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Breast cancer risk factors and survival by tumor subtype
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)
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
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation
FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium
Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
Genome-wide association studies identify four ER negative-specific breast cancer risk loci
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Functional Variants at the 11q13 Risk Locus for Breast Cancer Regulate Cyclin D1 Expression through Long-Range Enhancers