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Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Rare germline copy number variants (CNVs) and breast cancer risk
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer