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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
Breast cancer risk factors and survival by tumor subtype
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk
Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
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
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
