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Genome-wide association study identifies novel breast cancer susceptibility loci
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.
Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer
Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) C
Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers
Common Polymorphisms in ERCC2 (Xeroderma pigmentosum D) are not Associated with Breast Cancer Risk
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database
Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics
Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
Germ-line variation at a functional p53 binding site increases susceptibility to breast cancer development
