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Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival
The impact of coding germline variants on contralateral breast cancer risk and survival
FANCM missense variants and breast cancer riskn
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Gene-environment interactions relevant to estrogen and risk of breast cancer
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Breast cancer risk genes
CYP3A7*1C allele
Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis
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
Genome-wide association study of germline variants and breast cancer-specific mortality
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus