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Contribution of large genomic rearrangements in PALB2 to familial breast cancer: Implications for genetic testing

Somatic inactivation of breast cancer predisposition genes in tumors associated with pathogenic germline variants

Integration of tumour sequencing and case–control data to assess pathogenicity of RAD51C missense variants in familial breast cancer

Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study

Panel testing for familial breast cancer: calibrating the tension between research and clinical care

Reevaluation of RINT1 as a breast cancer predisposition gene

Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls

Reevaluation of the BRCA₂ truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context

Oncolysis of human ovarian cancers by echovirus type 1

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