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Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2018
Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity FrameworkBryce A Seifert, Jennifer L McGlaughon, Sarah A Jackson, et al.
International Journal of Cancer|December 7, 2005
Tamoxifen and contralateral breast cancer in BRCA1 and BRCA2 carriers: an updateJacek Gronwald, Nadine Tung, William D Foulkes, et al.
Human Mutation|October 13, 2018
Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genesMichael F Walsh, Deborah I Ritter, Chimene Kesserwan, et al.
Gynecologic Oncology|May 23, 2021
Achieving universal genetic assessment for women with ovarian cancer: Are we there yet? A systematic review and meta-analysisJenny Lin, Ravi N Sharaf, Rachel Saganty, et al.
Carcinogenesis|October 27, 2025
Symposium report-ethical and social considerations regarding return of secondary findings in atomic bomb survivorsNoriaki Yoshida, Douglas R Stewart, Arikuni Uchimura, et al.
European Journal of Human Genetics : EJHG|March 19, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screeningWybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
BMC Medical Research Methodology|August 19, 2020
Comparison of up-front cash cards and checks as incentives for participation in a clinician survey: a study within a trialLydia E Pace, Yeonsoo S Lee, Nadine Tung, et al.
European Journal of Human Genetics : EJHG|February 6, 2019
Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genesMykyta Artomov, Vijai Joseph, Grace Tiao, et al.
Nature Communications|November 23, 2022
Reversion mutations in germline BRCA1/2-mutant tumors reveal a BRCA-mediated phenotype in non-canonical histologiesYonina R Murciano-Goroff, Alison M Schram, Ezra Y Rosen, et al.
Human Genetics|April 30, 2018
High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputationTodd Lencz, Jin Yu, Cameron Palmer, et al.
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