Integration of genetic testing for risk associated genomic variants and rare predisposition genes into the management of high risk hereditary breast cancer families [ 2012 - 2015 ]

Research Grant

Researchers: A/Pr Paul James (Principal investigator) ,  Dr Gillian Mitchell ,  Dr Marion Harris ,  Dr Nina Hallowell ,  Ms Mary-Anne Young

Brief description Breast Cancer is a common disease with up to 20% of cases associated with a family history. This project aims to assess the contribution of recently identified risk associated genomic variants and rare predisposition genes to the heritability of familial breast cancer. The project will also assess the experience of clinicians and patients as we aim to use this information to help improve the process of risk assessment and genetic counselling in the specialist Familial Cancer Centres.

Funding Amount $AUD 645,457.40

Funding Scheme Project Grants

Notes Standard Project Grant