Faculty

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Stephen B Gruber, MD, PhD, MPH
Professor of Medicine
H. Leslie Hoffman and Elaine S. Hoffman Chair in Cancer Research
Director, Norris Comprehensive Cancer Center
Medicine
NOR 8302 Health Sciences Campus Los Angeles
+1 323 865 0816

Overview

Stephen B. Gruber, M.D., Ph.D., M.P.H., Director of the USC Norris Comprehensive Cancer Center, is a Professor of Medicine at the Keck School of Medicine of the University of Southern California, and the H. Leslie Hoffman and Elaine S. Hoffman Chair in Cancer Research.

Dr. Gruber is a board certified medical oncologist, cancer geneticist and epidemiologist whose research focuses on genetic and environmental contributions to cancer. His particular research interests include the genetic epidemiology of cancer, with emphasis on colorectal cancer; the molecular pathogenesis of cancer, integrated with genetic epidemiology; methods in genetic and molecular epidemiology; and clinical cancer genetics and translational research in cancer prevention. The goal of his research is to find new ways to prevent cancer and to improve treatment and care for cancer patients.

Dr. Gruber obtained his Bachelor’s Degree from the University of Pennsylvania in 1984 and subsequently a Master of Public Health Degree from Yale University in 1986. After completing his Doctorate Degree in Epidemiology at Yale in 1988, Dr. Gruber enrolled in the University of Pennsylvania Medical School and obtained his Medical Degree in 1992, where he also completed his internship and residency. He completed fellowships in medical oncology at Johns Hopkins Hospital and in clinical medical genetics at the University of Michigan.

He has received a variety of honors and awards and is the author of 158 peer-reviewed publications, many in very high quality journals attesting to his standing in the field of cancer genetics, particularly as it relates to colorectal cancer. In addition to serving on editorial boards for several professional journals, Dr. Gruber is active in national organizations. Since 2005, he has been chair of the Colorectal Family Registries Advisory Panel for the National Cancer Institute and for the past three years chaired the Cancer Genetics Education Committee of the American Society of Clinical Oncology.

Awards

USC: H. Leslie and Elaine S. Hoffman Cancer Research Chair, 2012

Alfred Stengel Memorial Prize

Penn Medical Scholar

Association of American Cancer Institute: Board of Directors, 2015

University of Michigan: League of Research Excellence, 2011

National Institute of Health: Cancer Training Grant, 1986-1988

American Society of Clinical Investigation: Elected Member, 2003

Jerome Conn Award for Excellence in Research

Collaborative Group of the Americas on Inherited Colorectal Cancer : Lifetime Achievement Award, 2013

Penn Pearls Teaching Award

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Collaborative Group of the Americas on Inherited Colorectal Cancer : award conferred by, 2013

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American Society of Clinical Investigation: award conferred by, 2003

National Institute of Health: award conferred by, 1986-1988

Association of American Cancer Institute: award conferred by, 2015

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University of Michigan: award conferred by, 2011

USC: award conferred by, 2012

National Institute of Health: ORNG Application Instance for Person, 1986-1988

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Association of American Cancer Institute: start date, 2015

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Collaborative Group of the Americas on Inherited Colorectal Cancer : is primary position, 2013

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In The News

National Institute of Health: In The News, 1986-1988

Collaborative Group of the Americas on Inherited Colorectal Cancer : In The News, 2013

In The News

USC: In The News, 2012

University of Michigan: In The News, 2011

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Association of American Cancer Institute: In The News, 2015

Department

Department

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Collaborative Group of the Americas on Inherited Colorectal Cancer : Department, 2013

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Collaborative Group of the Americas on Inherited Colorectal Cancer : Person, 2013

Gruber, Stephen

American Society of Clinical Investigation: Gruber, Stephen, 2003

Gruber, Stephen

Gruber, Stephen

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University of Michigan: Gruber, Stephen, 2011

Association of American Cancer Institute: Gruber, Stephen, 2015

USC: Gruber, Stephen, 2012

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links

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American Society of Clinical Investigation: links, 2003

Collaborative Group of the Americas on Inherited Colorectal Cancer : links, 2013

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American Society of Clinical Investigation: has ORNG Application Instance Data, 2003

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American Society of Clinical Investigation: In The News, 2003

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Keck School of Medicine of USC

Collaborative Group of the Americas on Inherited Colorectal Cancer : Keck School of Medicine of USC, 2013

Keck School of Medicine of USC

Keck School of Medicine of USC

Association of American Cancer Institute: Keck School of Medicine of USC, 2015

American Society of Clinical Investigation: Keck School of Medicine of USC, 2003

USC: Keck School of Medicine of USC, 2012

University of Michigan: Keck School of Medicine of USC, 2011

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Professor

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National Institute of Health: Professor, 1986-1988

American Society of Clinical Investigation: Professor, 2003

Collaborative Group of the Americas on Inherited Colorectal Cancer : Professor, 2013

USC: Professor, 2012

Association of American Cancer Institute: Professor, 2015

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Collaborative Group of the Americas on Inherited Colorectal Cancer : position in organization, 2013

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Collaborative Group of the Americas on Inherited Colorectal Cancer : award or honor for, 2013

American Society of Clinical Investigation: position in organization, 2003

Collaborative Group of the Americas on Inherited Colorectal Cancer : Professor of Medicine, 2013

Association of American Cancer Institute: Professor of Medicine, 2015

University of Michigan: Professor of Medicine, 2011

Professor of Medicine

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National Institute of Health: Professor of Medicine, 1986-1988

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Association of American Cancer Institute: preferred title, 2015

American Society of Clinical Investigation: preferred title, 2003

University of Michigan: preferred title, 2011

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Collaborative Group of the Americas on Inherited Colorectal Cancer : preferred title, 2013

Collaborative Group of the Americas on Inherited Colorectal Cancer : http://orng.info/ontology/orng#ApplicationInstance^^ORNG Application Instance^^1664-115, 2013

National Institute of Health: http://orng.info/ontology/orng#ApplicationInstance^^ORNG Application Instance^^1664-115, 1986-1988

American Society of Clinical Investigation: http://orng.info/ontology/orng#ApplicationInstance^^ORNG Application Instance^^1664-115, 2003

University of Michigan: http://orng.info/ontology/orng#ApplicationInstance^^ORNG Application Instance^^1664-115, 2011

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http://orng.info/ontology/orng#ApplicationInstance^^ORNG Application Instance^^1664-115

Association of American Cancer Institute: http://orng.info/ontology/orng#ApplicationInstance^^ORNG Application Instance^^1664-115, 2015

USC: http://orng.info/ontology/orng#ApplicationInstance^^ORNG Application Instance^^1664-115, 2012

Collaborative Group of the Americas on Inherited Colorectal Cancer : Medicine, 2013

Medicine

Association of American Cancer Institute: Medicine, 2015

USC: Medicine, 2012

American Society of Clinical Investigation: Medicine, 2003

Medicine

American Society of Clinical Investigation: Department, 2003

USC: has ORNG Application Instance Data, 2012

MediaLinks

National Institute of Health: MediaLinks, 1986-1988

University of Michigan: Medicine, 2011

National Institute of Health: Medicine, 1986-1988

Medicine

Medicine

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Collaborative Group of the Americas on Inherited Colorectal Cancer : Award or Honor Receipt, 2013

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American Society of Clinical Investigation: Award or Honor Receipt, 2003

Association of American Cancer Institute: Award or Honor Receipt, 2015

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Faculty Rank

American Society of Clinical Investigation: Faculty Rank, 2003

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Collaborative Group of the Americas on Inherited Colorectal Cancer : Gruber, Stephen, 2013

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Association of American Cancer Institute: has faculty rank, 2015

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American Society of Clinical Investigation: has faculty rank, 2003

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American Society of Clinical Investigation: position in department, 2003

Association of American Cancer Institute: position in department, 2015

USC: position in department, 2012

Collaborative Group of the Americas on Inherited Colorectal Cancer : position in department, 2013

ORNG Application Instance of Application

University of Michigan: ORNG Application Instance of Application, 2011

ORNG Application Instance of Application

ORNG Application Instance of Application

American Society of Clinical Investigation: ORNG Application Instance of Application, 2003

Collaborative Group of the Americas on Inherited Colorectal Cancer : ORNG Application Instance of Application, 2013

