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a likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Incorporating progesterone receptor expression into the PREDICT breast prognostic model
Rare germline copy number variants (CNVs) and breast cancer risk
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
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
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
Gene-environment interactions relevant to estrogen and risk of breast cancer
