PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

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

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

Genome-wide association studies identify four ER negative-specific breast cancer risk loci