A. Goldstein

N. Hu, M. Emmert-Buck, P. Albert, 2003, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Elevated antibodies against Epstein-Barr virus among individuals predicted to carry nasopharyngeal carcinoma susceptibility variants.

Chien-Jen Chen, A. Goldstein, A. Hildesheim, 2018, The Journal of general virology.

ASSOCIATION OF HUMAN LEUKOCYTE ANTIGENS (HLA) WITH NASOPHARYNGEAL CARCINOMA (NPC) IN HIGH-RISK MULTIPLEX FAMILIES IN TAIWAN

M. Carrington, Chien-Jen Chen, A. Goldstein, 2009 .

Distribution of Epstein‐Barr viral load in serum of individuals from nasopharyngeal carcinoma high‐risk families in Taiwan

Chien-Jen Chen, M. Gulley, A. Goldstein, 2006, International journal of cancer.

Evaluation of Human Leukocyte Antigen-A (HLA-A), Other Non-HLA Markers on Chromosome 6p21 and Risk of Nasopharyngeal Carcinoma

Chien-Jen Chen, A. Goldstein, A. Hildesheim, 2012, PloS one.

Association of MC1R Variants and Risk of Melanoma in Melanoma-Prone Families with CDKN2A Mutations

M. Tucker, A. Goldstein, M. Landi, 2005, Cancer Epidemiology Biomarkers & Prevention.

Sib‐pair linkage analyses of alcoholism: Dichotomous and quantitative measures

A. Goldstein, A. Bergen, K. Weissbecker, 1999, Genetic epidemiology.

Prognostic Utility of Anti-EBV Antibody Testing for Defining NPC Risk among Individuals from High-Risk NPC Families

Chien-Jen Chen, A. Goldstein, R. Pfeiffer, 2011, Clinical Cancer Research.

Epstein‐Barr virus seroreactivity among unaffected individuals within high‐risk nasopharyngeal carcinoma families in Taiwan

Chien-Jen Chen, A. Goldstein, A. Hildesheim, 2004, International journal of cancer.

Validation of family history of cancer in deceased family members.

M. Tucker, A. Goldstein, B. Novakovič, 1996, Journal of the National Cancer Institute.

Personal history of prostate cancer and increased risk of incident melanoma in the United States.

A. Qureshi, Jiali Han, M. Stampfer, 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

A Genome-First Approach to Estimate Prevalence of Germline Pathogenic Variants and Risk of Pancreatic Cancer in Select Cancer Susceptibility Genes

A. Goldstein, D. Carey, Jung Kim, 2022, Cancers.

Germline BAP1 mutations and tumor susceptibility

A. Goldstein, 2011, Nature Genetics.

Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome.

A. Goldstein, S. Bale, V. Kimonis, 1997, American journal of medical genetics.

A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma.

K. Stefánsson, M. Thun, J. Chang-Claude, 2011, American journal of human genetics.

Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families.

S. Puig, D. Bishop, D. Elder, 2016, The Journal of investigative dermatology.

A flexible multiplex bead-based assay for detecting germline CDKN2A and CDK4 variants in melanoma-prone kindreds.

S. Puig, N. Hayward, M. Tucker, 2011, The Journal of investigative dermatology.

Genetic Testing for Melanoma Predisposition: Current Challenges

M. Tucker, A. Goldstein, M. Gerstenblith, 2007, Cancer nursing.

Genetic Testing for Melanoma Predisposition

M. Tucker, A. Goldstein, M. Gerstenblith, 2007 .

Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity.

W. Clark, M. Tucker, A. Goldstein, 1993, American journal of human genetics.

Risks of Melanoma and Other Cancers in Melanoma-Prone Families over 4 Decades.

D. Elder, M. Tucker, A. Goldstein, 2018, The Journal of investigative dermatology.

Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma

F. Couch, S. Chanock, M. Yeager, 2022, Human mutation.

Cell-type-specific meQTL extends melanoma GWAS annotation beyond eQTL and 1 informs melanocyte gene regulatory mechanisms 2

K. Brown, M. Iles, A. Goldstein, 2021 .

Comprehensive evaluation of allele frequency differences of MC1R variants across populations.

A. Goldstein, K. Peris, M. Landi, 2006, Human mutation.

A Gene Expression Signature from Peripheral Whole Blood for Stage I Lung Adenocarcinoma

Nan Hu, Maria Teresa Landi, Neil E Caporaso, 2011, Cancer Prevention Research.

Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility.

G. Marti, S. Chanock, M. Yeager, 2016, Blood.

Characterization of large structural genetic mosaicism in human autosomes.

William Wheeler, Nan Hu, Peter Kraft, 2015, American journal of human genetics.

Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations

S. Chanock, M. Yeager, M. Tucker, 2010, Familial Cancer.

Frequency of CDKN2A mutation in Ligurian non-familial melanoma patients

A. Goldstein, P. Queirolo, M. Sertoli, 2004 .

Clustering of high density lipoprotein cholesterol levels in premenopausal and postmenopausal female twins

A. Goldstein, E. Harris, L. Park, 1993, Genetic epidemiology.

Sib‐pair linkage analyses of nuclear family data: Quantitative versus dichotomous disease classification

A. Goldstein, J. Korczak, 1997, Genetic epidemiology.

Identification of modifier genes for cutaneous malignant melanoma in melanoma‐prone families with and without CDKN2A mutations

S. Chanock, M. Yeager, M. Tucker, 2009, International journal of cancer.

A competitive enzyme-linked immunoassay (ELISA) for the measurement of soluble human interleukin-2 receptors (IL-2R, Tac protein).

B. Cullen, A. Goldstein, D. Nelson, 1988, Journal of immunological methods.

Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations.

A M Goldstein, N C Dracopoli, W. Clark, 1995, The New England journal of medicine.

Variation in cutaneous patterns of melanomagenesis according to germline CDKN2A/CDK4 status in melanoma-prone families.

M. Tucker, A. Goldstein, R. Pfeiffer, 2020, The Journal of investigative dermatology.

R. Sikorski, W. Clark, M. Tucker, 1998, Journal of the National Cancer Institute.

Hypermutability of UV-treated plasmids in dysplastic nevus/familial melanoma cell lines.

M. Tucker, A. Goldstein, R. Tarone, 1997, Cancer research.

Increased risk of neuroectodermal tumors and stomach cancer in relatives of patients with Ewing's sarcoma family of tumors.

