortia study (2023) (0)
- Abstract 1271: Genetic variants in the 16q24.3 region of melanocortin-1-receptor (MC1R)and prostate cancer risk: A Mendelian randomization analysis of 39,000 cases and 25,000 controls (2017) (0)
- Abstract 28: Resequence-analysis of 166kb KITLG region in eamilial testicular germ cell tumors (2011) (0)
- Genome-wide association study of susceptibility loci for breast cancer in Sardinian population (2015) (0)
- Proceedings of the fifth international Molecular Pathological Epidemiology (MPE) meeting (2019) (0)
- Abstract 826: Large-scale genome-wide association study identifies multiple novel germline susceptibility variants associated with bladder cancer risk (2021) (0)
- GST Polymorphisms and Atopic Dermatitis in an Inner City Cohort (2009) (0)
- DNA methylation age in paired tumor and adjacent normal breast tissue in Chinese women with breast cancer (2023) (0)
- ImmunoTyper-SR: A computational approach for genotyping immunoglobulin heavy chain variable genes using short-read data. (2022) (0)
- 1284-P: Genetic and Lifestyle Associations with Cardiometabolic Traits and Diabetes Risk Factors in Ethnically Diverse Africans (2022) (0)
- Author Correction: The evolutionary history of 2,658 cancers (2023) (0)
- Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (2019) (0)
- Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2019) (0)
- Probing the diabetes and colorectal cancer relationship using gene-environment interaction analyses (2022) (0)
- The genomic and epigenomic evolutionary history of papillary renal cell carcinomas (2020) (0)
- Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2019) (0)
- HGV2009 meeting: bigger and better studies provide more answers and more questions (2010) (0)
- Insulin-like growth factors and risk of testicular germ cell tumors (2007) (0)
- Abstract 1302: Genome-wide association study of glioma reveals specific differences in genetic susceptibility to glioblastoma and non-glioblastoma (2017) (0)
- Cancer Epidemiology in the 21 st Century Transforming Epidemiology for 21 st Century Medicine and Public Health (2013) (0)
- Abstract A88: Genome-wide association study identifies variants in several loci associated with circulating vitamin E levels (2010) (0)
- Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls (2018) (0)
- Genetic and treatment risks for diabetes mellitus (DM) in survivors of childhood cancer: A report from the Childhood Cancer Survivor Study (CCSS) and St. Jude Lifetime (SJLIFE) cohorts. (2021) (0)
- Promoter variants in the MSMB gene associated with prostate cancer regulate MSMB/NCOA4 fusion transcripts (2012) (0)
- Association between a Polygenic Risk Score for Multiple Myeloma Risk and Overall Survival (2019) (0)
- vRare VCAM1 Promoter Haplotypes Prevalent in African Americans Are Hyperinducible. (2006) (0)
- Abstract 811: Mosaic chromosome Y loss is not associated with testicular germ cell tumor risk (2016) (0)
- Variants in the TLR 4 and TLR 6-1-10 Genes and Prostate Cancer Risk . Results Based on Pooled Analysis from Three Independent Studies (2010) (0)
- Blood 1 J U L Y 2 0 1 0 I V O L U M E 1 1 5 , N U M B E R 2 6 (0)
- Gene expression profiling identifies two chordoma subtypes associated with distinct molecular mechanisms and clinical outcomes. (2022) (0)
- Abstract 4722: Evaluation of common genetic variation in 1,300 cancer-related candidate genes and endometrial cancer risk (2010) (0)
- Human Leukocyte Antigen Contributes to Childhood Endemic Burkitt Lymphoma in Eastern Africa: A Case-Control Association Study (2022) (0)
- Genetic variation and hematopoietic stem cell transplantation: expansion of the paradigm (2003) (0)
- Abstract 4680: Exploring the relationships between genetic variants within the UGT1A locus, cellular detoxification and risk of bladder cancer (2011) (0)
- Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer (2019) (0)
- Abstract 2203: Pathway analysis of genome-wide association study data highlights taste transduction and metabolic pathways and esophageal squamous cell carcinoma susceptibility (2014) (0)
- Abstract 1475: Uncovering the functional variants and target genes of the 7q32 pancreatic cancer risk locus (2022) (0)
- Interpretable, non-mechanistic forecasting using empirical dynamic modeling and interactive visualization (2022) (0)
- Genomics and Chip Technology (2006) (0)
- Abstract 2542: Evidence for large somatic structural events detected as autosomal genetic mosaicism in GWAS data. (2013) (0)
- Integrated Analysis of Co-expression and Exome Sequencing to Prioritize Susceptibility Genes for Familial Cutaneous Melanoma. (2022) (0)
- Incorporating Genetic Determinants of Prostate-Specific Antigen Levels Improves Prostate Cancer Screening (2022) (0)
- A Meta-Analysis Of Genome-Wide Association Studies Of Multiple Myeloma In Cases and Controls Of European Origin Identifies a Risk Locus In 12q23.1 (2013) (0)
- Germline Genes Specific to Chronic Lymphocytic Leukemia (CLL) and Genes Common to CLL, Lymphoplasmacytic Lymphoma/Waldenstrom's Macroglobulinemia, and Other Non-Hodgkin Lymphomas Are Important in Susceptibility (2008) (0)
- Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding. (2023) (0)
- Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia | NOVA. The University of Newcastle's Digital Repository (2014) (0)
- Abstract 2850: Endometrial cancer and genetic variation in PTEN, PIK3CA, AKT1, MLH1, and MSH2: results and replication in two case-control studies (2010) (0)
- Room 501 A-C, Los Angeles Convention Center Epidemiology 11 Inflammation, Immunity, and Novel Pathways (2007) (0)
- Cross-cancer genome-wide association analysis of lung, ovary, breast, prostate and colon cancer identifies a novel cancer locus at 1q22 (2015) (0)
- Replication of Five Prostate Cancer Loci Identi fi ed in an Asian Population — Results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3) Epidemiology,Biomarkers&Prevention (2011) (0)
- Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses (2020) (0)
- OP-JNCI190094 749..750 (2019) (0)
- Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (2019) (0)
- Abstract 2333: Possible prediction of tumor specific checkpoint inhibitor response based on TCGA somatic mutation load (2016) (0)
- Abstract 2077: Genome-wide association study identifies theGLDC/IL33locus associated with survival of osteosarcoma patients (2018) (0)
- Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank (2018) (0)
- Title : Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (0)
- Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2018) (0)
- Regions Bound by 119 Human Transcription Factors Sequence Features and Chromatin Structure around the Genomic Material Supplemental (2012) (0)
- Abstract 1202: Genetically inferred telomere length is associated with clonal copy number alterations in peripheral leukocytes (2020) (0)
- Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (2019) (0)
- Polymorphisms in cell cycle pathway genes and risk of non-Hodgkin’s lymphoma (2005) (0)
- BRCA1 mutations increase risk of prostate cancer (2012) (0)
- Protein-altering germline mutations implicate novel genes related to lung cancer development (2020) (0)
- Genome-Wide Analyses Characterize Shared Heritability Among Cancers and Identify Novel Cancer Susceptibility Regions. (2023) (0)
- Infections in Oncology GRANULOCYTE TRANSFUSIONS : TIME FOR A SECOND LOOK (2012) (0)
- Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men (2020) (0)
- Abstract 4726: Genetic determinants of serum retinol: A genome-wide association study (2011) (0)
- Polymorphisms in DNA repair genes and benzene hematotoxicity (2005) (0)
- Common Polymorphisms of the Interleukin-6 and Chitotriosidase Genes Are Associated with the Risk for Infection with Gram-Negative Bacteria in Children Undergoing Therapy for Acute Myeloid Leukemia. (2004) (0)
- Detectible mosaic truncating PPM1D mutations, age and breast cancer risk (2019) (0)
- Immune gene expression profiling reveals heterogeneity in luminal breast tumors (2019) (0)
- lymphoma survival Prognostic significance of host immune gene polymorphisms in follicular (2013) (0)
- Polymorphism of genes in the lipid metabolism pathway and the risk of biliary tract cancers: a population-based study in Shanghai, China (2005) (0)
- Human Variation 2.0: Using GWAS to Probe Intermediate Phenotypes (2013) (0)
- Abstract 3110: The aging genome: Genetic mosaicism and its relationship to cancer (2012) (0)
- Chromosomal Aberrations in Pre-HCT Blood Samples and Outcomes after Transplantation in Patients with Myelofibrosis (2020) (0)
- Selected issues in pediatric infection with human immunodeficiency virus (1989) (0)
- Abstract 865: Genomic and evolutionary classification of lung cancer in never smokers from the Sherlock-Lungstudy (2021) (0)
- Abstract 944: Translational implications of the 19q12 bladder cancer GWAS signal for aggressive bladder cancer (2014) (0)
- Genome-Wide Association Study Identifies an Immune-Related Etiology for Severe Aplastic Anemia (2019) (0)
- An R Package for Calculating Linkage Disequilibrium [R package LDlinkR version 1.0.2] (2020) (0)
- Genome-wide association study identifies novel loci associated with osteosarcoma (2013) (0)
- Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia (2014) (0)
- Abstract 5722: The mutational signatures of 100,477 targeted sequenced tumors (2023) (0)
- Abstract A111: Genetic variations in five estrogen metabolizing genes and endometrial cancer risk (2008) (0)
- Abstract A1-31: Molecular characteristics and predictors of poor prognosis in sporadic clear cell renal cancer among central/eastern European and United States patients (2015) (0)
- Abstract 4610: Functional characterization of a multicancer risk locus on chr5p15.33 reveals regulation ofTERTby ZNF148 (2015) (0)
- Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (0)
- Germline Single Nucleotide Polymorphisms (SNPs) in IL1A , IL6 , IL10 , and IFNGR2 in Combination with Clinical with Demographic Factors Predict Overall Survival in Diffuse Large B-Cell Lymphoma (DLBCL). (2006) (0)
