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1. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

2. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

3. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

4. Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

5. Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

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