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Personalized early detection and prevention of breast cancer: ENVISION consensus statement
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis
Towards controlled terminology for reporting germline cancer susceptibility variants: an ENIGMA report
Genome-wide association study of germline variants and breast cancer-specific mortality
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
MicroRNA Related Polymorphisms and Breast Cancer Risk
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
Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2
Genome-wide association analysis identifies three new breast cancer susceptibility loci
Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium
Confirmation of 5p12 As a Susceptibility Locus for Progesterone-Receptor-Positive, Lower Grade Breast Cancer