Meredith Yeager
#158,373
Most Influential Person Now
American geneticist
Meredith Yeager's AcademicInfluence.com Rankings
Meredith Yeagerbiology Degrees
Biology
#12913
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#16419
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#2664
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Genetics
#1454
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#1556
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#288
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Molecular Biology
#2182
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#2216
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#235
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Biology
Meredith Yeager's Degrees
- Bachelors Biology University of California, Berkeley
- PhD Genetics Stanford University
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Why Is Meredith Yeager Influential?
(Suggest an Edit or Addition)According to Wikipedia, Stella Meredith Yeager is an American geneticist who specializes in cancer genomics. She was the scientific director of the cancer genomics research laboratory at the National Cancer Institute. Yeager is an assistant professor of biology at Hood College.
Meredith Yeager'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
- A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer (2007) (1520)
- Genome-wide association study of prostate cancer identifies a second risk locus at 8q24 (2007) (1156)
- Multiple loci identified in a genome-wide association study of prostate cancer (2008) (970)
- Natural selection at major histocompatibility complex loci of vertebrates. (1998) (610)
- A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) (2009) (578)
- Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array (2012) (550)
- A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. (2009) (532)
- Detectable clonal mosaicism and its relationship to aging and cancer (2012) (512)
- 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)
- 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)
- Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium. (2006) (390)
- Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study (2011) (295)
- SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes (2005) (277)
- Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia (2012) (277)
- Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma (2014) (275)
- Genome-Wide and Candidate Gene Association Study of Cigarette Smoking Behaviors (2009) (262)
- Loci associated with skin pigmentation identified in African populations (2017) (253)
- 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)
- Global diversity and evidence for coevolution of KIR and HLA (2007) (233)
- Genome-wide association study of glioma and meta-analysis (2012) (225)
- 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)
- Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita (2013) (211)
- The 5p15.33 Locus Is Associated with Risk of Lung Adenocarcinoma in Never-Smoking Females in Asia (2010) (210)
- Genome-Wide Meta-Analysis Identifies Regions on 7p21 (AHR) and 15q24 (CYP1A2) As Determinants of Habitual Caffeine Consumption (2011) (204)
- Origin and dynamics of admixture in Brazilians and its effect on the pattern of deleterious mutations (2015) (201)
- 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)
- Genome-wide Association Study Identifies Multiple Risk Loci for Chronic Lymphocytic Leukemia (2013) (190)
- SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes (2004) (190)
- Cytokine polymorphisms in the Th1/Th2 pathway and susceptibility to non-Hodgkin lymphoma. (2006) (186)
- Genome-wide association study identifies new prostate cancer susceptibility loci. (2011) (183)
- HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis (2017) (183)
- Genome-wide Association Study Identifies Two Susceptibility Loci for Osteosarcoma (2013) (181)
- Solution State Characterization of Amyloid β-Derived Diffusible Ligands (2006) (177)
- Oxidative damage-related genes AKR1C3 and OGG1 modulate risks for lung cancer due to exposure to PAH-rich coal combustion emissions. (2004) (174)
- Evolution of the mammalian MHC: natural selection, recombination, and convergent evolution (1999) (167)
- Mass spectrometry and viral analysis. (1996) (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)
- High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays (2009) (152)
- Characterizing Associations and SNP-Environment Interactions for GWAS-Identified Prostate Cancer Risk Markers—Results from BPC3 (2011) (146)
- GWASdb v2: an update database for human genetic variants identified by genome-wide association studies (2015) (144)
- Genome-wide association study identifies multiple susceptibility loci for diffuse large B-cell lymphoma (2014) (140)
- Common genetic variants in proinflammatory and other immunoregulatory genes and risk for non-Hodgkin lymphoma. (2006) (136)
- Candidate genes for anorexia nervosa in the 1p33–36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa* (2003) (136)
- Association of Multiple DRD2 Polymorphisms with Anorexia Nervosa (2005) (134)
- Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations (2014) (133)
- Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types. (2015) (133)
- A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease. (2013) (131)
- Large-Scale Evaluation of Candidate Genes Identifies Associations between VEGF Polymorphisms and Bladder Cancer Risk (2007) (130)
- Genetic polymorphisms of interleukin-1B (IL-1B), IL-6, IL-8, and IL-10 and risk of prostate cancer. (2006) (128)
- HPV16 Sublineage Associations With Histology-Specific Cancer Risk Using HPV Whole-Genome Sequences in 3200 Women. (2016) (128)
- Polymorphisms in the DNA nucleotide excision repair genes and lung cancer risk in Xuan Wei, China (2005) (128)
- 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)
- A genome-wide association study identifies alleles in FGFR 2 associated with risk of sporadic postmenopausal breast cancer (2012) (122)
- 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)
- Widespread purifying selection at polymorphic sites in human protein-coding loci (2003) (119)
- A Recessive Founder Mutation in Regulator of Telomere Elongation Helicase 1, RTEL1, Underlies Severe Immunodeficiency and Features of Hoyeraal Hreidarsson Syndrome (2013) (117)
- Direct Activation of Protein Kinase C by 1α,25-Dihydroxyvitamin D3(*) (1995) (117)
- Mosaic loss of chromosome Y is associated with common variation near TCL1A (2016) (114)
- 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)
- Protein Kinase C Contains Two Activator Binding Sites That Bind Phorbol Esters and Diacylglycerols with Opposite Affinities (*) (1996) (110)
- Partitioning behavior of indocarbocyanine probes between coexisting gel and fluid phases in model membranes. (1990) (110)
- Genome-wide association study identifies common variants associated with circulating vitamin E levels (2011) (110)
- Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia (2016) (107)
- Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers (2008) (107)
- Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility (2009) (107)
- Common genetic polymorphisms modify the effect of smoking on absolute risk of bladder cancer. (2013) (104)
- 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)
- Polymorphisms in Th1-type cell-mediated response genes and risk of gastric cancer. (2007) (101)
- Nucleotide Excision Repair Gene Polymorphisms and Risk of Advanced Colorectal Adenoma: XPC Polymorphisms Modify Smoking-Related Risk (2006) (99)
- 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)
- Germline TP53 variants and susceptibility to osteosarcoma. (2015) (95)
- Sequence analysis of the mannose-binding lectin (MBL2) gene reveals a high degree of heterozygosity with evidence of selection (2004) (94)
- Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk. (2007) (93)
- Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma among women in Connecticut (2006) (93)
- Risk alleles for chronic hepatitis B are associated with decreased mRNA expression of HLA-DPA1 and HLA-DPB1 in normal human liver (2011) (92)
- Characterization of large structural genetic mosaicism in human autosomes. (2015) (91)
- Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours (2015) (91)
- Identification and Characterization of Vnx1p, a Novel Type of Vacuolar Monovalent Cation/H+ Antiporter of Saccharomyces cerevisiae* (2007) (89)
- Quantitative adenovirus neutralization assays based on the secreted alkaline phosphatase reporter gene: application in epidemiologic studies and in the design of adenovector vaccines. (2004) (89)
- A pooled investigation of Toll-like receptor gene variants and risk of non-Hodgkin lymphoma. (2009) (89)
- Two Susceptibility Loci Identified for Prostate Cancer Aggressiveness (2015) (88)
- Variation in KLK genes, prostate-specific antigen and risk of prostate cancer (2008) (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)
- Genome-wide association study identifies multiple risk loci for renal cell carcinoma (2017) (86)
- A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma. (2015) (85)
- Selected DNA repair polymorphisms and gastric cancer in Poland. (2005) (85)
- Polymorphisms in the DNA base excision repair genes APEX1 and XRCC1 and lung cancer risk in Xuan Wei, China. (2005) (84)
- Solution state characterization of amyloid beta-derived diffusible ligands. (2006) (83)
- Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes. (2006) (83)
- Interaction of Alcohols and Anesthetics with Protein Kinase Cα* (1997) (83)
- Coordinated Amino Acid Changes in the Evolution of Mammalian Defensins (1997) (82)
- Evolutionary instability of the major histocompatibility complex class I loci in New World primates. (1997) (82)
- PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3). (2010) (81)
- Lead, Genetic Susceptibility, and Risk of Adult Brain Tumors (2006) (80)
- Genetic variation in the sodium-dependent vitamin C transporters, SLC23A1, and SLC23A2 and risk for preterm delivery. (2006) (79)
- Pooled analysis of genetic variation at chromosome 8q24 and colorectal neoplasia risk. (2008) (79)
- Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families. (2014) (79)
- The new sequencer on the block: comparison of Life Technology’s Proton sequencer to an Illumina HiSeq for whole-exome sequencing (2013) (78)
- Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank (2018) (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)
- Variants in or near KITLG, BAK1, DMRT1, and TERT-CLPTM1L predispose to familial testicular germ cell tumour (2011) (78)
- Variants in inflammation genes and the risk of biliary tract cancers and stones: a population-based study in China. (2008) (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 variants in caspase genes and susceptibility to non-Hodgkin lymphoma. (2006) (75)
- Genetic variation in tumor necrosis factor and lymphotoxin-alpha (TNF–LTA) and breast cancer risk (2007) (72)
- Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome (2016) (72)
- Deep sequencing of HPV16 genomes: A new high-throughput tool for exploring the carcinogenicity and natural history of HPV16 infection (2015) (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)
- 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)
- Novel and known ribosomal causes of Diamond-Blackfan anaemia identified through comprehensive genomic characterisation (2017) (69)
- Association of variants in two vitamin e transport genes with circulating vitamin e concentrations and prostate cancer risk. (2009) (69)
- Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers. (2014) (69)
- Common genetic variants in the 9p21 region and their associations with multiple tumours (2013) (67)
- Natural selection and the evolutionary history of major histocompatibility complex loci. (1998) (67)
- Polymorphisms in cytokine and cellular adhesion molecule genes and susceptibility to hematotoxicity among workers exposed to benzene. (2005) (67)
- Risk of Non–Hodgkin Lymphoma Associated with Germline Variation in Genes that Regulate the Cell Cycle, Apoptosis, and Lymphocyte Development (2009) (66)
- Prostaglandin-endoperoxide synthase 2 (PTGS2) gene polymorphisms and risk of biliary tract cancer and gallstones: a population-based study in Shanghai, China. (2006) (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)
- 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)
- Colorectal cancer susceptibility loci as predictive markers of rectal cancer prognosis after surgery (2017) (63)
- A genome-wide association study of prostate cancer in West African men (2014) (63)
- The Intersection of HPV Epidemiology, Genomics and Mechanistic Studies of HPV-Mediated Carcinogenesis (2018) (62)
- Common genetic variation in TP53 and its flanking genes, WDR79 and ATP1B2, and susceptibility to breast cancer (2007) (62)
- Common Variation in Genes Related to Innate Immunity and Risk of Adult Glioma (2009) (62)
- Molecular evolution of the vertebrate immune system (1997) (62)
- Cigarette smoking, N-acetyltransferase genes and the risk of advanced colorectal adenoma. (2006) (61)
- LRRK 2 regulates mitochondrial dynamics and function through direct interaction with DLP 1 (2012) (61)
- Interleukin-8 Polymorphisms Are Not Associated with Gastric Cancer Risk in a Polish Population (2006) (60)
- A single nucleotide polymorphism tags variation in the arylamine N-acetyltransferase 2 phenotype in populations of European background (2010) (60)
- An Analysis of Growth, Differentiation and Apoptosis Genes with Risk of Renal Cancer (2009) (60)
- Testicular germ cell tumor susceptibility associated with the UCK2 locus on chromosome 1q23. (2013) (60)
- Genetic variation in sodium-dependent ascorbic acid transporters and risk of gastric cancer in Poland. (2009) (60)
- Neutralization of human papillomavirus (HPV) pseudovirions: a novel and efficient approach to detect and characterize HPV neutralizing antibodies. (2000) (60)
- Genome Analysis of Latin American Cervical Cancer: Frequent Activation of the PIK3CA Pathway (2015) (60)
- CYP1A1 Val462 and NQO1 Ser187 polymorphisms, cigarette use, and risk for colorectal adenoma. (2005) (60)
- Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies. (2012) (60)
- Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway. (2008) (59)
- A new statistic and its power to infer membership and phenotype in a genome-wide association study using genotype frequencies (2009) (59)
- Somatic Alterations Contributing to Metastasis of a Castration‐Resistant Prostate Cancer (2013) (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)
- Metabolic Gene Variants and Risk of Non-Hodgkin's Lymphoma (2006) (58)
- Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity. (2009) (58)
- Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer (2017) (58)
- GSTM1, GSTT1, and GSTP1 Polymorphisms and Risk of Advanced Colorectal Adenoma (2005) (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)
- Common Genetic Variants in Prostate Cancer Risk Prediction—Results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3) (2012) (56)
- 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)
- Hair dye use is not associated with risk for bladder cancer: evidence from a case-control study in Spain. (2006) (55)
- Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels (2011) (55)
- A genome-wide association study of marginal zone lymphoma shows association to the HLA region (2015) (55)
- Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies. (2009) (54)
- Sequence convergence in the peptide-binding region of primate and rodent MHC class Ib molecules. (1997) (54)
- Radiation-related genomic profile of papillary thyroid carcinoma after the Chernobyl accident (2021) (54)
- Efficient study design for next generation sequencing (2011) (54)
- Green tea consumption, genetic susceptibility, PAH-rich smoky coal, and the risk of lung cancer. (2005) (54)
- DRD2 genetic variation in relation to smoking and obesity in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (2006) (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)
- Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation (2016) (52)
- Microsomal epoxide hydrolase polymorphisms and risk for advanced colorectal adenoma. (2005) (52)
- Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma (2014) (51)
- High level of functional polymorphism indicates a unique role of natural selection at human immune system loci (2005) (51)
- The influence of obesity-related factors in the etiology of renal cell carcinoma—A mendelian randomization study (2019) (51)
- Germline variation in NCF4, an innate immunity gene, is associated with an increased risk of colorectal cancer (2014) (51)
- Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer. (2011) (51)
- A new taxonomy of mammalian MHC class I molecules. (1999) (51)
- Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN2A Mutations (2013) (50)
- Effect of pre-analytic variables on the reproducibility of qPCR relative telomere length measurement (2017) (49)
- Ovarian cancer risk and common variation in the sex hormone-binding globulin gene: a population-based case-control study (2007) (47)
- TNF polymorphisms and prostate cancer risk (2008) (47)
- Quantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium (BPC3). (2009) (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)
- Xenobiotic-metabolizing gene variants, pesticide use, and the risk of prostate cancer (2011) (45)
- Synonymous and Nonsynonymous Substitution Distances Are Correlated in Mouse and Rat Genes (1998) (45)
- Identification of modifier genes for cutaneous malignant melanoma in melanoma‐prone families with and without CDKN2A mutations (2009) (45)
- TET2 binds the androgen receptor and loss is associated with prostate cancer (2016) (45)
- Association of genetic variants in the calcium-sensing receptor with risk of colorectal adenoma. (2004) (44)
- Genetic Variation in Base Excision Repair Pathway Genes, Pesticide Exposure, and Prostate Cancer Risk (2011) (44)
- Risk of Meningioma and Common Variation in Genes Related to Innate Immunity (2010) (44)
- Human papillomavirus 16 sub-lineage dispersal and cervical cancer risk worldwide: Whole viral genome sequences from 7116 HPV16-positive women☆ (2019) (44)
- Pesticide use modifies the association between genetic variants on chromosome 8q24 and prostate cancer. (2010) (44)
- Insulin-like growth factor pathway genetic polymorphisms, circulating IGF1 and IGFBP3, and prostate cancer survival. (2014) (44)
- Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance (2020) (43)
- Pooled analysis of phosphatidylinositol 3-kinase pathway variants and risk of prostate cancer. (2010) (43)
- Haplotypes of the estrogen receptor beta gene and breast cancer risk (2008) (43)
- Improved imputation of common and uncommon SNPs with a new reference set (2011) (43)
- Transforming growth factor beta 1 (TGFB1) gene polymorphisms and risk of advanced colorectal adenoma. (2007) (42)
- Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations (2010) (42)
- Common genetic variants related to genomic integrity and risk of papillary thyroid cancer. (2011) (42)
- Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes. (2016) (42)
- Common genetic variants in candidate genes and risk of familial lymphoid malignancies (2009) (41)
- Integration of multiethnic fine-mapping and genomic annotation to prioritize candidate functional SNPs at prostate cancer susceptibility regions. (2015) (41)
- Smoky coal exposure, NBS1 polymorphisms, p53 protein accumulation, and lung cancer risk in Xuan Wei, China. (2005) (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)
- Factors associated with oxidative stress and cancer risk in the Breast and Prostate Cancer Cohort Consortium (2014) (40)
- Apolipoprotein E/C1 locus variants modify renal cell carcinoma risk. (2009) (40)
- Origins, admixture dynamics and homogenization of the African gene pool in the Americas (2019) (40)
- Folate metabolism genes, vegetable intake and renal cancer risk in central Europe (2007) (39)
- Polymorphisms in Cytokine Genes and Risk of Helicobacter pylori Infection among Jamaican Children (2006) (39)
- Addressing health disparities in Hispanic breast cancer: accurate and inexpensive sequencing of BRCA1 and BRCA2 (2015) (39)
- 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)
- COX1 and COX2 polymorphisms and gastric cancer risk in a Polish population. (2007) (38)
- Genetic polymorphisms in alcohol metabolism, alcohol intake and the risk of stomach cancer in Warsaw, Poland (2007) (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)
- 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)
- Iron Homeostasis and Distal Colorectal Adenoma Risk in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (2011) (38)
- Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women. (2016) (38)
- Genetic Variation in Sodium-Dependent Vitamin C Transporters SLC23A1 and SLC23A2 and Risk of Advanced Colorectal Adenoma (2008) (38)
- The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma. (2012) (37)
- Association of HPV35 with cervical carcinogenesis among women of African ancestry: Evidence of viral‐host interaction with implications for disease intervention (2020) (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)
- 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)
- 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)
- Peptide binding function and the paradox of HLA disease associations (1996) (37)
- Large-scale exploration of gene-gene interactions in prostate cancer using a multistage genome-wide association study. (2011) (37)
- Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia (2012) (36)
- Mosaic Y Loss Is Moderately Associated with Solid Tumor Risk. (2018) (36)
- Personal History of Diabetes, Genetic Susceptibility to Diabetes, and Risk of Brain Glioma: A Pooled Analysis of Observational Studies (2013) (36)
- Analysis of SNPs and Haplotypes in Vitamin D Pathway Genes and Renal Cancer Risk (2009) (36)
- Novel Breast Cancer Risk Alleles and Interaction with Ionizing Radiation among U.S. Radiologic Technologists (2010) (36)
- Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong (2010) (36)
- A pooled analysis of three studies evaluating genetic variation in innate immunity genes and non‐Hodgkin lymphoma risk (2011) (35)
- Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma. (2017) (35)
- Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men. (2012) (34)
- Genetic variation in nucleotide excision repair pathway genes, pesticide exposure and prostate cancer risk. (2012) (34)
- Polymorphic variants in PTGS2 and prostate cancer risk: results from two large nested case-control studies. (2007) (34)
- Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident (2021) (34)
- Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA) (2015) (34)
- Lipoprotein lipase in rat lung. Effect of dexamethasone. (1976) (34)
- Coevolution of the mammalian chemokines and their receptors (1999) (34)
- Genetic Susceptibility Loci, Pesticide Exposure and Prostate Cancer Risk (2013) (33)
- Genetic variants in T helper cell type 1, 2 and 3 pathways and gastric cancer risk in a Polish population. (2008) (33)
- Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family (2016) (33)
- Variants in blood pressure genes and the risk of renal cell carcinoma. (2010) (33)
- Evolution of multiple cell clones over a 29-year period of a CLL patient (2016) (33)
- DNA repair gene polymorphisms and tobacco smoking in the risk for colorectal adenomas. (2011) (33)
- Genetic variation in metabolic genes, occupational solvent exposure, and risk of non-hodgkin lymphoma. (2011) (33)
- Large-scale fine mapping of the HNF1B locus and prostate cancer risk. (2011) (33)
- A comprehensive resequence analysis of the KLK15–KLK3–KLK2 locus on chromosome 19q13.33 (2009) (32)
- Rare germline variants in known melanoma susceptibility genes in familial melanoma (2017) (32)
- Variants in hormone-related genes and the risk of biliary tract cancers and stones: a population-based study in China. (2009) (32)
- Somatic sequence alterations in twenty-one genes selected by expression profile analysis of breast carcinomas (2007) (31)
- Evaluating the Causal Link Between Malaria Infection and Endemic Burkitt Lymphoma in Northern Uganda: A Mendelian Randomization Study (2017) (31)
- Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene (2016) (31)
- Fluorescence quenching in model membranes: phospholipid acyl chain distributions around small fluorophores. (1990) (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)
- 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 susceptibility to diffuse large B‐cell lymphoma in a pooled study of three Eastern Asian populations (2015) (30)
- Polymorphisms of estrogen receptors and risk of biliary tract cancers and gallstones: a population-based study in Shanghai, China. (2010) (29)
- RNASEL Arg462Gln polymorphism and prostate cancer in PLCO (2007) (29)
- δ-Aminolevulinic Acid Dehydratase Polymorphism and Risk of Brain Tumors in Adults (2005) (29)
- Whole-Exome Sequencing of Nasopharyngeal Carcinoma Families Reveals Novel Variants Potentially Involved in Nasopharyngeal Carcinoma (2019) (28)
- Common Genetic Variation in TP53 and Risk of Human Papillomavirus Persistence and Progression to CIN3/Cancer Revisited (2009) (28)
- Dubowitz Syndrome Is a Complex Comprised of Multiple, Genetically Distinct and Phenotypically Overlapping Disorders (2014) (28)
- Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer. (2009) (28)
- Comprehensive Analysis of 5-Aminolevulinic Acid Dehydrogenase (ALAD) Variants and Renal Cell Carcinoma Risk among Individuals Exposed to Lead (2011) (27)
- Sex-specific gene and pathway modeling of inherited glioma risk (2017) (27)
- Association between adult height, genetic susceptibility and risk of glioma. (2012) (27)
- Promoter variants in the MSMB gene associated with prostate cancer regulate MSMB/NCOA4 fusion transcripts (2012) (27)
- Genetic variation of Cytochrome P450 1B1 (CYP1B1) and risk of breast cancer among Polish women (2006) (27)
- Genewindow: an interactive tool for visualization of genomic variation (2005) (27)
- Genotype frequency and FST analysis of polymorphisms in immunoregulatory genes in Chinese and Caucasian populations (2007) (27)
- Known glioma risk loci are associated with glioma with a family history of brain tumours—A case–control gene association study (2013) (27)
- XAF1 as a modifier of p53 function and cancer susceptibility (2020) (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)
- 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)
- A Germline Variant at 8q24 Contributes to Familial Clustering of Prostate Cancer in Men of African Ancestry. (2020) (26)
- Variation in innate immunity genes and risk of multiple myeloma (2011) (26)
- Comparative evolutionary rates of introns and exons in murine rodents (1997) (25)
- Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma risk (2013) (25)
- Immunodominance of a single CTL epitope in a primate species with limited MHC class I polymorphism. (1997) (25)
- Genome‐wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients (2018) (25)
- Refining the Prostate Cancer Genetic Association within the JAZF1 Gene on Chromosome 7p15.2 (2010) (24)
- Genome-wide SNP typing reveals signatures of population history. (2008) (24)
- Insulin Resistance-Related Genes and Advanced Left-Sided Colorectal Adenoma (2007) (24)
- Genetic variation in CLDN1 and susceptibility to hepatitis C virus infection (2010) (24)
- Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types (2015) (24)
- Alcohol, genetics and risk of breast cancer in the Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial (2012) (24)
- Characterising cis-regulatory variation in the transcriptome of histologically normal and tumour-derived pancreatic tissues (2017) (24)
- A comprehensive resequence‐analysis of 250 kb region of 8q24.21 in men of African ancestry (2014) (23)
- Comprehensive assessment of genetic variation of catechol-O-methyltransferase and breast cancer risk. (2006) (23)
- Pesticide Exposure and Inherited Variants in Vitamin D Pathway Genes in Relation to Prostate Cancer (2013) (23)
- A genome-wide pleiotropy scan for prostate cancer risk. (2015) (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)
- Stimulation of glucose transport and oxidation in adipocytes by fatty acids: evidence for a regulatory role in the cellular response to insulin. (1980) (22)
- Common Single Nucleotide Polymorphisms in Genes Related to Immune Function and Risk of Papillary Thyroid Cancer (2013) (22)
- Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut (2010) (22)
- Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China (2009) (22)
- Common Genetic Variation in GATA-Binding Protein 3 and Differential Susceptibility to Breast Cancer by Estrogen Receptor α Tumor Status (2007) (22)
- Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer (2009) (22)
- Genetic variants in DNA repair genes and the risk of cutaneous malignant melanoma in melanoma‐prone families with/without CDKN2A mutations (2012) (22)
- Genetic variation at chromosome 8q24 in osteosarcoma cases and controls. (2010) (22)
- The genetic structure and adaptation of Andean highlanders and Amazonians are influenced by the interplay between geography and culture. (2020) (21)
- Development of the TypeSeq Assay for Detection of 51 Human Papillomavirus Genotypes by Next-Generation Sequencing (2019) (21)
- Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men (2020) (21)
- NAT2 slow acetylation and GSTM1 null genotypes increase bladder cancer risk: results from the Spanish Bladder Cancer Study and meta-analyses (2008) (21)
- Characterization of HLA-DMB polymorphism (2004) (21)
- Polymorphisms in DNA repair genes and risk of non‐Hodgkin lymphoma in a pooled analysis of three studies (2010) (20)
- Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity (2009) (20)
- Polymorphisms in pattern‐recognition genes in the innate immunity system and risk of non‐Hodgkin lymphoma (2013) (19)
- Genetic signatures of gene flow and malaria-driven natural selection in sub-Saharan populations of the "endemic Burkitt Lymphoma belt" (2019) (19)
- Polymorphisms of an Innate Immune Gene, Toll-Like Receptor 4, and Aggressive Prostate Cancer Risk: A Systematic Review and Meta-Analysis (2014) (19)
- Sex specific associations in genome wide association analysis of renal cell carcinoma (2019) (19)
- Comprehensive Evaluation of One-Carbon Metabolism Pathway Gene Variants and Renal Cell Cancer Risk (2011) (18)
- Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility. (2016) (18)
- Evolutionary dynamics of the human NADPH oxidase genes CYBB, CYBA, NCF2, and NCF4: functional implications. (2013) (18)
- Age‐specific genome‐wide association study in glioblastoma identifies increased proportion of ‘lower grade glioma’‐like features associated with younger age (2018) (17)
- A mutation in KIR3DS1 that results in truncation and lack of cell surface expression (2007) (17)
- Direct activation of protein kinase C by 1 alpha,25-dihydroxyvitamin D3. (1995) (17)
- Mosaic chromosome 20q deletions are more frequent in the aging population. (2017) (17)
- Synergistic activation of protein kinase Calpha, -betaI, and -gamma isoforms induced by diacylglycerol and phorbol ester: roles of membrane association and activating conformational changes. (1999) (17)
- Polyunsaturation in cell membranes and lipid bilayers and its effects on membrane proteins (2007) (17)
- Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries (2022) (17)
- 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)
- Xenobiotic metabolizing genes, meat-related exposures, and risk of advanced colorectal adenoma. (2010) (16)
- Common genetic variation in GATA-binding protein 3 and differential susceptibility to breast cancer by estrogen receptor alpha tumor status. (2007) (16)
- Genetic variation in cell cycle and apoptosis related genes and multiple myeloma risk. (2009) (16)
- Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family (2015) (16)
- Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP (2014) (15)
- Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women. (2019) (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)
- Hemochromatosis gene mutations and distal adenomatous colorectal polyps. (2005) (15)
- Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry (2012) (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)
- Evaluation of TypeSeq, a Novel High-Throughput, Low-Cost, Next-Generation Sequencing-Based Assay for Detection of 51 Human Papillomavirus Genotypes (2019) (15)
- Polymorphisms in complement system genes and risk of non‐Hodgkin lymphoma (2012) (14)
- CYBB, an NADPH‐oxidase gene: restricted diversity in humans and evidence for differential long‐term purifying selection on transmembrane and cytosolic domains (2008) (14)
- Rare inactivating PDE11A variants associated with testicular germ cell tumors. (2015) (14)
- The population genetics of Quechuas, the largest native South American group: autosomal sequences, SNPs, and microsatellites evidence high level of diversity. (2012) (14)
- APOBEC Mutagenesis Is Concordant between Tumor and Viral Genomes in HPV-Positive Head and Neck Squamous Cell Carcinoma (2021) (14)
- A Two‐Platform Design for Next Generation Genome‐Wide Association Studies (2012) (14)
- Candidate gene analysis of the Price Foundation anorexia nervosa affected relative pair dataset. (2003) (14)
- Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays (2018) (13)
- Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia. (2020) (13)
- DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci (2014) (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)
- Prospective study of DNA methylation at chromosome 8q24 in peripheral blood and prostate cancer risk (2017) (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)
- SomaticCombiner: improving the performance of somatic variant calling based on evaluation tests and a consensus approach (2020) (12)
- Mosaic 13q14 deletions in peripheral leukocytes of non-hematologic cancer cases and healthy controls (2015) (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)
- Partitioning of gramicidin A' between coexisting fluid and gel phospholipid phases. (1993) (11)
- Genetic variants in the 8q24 locus and risk of testicular germ cell tumors (2008) (11)
- SLC6A3 and body mass index in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial (2009) (11)
- Class I and class II MHC bind self peptide sets that are strikingly different in their evolutionary characteristics (2000) (11)
- A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma. (2011) (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)
- CYP 1 A 1 Val 462 and NQO 1 Ser 187 polymorphisms , cigarette use , and risk for colorectal adenoma (2005) (11)
- Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia (2018) (11)
- Chromosomal Aberrations and Survival after Unrelated Donor Hematopoietic Stem Cell Transplant in Patients with Fanconi Anemia. (2018) (10)
- Polymorphisms in genes involved in Th1-type cell-mediated response and the risk of gastric cancer (2005) (10)
- Worldwide genetic structure in 37 genes important in telomere biology (2011) (10)
- Genetic Variation in a4GnT in Relation to Helicobacter pylori Serology and Gastric Cancer Risk (2009) (10)
- Innate immunity gene polymorphisms and the risk of colorectal neoplasia. (2013) (10)
- A custom 148 gene‐based resequencing chip and the SNP explorer software: new tools to study antibody deficiency (2010) (10)
- cis sequence effects on gene expression (2007) (10)
- Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families (2013) (10)
- Patterns of Human Leukocyte Antigen Class I and Class II Associations and Cancer (2020) (10)
- Genetic variants in frizzled-related protein (FRZB) and the risk of colorectal neoplasia (2009) (9)
- Interallelic recombination has not played a major role in the history of the HLA-C locus (1996) (9)
- The Interaction between Pesticide Use and Genetic Variants Involved in Lipid Metabolism on Prostate Cancer Risk (2012) (9)
- MBL2 and Hepatitis C Virus Infection among Injection Drug Users (2008) (9)
- The genetic structure and adaptation of Andean highlanders and Amazonian dwellers is influenced by the interplay between geography and culture (2020) (8)
- Detectable chromosome X mosaicism in males is rarely tolerated in peripheral leukocytes (2021) (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)
- Mechanism of hydrolysis of an unsymmetrical ketene O,O-acetal and of ketene O,S-acetals (1975) (8)
- Genomic diversity and phylogenetic relationships of human papillomavirus 16 (HPV16) in Nepal. (2016) (8)
- Oropharyngeal Squamous Cell Carcinoma Morphology and Subtypes by Human Papillomavirus Type and by 16 Lineages and Sublineages (2021) (7)
