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Now showing items 1-7 of 7
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.
Combined associations of a polygenic risk score and classical risk factors with breast cancer risk
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers.
Shared heritability and functional enrichment across six solid cancers
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer