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The New England Journal of Medicine|May 25, 2002
Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutationNoah D Kauff, Jaya M Satagopan, Mark E Robson, et al.Genes, Chromosomes & Cancer|January 17, 2002
Similar patterns of genomic alterations characterize primary mediastinal large-B-cell lymphoma and diffuse large-B-cell lymphomaNallasivam Palanisamy, Ashraf A Abou-Elella, Seeta R Chaganti, et al.Journal of the National Cancer Institute|October 16, 2003
Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemiaKenneth Offit, Orna Levran, Brian Mullaney, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2013
Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologiesKatrina A B Goddard, Evelyn P Whitlock, Jonathan S Berg, et al.European Urology|July 22, 2019
Familial Kidney Cancer: Implications of New Syndromes and Molecular InsightsMaria I Carlo, A Ari Hakimi, Grant D Stewart, et al.Breast Cancer Research and Treatment|February 3, 2017
Psychosocial factors associated with the uptake of contralateral prophylactic mastectomy among BRCA1/2 mutation noncarriers with newly diagnosed breast cancerJada G Hamilton, Margaux C Genoff, Melissa Salerno, et al.The American Journal of Surgical Pathology|October 25, 2003
Value of histopathology in predicting microsatellite instability in hereditary nonpolyposis colorectal cancer and sporadic colorectal cancerJinru Shia, Nathan A Ellis, Philip B Paty, et al.Plos One|July 11, 2013
Assessment of SLX4 Mutations in Hereditary Breast CancersSohela Shah, Yonghwan Kim, Irina Ostrovnaya, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2018
Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panelsKristy Lee, Bryce A Seifert, Hermela Shimelis, et al.Human Genetics|September 19, 2021
Patient and public preferences for being recontacted with updated genomic results: a mixed methods studyChloe Mighton, Marc Clausen, Agnes Sebastian, et al.Pageof 67