- HPV+ Oropharyngeal Squamous Cell Carcinomas from patients with two tumors display synchrony of viral genomes yet discordant mutational profiles and signatures. (2020) (7)
- The chromosome 2 p 21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma (2012) (7)
- Testicular germ cell tumor susceptibility associated with the UCK 2 locus on chromosome 1 q 23 (2013) (7)
- A Resequence Analysis of Genomic Loci on Chromosomes 1q32.1, 5p15.33, and 13q22.1 Associated With Pancreatic Cancer Risk (2013) (7)
- Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma (2020) (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)
- Comprehensive resequence analysis of a 123‐kb region of chromosome 11q13 associated with prostate cancer (2012) (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)
- Application of a Novel Score Test for Genetic Association Incorporating Gene-Gene Interaction Suggests Functionality for Prostate Cancer Susceptibility Regions (2011) (6)
- Polymorphisms in integrin genes and lymphoma risk. (2011) (6)
- Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study. (2021) (6)
- RPS29 is Mutated in a Multi-Case Diamond Blackfan Anemia Family (2012) (6)
- Quantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium ( BPC 3 ) (2009) (6)
- Candidate genes for anorexia nervosa in the 1p33-36 linkage region: Serotonin 1D and delta opioid receptors display significant association to anorexia nervosa [Conference Abstract] (2003) (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)
- Evaluation of Rare and Common Variants from Suspected Familial or Sporadic Nasopharyngeal Carcinoma (NPC) Susceptibility Genes in Sporadic NPC (2019) (5)
- Haplotypes of IL6 and IL10 and susceptibility to human T lymphotropic virus type I infection among children. (2006) (5)
- Improved Imputation of Common and Uncommon Single Nucleotide Polymorphisms (SNPs) with a New Reference Set (2011) (5)
- Genome diversity in Ukraine (2020) (5)
- Admixture/fine-mapping in Brazilians reveals a West African associated potential regulatory variant (rs114066381) with a strong female-specific effect on body mass- and fat mass-indexes (2019) (5)
- Validation of the performance of a comprehensive genotyping assay panel of single nucleotide polymorphisms in drug metabolism enzyme genes (2008) (4)
- Pre-HCT mosaicism increases relapse risk and lowers survival in acute lymphoblastic leukemia patients post-unrelated HCT. (2021) (4)
- Abstract LB-272: Genome-wide association study identifies multiple susceptibility loci for diffuse large B-cell lymphoma (2014) (4)
- Abstract 5574: High prevalence of germline TP53 mutations in young osteosarcoma cases (2015) (4)
- Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility (2021) (4)
- A mutation in KIR3DS1 that results in truncation and lack of cell surface expression (2007) (4)
- Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN 2 A Mutations (2013) (4)
- Fine mapping of 14q24.1 breast cancer susceptibility locus (2012) (4)
- Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case–Control Study within the Agricultural Health Study (2016) (4)
- KRLMM: an adaptive genotype calling method for common and low frequency variants (2014) (4)
- In search of genetic factors predisposing to familial hairy cell leukemia (HCL): exome-sequencing of four multiplex HCL pedigrees (2020) (4)
- Genetics and geography of leukocyte telomere length in sub-Saharan Africans (2020) (4)
- Abstract 2756: Whole-exome sequencing reveals a novel germline variant in CEBPA-associated familial acute myeloid leukemia: 45-year follow-up of a large family (2015) (3)
- Phylogenomic Analysis of Human Papillomavirus Type 31 and Cervical Carcinogenesis: A Study of 2093 Viral Genomes (2021) (3)
- Admixture/fine-mapping in Brazilians reveals a West African associated potential regulatory variant (rs114066381) with a strong female-specific effect on body mass and fat mass indexes (2021) (3)
- The D2 and D3 Sublineages of Human Papilloma Virus 16–Positive Cervical Cancer in Guatemala Differ in Integration Rate and Age of Diagnosis (2020) (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)
- The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature (2021) (3)
- Binding of β4γ5 by adenosine A1 and A2A receptors determined by stable isotope labeling with amino acids in cell culture and mass spectrometry. (2011) (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)
- Viral coinfection analysis using a MinHash toolkit (2019) (3)
- Invited commentary: more surprises from a gene desert. (2012) (3)
- Genetic variation within the human papillomavirus type 16 genome is associated with oropharyngeal cancer prognosis. (2022) (3)
- 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)
- Extrachromosomal Amplification of Human Papillomavirus Episomes as a Mechanism of Cervical Carcinogenesis (2021) (2)
- Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes (2022) (2)
- HPV16 E7 Nucleotide Variants Found in Cancer-Free Subjects Affect E7 Protein Expression and Transformation (2021) (2)
- SP16 Whole-Genome Association and Replication Studies in Prostate Cancer (2007) (2)
- Characterization of breakpoint regions of large structural autosomal mosaic events (2017) (2)
- 4-OR: Global diversity of KIR and HLA: Population-level evidence for co-evolution, natural selection, and signatures of demographic history (2007) (2)
- Germline-somatic JAK2 interactions are associated with clonal expansion in myelofibrosis (2022) (2)
- Risk of Non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair genes (2005) (2)
- Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA) (2015) (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)
- Rare inactivating PDE 11 A variants associated with testicular germ cell tumors (2015) (2)
- MBL 2 and Hepatitis C Virus Infection among Injection Drug Users (2016) (2)
- O689 - Trans-species polymorphism vs. Independent evolution of class II MHC sequence motifs (1996) (1)
- Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma (2022) (1)
- Polymorphism in the trifunctional enzyme coding gene MTHFD1 and the risk of stomach cancer (2006) (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)
- 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)
- 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)
- Combined somatic mutation and copy number analysis in the survival of familial CLL (2018) (1)
- Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility (2020) (1)
- Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma risk (2013) (1)
- Lead Exposure and Glioma Among Rural Residents: The Upper Midwest Health Study (2006) (1)
- Clonal Alterations and Survival after Unrelated Donor Allogeneic Hematopoietic Stem Cell Transplant in Patients with Fanconi Anemia (2018) (1)
- Interallellc recombination has not played a major role In the history of theHLA-C locus (2007) (1)
- Abstract 1300: Exploration of rare variants from exome sequencing in families with Waldenstrom macroglobulinemia (WM) (2014) (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)
- The future of pediatric cancer and complex diseases: Aren't they all? (2007) (1)
- GWAS Explorer: an open-source tool to explore, visualize, and access GWAS summary statistics in the PLCO Atlas (2023) (1)
- Development of the TypeSeq Assay for Detection of 51 HPV Genotypes by 1 Next Generation Sequencing 2 (2019) (1)
