This project is the first scholarship in Australia to support a dedicated Doctor of Medical Science scholar to focus on describing, understanding and improving diagnosis of Bone Marrow Failure Syndromes using genomics evaluation. More accurate diagnosis of Bone Marrow Failure Syndromes using genomics evaluation underpins targeted treatment/s which will be associated with a greater chance of cure while avoiding harms and costs of inappropriate therapies. Working closely with the Aplastic Anaemia Registry (AAR) team, this new research role will also provide a valuable clinical resource to the AAR project team and contribute to analysis of Australian data for presentation and publication.
2019-2023 (Co-funded VCA/Maddie Riewoldt’s Vision International Travelling Fellowship): Novel immunological assessment of Aplastic Anaemia and post transplant Graft Dysfunction for the purposes of targeted therapeutic intervention. Dr ...
Read more2017 – 2019 Fellowship / 2017 Grant-in-Aid, Towards targeted treatments for Fanconi Anaemia, Associate Professor Wayne Crismani, St Vincents Institute for Medical Research Fanconi Anaemia is an inherited disorder which can lead to bone ...
Read more2023- 2025 (Fellowship): The inaugural Captain Courageous Fellowship. A preclinical trial of next generation gene editing for the prevention of bone marrow failure in Fanconi Anaemia. Dr Astrid Glaser at the Genome Stability Unit of St Vincent’s ...
Read more2023- 2025 (Fellowship): Discovery of novel niche factors to improve long-term stem cell transplantation in bone marrow failure syndromes. Dr Vashe Chandrakanthan, The University of Adelaide. For many patients with Bone Marrow Failure Syndromes, ...
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