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Michelle de Silva

Associate Genetic Counsellor and Research Centre Manager

Michelle de Silva is a highly educated professional with a diverse background in medical research, genetic counseling, and research management.

With a PhD in Molecular Genetics and extensive experience in experimental research, Michelle has worked on projects related to gene discovery for attention deficit hyperactivity disorder, as well as cell regeneration therapies for hearing loss and heart disease.

Transitioning from a research-focused role, Michelle pursued training as a genetic counselor, leading to her current position as an Associate Genetic Counsellor at the Victorian Clinical Genetics Service (VCGS).

In her role as a genetic counsellor, Michelle provides vital resources and support to individuals and families navigating complex genetic information, contributing to their understanding and decision-making.

Currently serving as the Program Manager for the Rare Disease Flagship at the Murdoch Children's Research Institute, Michelle continues to excel in research management and is passionate about advancing genetic healthcare.

Michelle's educational background includes a Master’s Degree in Genetic Counselling, a BSc (Hons) in Molecular Genetics, a BSc in Genetics and Biochemistry, and a Doctor of Philosophy (PhD) in Molecular Genetics, all from esteemed Australian universities.

Throughout her career, Michelle has held various roles in prestigious organizations like the Murdoch Childrens Research Institute, VICTORIAN CLINICAL GENETICS SERVICES LIMITED, University of Melbourne, Baker IDI Heart and Diabetes Institute, where she has contributed significantly to genetics and genomics research.

Michelle de Silva
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Location

Melbourne, Australia