- Abstract A78: Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut (2008) (1)
- The genetic and evolutionary basis of gene expression variation in East Africans (2022) (1)
- Genetic variation in nucleotide excision repair (NER) and bladder cancer risk in the Spanish Bladder Cancer Study (2005) (1)
- Large-scale evaluation of candidate genes for urinary bladder cancer susceptibility using Illumina® in the Spanish Bladder Cancer Study (2006) (1)
- Novel and Known Ribosomal Causes of Diamond-Blackfan Anemia Identified through Comprehensive Genomic Characterization (2016) (1)
- KRLMM: an adaptive genotype calling method for common and low frequency variants (2014) (1)
- Mosaic loss of chromosome Y is associated with common variation near TCL 1 A 1 2 (2016) (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)
- Lead, Genetic Susceptibility and Risk of Adult Brain Tumors (2006) (1)
- Human papillomavirus 16 positive cervical cancer in Guatemala: The D2 and D3 sublineages differ in integration rate and age of diagnosis (2020) (1)
- Abstract A89: Association of genes involved in lipid metabolism-peroxidation and risk of renal cancer in the Central European Renal Cancer Case-Control Study (2008) (1)
- Genome-wide association study identifies novel loci associated with osteosarcoma (2013) (0)
- Functional Consequences Of RPS29 Germline Mutations In Diamond-Blackfan Anemia (2013) (0)
- Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry (2012) (0)
- Genome-Wide Association Study Identifies an Immune-Related Etiology for Severe Aplastic Anemia (2019) (0)
- Genetic variation in nu cleotide excision repair pathw ay ge nes, pesticide exposure, and prostate ca ncer ris k (2011) (0)
- Genome-wide association study of glioma and meta-analysis (2012) (0)
- Abstract 2553: Characterization of rare germline variants in somatically mutated melanoma genes in melanoma-prone families. (2013) (0)
- A genome-wide association study of prostate cancer in West African men (2013) (0)
- Original Contribution Genetic Variation in the Sodium-dependent Vitamin C Transporters, SLC23A1, and SLC23A2 and Risk for Preterm Delivery (2006) (0)
- Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma (2014) (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)
- Combining two genome wide association scans for seven smoking related phenotypes replicates published associations in the CHRNA3/5 region (2008) (0)
- Abstract 3379: Predictors of mosaic chromosome Y loss and associations with mortality in 223,338 men of the UK Biobank (2018) (0)
- Abstract 288: DNA methylation patterns in peripheral blood and the relationship with cancer susceptibility loci at chromosome 8q24 (2014) (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)
- Abstract 3273: rkmh: A MinHash toolbox for analyzing HPV coinfections (2018) (0)
- Genome-wide homozygosity and risk of four non-Hodgkin lymphoma subtypes (2021) (0)
- Germline-Somatic Interactions in Myelofibrosis Susceptibility (2021) (0)
- Abstract LB-330: Genetic variants in the 9p21 region in relation to the risk of multiple tumors (2012) (0)
- Abstract 4626: Genetic susceptibility to diffuse large B-cell lymphoma in a pooled study of three Eastern Asian populations (2015) (0)
- Abstract 2185: Multiple region whole-genome sequencing reveals intratumor heterogeneity and branching clonal architecture of non-clear-cell renal cell carcinoma (2018) (0)
- Abstract 2027: Anal cancer among African Americans associate with HPV16 lineage B and HIV (2020) (0)
- Abstract 2568: Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women (2016) (0)
- Abstract 1638: Whole-exome sequencing and protein interaction networks to prioritize candidate genes for cutaneous melanoma susceptibility (2019) (0)
- The SNP page for a typical SNP from the SNP500Cancer website, showing links to external resources, t (2011) (0)
- Abstract 2160: Immune escape mutations in HLA Class I,B2MandCASP8genes shape tumor evolution (2020) (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)
- Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia (2012) (0)
- Abstract PO-055: Molecular characterization of papillary thyroid cancer in relation to ionizing radiation dose following the Chernobyl accident (2021) (0)
- Whole-Exome Sequencing of Nasopharyngeal Carcinoma Families Reveals Novel Variants Potentially Involved in Nasopharyngeal Carcinoma (2019) (0)
- Acknowledgement to Reveiwers (2011) (0)
- Hierarchical clustering analysis of 194 breast tumor samples analyzed using the 'SAM264' patient sur (2011) (0)
- Divergence of HPV16 variants reflects loci undergoing inter-host positive selection, potentially immunologic selection (2017) (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)
- Pre-Transplant Clonal Mosaicism Is Associated with Increased Relapse and Lower Survival in Acute Lymphoblastic Leukemia Patients Undergoing Allogeneic Hematopoietic Cell Transplant (2020) (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 2966: A genome-wide scan identifies a new locus associated with pediatric rhabdomyosarcoma (2018) (0)
- Abstract 3974: A comprehensive resequence-analysis of 250kb region of 8q24 in Africans (2012) (0)
- ION TORRENT LIBRARY PREPARATION PROCESS USING KAPABIOSYSTEMS LIBRARY QUANTIFICATION KIT SIGNIFICANTLY INCREASES QUANTITATIVE SENSITIVITY AND IMPROVES SAMPLE POOLING FOR MULTIPLEXED SEQUENCING (2011) (0)
- The new sequencer on the block: comparison of Life Technology’s Proton sequencer to an Illumina HiSeq for whole-exome sequencing (2013) (0)
- Abstract 3930: Targeted cancer gene sequencing identifies potential causative novel candidate mutations among Caucasian colon carcinogenesis (2015) (0)
- Abstract 1867: DNA repair gene polymorphisms and tobacco smoking and the risk of colorectal adenoma (2010) (0)
- Erratum to: A genome-wide association study of prostate cancer in West African men (2013) (0)
- Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility (2018) (0)
- Detectable chromosome X mosaicism in males is rarely tolerated in peripheral leukocytes (2021) (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)
- In utero exposure to diethylstilbestrol and blood DNA methylation in adult women: Results from a meta-analysis of two cohort studies (2023) (0)
- Increased Frequency of Mosaic Chromosomal Alterations in Peripheral Blood Samples of Sub-Saharan African Children with Endemic Burkitt Lymphoma (2022) (0)
- Xenobiotic Metabolizing Genes, Meat-Related Exposures, and Risk of Advanced Colorectal Adenoma (2011) (0)
- Abstract LB-337: Synergistic effects of twelve common genetic polymorphisms and smoking habits on absolute risk of bladder cancer (2012) (0)
- Title: Sex Specific Associations in Genome Wide Association Analysis of Renal Cell Carcinoma (2019) (0)
- Abstract 683: Identification of common germline variants associated with pediatric rhabdomyosarcoma survival: A report from the Children's Oncology Group (COG) (2022) (0)
- Abstract 28: Resequence-analysis of 166kb KITLG region in eamilial testicular germ cell tumors (2011) (0)
- Erratum to: A genome-wide association study of prostate cancer in West African men (2014) (0)
- Erratum: A mutation in KIR3DS1 that results in truncation and lack of cell surface expression (Immunogenetics DOI: 10.1007/s00251-007-0240-8) (2007) (0)
- 730 HUMAN GENETIC VARIANTS LINKED TO CHRONIC HEPATITIS B ARE ASSOCIATED WITH EXPRESSION OF HLA-DPA1 AND HLA-DPB1 (2010) (0)
