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The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity
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
Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression
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
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation
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