Are BRCA1- and BRCA2-associated breast cancers different?OFFIT, Kenneth.Journal of clinical oncology. 2000, Vol 18, Num 21, pp 104s-106s, issn 0732-183X, SUPArticle

Inherited Predisposition to Cancer: Introduction and OverviewROBSON, Mark; OFFIT, Kenneth.Hematology/oncology clinics of North America. 2010, Vol 24, Num 5, issn 0889-8588, vii, 793-797 [6 p.]Article

Genetic Predisposition to CancerOFFIT, Kenneth; ROBSON, Mark.Hematology/oncology clinics of North America. 2010, Vol 24, Num 5, issn 0889-8588, 221 p.Serial Issue

Management of an inherited predisposition to breast cancerROBSON, Mark; OFFIT, Kenneth.The New England journal of medicine. 2007, Vol 357, Num 2, pp 154-162, issn 0028-4793, 9 p.Article

Endocrine Cancer Predisposition Syndromes: Hereditary Paraganglioma, Multiple Endocrine Neoplasia Type 1, Multiple Endocrine Neoplasia Type 2, and Hereditary Thyroid CancerRUBINSTEIN, Wendy S.Hematology/oncology clinics of North America. 2010, Vol 24, Num 5, issn 0889-8588, viii-ix, 907-937 [33 p.]Article

Personalized medicine: new genomics, old lessonsOFFIT, Kenneth.Human genetics. 2011, Vol 130, Num 1, pp 3-14, issn 0340-6717, 12 p.Article

Ethical and legal aspects of cancer genetic testingOFFIT, Kenneth; THOM, Peter.Seminars in oncology. 2007, Vol 34, Num 5, pp 435-443, issn 0093-7754, 9 p.Article

Hereditary cancer predisposition syndromesGARBER, Judy E; OFFIT, Kenneth.Journal of clinical oncology. 2005, Vol 23, Num 2, pp 276-292, issn 0732-183X, 17 p.Article

Upper Gastrointestinal Cancer Predisposition SyndromesSHAH, Manish A; KURTZ, Robert C.Hematology/oncology clinics of North America. 2010, Vol 24, Num 5, issn 0889-8588, vii, 815-835 [22 p.]Article

Breast Cancer Predisposition SyndromesHEMEL, Deborah; DOMCHEK, Susan M.Hematology/oncology clinics of North America. 2010, Vol 24, Num 5, issn 0889-8588, vii, 799-814 [17 p.]Article

Heritability of Hematologic Malignancies: From Pedigrees to GenomicsCHURPEK, Jane E; ONEL, Kenan.Hematology/oncology clinics of North America. 2010, Vol 24, Num 5, issn 0889-8588, ix, 939-972 [35 p.]Article

Gene Patents and Personalized Cancer Care: Impact of the Myriad Case on Clinical OncologyOFFIT, Kenneth; BRADBURY, Angela; STORM, Courtney et al.Journal of clinical oncology. 2013, Vol 31, Num 21, pp 2743-2748, issn 0732-183X, 6 p.Article

Quality of life in women at risk for ovarian cancer who have undergone risk-reducing oophorectomyROBSON, Mark; HENSLEY, Martee; BARAKAT, Richard et al.Gynecologic oncology (Print). 2003, Vol 89, Num 2, pp 281-287, issn 0090-8258, 7 p.Article

Cancer Genomics and Inherited RiskSTADLER, Zsofia K; SCHRADER, Kasmintan A; VIJAI, Joseph et al.Journal of clinical oncology. 2014, Vol 32, Num 7, pp 687-698, issn 0732-183X, 12 p.Article

The Duty to warn a patient's family members about hereditary disease risksOFFIT, Kenneth; GROEGER, Elizabeth; TURNER, Sam et al.JAMA, the journal of the American Medical Association. 2004, Vol 292, Num 12, pp 1469-1473, issn 0098-7484, 5 p.Article

Genitourinary Cancer Predisposition SyndromesGALLAGHER, David J; FEIFER, Andrew; COLEMAN, Jonathan A et al.Hematology/oncology clinics of North America. 2010, Vol 24, Num 5, issn 0889-8588, viii, 861-883 [23 p.]Article

Clinical Genetics of Hereditary Colorectal CancerPOWER, Derek G; GLOGLOWSKI, Emily; LIPKIN, Steven M et al.Hematology/oncology clinics of North America. 2010, Vol 24, Num 5, issn 0889-8588, vii-viii, 837-859 [25 p.]Article

Hereditary Genodermatoses with Cancer PredispositionGERSTENBLITH, Meg R; GOLDSTEIN, Alisa M; TUCKER, Margaret A et al.Hematology/oncology clinics of North America. 2010, Vol 24, Num 5, issn 0889-8588, viii, 885-906 [13 p.]Article

Genome-wide Association Studies of Cancer PredispositionSTADLER, Zsofia K; VIJAI, Joseph; THOM, Peter et al.Hematology/oncology clinics of North America. 2010, Vol 24, Num 5, issn 0889-8588, ix, 973-996 [25 p.]Article

The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriersLAITMAN, Yael; KUCHENBAECKER, Karoline B; SCHMUTZLER, Rita K et al.Breast cancer research and treatment. 2012, Vol 132, Num 3, pp 1119-1126, issn 0167-6806, 8 p.Article

Germline mutations in BAP1 predispose to melanocytic tumorsWIESNER, Thomas; OBENAUF, Anna C; VIALE, Agnes et al.Nature genetics. 2011, Vol 43, Num 10, pp 1018-1021, issn 1061-4036, 4 p.Article

BRCA Germline Mutations in Jewish Patients With Pancreatic AdenocarcinomaFERRONE, Cristina R; LEVINE, Douglas A; TANG, Laura H et al.Journal of clinical oncology. 2009, Vol 27, Num 3, pp 433-438, issn 0732-183X, 6 p.Article

Breast cancer risk following bilateral oophorectomy in BRCA1 and BRCA2 mutation carriers : An international case-control studyEISEN, Andrea; LUBINSKI, Jan; FOULKES, William D et al.Journal of clinical oncology. 2005, Vol 23, Num 30, pp 7491-7496, issn 0732-183X, 6 p.Article

Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish populationSHAAG, Avraham; WALSH, Tom; OFFIT, Kenneth et al.Human molecular genetics (Print). 2005, Vol 14, Num 4, pp 555-563, issn 0964-6906, 9 p.Article

Frequency of BRCA1 and BRCA2 mutations in unselected Ashkenazi Jewish patients with colorectal cancerKIRCHHOFF, Tomas; SATAGOPAN, Java M; KAUFF, Noah D et al.Journal of the National Cancer Institute. 2004, Vol 96, Num 1, pp 68-70, issn 0027-8874, 3 p.Article