ORNG Application Instance of Application

Association of American Cancer Institute: ORNG Application Instance of Application, 2015

National Institute of Health: ORNG Application Instance of Application, 1986-1988

USC: ORNG Application Instance of Application, 2012

Publications

T-Cell Transfer Therapy Targeting Mutant KRAS. N Engl J Med. 2017 02 16; 376(7):e11. View in: PubMed

Variants in autophagy-related genes and clinical characteristics in melanoma: a population-based study. Cancer Med. 2016 Oct 17. View in: PubMed

Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. Cancer Res. 2016 Sep 1; 76(17):5103-14. View in: PubMed

Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses. PLoS Med. 2016 Sep; 13(9):e1002118. View in: PubMed

Tumor-Infiltrating Lymphocytes, Crohn's-Like Lymphoid Reaction, and Survival From Colorectal Cancer. J Natl Cancer Inst. 2016 Aug; 108(8). View in: PubMed

Association of Interferon Regulatory Factor-4 Polymorphism rs12203592 With Divergent Melanoma Pathways. J Natl Cancer Inst. 2016 Jul; 108(7). View in: PubMed

Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. Gastroenterology. 2016 Jun; 150(7):1633-45. View in: PubMed

Mendelian randomization study of adiposity-related traits and risk of breast, ovarian, prostate, lung and colorectal cancer. Int J Epidemiol. 2016 Jun; 45(3):896-908. View in: PubMed

Increased yield of actionable mutations using multi-gene panels to assess hereditary cancer susceptibility in an ethnically diverse clinical cohort. Cancer Genet. 2016 Apr; 209(4):130-7. View in: PubMed

Coffee Consumption and the Risk of Colorectal Cancer. Cancer Epidemiol Biomarkers Prev. 2016 Apr; 25(4):634-9. View in: PubMed

A novel BAP1 mutation is associated with melanocytic neoplasms and thyroid cancer. Cancer Genet. 2016 Mar; 209(3):75-81. View in: PubMed

Tests for Gene-Environment Interactions and Joint Effects With Exposure Misclassification. Am J Epidemiol. 2016 Feb 1; 183(3):237-47. View in: PubMed

Vitamin D receptor polymorphisms and survival in patients with cutaneous melanoma: a population-based study. Carcinogenesis. 2016 Jan; 37(1):30-8. View in: PubMed

A Cross-Cancer Genetic Association Analysis of the DNA Repair and DNA Damage Signaling Pathways for Lung, Ovary, Prostate, Breast, and Colorectal Cancer. Cancer Epidemiol Biomarkers Prev. 2016 Jan; 25(1):193-200. View in: PubMed

A Germline Variant on Chromosome 4q31. 1 Associates with Susceptibility to Developing Colon Cancer Metastasis. PLoS One. 2016; 11(1):e0146435. View in: PubMed

Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer. J Natl Cancer Inst. 2015 Nov; 107(11). View in: PubMed

A genome-wide association study for colorectal cancer identifies a risk locus in 14q23. 1. Hum Genet. 2015 Nov; 134(11-12):1249-62. View in: PubMed

Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study. Hum Mol Genet. 2015 Sep 15; 24(18):5356-66. View in: PubMed

Inherited genetic variants associated with occurrence of multiple primary melanoma. Cancer Epidemiol Biomarkers Prev. 2015 Jun; 24(6):992-7. View in: PubMed

A model to determine colorectal cancer risk using common genetic susceptibility Loci. Gastroenterology. 2015 Jun; 148(7):1330-1339. e14. View in: PubMed

Association Between NRAS and BRAF Mutational Status and Melanoma-Specific Survival Among Patients With Higher-Risk Primary Melanoma. JAMA Oncol. 2015 Jun; 1(3):359-68. View in: PubMed

Inherited variation at MC1R and ASIP and association with melanoma-specific survival. Int J Cancer. 2015 Jun 1; 136(11):2659-67. View in: PubMed

A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype. J Med Genet. 2015 May; 52(5):348-52. View in: PubMed

The impact of exposure-biased sampling designs on detection of gene-environment interactions in case-control studies with potential exposure misclassification. Eur J Epidemiol. 2015 May; 30(5):413-23. View in: PubMed

Hereditary colorectal cancer syndromes: american society of clinical oncology clinical practice guideline endorsement of the familial risk-colorectal cancer: European society for medical oncology clinical practice guidelines. J Clin Oncol. 2015 Jan 10; 33(2):209-17. View in: PubMed

Inherited Variation at MC1R and Histological Characteristics of Primary Melanoma. PLoS One. 2015; 10(3):e0119920. View in: PubMed

Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nat Commun. 2015; 6:8739. View in: PubMed

Genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nat Commun. 2015; 6:7138. View in: PubMed

MicroRNA Polymorphisms and Risk of Colorectal Cancer. Cancer Epidemiol Biomarkers Prev. 2015 Jan; 24(1):65-72. View in: PubMed

Screening for germline mismatch repair mutations following diagnosis of sebaceous neoplasm. JAMA Dermatol. 2014 Dec; 150(12):1315-21. View in: PubMed

Comparison of clinicopathologic features and survival of histopathologically amelanotic and pigmented melanomas: a population-based study. JAMA Dermatol. 2014 Dec; 150(12):1306-314. View in: PubMed

A novel colorectal cancer risk locus at 4q32. 2 identified from an international genome-wide association study. Carcinogenesis. 2014 Nov; 35(11):2512-9. View in: PubMed

Sun Exposure and Melanoma Survival: A GEM Study. Cancer Epidemiol Biomarkers Prev. 2014 Oct; 23(10):2145-52. View in: PubMed

The Clinical Phenotype of SDHC-Associated Hereditary Paraganglioma Syndrome (PGL3). J Clin Endocrinol Metab. 2014 Aug; 99(8):E1482-6. View in: PubMed

An oncocytic adrenal tumour in a patient with Birt-Hogg-Dubé syndrome. Clin Endocrinol (Oxf). 2014 Jun; 80(6):925-7. View in: PubMed

Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. Nat Genet. 2014 Jun; 46(6):533-42. View in: PubMed

MITF E318K's effect on melanoma risk independent of, but modified by, other risk factors. Pigment Cell Melanoma Res. 2014 May; 27(3):485-8. View in: PubMed

Cumulative exposure to medical radiation for children requiring surgery for congenital heart disease. J Pediatr. 2014 Apr; 164(4):789-794. e10. View in: PubMed

Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A. Nat Commun. 2014; 5:4613. View in: PubMed

Tumor-infiltrating lymphocyte grade in primary melanomas is independently associated with melanoma-specific survival in the population-based genes, environment and melanoma study. J Clin Oncol. 2013 Nov 20; 31(33):4252-9. View in: PubMed

Transcriptome profiling identifies HMGA2 as a biomarker of melanoma progression and prognosis. J Invest Dermatol. 2013 Nov; 133(11):2585-92. View in: PubMed

Interaction of Fatty Acid genotype and diet on changes in colonic Fatty acids in a mediterranean diet intervention study. Cancer Prev Res (Phila). 2013 Nov; 6(11):1212-21. View in: PubMed

Distinct molecular features of colorectal cancer in Ghana. Cancer Epidemiol. 2013 Oct; 37(5):556-61. View in: PubMed

Adrenocortical carcinoma is a lynch syndrome-associated cancer. J Clin Oncol. 2013 Aug 20; 31(24):3012-8. View in: PubMed

Survival for patients with single and multiple primary melanomas: the genes, environment, and melanoma study. JAMA Dermatol. 2013 Aug; 149(8):921-7. View in: PubMed

Elevated risk of prostate cancer among men with Lynch syndrome. J Clin Oncol. 2013 May 10; 31(14):1713-8. View in: PubMed

Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. Gastroenterology. 2013 Apr; 144(4):799-807. e24. View in: PubMed

Inflammatory bowel disease and familial adenomatous polyposis. J Crohns Colitis. 2013 Apr 1; 7(3):e103-7. View in: PubMed

BAYESIAN SEMIPARAMETRIC ANALYSIS FOR TWO-PHASE STUDIES OF GENE-ENVIRONMENT INTERACTION. Ann Appl Stat. 2013 Mar; 7(1):543-569. View in: PubMed

Contemporary outcomes of surgical ventricular septal defect closure. J Thorac Cardiovasc Surg. 2013 Mar; 145(3):641-7. View in: PubMed

Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinoma. J Clin Endocrinol Metab. 2013 Jan; 98(1):E119-25. View in: PubMed

Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome. Gynecol Oncol. 2012 Dec; 127(3):544-51. View in: PubMed

MLH1 methylation screening is effective in identifying epimutation carriers. Eur J Hum Genet. 2012 Dec; 20(12):1256-64. View in: PubMed

Common MUTYH mutations and colorectal cancer risk in multiethnic populations. Fam Cancer. 2012 Sep; 11(3):329-35. View in: PubMed

MLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness study. Eur J Hum Genet. 2012 Jul; 20(7):762-8. View in: PubMed

Risk of non-melanoma cancers in first-degree relatives of CDKN2A mutation carriers. J Natl Cancer Inst. 2012 Jun 20; 104(12):953-6. View in: PubMed

Breast cancer phenotype in women with TP53 germline mutations: a Li-Fraumeni syndrome consortium effort. Breast Cancer Res Treat. 2012 Jun; 133(3):1125-30. View in: PubMed

An American founder mutation in MLH1. Int J Cancer. 2012 May 1; 130(9):2088-95. View in: PubMed

Clinicopathologic features of incident and subsequent tumors in patients with multiple primary cutaneous melanomas. Ann Surg Oncol. 2012 Mar; 19(3):1024-33. View in: PubMed

Familial renal cancer as an indicator of hereditary leiomyomatosis and renal cell cancer syndrome. Fam Cancer. 2012 Mar; 11(1):115-21. View in: PubMed

Meta-analysis of new genome-wide association studies of colorectal cancer risk. Hum Genet. 2012 Feb; 131(2):217-34. View in: PubMed

Testing gene-environment interaction in large-scale case-control association studies: possible choices and comparisons. Am J Epidemiol. 2012 Feb 1; 175(3):177-90. View in: PubMed

Vitamin D receptor polymorphisms in patients with cutaneous melanoma. Int J Cancer. 2012 Jan 15; 130(2):405-18. View in: PubMed

A pilot study of microsatellite instability and endometrial cancer survival in white and African American women. Int J Gynecol Pathol. 2012 Jan; 31(1):66-72. View in: PubMed

Genome-wide search for gene-gene interactions in colorectal cancer. PLoS One. 2012; 7(12):e52535. View in: PubMed

Interaction of CDKN2A and sun exposure in the etiology of melanoma in the general population. J Invest Dermatol. 2011 Dec; 131(12):2500-3. View in: PubMed

Gene expression differences between colon and rectum tumors. Clin Cancer Res. 2011 Dec 1; 17(23):7303-12. View in: PubMed

Bayesian modeling for genetic anticipation in presence of mutational heterogeneity: a case study in Lynch syndrome. Biometrics. 2011 Dec; 67(4):1627-37. View in: PubMed

Micromanaging the Classification of Colon Cancer: The Role of the microRNAome. Clin Cancer Res. 2011 Dec 1; 17(23):7207-9. View in: PubMed

Personalized oncology through integrative high-throughput sequencing: a pilot study. Sci Transl Med. 2011 Nov 30; 3(111):111ra121. View in: PubMed

Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer. PLoS Biol. 2011 Nov; 9(11):e1001199. View in: PubMed

Clinical implications of UGT1A1*28 genotype testing in colorectal cancer patients. Cancer. 2011 Jul 15; 117(14):3156-62. View in: PubMed

Missing exposure data in steregtype regression model: applicataon to matched case-control studq with disease subclassification Biometrics. 2011 Jun; 67(2):546-58. View in: PubMed

Missing exposure data in stereotype regression model: application to matched case-control study with disease subclassification. Biometrics. 2011 Jun; 67(2):546-58. View in: PubMed

High risk of colorectal and endometrial cancer in Ashkenazi families with the MSH2 A636P founder mutation. Gastroenterology. 2011 Jun; 140(7):1919-26. View in: PubMed

Risk of colorectal cancer in self-reported inflammatory bowel disease and modification of risk by statin and NSAID use. Cancer. 2011 Apr 15; 117(8):1640-8. View in: PubMed

AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome. Am J Med Genet A. 2011 Apr; 155A(4):898-902. View in: PubMed

MRE11 deficiency increases sensitivity to poly(ADP-ribose) polymerase inhibition in microsatellite unstable colorectal cancers. Cancer Res. 2011 Apr 1; 71(7):2632-42. View in: PubMed

Use of bisphosphonates and reduced risk of colorectal cancer. J Clin Oncol. 2011 Mar 20; 29(9):1146-50. View in: PubMed

Hereditary prostate cancer as a feature of Lynch syndrome. Fam Cancer. 2011 Mar; 10(1):37-42. View in: PubMed

Disclosing individual CDKN2A research results to melanoma survivors: interest, impact, and demands on researchers. Cancer Epidemiol Biomarkers Prev. 2011 Mar; 20(3):522-9. View in: PubMed

Higher micronutrient intake is associated with human papillomavirus-positive head and neck cancer: a case-only analysis. Nutr Cancer. 2011; 63(5):734-42. View in: PubMed

Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population. Cancer Prev Res (Phila). 2011 Jan; 4(1):9-22. View in: PubMed

Nonsteroidal anti-inflammatory drugs and risk of melanoma. J Skin Cancer. 2011; 2011:598571. View in: PubMed

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas. JAMA. 2010 Dec 15; 304(23):2611-9. View in: PubMed

Head circumference in the clinical detection of PTEN hamartoma tumor syndrome in a clinic population at high-risk of breast cancer. Breast Cancer Res Treat. 2010 Nov; 124(2):459-65. View in: PubMed

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Multiple forms of genetic instability within a 2-Mb chromosomal segment of 3q26. 3-q27 are associated with development of esophageal adenocarcinoma. Genes Chromosomes Cancer. 2006 Apr; 45(4):319-31. View in: PubMed

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Truncating BRCA1 mutations are uncommon in a cohort of hereditary prostate cancer families with evidence of linkage to 17q markers. Clin Cancer Res. 2004 Sep 15; 10(18 Pt 1):5975-80. View in: PubMed

The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer. Nat Genet. 2004 Jul; 36(7):694-9. View in: PubMed

Relative frequency and morphology of cancers in STK11 mutation carriers. Gastroenterology. 2004 Jun; 126(7):1788-94. View in: PubMed

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Merkel cell carcinoma and the controversial role of adjuvant radiation therapy: clinical choices in the absence of statistical evidence. J Am Acad Dermatol. 2004 Mar; 50(3):435-7; discussion 437-8. View in: PubMed

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BRCA1 and BRCA2 founder mutations and the risk of colorectal cancer. J Natl Cancer Inst. 2004 Jan 7; 96(1):15-21. View in: PubMed

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Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: evidence of genetic drift within the Ashkenazim. Am J Hum Genet. 2003 Dec; 73(6):1250-60. View in: PubMed

Accurate molecular classification of human cancers based on gene expression using a simple classifier with a pathological tree-based framework. Am J Pathol. 2003 Nov; 163(5):1985-95. View in: PubMed

Prostate cancer early detection practices among men with a family history of disease. Urology. 2003 Sep; 62(3):470-5. View in: PubMed

Cyclooxygenase 2 expression and molecular alterations in Peutz-Jeghers hamartomas and carcinomas. Clin Cancer Res. 2003 Aug 1; 9(8):3065-72. View in: PubMed

Phenotype of microsatellite unstable colorectal carcinomas: Well-differentiated and focally mucinous tumors and the absence of dirty necrosis correlate with microsatellite instability. Am J Surg Pathol. 2003 May; 27(5):563-70. View in: PubMed

R726L androgen receptor mutation is uncommon in prostate cancer families in the united states. Prostate. 2003 Mar 1; 54(4):306-9. View in: PubMed

The genetics of hereditary non-polyposis colorectal cancer. J Natl Compr Canc Netw. 2003 Jan; 1(1):137-44. View in: PubMed

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Cancer risks in BRCA1 carriers: time for the next generation of studies. J Natl Cancer Inst. 2002 Sep 18; 94(18):1344-5. View in: PubMed

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