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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

4. Incorporating patient perspectives in the development of a core outcome set for reproductive genetic carrier screening: a sequential systematic review.

7. Connecting patients, researchers and clinical genetics services: the experiences of participants in the Australian Ovarian Cancer Study (AOCS).

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