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Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Physical activity, sedentary time and breast cancer risk
Rare germline copy number variants (CNVs) and breast cancer risk
Common variants in breast cancer risk loci predispose to distinct tumor subtypes
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes