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(41 - 60 of 133)

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BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3
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
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
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
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression
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
Age- and Tumor Subtype Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing
RAD51B in Familial Breast Cancer
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Genetic predisposition to ductal carcinoma in situ of the breast
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2

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