Alisa M. Goldstein
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American genetic epidemiologist
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Alisa M. Goldstein's Degrees
- Bachelors Biology University of California, Berkeley
- PhD Genetic Epidemiology Stanford University
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Why Is Alisa M. Goldstein Influential?
(Suggest an Edit or Addition)According to Wikipedia, Alisa Miriam Goldstein is an American genetic epidemiologist who researches the genetic and environmental causes of cancer. She is a senior investigator at the National Cancer Institute. Life Goldstein received a Ph.D. in genetic epidemiology from the University of California, Los Angeles in 1988. Her dissertation was titled, A genetic epidemiologic investigation of breast cancer in families with bilateral breast cancer. Robert Haile was her doctoral advisor. Goldstein completed a fellowship in the National Institutes of Health InterInstitute Medical Genetics Program, and is board certified in medical genetics.
Alisa M. Goldstein'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
- Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome (1996) (1990)
- Germline p16 mutations in familial melanoma (1994) (1309)
- Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome. (1997) (878)
- Chordoma: incidence and survival patterns in the United States, 1973–1995 (2004) (818)
- Mutations in SUFU predispose to medulloblastoma (2002) (808)
- Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma (1996) (803)
- Localization of the gene for Cowden disease to chromosome 10q22–23 (1996) (641)
- Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations. (1995) (611)
- 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)
- Geographical variation in the penetrance of CDKN2A mutations for melanoma. (2002) (484)
- A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma (2010) (469)
- Genome-wide association study identifies three loci associated with melanoma risk (2009) (444)
- Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish (1989) (415)
- High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. (2006) (401)
- Diabetes mellitus, other medical conditions and familial history of cancer as risk factors for pancreatic cancer (1999) (388)
- Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents (2006) (384)
- Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair (2010) (383)
- Two newly identified genetic determinants of pigmentation in Europeans (2008) (349)
- ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma (2008) (335)
- MicroRNA Expression Differentiates Histology and Predicts Survival of Lung Cancer (2010) (324)
- Mutations associated with familial melanoma impair p16INK4 function (1995) (288)
- Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma (2014) (275)
- Melanoma etiology: where are we? (2003) (272)
- Follow-up study of twenty-four families with Li-Fraumeni syndrome. (1991) (272)
- T (brachyury) gene duplication confers major susceptibility to familial chordoma (2009) (261)
- Genome-wide association study identifies three new melanoma susceptibility loci (2011) (252)
- Acral lentiginous melanoma: incidence and survival patterns in the United States, 1986-2005. (2009) (240)
- Common sequence variants on 20q11.22 confer melanoma susceptibility (2008) (238)
- Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions (2012) (227)
- CDKN2A mutations in multiple primary melanomas. (1998) (227)
- Evaluation of Risk Factors for Nasopharyngeal Carcinoma in High-Risk Nasopharyngeal Carcinoma Families in Taiwan (2005) (207)
- Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma (2015) (199)
- Increased risk of second primary cancers after a diagnosis of melanoma. (2010) (198)
- Global Gene Expression Profiling and Validation in Esophageal Squamous Cell Carcinoma and Its Association with Clinical Phenotypes (2011) (197)
- Genotype-phenotype relationships in U.S. melanoma-prone families with CDKN2A and CDK4 mutations. (2000) (191)
- Selection criteria for genetic assessment of patients with familial melanoma. (2009) (168)
- MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population. (2005) (161)
- Chronic Obstructive Pulmonary Disease and Altered Risk of Lung Cancer in a Population-Based Case-Control Study (2009) (156)
- Genome wide analysis of DNA copy number neutral loss of heterozygosity (CNNLOH) and its relation to gene expression in esophageal squamous cell carcinoma (2010) (147)
- Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3 (2011) (146)
- Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients. (1996) (138)
- Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types. (2015) (133)
- Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations (2014) (133)
- A natural history of melanomas and dysplastic nevi (2002) (131)
- Risk of melanoma and other cancers in melanoma-prone families. (1993) (130)
- Genetic epidemiology of cutaneous melanoma: a global perspective. (2001) (127)
- International cancer seminars: a focus on esophageal squamous cell carcinoma (2017) (126)
- Environment And Genetics in Lung cancer Etiology (EAGLE) study: An integrative population-based case-control study of lung cancer (2008) (124)
- Localization of a novel melanoma susceptibility locus to 1p22. (2003) (124)
- Risk factors for esophageal and gastric cancers in Shanxi Province, China: a case-control study. (2011) (123)
- Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants (2013) (121)
- Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity. (1994) (120)
- A variant in FTO shows association with melanoma risk not due to BMI (2013) (120)
- Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity. (1993) (119)
- Phase I Metabolic Genes and Risk of Lung Cancer: Multiple Polymorphisms and mRNA Expression (2009) (117)
- Epidemiologic and genetic approaches in the study of gene-environment interaction: an overview of available methods. (1998) (115)
- Genome-wide association study in esophageal cancer using GeneChip mapping 10K array. (2005) (114)
- Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study (2010) (113)
- Allelic imbalance, including deletion of PTEN/MMAC1, at the Cowden disease locus on 10q22‐23, in hamartomas from patients with cowden syndrome and germline PTEN mutation (1998) (112)
- Familial melanoma, pancreatic cancer and germline CDKN2A mutations (2004) (112)
- Family history of gallstones and the risk of biliary tract cancer and gallstones: A population‐based study in Shanghai, China (2007) (111)
- A genome‐wide search for loci contributing to smoking and alcoholism (1999) (110)
- Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous‐cell carcinoma in a high‐risk Chinese population (2000) (110)
- Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33. (1998) (108)
- Genetic testing for melanoma. (2002) (104)
- Family history of cancer and risk for esophageal and gastric cancer in Shanxi, China (2009) (104)
- The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length (2014) (103)
- Molecular Characterization of the Human Stomach Microbiota in Gastric Cancer Patients (2017) (101)
- Prognostic Factors and Secondary Malignancies in Childhood Medulloblastoma (2001) (100)
- Association of MC1R variants and risk of melanoma in melanoma-prone families with CDKN2A mutations. (2005) (100)
- Comprehensive evaluation of allele frequency differences of MC1R variants across populations. (2006) (96)
- Frequent inactivation of the TP53 gene in esophageal squamous cell carcinoma from a high-risk population in China. (2001) (94)
- Comparison of Global Gene Expression of Gastric Cardia and Noncardia Cancers from a High-Risk Population in China (2013) (94)
- Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer. (2017) (93)
- Familial risk in oral and pharyngeal cancer. (1994) (92)
- Assessment of Human Papillomavirus in Lung Tumor Tissue (2011) (91)
- Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours (2015) (91)
- Characterization of large structural genetic mosaicism in human autosomes. (2015) (91)
- Second cancers after medulloblastoma: population-based results from the United States and Sweden (1997) (91)
- Dysplastic Nevi and Melanoma (2013) (90)
- 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)
- The genetics of melanoma: recent advances. (2013) (88)
- Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility (2020) (87)
- Comprehensive Characterization of Annexin I Alterations in Esophageal Squamous Cell Carcinoma (2004) (86)
- Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer. (2008) (85)
- A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families. (2000) (84)
- Mutation screening of the CDKN2A promoter in melanoma families (2000) (82)
- High prevalence of the G101W germline mutation in the CDKN2A (P16(ink4a)) gene in 62 Italian malignant melanoma families. (2002) (80)
- Rising Melanoma Incidence Rates of the Trunk among Younger Women in the United States (2010) (79)
- Genetic epidemiology of familial melanoma. (1995) (79)
- A mutation hotspot at the p14ARF splice site (2005) (76)
- Genetic variants in DNA repair pathway genes and risk of esophageal squamous cell carcinoma and gastric adenocarcinoma in a Chinese population. (2013) (75)
- Index‐based dietary patterns and risk of incident hepatocellular carcinoma and mortality from chronic liver disease in a prospective study (2014) (74)
- Index-based dietary patterns and risk of esophageal and gastric cancer in a large cohort study. (2013) (74)
- Gene expression analysis of esophageal squamous cell carcinoma reveals consistent molecular profiles related to a family history of upper gastrointestinal cancer. (2003) (72)
- Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome (2016) (72)
- Familial chordoma, a tumor of notochordal remnants, is linked to chromosome 7q33. (2001) (70)
- Lung cancer prognosis before and after recurrence in a population-based setting. (2015) (70)
- Comprehensive evaluation of allele frequency differences of MC1R variants across populations (2007) (70)
- Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers. (2014) (69)
- Evaluation of BRCA2 in the genetic susceptibility of familial esophageal cancer (2004) (69)
- Prospective risk of cancer in CDKN2A germline mutation carriers (2004) (68)
- Rarity of CDK4 germline mutations in familial melanoma (2002) (68)
- A Gene Expression Signature from Peripheral Whole Blood for Stage I Lung Adenocarcinoma (2011) (67)
- Common genetic variants in the 9p21 region and their associations with multiple tumours (2013) (67)
- Dietary quercetin, quercetin-gene interaction, metabolic gene expression in lung tissue and lung cancer risk. (2010) (66)
- Localization of the gene for the nevoid basal cell carcinoma syndrome. (1994) (65)
- Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies (2015) (65)
- Clinical findings in two African-American families with the nevoid basal cell carcinoma syndrome (NBCC). (1994) (64)
- Mutation testing in melanoma families: INK4A, CDK4 and INK4D (1999) (63)
- Genomic characterization of esophageal squamous cell carcinoma from a high-risk population in China. (2009) (63)
- Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer. (1999) (62)
- Genomic Landscape of Somatic Alterations in Esophageal Squamous Cell Carcinoma and Gastric Cancer. (2016) (62)
- Sporadic multiple primary melanoma cases: CDKN2A germline mutations with a founder effect (2001) (61)
- Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies. (2012) (60)
- Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations (1998) (59)
- Sun exposure and basal cell carcinomas in the nevoid basal cell carcinoma syndrome. (1993) (59)
- Epstein‐Barr virus seroreactivity among unaffected individuals within high‐risk nasopharyngeal carcinoma families in Taiwan (2004) (58)
- Nested PCR Biases in Interpreting Microbial Community Structure in 16S rRNA Gene Sequence Datasets (2015) (57)
- Prognostic Utility of Anti-EBV Antibody Testing for Defining NPC Risk among Individuals from High-Risk NPC Families (2011) (57)
- HLA-DR, HLA-DQ, and TAP genes in familial Hodgkin disease. (2002) (56)
- Alcohol consumption and lung cancer risk in the Environment and Genetics in Lung Cancer Etiology (EAGLE) study. (2010) (55)
- Cleft lip with or without cleft palate: Reanalysis of a three‐generation family study from England (1986) (55)
- Genomic regions linked to alcohol consumption in the Framingham Heart Study (2003) (54)
- Familial and sporadic cases of nasopharyngeal carcinoma in Taiwan. (1999) (54)
- Two-locus linkage analysis of cutaneous malignant melanoma/dysplastic nevi. (1996) (54)
- Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries (2007) (53)
- Index-based dietary patterns and risk of head and neck cancer in a large prospective study. (2014) (53)
- Screening for CDKN2A mutations in hereditary melanoma. (1997) (53)
- Family history of cancer and nonmalignant lung diseases as risk factors for lung cancer (2009) (52)
- Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma (2014) (51)
- Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN2A Mutations (2013) (50)
- Cell-type–specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes (2017) (50)
- Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome‐associated medulloblastoma (1999) (47)
- Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array (2006) (47)
- Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies (2018) (46)
- Identification of modifier genes for cutaneous malignant melanoma in melanoma‐prone families with and without CDKN2A mutations (2009) (45)
- High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern China. (2000) (45)
- Genetic susceptibility in familial melanoma from northeastern Italy (2004) (45)
- Germline BAP1 mutations and tumor susceptibility (2011) (45)
- Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence (2021) (45)
- Increased matrix metalloproteinase activation in esophageal squamous cell carcinoma (2010) (45)
- Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. (2006) (44)
- Age at diagnosis and transmission of invasive melanoma in 23 families with cutaneous malignant melanoma/dysplastic nevi. (1994) (43)
- Clinical features distinguish childhood chordoma associated with tuberous sclerosis complex (TSC) from chordoma in the general paediatric population (2011) (43)
- Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations (2010) (42)
- Gene-covariate interaction between dysplastic nevi and the CDKN2A gene in American melanoma-prone families. (2000) (40)
- Validation of family history of cancer in deceased family members. (1996) (40)
- Family history as a co‐factor for adenocarcinoma and squamous cell carcinoma of the uterine cervix: Results from two studies conducted in Costa Rica and the United States (2005) (40)
- Germline splicing mutations of CDKN2A predispose to melanoma (2003) (40)
- Personal history of prostate cancer and increased risk of incident melanoma in the United States. (2013) (40)
- Distribution of Epstein‐Barr viral load in serum of individuals from nasopharyngeal carcinoma high‐risk families in Taiwan (2006) (39)
- Heterogeneity of risk for melanoma and pancreatic and digestive malignancies (2004) (39)
- Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma (2018) (39)
- Nevoid basal cell carcinoma syndrome with medulloblastoma in an African-American boy: a rare case illustrating gene-environment interaction. (1997) (37)
- Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148 (2017) (37)
- Counter-matching in studies of gene-environment interaction: efficiency and feasibility. (2001) (37)
- A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL). (2008) (37)
- Sun-related risk factors in melanoma-prone families with CDKN2A mutations. (1998) (37)
- Nucleotide diversity and population differentiation of the Melanocortin 1 Receptor gene, MC1R (2008) (36)
- MicroRNA analysis of microdissected normal squamous esophageal epithelium and tumor cells. (2011) (36)
- Evaluation of Human Leukocyte Antigen-A (HLA-A), Other Non-HLA Markers on Chromosome 6p21 and Risk of Nasopharyngeal Carcinoma (2012) (36)
- Detection of interaction involving identified genes: available study designs. (1999) (34)
- Allelic loss on chromosome bands 13q11‐q13 in esophageal squamous cell carcinoma (2001) (33)
- Quantitative real-time RT-PCR validation of differential mRNA expression of SPARC, FADD, Fascin, COL7A1, CK4, TGM3, ECM1, PPL and EVPL in esophageal squamous cell carcinoma (2006) (33)
- Genetic variants in sex hormone metabolic pathway genes and risk of esophageal squamous cell carcinoma. (2013) (33)
- Affected members of melanoma‐prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19ARF (1997) (32)
- Rare germline variants in known melanoma susceptibility genes in familial melanoma (2017) (32)
- Integrated analysis of genome-wide miRNAs and targeted gene expression in esophageal squamous cell carcinoma (ESCC) and relation to prognosis (2020) (32)
- Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions (2014) (32)
- Association of human leukocyte antigens with nasopharyngeal carcinoma in high-risk multiplex families in Taiwan. (2009) (32)
- Familial eosinophilia: clinical and laboratory results on a U.S. kindred. (1998) (32)
- High frequency of CDKN2A alterations in esophageal squamous cell carcinoma from a high‐risk Chinese population (2004) (32)
- PLCE1 mRNA and Protein Expression and Survival of Patients with Esophageal Squamous Cell Carcinoma and Gastric Adenocarcinoma (2014) (31)
- Identification of somatic mutations of the RNF6 gene in human esophageal squamous cell carcinoma. (2002) (31)
- Gastric microbiota features associated with cancer risk factors and clinical outcomes: A pilot study in gastric cardia cancer patients from Shanxi, China (2017) (31)
- Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene (2016) (31)
- CDKN2A point mutations D153spl(c.457G>T) and IVS2+1G>T result in aberrant splice products affecting both p16INK4a and p14ARF (2003) (31)
- Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival (2021) (31)
- CDKN2A mutations and melanoma risk in the Icelandic population (2008) (31)
- Retrospective family study of childhood medulloblastoma (2005) (31)
- Influence of Genetic Background and Tissue Types on Global DNA Methylation Patterns (2010) (30)
- A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families (2001) (30)
- Overexpression of CDC25B and LAMC2 mRNA and Protein in Esophageal Squamous Cell Carcinomas and Premalignant Lesions in Subjects from a High-Risk Population in China (2008) (30)
- Early onset may predict G101W CDKN2A founder mutation carrier status in Ligurian melanoma patients (2004) (30)
- Influence of glutathione-S-transferase (GSTM1, GSTP1, GSTT1) and cytochrome p450 (CYP1A1, CYP2D6) polymorphisms on numbers of basal cell carcinomas (BCCs) in families with the naevoid basal cell carcinoma syndrome (2005) (29)
- Genetic variants in fas signaling pathway genes and risk of gastric cancer (2014) (29)
- Common genetic variants of TP53 and BRCA2 in esophageal cancer patients and healthy individuals from low and high risk areas of northern China. (2003) (28)
- Infrequent mutation in the BRCA2 gene in esophageal squamous cell carcinoma. (2002) (28)
- Cancer patterns in nasopharyngeal carcinoma multiplex families in Taiwan (2009) (28)
- Whole-Exome Sequencing of Nasopharyngeal Carcinoma Families Reveals Novel Variants Potentially Involved in Nasopharyngeal Carcinoma (2019) (28)
- Allelic loss on chromosome 13q14 and mutation in deleted in cancer 1 gene in esophageal squamous cell carcinoma (2003) (27)
- Detecting gene‐environment interactions using a case‐control design (1997) (27)
- Identification of unique expression signatures and therapeutic targets in esophageal squamous cell carcinoma (2012) (27)
- Recent tanning bed use: a risk factor for melanoma. (2006) (27)
- Familiality of breast cancer and socioeconomic status in blacks. (1991) (26)
- Lack of germline CDK6 mutations in familial melanoma (2000) (26)
- Corroboration of a familial chordoma locus on chromosome 7q and evidence of genetic heterogeneity using single nucleotide polymorphisms (SNPs) (2005) (26)
- Affected members of melanoma-prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19ARF. (1997) (26)
- Increased risk of neuroectodermal tumors and stomach cancer in relatives of patients with Ewing's sarcoma family of tumors. (1994) (26)
- A genome-wide linkage scan for body mass index on Framingham Heart Study families (2003) (25)
- Evidence for a familial esophageal cancer susceptibility gene on chromosome 13. (2003) (25)
- Parenchymal-stromal interactions in neoplasia. Theoretical considerations and observations in melanocytic neoplasia. (1995) (24)
- Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9q. (1994) (24)
- Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types (2015) (24)
- Intracranial calcifications in childhood medulloblastoma: relation to nevoid basal cell carcinoma syndrome. (2000) (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)
- Use of relatives of cases as controls to identify risk factors when an interaction between environmental and genetic factors exists. (1996) (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)
- Integrative genomics analysis of genes with biallelic loss and its relation to the expression of mRNA and micro-RNA in esophageal squamous cell carcinoma (2015) (23)
- Hypermutability of UV-treated plasmids in dysplastic nevus/familial melanoma cell lines. (1997) (22)
- Genetic variants in DNA repair genes and the risk of cutaneous malignant melanoma in melanoma‐prone families with/without CDKN2A mutations (2012) (22)
- Epstein–Barr virus microRNAs and lung cancer (2011) (21)
- Histologic features of melanoma associated with CDKN2A genotype. (2015) (21)
- High‐risk pregnancy and neonatal complications in the DNA repair and transcription disorder trichothiodystrophy: report of 27 affected pregnancies (2011) (21)
- Etiology, epidemiology, risk factors, and public health issues of melanoma (1993) (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)
- Genetic Testing for Melanoma Predisposition: Current Challenges (2007) (19)
- The case-combined-control design was efficient in detecting gene-environment interactions. (2004) (19)
- An interstitial deletion within 9p21.3 and extending beyond CDKN2A predisposes to melanoma, neural system tumours and possible haematological malignancies (2016) (18)
- On the Interplay of Telomeres, Nevi and the Risk of Melanoma (2012) (18)
