Our expansive research facilities, state-of-the-art technologies and unique location within The Royal Children’s Hospital, are some of the reasons we’re home to over 1,800 leading researchers and scientists.
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Our research provides evidence for policy and clinical practice to improve child health outcomes in resource-poor settings in the Asia-Pacific region.
By combining expertise in epidemiology, psychology, genetics, and maternal fetal medicine we will measure, monitor, and maximise longitudinal health outcomes associated with prenatal risk factors.
Differences of sexual development (DSDs) are surprisingly common and often result in genital abnormalities, gender misassignment, infertility and psychological trauma.
Our group aims to improve current and future health outcomes in children with skeletal disorders by conducting clinical trials utilising new precision therapies.
Our research promotes understanding of genetics and genomics, and informs evidence-based practice, among families, health professionals and the community.
Our emphasis is on the research and development of unique technologies to improve services provided by Victorian Clinical Genetic Services (VCGS) Pathology, a wholly-owned subsidiary of Murdoch Children's Research Institute.
Our vision is that genomic information should be available to enable comprehensive disease prediction, accurate diagnosis, and effective therapeutics for all the diverse peoples of Australia.
Our group was established in 2004 to develop laboratory-based molecular neuroscience research within the Murdoch Children's Research Institute and enhance the established clinical and public health research activities of the Bruce Lefroy Centre (BLC). We research gene discovery and functional
Health, wellbeing, access and equity for children and adults living with genetic diseases.
Improving diagnosis and outcomes for children and families with rare inherited mitochondrial and neurogenetic diseases.
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