M. Tucker, A. Goldstein, L. Wexler, 1994, Journal of the National Cancer Institute.

Cytogenetics of familial Waldenstrom's macroglobulinemia: in pursuit of an understanding of genetic predisposition.

M. Tucker, A. Goldstein, M. McMaster, 2005, Clinical lymphoma.

The inheritance pattern of dysplastic naevi in families of dysplastic naevus patients.

P. Hartge, M. Tucker, A. Goldstein, 1993, Melanoma research.

Rarity of CDK4 germline mutations in familial melanoma

A. Halpern, D. Elder, D. Guerry, 2002, Melanoma research.

Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes

M. Tucker, A. Goldstein, Xiaohong R. Yang, 2008, BMC Research Notes.

EDITORIALS Screening for CDKN2A Mutations in Hereditary Melanoma

M. Tucker, A. Goldstein, 1997 .

Phenocopies in melanoma-prone families with germ-line CDKN2A mutations

H. Olsson, M. Tucker, A. Goldstein, 2017, Genetics in Medicine.

A piece of the melanoma puzzle.

M. Tucker, A. Goldstein, 2005, Journal of the National Cancer Institute.

High‐risk pregnancy and neonatal complications in the DNA repair and transcription disorder trichothiodystrophy: report of 27 affected pregnancies

Sikandar G. Khan, M. Tucker, A. Goldstein, 2011, Prenatal diagnosis.

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

M. Tucker, A. Goldstein, D. Hogg, 1997 .

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.

M. Tucker, A. Goldstein, D. Hogg, 1997, Genes, chromosomes & cancer.

Etiology, epidemiology, risk factors, and public health issues of melanoma

M. Tucker, A. Goldstein, 1993, Current opinion in oncology.

Association of MC 1 R Variants and Risk of Melanoma in Melanoma-Prone Families with CDKN 2 A Mutations

M. Tucker, A. Goldstein, M. Landi, 2005 .

Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients.

A. Goldstein, S. Bale, J. DiGiovanna, 1996, Cancer research.

DR2/DQwl Inheritance and haplotype sharing in affected siblings from multiple sclergis families

A. Goldstein, H. McFarland, R. Voskuhl, 1996 .

A genome‐wide search for loci contributing to smoking and alcoholism

A. Goldstein, A. Bergen, K. Weissbecker, 1999, Genetic epidemiology.

CSMD1 Shows Complex Patterns of Somatic Copy Number Alterations and Expressions of mRNAs and Target Micro RNAs in Esophageal Squamous Cell Carcinoma

N. Hu, A. Goldstein, P. Taylor, 2022, Cancers.

Germline Mutations in PALB 2 , BRCA 1 , and RAD 51 C , Which Regulate DNA Recombination Repair , in Patients With Gastric Cancer

C. Yau, N. Hu, A. Goldstein, 2017 .

Associations of pigmentary and naevus phenotype with melanoma risk in two populations with comparable ancestry but contrasting levels of ambient sun exposure

J. Barrett, D. Bishop, D. Elder, 2019, Journal of the European Academy of Dermatology and Venereology : JEADV.

Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in CDKN2A and Pancreatic Cancer.

S. Chanock, M. Tucker, N. Freedman, 2022, JCO precision oncology.

Infrequent mutation in the BRCA2 gene in esophageal squamous cell carcinoma.

Quan-hong Wang, Jing Huang, N. Hu, 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.

Linkage analysis of anti-CCP levels as dichotomized and quantitative traits using GAW15 single-nucleotide polymorphism scan of NARAC families

A. Goldstein, A. Bergen, L. Goldin, 2007, BMC proceedings.

Linkage analysis of melanoma alone and chromosome 1p markers PND, D1S47, and LMYC.

M. Tucker, A. Goldstein, S. Bale, 1992, Cytogenetics and cell genetics.

Correction: Hereditary cutaneous malignant melanoma-dysplastic nevus.

M. Tucker, A. Goldstein, S. Bale, 1991, The New England journal of medicine.

Localization of the gene for the nevoid basal cell carcinoma syndrome.

A. Goldstein, C. Stewart, A. Bale, 1994, American journal of human genetics.

Integrative molecular characterization of gallbladder cancer reveals microenvironment-associated subtypes.

S. Chanock, A. Goldstein, A. Rashid, 2020, Journal of hepatology.

Detection of interaction involving identified genes: available study designs.

A. Goldstein, N. Andrieu, Alisa M. Goldstein, 1999, Journal of the National Cancer Institute. Monographs.

Genetic testing for inherited predisposition to melanoma: has the time come?

M. Tucker, A. Goldstein, M. Fraser, 2004, Journal of drugs in dermatology : JDD.

High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.

S. Puig, E. Gillanders, D. Bishop, 2006, Cancer research.

Cleft lip with or without cleft palate: Reanalysis of a three‐generation family study from England

M. Spence, A. Goldstein, D. Rao, 1986, Genetic epidemiology.

RESPONSE: Re: MC1R, ASIP, and DNA Repair in Sporadic and Familial Melanoma in a Mediterranean Population

A. Goldstein, R. Pfeiffer, M. Landi, 2006 .

Nested PCR Biases in Interpreting Microbial Community Structure in 16S rRNA Gene Sequence Datasets

J. Goedert, J. Ravel, A. Goldstein, 2015, PloS one.

Localization of the gene for Cowden disease to chromosome 10q22–23

E. Mariman, D. Easton, R. Eeles, 1996, Nature Genetics.

Acral lentiginous melanoma: incidence and survival patterns in the United States, 1986-2005.

M. Tucker, A. Goldstein, M. McMaster, 2009, Archives of dermatology.

Nevoid basal cell carcinoma syndrome with medulloblastoma in an African-American boy: a rare case illustrating gene-environment interaction.

A. Goldstein, J. DiGiovanna, L. Wexler, 1997, American journal of medical genetics.

Survival among children with medulloblastoma in Greece: gains from transition to chemotherapy and socio-economic differentials

A. Goldstein, E. Petridou, F. Tzortzatou-Stathopoulou, 2007, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Retrospective family study of childhood medulloblastoma

A. Goldstein, J. Rutka, B. Gold, 2005, American journal of medical genetics. Part A.

Prognostic Factors and Secondary Malignancies in Childhood Medulloblastoma

A. Goldstein, G. Reaman, R. Packer, 2001, Journal of pediatric hematology/oncology.

Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome

Michael Dean, Georgia Chenevix-Trench, Susan Shanley, 1996, Cell.

Clinical findings in two African-American families with the nevoid basal cell carcinoma syndrome (NBCC).

A. Goldstein, S. Bale, J. DiGiovanna, 1994, American journal of medical genetics.

Sebaceous Carcinoma Epidemiology and Genetics: Emerging Concepts and Clinical Implications for Screening, Prevention, and Treatment

M. Tucker, A. Goldstein, E. Engels, 2020, Clinical Cancer Research.

Chordoma: incidence and survival patterns in the United States, 1973–1995

A. Goldstein, D. Parry, M. McMaster, 2004, Cancer Causes & Control.

Genotype-phenotype relationships in U.S. melanoma-prone families with CDKN2A and CDK4 mutations.

J. Struewing, M. Tucker, A. Goldstein, 2000, Journal of the National Cancer Institute.

Histologic features of melanoma associated with CDKN2A genotype.

S. Puig, D. Elder, G. Mann, 2015, Journal of the American Academy of Dermatology.

Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair

Sikandar G. Khan, M. Tucker, A. Goldstein, 2010, Journal of Medical Genetics.

Sun exposure and basal cell carcinomas in the nevoid basal cell carcinoma syndrome.

A. Goldstein, S. Bale, J. DiGiovanna, 1993, Journal of the American Academy of Dermatology.

Intracranial calcifications in childhood medulloblastoma: relation to nevoid basal cell carcinoma syndrome.

A. Goldstein, G. Reaman, G. Vezina, 2000, AJNR. American journal of neuroradiology.

Mutations in SUFU predispose to medulloblastoma

David Hogg, S. Scherer, A. Goldstein, 2002, Nature Genetics.

Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome‐associated medulloblastoma

A. Vortmeyer, A. Goldstein, R. Weil, 1999, Cancer.

Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel‐type zinc finger sequence on chromosome segment 9q22.3

A. Goldstein, M. Dean, I. Chumakov, 1997, Genes, chromosomes & cancer.

Whole‐exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data

A. Goldstein, L. Mirabello, K. Jones, 2018, Molecular genetics & genomic medicine.

Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9q.

A. Goldstein, S. Bale, M. Turner, 1994, The Journal of investigative dermatology.

Germline p16 mutations in familial melanoma

W. Clark, J. Struewing, M. Tucker, 1994, Nature Genetics.

A natural history of melanomas and dysplastic nevi

W. Clark, J. Struewing, M. Tucker, 2002, Cancer.

MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population.

Maria Teresa Landi, Mohammad Hedayati, Ruth M Pfeiffer, 2005, Journal of the National Cancer Institute.

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

Marko Hočevar, Kevin M. Brown, Florence Demenais, 2015, Nature Genetics.

Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma

N. Hayward, M. Tucker, A. Goldstein, 1996, Nature Genetics.

Comprehensive evaluation of allele frequency differences of MC1R variants across populations

A. Goldstein, K. Peris, M. Landi, 2007 .

Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility

Blair H. Smith, Jeffrey E. Lee, G. Abecasis, 2020, Nature Genetics.

A variant in FTO shows association with melanoma risk not due to BMI

Marko Hočevar, Florence Demenais, Kari Stefansson, 2013, Nature Genetics.

An interstitial deletion within 9p21.3 and extending beyond CDKN2A predisposes to melanoma, neural system tumours and possible haematological malignancies

A. Goldstein, J. Drabick, P. L. Gordon, 2016, Journal of Medical Genetics.

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

Jianxin Shi, Florence Demenais, Maria Teresa Landi, 2014, Nature Genetics.

Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN2A Mutations

S. Chanock, M. Yeager, M. Tucker, 2013, PloS one.

Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants

L. Thomas, N. Hayward, M. Tucker, 2013, Journal of Medical Genetics.

Lack of inherited mutations of PTPRD in familial melanoma and melanoma‐astrocytoma syndrome

M. Tucker, A. Goldstein, Y. Samuels, 2009, Pigment cell & melanoma research.

Familial melanoma, pancreatic cancer and germline CDKN2A mutations

A. Goldstein, 2004, Human mutation.

Geographical variation in the penetrance of CDKN2A mutations for melanoma.

Florence Demenais, Johan Hansson, Paola Ghiorzo, 2002, Journal of the National Cancer Institute.

Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families

S. Chanock, M. Yeager, M. Tucker, 2013, The Journal of investigative dermatology.

Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer.

C. Yau, N. Hu, A. Goldstein, 2017, Gastroenterology.

Genomic characterization of esophageal squamous cell carcinoma from a high-risk population in China.

Nan Hu, Maxwell P Lee, Quan-hong Wang, 2009, Cancer research.

Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish

K. Kidd, J. Kelsoe, S. Paul, 1989, Nature.

A mutation hotspot at the p14ARF splice site

J. A. Bishop, D. Bishop, M. Tucker, 2005, Oncogene.

Cell-type–specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes

Jianxin Shi, Stuart MacGregor, David L Duffy, 2017, bioRxiv.

A Systematic Literature Review of Whole Exome and Genome Sequencing Population Studies of Genetic Susceptibility to Cancer

Leah E. Mechanic, E. Gillanders, T. Lam, 2020, Cancer Epidemiology, Biomarkers & Prevention.

Rare germline variants in known melanoma susceptibility genes in familial melanoma

S. Chanock, Jiali Han, M. Yeager, 2017, Human molecular genetics.

Mutation screening of the CDKN2A promoter in melanoma families

D. Bishop, G. Mann, M. Tucker, 2000, Genes, chromosomes & cancer.

Nucleotide diversity and population differentiation of the Melanocortin 1 Receptor gene, MC1R

A. Goldstein, K. Peris, L. Mirabello, 2008, BMC Genetics.

Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility

Blair H. Smith, Jeffrey E. Lee, G. Abecasis, 2020, Nature Genetics.

Risk factors for esophageal and gastric cancers in Shanxi Province, China: a case-control study.

Nan Hu, Ti Ding, N. Hu, 2011, Cancer epidemiology.

International cancer seminars: a focus on esophageal squamous cell carcinoma

R. Malekzadeh, C. Mathew, V. McCormack, 2017, Annals of oncology : official journal of the European Society for Medical Oncology.

Gastric microbiota features associated with cancer risk factors and clinical outcomes: A pilot study in gastric cardia cancer patients from Shanxi, China

N. Hu, J. Ravel, C. Abnet, 2017, International journal of cancer.

Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies

Hongbing Shen, N. Hu, S. Chanock, 2015, Gut.

Common genetic variants in epigenetic machinery genes and risk of upper gastrointestinal cancers.

William Wheeler, Nan Hu, Christian C Abnet, 2015, International journal of epidemiology.

Genetic Variants in Epidermal Growth Factor Receptor Pathway Genes and Risk of Esophageal Squamous Cell Carcinoma and Gastric Cancer in a Chinese Population

N. Hu, S. Chanock, Y. Wang, 2013, PloS one.

Family history of cancer and risk for esophageal and gastric cancer in Shanxi, China

N. Hu, T. Ding, A. Goldstein, 2009, BMC Cancer.

Familial melanoma and its management

M. Tucker, A. Goldstein, 1996 .

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

R. Eeles, A. Goldstein, C. Eng, 1998, Genes, chromosomes & cancer.

Genetic susceptibility in familial melanoma from northeastern Italy

A. Goldstein, W. Modi, R. Steighner, 2004, Journal of Medical Genetics.

CDKN2A point mutations D153spl(c.457G>T) and IVS2+1G>T result in aberrant splice products affecting both p16INK4a and p14ARF

J. Struewing, M. Tucker, A. Goldstein, 2003, Oncogene.

Genetic epidemiology of cutaneous melanoma: a global perspective.

M. Tucker, A. Goldstein, 2001, Archives of dermatology.

Sporadic multiple primary melanoma cases: CDKN2A germline mutations with a founder effect

A. Goldstein, T. Frebourg, A. Chompret, 2001, Genes, chromosomes & cancer.

Lack of phospholipase A2 mutations in neuroblastoma, melanoma and colon‐cancer cell lines

D. Housman, A. Goldstein, F. Haluska, 1997, International journal of cancer.

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

S. Chanock, H. Olsson, M. Yeager, 2016, Human Genetics.

Evaluation of Risk Factors for Nasopharyngeal Carcinoma in High-Risk Nasopharyngeal Carcinoma Families in Taiwan

Chien-Jen Chen, A. Goldstein, M. Dosemeci, 2005, Cancer Epidemiology Biomarkers & Prevention.

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

Quan-hong Wang, N. Hu, M. Emmert-Buck, 2008, Cancer Epidemiology Biomarkers & Prevention.

Follow-up study of twenty-four families with Li-Fraumeni syndrome.

J. Fraumeni, A. Goldstein, J. Garber, 1991, Cancer research.

Hereditary genodermatoses with cancer predisposition.

M. Tucker, A. Goldstein, M. Gerstenblith, 2010, Hematology/oncology clinics of North America.

Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma

Jianxin Shi, S. Chanock, M. Yeager, 2014, Human Genetics.

Genetic variants in DNA repair pathway genes and risk of esophageal squamous cell carcinoma and gastric adenocarcinoma in a Chinese population.

N. Hu, S. Chanock, Zhaoming Wang, 2013, Carcinogenesis.

Cell-type-specific meQTL extends melanoma GWAS annotation beyond eQTL and informs melanocyte gene regulatory mechanisms

Michael A. Kovacs, Jianxin Shi, K. Brown, 2021, bioRxiv.

The genetics of melanoma: recent advances.

A. Goldstein, J. Gartner, V. Hill, 2013, Annual review of genomics and human genetics.

Allelic loss on chromosome 13q14 and mutation in deleted in cancer 1 gene in esophageal squamous cell carcinoma

N. Hu, M. Emmert-Buck, A. Goldstein, 2003, Oncogene.

Common genetic variants of TP53 and BRCA2 in esophageal cancer patients and healthy individuals from low and high risk areas of northern China.

N. Hu, M. Emmert-Buck, P. Albert, 2003, Cancer detection and prevention.

Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148

Geoffrey S. Tobias, K. Nielsen, J. Malvehy, 2017, Nature Communications.

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.

Jian Su, Wen Tan, Paolo Vineis, 2015, Journal of the National Cancer Institute.

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types

Alison P. Klein, William Wheeler, Li Jin, 2015 .

Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers.

Jianxin Shi, N. Hu, S. Chanock, 2014, Carcinogenesis.

The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length

Jeffrey E. Lee, S. Puig, E. Gillanders, 2014, Journal of the National Cancer Institute.

MicroRNA Expression Differentiates Histology and Predicts Survival of Lung Cancer

Yingdong Zhao, Neil E. Caporaso, Maria Teresa Landi, 2010, Clinical Cancer Research.

Family history of cancer and nonmalignant lung diseases as risk factors for lung cancer

Maria Teresa Landi, Neil E Caporaso, Sholom Wacholder, 2009, International journal of cancer.

Phase I Metabolic Genes and Risk of Lung Cancer: Multiple Polymorphisms and mRNA Expression

Nilanjan Chatterjee, Neil E. Caporaso, Maria Teresa Landi, 2009, PloS one.

Localization of a novel melanoma susceptibility locus to 1p22.

E. Gillanders, J. Trent, G. Mann, 2003, American journal of human genetics.

Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer.

W. Linehan, M. Tucker, M. Merino, 2008, Archives of dermatology.

Detectable clonal mosaicism and its relationship to aging and cancer

William Wheeler, Nan Hu, Peter Kraft, 2012, Nature Genetics.

Identification of unique expression signatures and therapeutic targets in esophageal squamous cell carcinoma

Nan Hu, Jason Hipp, Jaime Rodriguez-Canales, 2012, BMC Research Notes.

Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma.

Jianxin Shi, S. Chanock, M. Yeager, 2016, The Journal of investigative dermatology.

Interrogation of Chromosome 13q12-14 in Esophageal Squamous Cell Carcinoma

N. Hu, M. Emmert-Buck, P. Albert, 2012 .

Interrogation of Chromosome 13 q 12-14 in Esophageal Squamous Cell Carcinoma

N. Hu, M. Emmert-Buck, P. Albert, 2012 .

Genome-wide association study in esophageal cancer using GeneChip mapping 10K array.

Nan Hu, Kenneth H Buetow, Maxwell P Lee, 2005, Cancer research.

Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous‐cell carcinoma in a high‐risk Chinese population

Quan-hong Wang, N. Hu, M. Emmert-Buck, 2000, Genes, chromosomes & cancer.

Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer.

N. Hu, M. Emmert-Buck, T. Ding, 1999, Clinical cancer research : an official journal of the American Association for Cancer Research.

Familial eosinophilia: clinical and laboratory results on a U.S. kindred.

M. Tucker, A. Goldstein, T. Knutsen, 1998, American journal of medical genetics.

Integrated analysis of genome-wide miRNAs and targeted gene expression in esophageal squamous cell carcinoma (ESCC) and relation to prognosis

N. Hu, A. Goldstein, P. Taylor, 2020, BMC Cancer.

Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival

X. Hua, Jianxin Shi, A. Goldstein, 2021, Nature Communications.

Dysplastic Nevi and Melanoma

M. Tucker, A. Goldstein, 2013, Cancer Epidemiology, Biomarkers & Prevention.

Diabetes mellitus, other medical conditions and familial history of cancer as risk factors for pancreatic cancer

K. Lillemoe, D. Silverman, R. Hoover, 1999, British Journal of Cancer.

Lung cancer prognosis before and after recurrence in a population-based setting.

M. Gail, S. Wacholder, M. Tucker, 2015, Journal of the National Cancer Institute.

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

A. Goldstein, R. Pfeiffer, X. R Yang, 2005, Journal of Medical Genetics.

Jasmine tea consumption and upper gastrointestinal cancer in China

N. Hu, T. Ding, A. Goldstein, 2009, Cancer Causes & Control.

Identification of unique expression signatures and therapeutic targets in esophageal squamous cell carcinoma

J. Hipp, N. Hu, M. Emmert-Buck, 2012, BMC Research Notes.

Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family

R. Nussinov, N. Hayward, M. Tucker, 2021, Familial Cancer.

Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family

R. Nussinov, S. Puig, K. Brown, 2021, medRxiv.

First international workshop of the ATM and cancer risk group (4-5 December 2019)

F. Couch, R. Eeles, Z. Kote-Jarai, 2021, Familial Cancer.

Assessment of Human Papillomavirus in Lung Tumor Tissue

S. Wacholder, A. Goldstein, P. Taylor, 2011, Journal of the National Cancer Institute.

Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene

S. Chanock, M. Yeager, M. Tucker, 2016, Haematologica.

Genetic variants in fas signaling pathway genes and risk of gastric cancer

N. Hu, S. Chanock, Zhaoming Wang, 2014, International journal of cancer.

Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33.

M. Daly, E. Lander, T. Hudson, 1998, American journal of human genetics.

Common genetic variants in the 9p21 region and their associations with multiple tumours

Summer S. Han, R. Hayes, N. Hu, 2013, British Journal of Cancer.

Association of MC1R variants and risk of melanoma in melanoma-prone families with CDKN2A mutations.

M. Tucker, A. Goldstein, M. Landi, 2005, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Melanoma etiology: where are we?

M. Tucker, A. Goldstein, 2003, Oncogene.

Histological Features of Melanoma Associated with CDKN 2 A Genotype

D. Elder, G. Mann, N. Hayward, 2015 .

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.

A. Goldstein, N. Patronas, M. Quezado, 2020, Journal of neurosurgery.

T (brachyury) gene duplication confers major susceptibility to familial chordoma

A. Goldstein, M. Kelley, D. Alcorta, 2009, Nature Genetics.

Genetic variants in sex hormone metabolic pathway genes and risk of esophageal squamous cell carcinoma.

N. Hu, S. Chanock, Kai Yu, 2013, Carcinogenesis.

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

William Wheeler, Nan Hu, Peter Kraft, 2016, Nature Communications.

Genetic epidemiology of bilateral breast cancer: A linkage analysis using the affected‐pedigree‐member method

D. Weeks, A. Goldstein, D. Rao, 1990, Genetic epidemiology.

Whole-Exome Sequencing of Nasopharyngeal Carcinoma Families Reveals Novel Variants Potentially Involved in Nasopharyngeal Carcinoma

Chien-Jen Chen, M. Yeager, A. Goldstein, 2019, Scientific Reports.

Evaluation of Rare and Common Variants from Suspected Familial or Sporadic Nasopharyngeal Carcinoma (NPC) Susceptibility Genes in Sporadic NPC

Chien-Jen Chen, M. Yeager, A. Goldstein, 2019, Cancer Epidemiology, Biomarkers & Prevention.

Gene expression analysis of esophageal squamous cell carcinoma reveals consistent molecular profiles related to a family history of upper gastrointestinal cancer.

Nan Hu, Eric Y Chuang, Michael R Emmert-Buck, 2003, Cancer research.

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

M. Tucker, A. Goldstein, M. Nelson, 2002, International journal of cancer.

Frequent inactivation of the TP53 gene in esophageal squamous cell carcinoma from a high-risk population in China.

N. Hu, M. Emmert-Buck, T. Ding, 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.

Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN2A Mutations

S. Chanock, M. Yeager, M. Tucker, 2013, PloS one.

Molecular Characterization of the Human Stomach Microbiota in Gastric Cancer Patients

N. Hu, J. Ravel, C. Abnet, 2017, Front. Cell. Infect. Microbiol..

Novel loss-of-function variant in DENND5A impedes melanosomal cargo transport and predisposes to familial cutaneous melanoma.

M. Tucker, A. Goldstein, J. Lundeberg, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

A UVB-responsive common variant at chr7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor gene (AHR)

Michael A. Kovacs, Ashley A. Jermusyk, S. Grant, 2021, bioRxiv.

Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study

S. Puig, E. Gillanders, D. Elder, 2010, Journal of the National Cancer Institute.

Identifying rheumatoid arthritis susceptibility genes using high-dimensional methods

T. Lam, A. Goldstein, Qizhai Li, 2009, BMC proceedings.

Oesophageal squamous cell carcinoma in high-risk Chinese populations: Possible role for vascular epithelial growth factor A.

T. Beaty, N. Hu, I. Ruczinski, 2014, European journal of cancer.

Pediatric melanoma in melanoma‐prone families

M. Tucker, A. Goldstein, Xiaohong R. Yang, 2018, Cancer.

Evaluation of BRCA2 in the genetic susceptibility of familial esophageal cancer

N. Hu, M. Emmert-Buck, A. Goldstein, 2004, Oncogene.

Genomic regions linked to alcohol consumption in the Framingham Heart Study

A. Goldstein, A. Bergen, M. Beerman, 2003, BMC Genetics.

Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies

K. Brown, J. Barrett, D. Bishop, 2018, The Journal of investigative dermatology.

CDKN2A mutations and melanoma risk in the Icelandic population

U. Thorsteinsdóttir, A. Kong, K. Stefánsson, 2008, Journal of Medical Genetics.

Icelandic population mutations and melanoma risk in the CDKN2A

J. Gulcher, U. Thorsteinsdóttir, P. Sulem, 2008 .

Familial chordoma, a tumor of notochordal remnants, is linked to chromosome 7q33.

A. Goldstein, M. Kelley, E. Sheridan, 2001, American journal of human genetics.

Risk of melanoma and other cancers in melanoma-prone families.

D. Elder, D. Guerry, M. Tucker, 1993, The Journal of investigative dermatology.

Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia

S. Puig, D. Elder, N. Hayward, 2021, Genetics in Medicine.

The Impact of Longitudinal Surveillance on Tumor Thickness for Melanoma-Prone Families with and without Pathogenic Germline Variants of CDKN2A and CDK4

D. Elder, M. Tucker, A. Goldstein, 2021, Cancer Epidemiology, Biomarkers & Prevention.

Index‐based dietary patterns and risk of incident hepatocellular carcinoma and mortality from chronic liver disease in a prospective study

N. Freedman, A. Goldstein, P. Taylor, 2014, Hepatology.

Epstein–Barr virus microRNAs and lung cancer

F. Marincola, M. Gulley, A. Goldstein, 2011, British Journal of Cancer.

Influence of Genetic Background and Tissue Types on Global DNA Methylation Patterns

Nan Hu, Barbara K. Dunn, Ti Ding, 2010, PloS one.

Constitutional promoter methylation and risk of familial melanoma

M. Tucker, A. Goldstein, R. Pfeiffer, 2014, Epigenetics.

LINE-1 methylation in peripheral blood and the risk of melanoma in melanoma-prone families with and without CDKN2A mutations

M. Tucker, A. Goldstein, R. Pfeiffer, 2013, Melanoma research.

High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern China.

N. Hu, M. Emmert-Buck, T. Ding, 2000, Carcinogenesis.

Counter-matching in studies of gene-environment interaction: efficiency and feasibility.

B Langholz, N Andrieu, A M Goldstein, 2001, American journal of epidemiology.

Epidemiologic and genetic approaches in the study of gene-environment interaction: an overview of available methods.

N Andrieu, A M Goldstein, A. Goldstein, 1998, Epidemiologic reviews.

Histologic features of melanoma associated with germline mutations of CDKN2A, CDK4, and POT1 in melanoma-prone families from the United States, Italy, and Spain.

S. Puig, D. Elder, M. Tucker, 2020, Journal of the American Academy of Dermatology.

Second cancers after medulloblastoma: population-based results from the United States and Sweden

M. Tucker, A. Goldstein, J. Yuen, 1997, Cancer Causes & Control.

Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

S. Steinberg, D. Gudbjartsson, L. Kiemeney, 2008, Nature Genetics.

Genetic testing for melanoma.

S. Puig, D. Elder, N. Hayward, 2002, The Lancet. Oncology.

Risk factors for melanoma by anatomical site: an evaluation of aetiological heterogeneity *

D. Bishop, M. Iles, G. Giles, 2020, The British journal of dermatology.

Early onset may predict G101W CDKN2A founder mutation carrier status in Ligurian melanoma patients

M. Sormani, A. Goldstein, P. Queirolo, 2004, Melanoma research.

Parenchymal-stromal interactions in neoplasia. Theoretical considerations and observations in melanocytic neoplasia.

W. Clark, M. Tucker, A. Goldstein, 1995, Acta oncologica.

Meeting report: consensus from the first and second Global Workshops in Melanoma November 19–20, 2008

A. Hauschild, D. Schadendorf, A. Halpern, 2009, Pigment cell & melanoma research.

A genome-wide linkage scan for body mass index on Framingham Heart Study families

A. Goldstein, A. Bergen, R. Moslehi, 2003, BMC Genetics.

Body mass index and height and risk of cutaneous melanoma: Mendelian randomization analyses.

M. Iles, A. Goldstein, D. Whiteman, 2020, International journal of epidemiology.

Linkage analysis of the GAW14 simulated dataset with microsatellite and single-nucleotide polymorphism markers in large pedigrees

Andrew W Bergen, K. Jacobs, A. Goldstein, 2005, BMC Genetics.

Integrative genomics analysis of genes with biallelic loss and its relation to the expression of mRNA and micro-RNA in esophageal squamous cell carcinoma

N. Hu, T. Ding, A. Goldstein, 2015, BMC Genomics.

Allelotyping of esophageal squamous‐cell carcinoma on chromosome 13 defines deletions related to family history

N. Hu, M. Emmert-Buck, A. Goldstein, 2005, Genes, chromosomes & cancer.

Comprehensive Characterization of Annexin I Alterations in Esophageal Squamous Cell Carcinoma

N. Hu, M. Emmert-Buck, A. Goldstein, 2004, Clinical Cancer Research.

Identification of somatic mutations of the RNF6 gene in human esophageal squamous cell carcinoma.

N. Hu, A. Goldstein, P. Taylor, 2002, Cancer research.

Index-based dietary patterns and risk of head and neck cancer in a large prospective study.

C. Abnet, N. Freedman, A. Goldstein, 2014, The American journal of clinical nutrition.

Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data.

N. Hu, S. Chanock, Zhaoming Wang, 2016, International journal of epidemiology.

Global Gene Expression Profiling and Validation in Esophageal Squamous Cell Carcinoma and Its Association with Clinical Phenotypes

Nan Hu, Stephen M. Hewitt, Quan-hong Wang, 2011, Clinical Cancer Research.

Genome wide analysis of DNA copy number neutral loss of heterozygosity (CNNLOH) and its relation to gene expression in esophageal squamous cell carcinoma

Nan Hu, Maxwell P Lee, Ti Ding, 2010, BMC Genomics.

GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer

N. Hu, S. Chanock, Zhaoming Wang, 2017, Scientific Reports.

Replication of a genome‐wide case–control study of esophageal squamous cell carcinoma

N. Hu, A. Goldstein, P. Taylor, 2008, International journal of cancer.

Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours

P. Zhang, N. Hu, S. Chanock, 2015, Gut.

PLCE1 mRNA and Protein Expression and Survival of Patients with Esophageal Squamous Cell Carcinoma and Gastric Adenocarcinoma

N. Hu, C. Abnet, T. Ding, 2014, Cancer Epidemiology, Biomarkers & Prevention.

Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence

David C. Jones, Lia S. Campos, R. Malekzadeh, 2021, Nature Genetics.

Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions

S. Puig, E. Gillanders, K. Brown, 2014, International journal of cancer.

Integrated Analysis of Co-expression and Exome Sequencing to Prioritize Susceptibility Genes for Familial Cutaneous Melanoma.

K. Brown, S. Chanock, M. Yeager, 2022, The Journal of investigative dermatology.

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

Quan-hong Wang, N. Hu, M. Emmert-Buck, 2006, BMC Cancer.

Gene-covariate interaction between dysplastic nevi and the CDKN2A gene in American melanoma-prone families.

M. Tucker, A. Goldstein, F. Demenais, 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

A systematic review of the prevalence of germline pathogenic variants in patients with pancreatic cancer

A. Goldstein, Esteban Astiazaran-Symonds, 2021, Journal of Gastroenterology.

Familial risk in oral and pharyngeal cancer.

D. Winn, J. Fraumeni, A. Goldstein, 1994, European journal of cancer. Part B, Oral oncology.

Familial melanoma aggregation in north-eastern Italy.

A M Goldstein, M T Landi, A. Goldstein, 2000, The Journal of investigative dermatology.

Familiality of breast cancer and socioeconomic status in blacks.

C. Amos, A. Goldstein, E. Harris, 1991, Cancer research.

Dietary quercetin, quercetin-gene interaction, metabolic gene expression in lung tissue and lung cancer risk.

S. Chanock, T. Lam, S. Wacholder, 2010, Carcinogenesis.

Familial and sporadic cases of nasopharyngeal carcinoma in Taiwan.

C. J. Chen, A. Goldstein, L. Brinton, 1999, Anticancer research.

Family history of gallstones and the risk of biliary tract cancer and gallstones: A population‐based study in Shanghai, China

Jinbo Chen, J. Fraumeni, A. Goldstein, 2007, International journal of cancer.

Association of high-evidence gastric cancer susceptibility loci and somatic gene expression levels with survival

N. Hu, A. Goldstein, P. Taylor, 2017, Carcinogenesis.

Association of human leukocyte antigens with nasopharyngeal carcinoma in high-risk multiplex families in Taiwan.

M. Carrington, Chien-Jen Chen, A. Goldstein, 2009, Human immunology.

Constitutive mitochondrial DNA copy number in peripheral blood of melanoma families with and without CDKN2A mutations.

M. Tucker, A. Goldstein, J. Yuenger, 2014, Journal of carcinogenesis & mutagenesis.

Index-based dietary patterns and risk of esophageal and gastric cancer in a large cohort study.

C. Abnet, N. Freedman, A. Goldstein, 2013, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer

S. Chanock, M. Yeager, M. Tucker, 2011, Familial Cancer.

Alcohol consumption and lung cancer risk in the Environment and Genetics in Lung Cancer Etiology (EAGLE) study.

T. Lam, S. Wacholder, M. Tucker, 2010, American journal of epidemiology.

ABO genotypes and the risk of esophageal and gastric cancers

N. Hu, Kai Yu, C. Abnet, 2021, BMC Cancer.

Abstract 1333: Specific RB1 mutations and risk of subsequent neoplasms among survivors of hereditary retinoblastoma.

B. Gallie, M. Tucker, A. Goldstein, 2013 .

Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma

Jianxin Shi, S. Chanock, M. Yeager, 2014, Human Genetics.

Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study.

Stephen W. Hartley, S. Chanock, D. Karyadi, 2021, JNCI cancer spectrum.

Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility

S. Chanock, M. Yeager, N. Freedman, 2021, Cancers.

Cancer patterns in nasopharyngeal carcinoma multiplex families in Taiwan

Chien-Jen Chen, A. Goldstein, R. Pfeiffer, 2009, International journal of cancer.

DR2/DQw1 inheritance and haplotype sharing in affected siblings from multiple sclerosis families.

A. Goldstein, H. McFarland, R. Voskuhl, 1996, Annals of Neurology.

Corroboration of a familial chordoma locus on chromosome 7q and evidence of genetic heterogeneity using single nucleotide polymorphisms (SNPs)

S. Chanock, A. Goldstein, A. Bergen, 2005, International journal of cancer.

Prospectives for cutaneous malignant melanoma. Considerations of the precursor state and heritability.

W. Clark, M. Tucker, A. Goldstein, 1995, British medical bulletin.

No evidence for linkage between an insulin‐dependent diabetes mellitus‐susceptibility locus and immunoglobulin loci KM or GM

M. Spence, A. Goldstein, D. Rao, 1984, Genetic epidemiology.

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

S. Wacholder, J. Lubin, A. Goldstein, 2010 .

Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT.

S. Puig, D. Bishop, D. Elder, 2019, Journal of the American Academy of Dermatology.

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

M. Sherman, A. Goldstein, R. Burk, 2005, International journal of cancer.

Ambient Ultraviolet Radiation and Sebaceous Carcinoma Incidence in the United States, 2000-2016.

M. Tucker, A. Goldstein, R. Pfeiffer, 2020, JNCI cancer spectrum.

Inflated expectations: Rare-variant association analysis using public controls

Stephen W. Hartley, S. Chanock, D. Karyadi, 2023, PloS one.

HLA-DR, HLA-DQ, and TAP genes in familial Hodgkin disease.

M. Carrington, E. Jaffe, M. Tucker, 2002, Blood.

Apparent anticipation in familial melanoma

W. Clark, M. Tucker, A. Goldstein, 1996, Melanoma research.

Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma‐prone family

S. Puig, N. Hayward, M. Tucker, 2012, Pigment cell & melanoma research.

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

S. Puig, S. Chanock, M. Greene, 2018, Genome Medicine.

PLCE1mRNAandProteinExpressionandSurvivalofPatients with Esophageal Squamous Cell Carcinoma and Gastric Adenocarcinoma

N. Hu, C. Abnet, T. Ding, 2014 .

Use of relatives of cases as controls to identify risk factors when an interaction between environmental and genetic factors exists.

A. Goldstein, N. Andrieu, 1996, International journal of epidemiology.

Low Epstein–Barr Virus Prevalence in Cardia Gastric Cancer Among a High-Incidence Chinese Population

N. Hu, M. Gulley, A. Goldstein, 2020, Digestive Diseases and Sciences.

Gene expression profiling identifies two chordoma subtypes associated with distinct molecular mechanisms and clinical outcomes.

Tengyu Ma, S. Chanock, A. Goldstein, 2022, Clinical cancer research : an official journal of the American Association for Cancer Research.

Detecting gene‐environment interactions using a case‐control design

J H Lubin, A M Goldstein, J. Lubin, 1997, Genetic epidemiology.

Correlates of anti-EBV EBNA1 IgA positivity among unaffected relatives from nasopharyngeal carcinoma multiplex families

C. J. Chen, A. Goldstein, P. Lou, 2011, British Journal of Cancer.

An international report on bacterial communities in esophageal squamous cell carcinoma

Charles J. Vaske, R. Malekzadeh, M. Meyerson, 2021, bioRxiv.

