Gareth focuses on equitable and community engaged health innovation and implementation through public-private-philanthropic partnerships and under a precision public health paradigm. He is Head of the Western Australian Register of Developmental Anomalies (combined birth defects and cerebral palsy registers); a Clinical Geneticist at Genetic Services of Western Australia; an Adjunct Policy Advisor on Clinical Genomics at the WA Department of Health; and Director of the Undiagnosed Diseases Program (UDP) WA . He is a founding member of the Board of Directors of the Undiagnosed Diseases Network – International; Vice-Chair of the Diagnostics Scientific Committee of the International Rare Diseases Research Consortium; a member of the Governance Council of the International Cerebral Palsy Genomics Consortium; and a Director of the Academy for Child and Adolescent Health. He is a Clinical A/Prof at the School of Paediatrics and Child Health, University of Western Australia; the Institute for Immunology and Infectious Diseases , Murdoch University; at Spatial Sciences, Curtin University; and at the School of Population and Global Health, University of Melbourne. He Co-Directs the Genetic and Rare Diseases Program at Telethon Kids Institute. His PhD was in genetic modifiers of vaccine response in children and he leads a 3D facial analysis team. He translated, to public health system implementation, the first Aboriginal genomic reference range in Western Australia and supervises the first genetic counsellor dedicated to Australian Aboriginal genetic health care. He led the implementation of a knowledge management platform for rare diseases in the WA Health System, Patient Archive. He is on the Scientific Advisory Board for Solve-RD. He is a Board Member of the Genetic and Rare Diseases Network, WA and a member of the Rare Voices Australia Scientific and Medical Advisory Committee.