- Abstract 58: Associations between breast cancer susceptibility markers and terminal duct lobular unit involution in normal breast tissues among women from the Susan G. Komen for the Cure® Tissue Bank. (2012) (0)
- ABO blood group and risk of epithelial ovarian cancer within the Ovarian Cancer Association Consortium (2012) (0)
- Genome-wide association study of glioma and meta-analysis (2012) (0)
- Transcriptome-Wide Association Analysis Identifies Novel Candidate Susceptibility Genes for Prostate-Specific Antigen Levels in Men Without Prostate Cancer (2023) (0)
- Abstract 3436: Pan-cancer analysis of the HIF-transcriptional pathway and its association with genetic susceptibility to cancer (2020) (0)
- Abstract PR05: A meta-analysis of genome-wide association study and eQTL analysis of multiple myeloma among African Americans (2020) (0)
- Comprehensive Investigation of White Blood Cell and Gene Expression Profiles As Risk Factors for Multiple Myeloma in African Americans (2019) (0)
- Abstract SY25-01: Identification of enhancer elements at kidney cancer susceptibility loci using genome-wide approaches in which post-GWAS functional studies implicate the SWI/SNF DPF3 gene for the 14q24 risk locus (2019) (0)
- Human variation 2.0: using GWAS to probe intermediate phenotypes. (2013) (0)
- Abstract 3273: rkmh: A MinHash toolbox for analyzing HPV coinfections (2018) (0)
- Breast cancer risks associated with missense variants in breast cancer susceptibility genes (2022) (0)
- Abstract 3379: Predictors of mosaic chromosome Y loss and associations with mortality in 223,338 men of the UK Biobank (2018) (0)
- Abstract PR-6: Variation in VDR pathway genes and renal cancer risk (2008) (0)
- Breast cancer risk in women from Ghana carrying rare germline pathogenic mutations. (2022) (0)
- A genome-wide association study of prostate cancer in West African men (2013) (0)
- Correction: Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2017) (0)
- Publisher Correction: Mendelian randomisation study of the relationship between vitamin D and risk of glioma (2019) (0)
- HBB rs334, ABO R s8176703 and Plasmodium Falciparum Positivity at Enrollment Are Independently Associated with Lower Risk for Endemic Burkitt Lymphoma in Uganda, Tanzania, Kenya, and Malawi (2022) (0)
- DNA repair and related genes Risk of Non-Hodgkin lymphoma (NHL) in relation to germline variation in (2013) (0)
- Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry (2023) (0)
- Prevention and Epidemiology LIN 28 B Polymorphisms Influence Susceptibility to Epithelial Ovarian Cancer (2011) (0)
- FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. (2023) (0)
- Cancer-om-atics: Multilevel interpretation of cancer genome data (2011) (0)
- A UVB-responsive common variant at chr7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor gene (AHR) (2021) (0)
- Author Correction: Patterns of somatic structural variation in human cancer genomes (2020) (0)
- Abstract 1272: Prostate cancer risk and vitamin a related genetic variants in the PRACTICAL Consortium (2017) (0)
- Null Results in Brief Association of CYP 1 B 1 Haplotypes and Breast Cancer Risk in Caucasian Women (2009) (0)
- A genome-wide association study of renal cell carcinoma among African Americans Running title: RCC GWAS among African Americans (2013) (0)
- Abstract 1187: Comparison of intra-tumor heterogeneity and clonal evolution across lung cancer subtypes by multi-region whole genome sequencing (2018) (0)
- Principles of High-Quality Genotyping (2016) (0)
- Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (2023) (0)
- CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers (2021) (0)
- Brief report PRRC2A and BCL2L11 gene variants influence risk of non-Hodgkin lymphoma: results from the InterLymph consortium (2012) (0)
- Abstract 32: PER3 gene in association with plasma melatonin in Caucasian men. (2012) (0)
- Rapid development of multiple liver metastases in a child with medullary carcinoma of the kidney and sickle cell trait (2000) (0)
- Abstract 1298: Genetic variants related to longer telomere length are associated with increased risk of renal cell carcinoma (2017) (0)
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Other Resources About Stephen Chanock
What Schools Are Affiliated With Stephen Chanock?
Stephen Chanock is affiliated with the following schools:
- University of British Columbia
- Albert Einstein College of Medicine
- University of South Florida
- Chinese Center for Disease Control and Prevention
- Lund University
- University of Washington
- University of Miami
- University of Cambridge
- Harvard University
- University of California, Santa Cruz
- University of California, Berkeley
- Indiana University
- University of Bristol
- University of Oxford
- University of Alberta
- Wake Forest University
- Charles University
- University of the West Indies
- Princeton University
- Technical University of Munich
- University of California, San Francisco
- Queensland University of Technology
- Washington University in St. Louis
- Yale University
- Indiana University Bloomington
