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a likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Physical activity, sedentary time and breast cancer risk
Rare germline copy number variants (CNVs) and breast cancer risk
Common variants in breast cancer risk loci predispose to distinct tumor subtypes
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
Genetic insights into biological mechanisms governing human ovarian ageing
Mendelian randomisation study of smoking exposure in relation to breast cancer risk
Breast cancer risk factors and survival by tumor subtype
CYP3A7*1C allele
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
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
Two truncating variants in FANCC and breast cancer risk
Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
Genome-wide association study of germline variants and breast cancer-specific mortality