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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Melbourne researchers have discovered gender-affirming hormone therapy can alter body proteins to match a person’s gender identity, potentially affecting susceptibility to certain health conditions. The research, led by Murdoch Children’s Research Institute (MCRI) and the University of
Murdoch Children’s Research Institute (MCRI) Director Professor Kathryn North AC has been appointed the new Chair of the Australian Medical Research Advisory Board (AMRAB). AMRAB sets the priorities for the Federal Government’s Medical Research Future Fund (MRFF), which oversees $650 million
This project is harnessing the power of stem cell technology to develop advanced infection models to find new treatments for antibiotic resistant infections in people with cystic fibrosis (CF). Our team at MCRI has developed a world first model of macrophage-resident mycobacteria that can be
Murdoch Children’s Research Institute (MCRI) has proudly become a member of the Victorian Aboriginal Health, Medical and Wellbeing Research Accord, marking a significant step forward in ethical, culturally safe research practices for Aboriginal and Torres Strait Islander communities in
Australian teenagers are being sought for a new study that will monitor the impact of a world first social media ban on their phone use, screentime, mental health and wellbeing. The Connected Minds Study, by Murdoch Children’s Research Institute (MCRI) and Deakin University, is seeking 13- to
We will co-create an innovative pain education intervention for children with cerebral palsy and chronic pain by partnering with people with lived experience of cerebral palsy. This national program of research focuses on understanding the pain experience of children with cerebral palsy and
Advancing world-class developmental imaging research on the Melbourne Children’s Campus through the purchase of the Siemens 3T Cima.X MRI system.
Developing a bedside genomic test for safer, paediatric antibiotic use. Our project aims to evaluate the role of genetic testing to prevent permanent drug-related hearing loss in children receiving aminoglycoside antibiotic treatment with a view to developing a rapid bedside, point-of-care
If it weren’t for a test that screens for genetic conditions, Giselle may not be the lively, cheeky toddler her parents know today. Giselle, 14 months, is a ball of energy, not quite walking unassisted yet, but she’s close. The picture of health is a far cry from the fragile baby her parents
Adding genomic sequencing to newborn blood screening would detect hundreds of additional childhood conditions, providing much earlier diagnosis and treatment, according to a new study. A baby’s genome, which stays with them for life, could also be re-examined if a health issue arises during their
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