- Allelotyping of esophageal squamous‐cell carcinoma on chromosome 13 defines deletions related to family history (2005) (18)
- Lack of phospholipase A2 mutations in neuroblastoma, melanoma and colon‐cancer cell lines (1997) (18)
- Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility. (2016) (18)
- Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families. (2017) (18)
- Apparent anticipation in familial melanoma (1996) (18)
- Insights into Genetic Susceptibility to Melanoma by Gene Panel Testing: Potential Pathogenic Variants in ACD, ATM, BAP1, and POT1 (2020) (17)
- Lower Risk of Lung Cancer after Multiple Pneumonia Diagnoses (2010) (16)
- Familial melanoma and its management (1996) (16)
- Replication of a genome‐wide case–control study of esophageal squamous cell carcinoma (2008) (16)
- Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT. (2019) (16)
- Jasmine tea consumption and upper gastrointestinal cancer in China (2009) (15)
- Approaches to complex pathways in molecular epidemiology: summary of a special conference of the American Association for Cancer Research. (2008) (15)
- Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma‐prone family (2012) (15)
- Hereditary genodermatoses with cancer predisposition. (2010) (15)
- Effect of mutations in XPD(ERCC2) on pregnancy and prenatal development in mothers of patients with trichothiodystrophy or xeroderma pigmentosum (2012) (15)
- Variants Associated with Susceptibility to Pancreatic Cancer and Melanoma Do Not Reciprocally Affect Risk (2014) (14)
- Pediatric melanoma in melanoma‐prone families (2018) (14)
- Body mass index and height and risk of cutaneous melanoma: Mendelian randomization analyses. (2020) (14)
- Risks of Melanoma and Other Cancers in Melanoma-Prone Families over 4 Decades. (2018) (14)
- Germline Mutations in PALB 2 , BRCA 1 , and RAD 51 C , Which Regulate DNA Recombination Repair , in Patients With Gastric Cancer (2017) (13)
- Integrative molecular characterization of gallbladder cancer reveals microenvironment-associated subtypes. (2020) (13)
- Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data. (2016) (13)
- Cytogenetics of familial Waldenstrom's macroglobulinemia: in pursuit of an understanding of genetic predisposition. (2005) (13)
- Constitutional promoter methylation and risk of familial melanoma (2014) (13)
- DR2/DQwl Inheritance and haplotype sharing in affected siblings from multiple sclergis families (1996) (13)
- Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma. (2016) (12)
- A flexible multiplex bead-based assay for detecting germline CDKN2A and CDK4 variants in melanoma-prone kindreds. (2011) (12)
- Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families. (2016) (12)
- LINE-1 methylation in peripheral blood and the risk of melanoma in melanoma-prone families with and without CDKN2A mutations (2013) (12)
- The inheritance pattern of dysplastic naevi in families of dysplastic naevus patients. (1993) (11)
- Analysis of mutations and identification of several polymorphisms in the putative promoter region of the P34CDC2‐related CDC2L1 gene located at 1P36 in melanoma cell lines and melanoma families (2002) (11)
- Associations of pigmentary and naevus phenotype with melanoma risk in two populations with comparable ancestry but contrasting levels of ambient sun exposure (2019) (11)
- Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes (2008) (11)
- Whole‐exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data (2018) (11)
- Sebaceous Carcinoma Epidemiology and Genetics: Emerging Concepts and Clinical Implications for Screening, Prevention, and Treatment (2020) (11)
- Variation in cutaneous patterns of melanomagenesis according to germline CDKN2A/CDK4 status in melanoma-prone families. (2020) (11)
- Association of MC 1 R Variants and Risk of Melanoma in Melanoma-Prone Families with CDKN 2 A Mutations (2005) (11)
- A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma. (2011) (11)
- Association of MC1R Variants and Risk of Melanoma in Melanoma-Prone Families with CDKN2A Mutations (2005) (10)
- GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer (2017) (10)
- Unconditional analyses can increase efficiency in assessing gene-environment interaction of the case-combined-control design. (2006) (10)
- Ancient origin of a Japanese xeroderma pigmentosum founder mutation. (2013) (10)
- A competitive enzyme-linked immunoassay (ELISA) for the measurement of soluble human interleukin-2 receptors (IL-2R, Tac protein). (1988) (10)
- Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia (2021) (10)
- A systematic review of the prevalence of germline pathogenic variants in patients with pancreatic cancer (2021) (10)
- DR2/DQw1 inheritance and haplotype sharing in affected siblings from multiple sclerosis families. (1996) (10)
- Association of high-evidence gastric cancer susceptibility loci and somatic gene expression levels with survival (2017) (10)
- Common genetic variants in epigenetic machinery genes and risk of upper gastrointestinal cancers. (2015) (10)
- Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families (2013) (10)
- Clinical characteristics of 20 Italian melanoma-prone families. (1999) (9)
- Familial melanoma aggregation in north-eastern Italy. (2000) (9)
- Constitutive mitochondrial DNA copy number in peripheral blood of melanoma families with and without CDKN2A mutations. (2014) (9)
- Ambient Ultraviolet Radiation and Sebaceous Carcinoma Incidence in the United States, 2000-2016. (2020) (9)
- First international workshop of the ATM and cancer risk group (4-5 December 2019) (2021) (9)
- Linkage analysis of the GAW14 simulated dataset with microsatellite and single-nucleotide polymorphism markers in large pedigrees (2005) (9)
- Sib‐pair linkage analyses of nuclear family data: Quantitative versus dichotomous disease classification (1997) (8)
- A Systematic Literature Review of Whole Exome and Genome Sequencing Population Studies of Genetic Susceptibility to Cancer (2020) (8)
- Sebaceous Carcinoma Incidence and Survival Among Solid Organ Transplant Recipients in the United States, 1987-2017. (2020) (8)
- Phenocopies in melanoma-prone families with germ-line CDKN2A mutations (2018) (8)
- Oesophageal squamous cell carcinoma in high-risk Chinese populations: Possible role for vascular epithelial growth factor A. (2014) (8)
- Common genetic variants related to vitamin D status are not associated with esophageal squamous cell carcinoma risk in China. (2015) (7)
- Risk factors for melanoma by anatomical site: an evaluation of aetiological heterogeneity * (2020) (7)
- Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel‐type zinc finger sequence on chromosome segment 9q22.3 (1997) (7)
- Identifying rheumatoid arthritis susceptibility genes using high-dimensional methods (2009) (7)
- Linkage analysis of melanoma alone and chromosome 1p markers PND, D1S47, and LMYC. (1992) (7)
- Survival among children with medulloblastoma in Greece: gains from transition to chemotherapy and socio-economic differentials (2007) (6)
- Cell-type-specific meQTL extends melanoma GWAS annotation beyond eQTL and informs melanocyte gene regulatory mechanisms (2021) (6)
- Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study. (2021) (6)
- Lack of inherited mutations of PTPRD in familial melanoma and melanoma‐astrocytoma syndrome (2009) (6)
- Use of Big Data to Estimate Prevalence of Defective DNA Repair Variants in the US Population (2019) (6)
- Increased power to detect gene-environment interaction using siblings controls. (2005) (6)
- Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer (2011) (5)
- Three-dimensional mRNA measurements reveal minimal regional heterogeneity in esophageal squamous cell carcinoma. (2013) (5)
- Evaluation of Rare and Common Variants from Suspected Familial or Sporadic Nasopharyngeal Carcinoma (NPC) Susceptibility Genes in Sporadic NPC (2019) (5)
- No evidence for linkage between an insulin‐dependent diabetes mellitus‐susceptibility locus and immunoglobulin loci KM or GM (1984) (5)
- Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility (2020) (5)
- Reproductive Health in Xeroderma Pigmentosum: Features of Premature Aging. (2019) (5)
- A piece of the melanoma puzzle. (2005) (5)
- Comparison of the affected-pedigree-member and lod-score methods. (1989) (4)
- Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN 2 A Mutations (2013) (4)
- ABO genotypes and the risk of esophageal and gastric cancers (2021) (4)
- Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma (2008) (4)
- Use of Weighted p‐Values in Regional Inference Procedures (2001) (4)
- Genetic epidemiology of bilateral breast cancer: A linkage analysis using the affected‐pedigree‐member method (1990) (4)
- Elevated antibodies against Epstein-Barr virus among individuals predicted to carry nasopharyngeal carcinoma susceptibility variants. (2018) (4)
- Genetic testing for inherited predisposition to melanoma: has the time come? (2004) (4)
- Histologic features of melanoma associated with germline mutations of CDKN2A, CDK4, and POT1 in melanoma-prone families from the United States, Italy, and Spain. (2020) (4)
- Prospectives for cutaneous malignant melanoma. Considerations of the precursor state and heritability. (1995) (4)
- Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility (2021) (4)
- Low Epstein–Barr Virus Prevalence in Cardia Gastric Cancer Among a High-Incidence Chinese Population (2020) (4)
- Correlates of anti-EBV EBNA1 IgA positivity among unaffected relatives from nasopharyngeal carcinoma multiplex families (2011) (4)
- Comparison of Likelihood Approaches for Combined Segregation and Linkage Analysis of a Complex Disease and a Candidate Gene Marker Under Different Ascertainment Schemes (2001) (4)
- An international report on bacterial communities in esophageal squamous cell carcinoma (2021) (3)
- Clustering of high density lipoprotein cholesterol levels in premenopausal and postmenopausal female twins (1993) (3)
- No Evidence for Linkage with Melanoma in Italian Melanoma-Prone Families (2008) (3)
- Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility (2020) (3)
- Gene×Environment Interaction from Case‐Control and Case‐Case Approaches (2001) (3)
- RPA2, a gene for the 32 kDa subunit of replication protein A on chromosome 1p35—36, is not mutated in patients with familial melanoma linked to chromosome 1p36 (1998) (3)
- Clinical findings in families with chordoma with and without T gene duplications and in patients with sporadic chordoma reported to the Surveillance, Epidemiology, and End Results program. (2020) (3)
- 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)
- EDITORIALS Screening for CDKN2A Mutations in Hereditary Melanoma (1997) (2)
- The Impact of Longitudinal Surveillance on Tumor Thickness for Melanoma-Prone Families with and without Pathogenic Germline Variants of CDKN2A and CDK4 (2021) (2)
- Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2019) (2)
- Linkage analysis of anti-CCP levels as dichotomized and quantitative traits using GAW15 single-nucleotide polymorphism scan of NARAC families (2007) (2)
- Corrigendum: Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions (2014) (2)
- Flexible Two-Phase studies for rare exposures: Feasibility, planning and efficiency issues of a new variant (2008) (2)
- A problem in identifying risk factors for disease using surrogate exposure variables that are under genetic control. (1990) (2)
- A Genome-First Approach to Estimate Prevalence of Germline Pathogenic Variants and Risk of Pancreatic Cancer in Select Cancer Susceptibility Genes (2022) (2)
- Description of the National Cancer Institute melanoma families. (1992) (2)
- The genetics of melanoma. (1997) (2)
- Genetic Epidemiology of Cutaneous Melanoma (2015) (2)
- Meeting report: consensus from the first and second Global Workshops in Melanoma November 19–20, 2008 (2009) (2)
- Histological Features of Melanoma Associated with CDKN 2 A Genotype (2015) (2)
- Reply: To PMID 24715615. (2015) (1)
- Sib‐pair linkage analyses of alcoholism: Dichotomous and quantitative measures (1999) (1)
- Correction: Hereditary cutaneous malignant melanoma-dysplastic nevus. (1991) (1)
- Inflated expectations: Rare-variant association analysis using public controls (2023) (1)
- Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation (2022) (1)
- Frequency of CDKN2A mutation in Ligurian non-familial melanoma patients (2004) (1)
- Abstract 2755: Germline copy number variations in melanoma families with/without CDKN2A/CDK4 mutations (2015) (1)
- Abstract 1333: Specific RB1 mutations and risk of subsequent neoplasms among survivors of hereditary retinoblastoma. (2013) (1)
- Patients with multiple primary melanomas may have germline CDKN24 mutations and an occult family history of the disease: 467 (1997) (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)
- Abstract #LB-139: A comprehensive genome-wide association study of lung cancer (2009) (1)
- ASSOCIATION OF HUMAN LEUKOCYTE ANTIGENS (HLA) WITH NASOPHARYNGEAL CARCINOMA (NPC) IN HIGH-RISK MULTIPLEX FAMILIES IN TAIWAN (2009) (1)
- RESPONSE: Re: MC1R, ASIP, and DNA Repair in Sporadic and Familial Melanoma in a Mediterranean Population (2006) (1)
- Abstract B27: DNA polymorphisms in sex hormone pathway genes and risk of esophageal squamous cell carcinoma (2010) (1)
- Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family (2021) (1)
- Abstract 4289: Whole-exome sequencing study of nevoid basal cell carcinoma syndrome (NBCCS) families to identify disease-causing exonic mutations (2017) (1)
- Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma (2022) (1)
- Identification of susceptibility loci for complex diseases in a case-control association study using the Genetic Analysis Workshop 14 dataset (2005) (1)
- A retrospective family study of childhood medulloblastoma (Am J Med Genet 134A(4): 399–403) (2005) (1)
- Contributors and Participants (1982) (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)
- Novel loss-of-function variant in DENND5A impedes melanosomal cargo transport and predisposes to familial cutaneous melanoma. (2021) (0)
- Family history of cancer and family history of smoking in lung cancer risk by histology (2008) (0)
- First international workshop of the ATM and cancer risk group (4-5 December 2019) (2021) (0)
- Genetic and epidemiologic factors in hereditary melanoma: 050 (1997) (0)
- Abstract 2553: Characterization of rare germline variants in somatically mutated melanoma genes in melanoma-prone families. (2013) (0)
- 126 Anatomic distribution of cutaneous melanoma in patients with and without germline CDKN2A and CDK4 mutations (2019) (0)
- Abstract B1: Genome-wide LOH and copy number alterations show heterogeneity in esophageal squamous cell carcinoma (2008) (0)
- Integrated Analysis of Co-expression and Exome Sequencing to Prioritize Susceptibility Genes for Familial Cutaneous Melanoma. (2022) (0)
- Phenocopies in melanoma-prone families with germ-line CDKN2A mutations (2017) (0)
- 308 Host characteristics and risk of atypical nevi (2018) (0)
- Abstract 4805: Index-based dietary patterns and risk of esophageal cancer and gastric cancer in the NIH-AARP diet and health study. (2013) (0)
- Interrogation of Chromosome 13 q 12-14 in Esophageal Squamous Cell Carcinoma (2012) (0)
- p16 Mutations in hereditary melanomas (1994) (0)
- Abstract 2206: Genetic variants in selenoprotein genes and risk of esophageal squamous cell carcinoma and gastric cancer in a Chinese population (2014) (0)
- Table 2 . ORs and 95 % CIs for associations of lung cancer with pneumonia and tuberculosis diagnosed at least 1 y prior to entry into the EAGLE case-control study , both overall and stratified by smoking status (2010) (0)
- Integrated analysis of genome-wide miRNAs and targeted gene expression in esophageal squamous cell carcinoma (ESCC) and relation to prognosis (2020) (0)
- Reply (2015) (0)
- Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma (2014) (0)
- Variation in second cancer risk by melanoma subtype among survivors. (2022) (0)
- Abstract 1600: A literature review of whole exome and genome sequencing population studies for identifying novel germline mutations in relation to cancer risk (2019) (0)
- Molecular Analysis ofChromosome9qDeletions inTwoGorlin Syndrome Patients (1996) (0)
- Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in CDKN2A and Pancreatic Cancer. (2022) (0)
- Abstract 2589: Identifying cancer susceptibility variants and genes using whole exome and genome sequencing: a literature review (2017) (0)
- Abstract 869: Characterization of malignant melanoma families withCDK4germ-line mutation (2011) (0)
- Abstract 2294: Atypical nevi and risk of incident skin cancer in US men: a prospective study (2017) (0)
- Gene expression profiling identifies two chordoma subtypes associated with distinct molecular mechanisms and clinical outcomes. (2022) (0)
- Cell-type-specific meQTL extends melanoma GWAS annotation beyond eQTL and 1 informs melanocyte gene regulatory mechanisms 2 (2021) (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)
- Whole-Exome Sequencing of Nasopharyngeal Carcinoma Families Reveals Novel Variants Potentially Involved in Nasopharyngeal Carcinoma (2019) (0)
- Icelandic population mutations and melanoma risk in the CDKN2A (2008) (0)
- GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer (2017) (0)
- Abstract 866: Changing anatomic site trends of melanoma in the United States among young women (2010) (0)
- Sa1933 PLCE1 mRNA and Protein Expression and Survival of Patients With Esophageal Squamous Cell Carcinoma and Gastric Adenocarcinoma (2014) (0)
- Genetic Testing for Melanoma Predisposition (2007) (0)
- Abstract 941: Exome sequencing identifiedPOT1, a telomere shelterin gene, as a major susceptibility gene for familial cutaneous malignant melanoma (2014) (0)
- Abstract 2561: Integrated analysis of ESCC tumor/normal tissues and patient blood samples using expression, genotypes and DNA somatic change data (2016) (0)
- Clinical findings in chordoma families with and without T gene duplications and chordoma patients reported to the Surveillance, Epidemiology and End Results Program (2021) (0)
- Abstract A105: Dietary quercetin, quercetin‐gene interaction, metabolic gene expression in lung tissue, and lung cancer risk (2010) (0)
- Abstract 4824: Little evidence of human papillomavirus in lung tumor tissue (2010) (0)
- Cancer patterns in nasopharyngeal carcinoma multiplex families over 15 years (2021) (0)
- CLINICAL FEATURES IN CHILDREN WITH NEVOID BASAL CELL CARCINOMA SYNDROME.• 863 (1996) (0)
- PLCE1mRNAandProteinExpressionandSurvivalofPatients with Esophageal Squamous Cell Carcinoma and Gastric Adenocarcinoma (2014) (0)
- Linkage analysis of GAW14 simulated dataset with microsatellite and SNP markers in large pedigrees. (2005) (0)
- Abstract LB-330: Genetic variants in the 9p21 region in relation to the risk of multiple tumors (2012) (0)
- Erratum: Analysis of mutations and identification of several polymorphisms in the putative promoter region of the P34CDC2-related CDC2L1 gene located at 1P36 in melanoma cell lines and melanoma families (International Journal of Cancer (2002) 99 (834-838)) (2002) (0)
- Mutations in genes controlling the G1 checkpoint in familial melanoma: 028 (1997) (0)
- Impact of Transcript (p16/p14ARF) Alteration on Cancer Risk in CDKN2A Germline Pathogenic Variant Carriers. (2022) (0)
- Abstract 1638: Whole-exome sequencing and protein interaction networks to prioritize candidate genes for cutaneous melanoma susceptibility (2019) (0)
- Association of germline variants in telomere maintenance genes (POT1, TERF2IP, ACD, and TERT) with spitzoid morphology in familial melanoma: A multi-center case series (2023) (0)
- Abstract 3257: Molecular characterization of the human stomach microbiota in gastric cancer patients (2017) (0)
- CSMD1 Shows Complex Patterns of Somatic Copy Number Alterations and Expressions of mRNAs and Target Micro RNAs in Esophageal Squamous Cell Carcinoma (2022) (0)
- Correction to: Overlapping genetic architecture between Parkinson disease and melanoma (2020) (0)
- M1990 Over-Expression of CDC25B and LAMC2 mRNA and Protein in Esophageal Squamous Cell Carcinomas and Pre-Malignant Lesions in Subjects from a High-Risk Population in China (2008) (0)
- Identification of unique expression signatures and therapeutic targets in esophageal squamous cell carcinoma (2012) (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)
- Abstract LB-158: Germline mutations inPALB2,BRCA1andRAD51Cobserved in gastric cancer cases (2017) (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)
- ng Melanoma Incidence Rates of the Trunk among B & P nger Women in the United States (2010) (0)
- Abstract 4710: A candidate gene expression signature of early stage lung adenocarcinoma from peripheral whole blood (2010) (0)
- Abstract 2632: Genetic variants of iron-dependent metabolism genes and risk of upper gastrointestinal cancers (2012) (0)
- Abstract 234: Understanding melanoma susceptibility through GWAS of risk phenotypes (2018) (0)
- Protein Intake , Chronic Liver Diseases , and Hepatocellular Carcinoma To the (2015) (0)
- ABO genotypes and the risk of esophageal and gastric cancers (2021) (0)
- Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2018) (0)
- Integrative genomics analysis of genes with biallelic loss and its relation to the expression of mRNA and micro-RNA in esophageal squamous cell carcinoma (2015) (0)
- Abstract 688: Promoter methylation of death receptor decoy genes in blood and risk of melanoma in melanoma-prone families . (2013) (0)
- Abstract 2168: Molecular pathway analysis of esophageal squamous cell differentiation versus carcinoma formation (2010) (0)
- Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family (2021) (0)
- Interrogation of Chromosome 13q12-14 in Esophageal Squamous Cell Carcinoma (2012) (0)
- SeqPlus sequencing methodology enables robust whole-genome sequencing, true variant detection, and novel genomic insights from archival esophageal carcinoma FFPE samples. (2019) (0)
- Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2019) (0)
- Genome-Wide Analyses Characterize Shared Heritability Among Cancers and Identify Novel Cancer Susceptibility Regions. (2023) (0)
- Abstract 228: Association analysis across different populations identifies 26 new cutaneous melanoma risk loci (2018) (0)
- Preface (0)
- Abstract A84: Reduced LINE-1 methylation in peripheral blood mononuclear cells is associated with risk of melanoma in families segregating CDKN2A germline mutations (2011) (0)
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