About
Steve Wilton is a Professor and Adjunct Professor at the University of Western Australia (UWA), affiliated with the UWA Medical School and the Centre for Neuromuscular and Neurological Disorders (Perron Institute). He holds a BSc and PhD from Adel.
His research focuses on genetic therapies, molecular medicine, and neuromuscular disorders such as muscular dystrophy and Parkinson’s disease. Key interests include antisense oligonucleotides, exon skipping, and neurogenetics. His work contributes to UN Sustainable Development Goals related to health and well-being.
Recent publications highlight advancements in Parkinson’s disease therapies, APOC3 isoform discovery, and allele-selective treatments for ALS. Over 235 research outputs and 30 grants underscore his extensive contributions, including projects funded by NHMRC, the University of Queensland, and the Muscular Dystrophy Association of America.
As a principal investigator, he has led initiatives such as personalized exon skipping strategies for Duchenne Muscular Dystrophy and preclinical assessments of splice-switching oligomers. His collaborative networks span international research institutions.
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