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Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction
Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer