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JAMA|September 24, 2004
The "duty to warn" a patient's family members about hereditary disease risksKenneth Offit, Elizabeth Groeger, Sam Turner, et al.Mutation Research|December 17, 2008
cDNA analysis demonstrates that the BRCA2 intronic variant IVS4-12del5 is a deleterious mutationLiying Zhang, Ruben Bacares, Sherry Boyar, et al.Familial Cancer|May 2, 2020
Characterization of a germline splice site variant MLH1 c.678-3T>A in a Lynch syndrome familyCiyu Yang, Margaret Sheehan, Ester Borras, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 1, 2006
Sharing BRCA1/2 test results with first-degree relatives: factors predicting who women tellAndrea Farkas Patenaude, Michel Dorval, Lisa S DiGianni, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 15, 2003
Complementary medicine use among women enrolled in a genetic testing programLisa M DiGianni, Haesook T Kim, Karen Emmons, et al.Familial Cancer|May 14, 2011
Attitudes toward childbearing and prenatal testing in individuals undergoing genetic testing for Lynch syndromeAkriti Dewanwala, Anu Chittenden, Margery Rosenblatt, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 23, 2014
Cancer genomics and inherited riskZsofia K Stadler, Kasmintan A Schrader, Joseph Vijai, et al.Familial Cancer|November 2, 2004
Hereditary ovarian cancer in Ashkenazi JewsLuis Robles-Díaz, Deborah J Goldfrank, Noah D Kauff, et al.Cancer|January 26, 2011
Clinical outcome of triple negative breast cancer in BRCA1 mutation carriers and noncarriersLarissa J Lee, Brian Alexander, Stuart J Schnitt, et al.Breast Cancer Research and Treatment|September 13, 2005
Sex ratio distortion in offspring of families with BRCA1 or BRCA2 mutant alleles: an ascertainment bias phenomenon?Judith Balmaña, Orland Díez, Berta Campos, et al.Pageof 68