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Outstanding mentor named Eureka prize finalistLeading infectious diseases researcher, Clinical Associate Professor Deborah Lehmann AO, has been named a finalist for the Australian Museum Eureka Prizes for her work training and mentoring a new generation of researchers.
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Video intervention offers promising language boost for kids showing early signs of autismThe first rigorous trial of a pre-emptive behavioural intervention for babies showing early signs of autism has found the therapy can improve early language development.
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State-first program to accelerate digital health in WAA consortium of partners across the WA medical research sector will develop and deliver the State’s first digital health-specific program.
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“Correlation doesn’t equal causation”: Autism and caesarean sectionsA new study that combines data from over 20 million births has found that a caesarean section delivery is associated with autism spectrum disorder (autism) and attention-deficit hyperactivity disorder (ADHD).
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Major grant empowers community voices to drive reduction in skin infectionsAboriginal community members throughout the Kimberley will take a lead role in driving healthy skin messages within their own communities thanks to a major funding boost to The Kids Research Institute Australia’s SToP Trial.
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Meet Baxter HutchinsonBaxter Hutchinson was diagnosed with two life-threatening brain tumours a year ago, aged 17. Since then he has undergone surgery, radiotherapy and chemotherapy in his journey to beat the cancer.
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One-of-a-kind autism service offers new hope to familiesWestern Australian babies and children with autism and developmental delay will be able to access world-first therapies and interventions backed by the latest research, thanks a unique clinical service developed by The Kids Research Institute Australia.
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Vaccination reminder program to boost immunisation rates across AustraliaFamilies throughout the country will trial a new text message vaccination reminder program designed to safeguard kids against infectious diseases thanks to a generous funding boost from the Ramaciotti Foundation.
MECP2 duplication syndrome is a rare disorder neurodevelopmental disorder that, unlike Rett syndrome, mostly affects boys.
Our research covers a broad range of areas from the influence of mutation type on health outcomes to factors impacting on the lives of familes.