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Journal of the National Cancer Institute|November 21, 2015
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian CancersHuong D Meeks, Honglin Song, Kyriaki Michailidou, et al.Plos Genetics|April 2, 2013
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer riskFergus J Couch, Xianshu Wang, Lesley McGuffog, et al.European Journal of Human Genetics : EJHG|January 14, 2022
Polygenic risk modeling for prediction of epithelial ovarian cancer riskEileen O Dareng, Jonathan P Tyrer, Daniel R Barnes, et al.NPJ Breast Cancer|November 9, 2019
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancerGisella Figlioli, Massimo Bogliolo, Irene Catucci, et al.Nature Genetics|January 13, 2015
Identification of six new susceptibility loci for invasive epithelial ovarian cancerKaroline B Kuchenbaecker, Susan J Ramus, Jonathan Tyrer, et al.Nature Communications|September 8, 2016
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locusKate Lawrenson, Siddhartha Kar, Karen McCue, et al.Nature Genetics|May 20, 2020
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analysesHaoyu Zhang, Thomas U Ahearn, Julie Lecarpentier, et al.Nature Communications|September 25, 2019
Publisher Correction: Shared heritability and functional enrichment across six solid cancersXia Jiang, Hilary K Finucane, Fredrick R Schumacher, et al.Journal of Medical Genetics|September 7, 2016
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGSMelissa C Southey, David E Goldgar, Robert Winqvist, et al.Nature Communications|January 27, 2019
Shared heritability and functional enrichment across six solid cancersXia Jiang, Hilary K Finucane, Fredrick R Schumacher, et al.Pageof 28