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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
