Research output per year
Research output per year
Personal profile
Research expertise keywords
- Genetic therapies
- Molecular medicine
- Muscular dystrophy
- Neuroscience: genetics
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Dive into the research topics where Steve Wilton is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Research output
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A personalised and comprehensive approach is required to suppress or replenish SNCA for Parkinson's disease
Li, D., Yau, W. Y., Chen, S., Wilton, S. & Mastaglia, F., Dec 2025, In: Npj Parkinsons Disease. 11, 1, 8 p., 42.Research output: Contribution to journal › Review article › peer-review
Open Access2 Citations (Scopus) -
Characterization of severe COL6-related dystrophy due to the recurrent variant COL6A1 c.930+189C>T
Foley, A. R., Bolduc, V., Guirguis, F., Donkervoort, S., Hu, Y., Orbach, R., Mccarty, R. M., Sarathy, A., Norato, G., Cummings, B. B., Lek, M., Sarkozy, A., Butterfield, R. J., Kirschner, J., Nascimento, A., Natera-De Benito, D., Quijano-Roy, S., Stojkovic, T., Merlini, L. & Comi, G. & 49 others, , Sept 2025, In: Brain. 148, 9, p. 3215-3227 13 p.Research output: Contribution to journal › Article › peer-review
1 Citation (Scopus) -
Discovery of Novel APOC3 Isoforms in Hepatic and Intestinal Cell Models Using Long-Read RNA Sequencing
Farstad-O’Halloran, K., Sooda, A., Iqbal, T., Wilton, S. & Aung-Htut, M. T., Apr 2025, In: Genes. 16, 4, p. 1-12 12 p., 412.Research output: Contribution to journal › Article › peer-review
Open Access -
Allele-Selective Thiomorpholino Antisense Oligonucleotides as a Therapeutic Approach for Fused-in-Sarcoma Amyotrophic Lateral Sclerosis
Mejzini, R., Caruthers, M. H., Schafer, B., Kostov, O., Sudheendran, K., Ciba, M., Danielsen, M., Wilton, S., Akkari, P. A. & Flynn, L. L., 3 Aug 2024, In: International Journal of Molecular Sciences. 25, 15, 20 p., 8495.Research output: Contribution to journal › Article › peer-review
Open Access2 Citations (Scopus) -
Antisense oligonucleotides and their applications in rare neurological diseases
McDowall, S., Aung-Htut, M., Wilton, S. & Li, D., 23 Sept 2024, In: Frontiers in Neuroscience. 18, 13 p., 1414658.Research output: Contribution to journal › Review article › peer-review
Open Access9 Citations (Scopus)
Datasets
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Data from: Functional improvement of dystrophic muscle by repression of utrophin: let-7c interaction
Mishra, M. K. (Creator), Loro, E. (Creator), Sengupta, K. (Creator), Wilton, S. D. (Creator) & Khurana, T. S. (Creator), Figshare, 16 Sept 2017
https://figshare.com/s/974a72223a0d313aea74
Dataset
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The L-type calcium channel as a reporter of successful morpholino oligomer therapy in treatment of Duchenne Muscular Dystrophy cardiomyopathy
Hool, L. (Investigator 01), Fletcher, S. (Investigator 02) & Wilton, S. (Investigator 03)
NHMRC National Health and Medical Research Council
1/01/14 → 31/12/16
Project: Research
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Development of a nucleolus-homing peptide for targeting RNA-therapeutics in gene therapy
Rothnagel, J. (Investigator 01) & Wilton, S. (Investigator 02)
1/01/13 → 31/12/13
Project: Research
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2011 - Bypassing Mutations in the 5' Region of the Dystrophin Gene by Promoting Alternative Translation Initiation Codons using Antisense Oligonucleotides
Adkin, C. (Investigator 01), Wilton, S. (Investigator 02) & Fletcher, S. (Investigator 03)
The University of Western Australia
1/01/11 → 31/12/11
Project: Research
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Personalized Exon Skipping Strategies for the Treatment of DMD
Wilton, S. (Investigator 01), Adkin, C. (Investigator 02), Ohlendieck, K. (Investigator 03) & Fletcher, S. (Investigator 04)
1/08/10 → 30/09/13
Project: Research
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Preclinical Assessment of Splice Switching Oligomers
Wilton, S. (Investigator 01) & Ohlendieck, K. (Investigator 02)
Muscular Dystrophy Association of America
1/07/10 → 30/06/13
Project: Research