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Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer
BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
BRCA1 Circos: a visualisation resource for functional analysis of missense variants