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a likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants
Common variants in breast cancer risk loci predispose to distinct tumor subtypes
Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Characterization of male breast cancer: results of the EORTC 10085/TBCRC/BIG/NABCG International Male Breast Cancer Program