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Genome-wide association study identifies novel breast cancer susceptibility loci
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.
Characterizing genetic variants for clinical action
Evaluation of Fanconi Anemia genes in familial breast cancer predisposition
The ICR639 CPG NGS validation series: A resource to assess analytical sensitivity of cancer predisposition gene testing
The emerging landscape of breast cancer susceptibility
THE GENETICS OF BREAST CANCER SUSCEPTIBILITY
Corrigendum: Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth
