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(1 - 24 of 39)
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Common variants in breast cancer risk loci predispose to distinct tumor subtypes
Breast cancer risk genes
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis
Two truncating variants in FANCC and breast cancer risk
Genome-wide association study of germline variants and breast cancer-specific mortality
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Association analysis identifies 65 new breast cancer risk loci
BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer
BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer
Genetic modifiers of CHEK2*1100delC-associated breast cancer risk
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21
Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer
Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent
Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
RAD51B in Familial Breast Cancer
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Genetic predisposition to ductal carcinoma in situ of the breast
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