Use of Big Data to Estimate Prevalence of Defective DNA Repair Variants in the US Population

Sikandar G. Khan, A. Goldstein, M. Landi, 2019, JAMA dermatology.

Integrated analysis of genome-wide miRNAs and targeted gene expression in esophageal squamous cell carcinoma (ESCC) and relation to prognosis

N. Hu, A. Goldstein, P. Taylor, 2020, BMC Cancer.

Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation

N. Hu, A. Goldstein, P. Taylor, 2022, Cancers.

Increased power to detect gene-environment interaction using siblings controls.

A. Goldstein, N. Andrieu, M. Dondon, 2005, Annals of epidemiology.

No Evidence for Linkage with Melanoma in Italian Melanoma-Prone Families

A. Goldstein, K. Peris, R. Steighner, 2008, Cancer Epidemiology Biomarkers & Prevention.

Clinical findings in chordoma families with and without T gene duplications and chordoma patients reported to the Surveillance, Epidemiology and End Results Program

A. Goldstein, M. Quezado, D. Parry, 2021 .

GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer

N. Hu, S. Chanock, Zhaoming Wang, 2017, Scientific Reports.

Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma

M. Tucker, A. Goldstein, G. Peters, 2005, Journal of Medical Genetics.

Contributors and Participants

D. Cox, A. Kong, N. Mendell, 1982 .

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

David M. Evans, A. Uitterlinden, T. Spector, 2017, Nature Communications.

A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families

J. Struewing, M. Tucker, A. Goldstein, 2001, British Journal of Cancer.

Selection bias in case-control studies using relatives as the controls.

S. Hodge, A. Goldstein, R. Haile, 1989, International journal of epidemiology.

Identification of susceptibility loci for complex diseases in a case-control association study using the Genetic Analysis Workshop 14 dataset

K. Jacobs, A. Goldstein, A. Bergen, 2005, BMC Genetics.

A problem in identifying risk factors for disease using surrogate exposure variables that are under genetic control.

A. Goldstein, R. Falk, S. Hodge, 1990, American Journal of Epidemiology.

Estimated Prevalence, Tumor Spectrum, and Neurofibromatosis Type 1-Like Phenotype of CDKN2A-Related Melanoma-Astrocytoma Syndrome.

M. Tucker, A. Goldstein, M. Yohe, 2023, JAMA dermatology.

Comparison of the affected-pedigree-member and lod-score methods.

D. Weeks, A. Goldstein, V. Cortessis, 1989, Progress in clinical and biological research.

Unconditional analyses can increase efficiency in assessing gene-environment interaction of the case-combined-control design.

A. Goldstein, N. Andrieu, Marie-Gabrielle Dondon, 2006, International journal of epidemiology.

Joint analysis of three genome- wide association studies of esophageal squamous cell carcinoma in Chinese populations

Hongbing Shen, N. Hu, S. Chanock, 2014 .

Corrigendum: Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions

L. Liang, Hongbing Shen, N. Hu, 2014, Nature Genetics.

Gene×Environment Interaction from Case‐Control and Case‐Case Approaches

A. Goldstein, L. Goldin, Yan Bei, 2001, Genetic Epidemiology.

Comparison of Likelihood Approaches for Combined Segregation and Linkage Analysis of a Complex Disease and a Candidate Gene Marker Under Different Ascertainment Schemes

J. O’Connell, A. Goldstein, Maria Martinez, 2001, Genetic epidemiology.

Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations

Shu Han Chen, Wei Zhang, P. Zhang, 2014, Nature Genetics.

The genomics of emerging pathogens.

J. Hirschhorn, A. Goldstein, K. Christensen, 2013, Annual review of genomics and human genetics.

Human Cancer Biology Microrna Expression Differentiates Histology and Predicts Survival of Lung Cancer Clinical Cancer Research Authors' Affiliations: Divisions of 1 Cancer Epidemiology and Genetics and 2 Cancer Treatment and Diagnosis

F. Marincola, M. Tucker, A. Goldstein, 2022 .

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

Quan-hong Wang, N. Hu, M. Emmert-Buck, 2008, Cancer Epidemiology Biomarkers & Prevention.

Dietary quercetin, quercetin-gene interaction, metabolic gene expression in lung tissue and lung cancer risk.

S. Chanock, T. Lam, S. Wacholder, 2010, Carcinogenesis.

Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.

David M. Thomas, Krista A. Zanetti, Geoffrey S. Tobias, 2014, Human molecular genetics.

Reproductive Health in Xeroderma Pigmentosum: Features of Premature Aging.

Sikandar G. Khan, A. Goldstein, K. Kraemer, 2019, Obstetrics and gynecology.

Characterization of large structural genetic mosaicism in human autosomes.

Krista A. Zanetti, Geoffrey S. Tobias, Sarah C. Nelson, 2015, American journal of human genetics.

Index-based dietary patterns and risk of esophageal and gastric cancer in a large cohort study.

C. Abnet, N. Freedman, A. Goldstein, 2013, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Index‐based dietary patterns and risk of incident hepatocellular carcinoma and mortality from chronic liver disease in a prospective study

N. Freedman, A. Goldstein, P. Taylor, 2014, Hepatology.

Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies.

N. Hu, S. Chanock, K. Jacobs, 2012, Human Molecular Genetics.

PLCE1 mRNA and Protein Expression and Survival of Patients with Esophageal Squamous Cell Carcinoma and Gastric Adenocarcinoma

N. Hu, C. Abnet, T. Ding, 2014, Cancer Epidemiology, Biomarkers & Prevention.

Acral lentiginous melanoma: incidence and survival patterns in the United States, 1986-2005.

M. Tucker, A. Goldstein, M. McMaster, 2009, Archives of dermatology.

Genetic susceptibility in familial melanoma from northeastern Italy

A. Goldstein, W. Modi, R. Steighner, 2004, Journal of Medical Genetics.

Association of germline variants in telomere maintenance genes (POT1, TERF2IP, ACD, and TERT) with spitzoid morphology in familial melanoma: A multi-center case series

D. Bishop, D. Elder, G. Mann, 2023, JAAD international.

Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence

N. Hu, J. Teague, L. Alexandrov, 2021, Nature Genetics.

Genomic Landscape of Somatic Alterations in Esophageal Squamous Cell Carcinoma and Gastric Cancer.

N. Hu, Hailong Wu, A. Hutchinson, 2016, Cancer research.