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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Association of genomic domains in BRCA1 and BRCA2 with prostate cancer risk and aggressiveness
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Cancer Risks for PMS2-Associated Lynch Syndrome
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)