- Subject Index Vol 3, 2010 (2011) (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)
- Fine mapping of 14q24.1 breast cancer susceptibility locus (2011) (0)
- Abstract 1442: Analysis ofcis-eQTLs in normal and tumor-derived pancreatic tissues reveals functional insights, including for the 9q34.1ABOpancreatic cancer risk locus (2017) (0)
- Abstract 607: Clonal hematopoiesis alters blood cell counts in the UK Biobank (2019) (0)
- Abstract B51: Genetic variation in nucleotide excision repair pathway genes, pesticide exposure, and prostate cancer risk (2011) (0)
- Illumina® - based multiplexed genotyping indicates a role for altered DNA repair and genomic maintenance in susceptibility to benzene toxicity (2006) (0)
- A Case of HPV-Associated Oropharyngeal Squamous Cell Carcinoma with Block-Like, Partial Loss of p16 Expression (2022) (0)
- Abstract 4871: Whole-exome sequencing identifies a high frequency of germline deleterious variants in cancer predisposition genes in individuals with osteosarcoma (2017) (0)
- Sa1942 Targeted Cancer Gene Sequencing Identifies Potential Causative Novel Candidate Mutations in African Americans Colon Carcinogenesis (2015) (0)
- Abstract 1668: Understanding cancer associated SNPs in the TERT-CLPTM1L locus through population genetics (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)
- Sex specific associations in genome wide association analysis of renal cell carcinoma (2019) (0)
- Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays (2018) (0)
- Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita (2013) (0)
- Linkage disequlibrium (LD) representation of the SERPINA5 gene. (2013) (0)
- Reply to ‘Mosaic loss of chromosome Y in leukocytes matters’ (2018) (0)
- Germline Mutations in Patients Receiving Unrelated Donor Hematopoietic Cell Transplant for Severe Aplastic Anemia (2016) (0)
- Abstract 355: TET2-loss modifies androgen signaling in prostate cancer (2017) (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)
- Contents Vol 3, 2010 (2011) (0)
- A comprehensive database for GWAS¬identified human genetic variants: an update of GWASdb (2015) (0)
- OP-MOLB200033 1647..1656 (2020) (0)
- Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia (2018) (0)
- Viral coinfection analysis using a MinHash toolkit (2019) (0)
- Characterization of population-based variation and putative functional elements for the multiple-cancer susceptibility loci at 5p15.33 (2014) (0)
- Breast Cancer Risk in Women from Ghana Carrying Rare Germline Pathogenic Mutations: A Resource for Genetic Counseling of West African Women (2021) (0)
- Abstract B129: Xenobiotic metabolizing genes, meat intake and risk of advanced colorectal adenoma (2008) (0)
- From copy number alterations to structural variants: the evolutionary cascade of papillary renal cell carcinomas (2018) (0)
- Abstract 941: Exome sequencing identifiedPOT1, a telomere shelterin gene, as a major susceptibility gene for familial cutaneous malignant melanoma (2014) (0)
- Abstract 2970: Multiple new susceptibility loci identified in genome-wide association study of Ewing sarcoma (2018) (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)
- Germline Genetic Variants and Pediatric Rhabdomyosarcoma Outcomes: A Report from the Children's Oncology Group. (2023) (0)
- Partitioning of Gramicidin A’ Between Coexisting Phases within Phospholipid Bilayers (1991) (0)
- Managing Fats, Oil, and Grease from the Food Service Industry (2000) (0)
- Abstract 4604: DNA methylation at chromosome 8q24 in peripheral blood and prostate cancer risk (2015) (0)
- Mo1028 HPV16 LINEAGE B IS ASSOCIATED WITH ANAL CANCER IN AFRICAN AMERICANS (2020) (0)
- Nucleotide excision repair polymorphisms and risk of colorectal adenoma (2004) (0)
- Abstract B42: A comprehensive resequence-analysis of 250kb region of 8q24 in Africans (2011) (0)
- Genetic variation within the human papillomavirus type 16 genome is associated with oropharyngeal cancer prognosis (2021) (0)
- donors graft-versus-host disease after marrow transplantation from unrelated methotrexate and cyclosporine for prophylaxis of acute Phase 3 study comparing methotrexate and tacrolimus with (2011) (0)
- Abstract PR-6: Variation in VDR pathway genes and renal cancer risk (2008) (0)
- A mutation in KIR3DS1 that results in truncation and lack of cell surface expression (2007) (0)
- Germline Mutations in RTEL1 cause Dyskeratosis Congenita (2012) (0)
- Abstract A88: Genome-wide association study identifies variants in several loci associated with circulating vitamin E levels (2010) (0)
- Promoter variants in the MSMB gene associated with prostate cancer regulate MSMB/NCOA4 fusion transcripts (2012) (0)
- Abstract 1302: Genome-wide association study of glioma reveals specific differences in genetic susceptibility to glioblastoma and non-glioblastoma (2017) (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)
- Abstract 4488: Targeted sequencing revealed distinctive and pathogenic mutations in African Americans with colorectal cancer (2016) (0)
- Human Leukocyte Antigen Contributes to Childhood Endemic Burkitt Lymphoma in Eastern Africa: A Case-Control Association Study (2022) (0)
- Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding. (2023) (0)
- Comprehensive Comparison of Normalization Methods for Human Methylation 450K Array (2016) (0)
- Five Novel Deleterious Variants in FANCA, FANCF and FANCG Identified in Pakistani Fanconi Anemia Families Using Exome Sequencing (2020) (0)
- Abstract 2542: Evidence for large somatic structural events detected as autosomal genetic mosaicism in GWAS data. (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)
- Genome-Wide Association Studies: Admixture mapping for disease gene discovery (2016) (0)
- Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family (2015) (0)
- Integrated Analysis of Co-expression and Exome Sequencing to Prioritize Susceptibility Genes for Familial Cutaneous Melanoma. (2022) (0)
- Abstract 2077: Genome-wide association study identifies theGLDC/IL33locus associated with survival of osteosarcoma patients (2018) (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)
- Room 501 A-C, Los Angeles Convention Center Epidemiology 11 Inflammation, Immunity, and Novel Pathways (2007) (0)
- Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank (2018) (0)
- Abstract C121: Genomic characterization of invasive cervical cancer in Guatemala and Venezuela: Common activation of the PIK3CA pathway. (2013) (0)
- The genomic and epigenomic evolutionary history of papillary renal cell carcinomas (2020) (0)
- Polymorphisms in DNA repair genes and benzene hematotoxicity (2005) (0)
- Breast cancer risk in women from Ghana carrying rare germline pathogenic mutations. (2022) (0)
- Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men (2020) (0)
- Abstract 3110: The aging genome: Genetic mosaicism and its relationship to cancer (2012) (0)
- DNA repair and related genes Risk of Non-Hodgkin lymphoma (NHL) in relation to germline variation in (2013) (0)
- Abstract 4249: Evidence of APOBEC3 editing in the HPV16 genome (2017) (0)
- Chromosomal Aberrations in Pre-HCT Blood Samples and Outcomes after Transplantation in Patients with Myelofibrosis (2020) (0)
- Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance (2020) (0)
- Determination of polymorphism in DMB (1992) (0)
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