Research output per year
Research output per year
Personal profile
Research expertise keywords
- Genetic therapies
- Molecular medicine
- Muscular dystrophy
- RNA biology
- Neurodegeneration
- Neuromuscular and neurological disorders
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Dive into the research topics where Susan Fletcher 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
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Expression and Site-Specific Biotinylation of Human Cytosolic 5′-Nucleotidase 1A in Escherichia coli
Slater, N., Sooda, A., Mastaglia, F. L., Fletcher, S., Watson, M., Needham, M. & Coudert, J. D., Jun 2025, In: Methods and protocols. 8, 3, 66.Research output: Contribution to journal › Article › peer-review
Open Access2 Link opens in a new tab Citations (Scopus) -
Skipping of Duplicated Dystrophin Exons: In Vitro Induction and Assessment
Greer, K., Fletcher, S. & Wilton, S. D., 29 Jul 2025, (E-pub ahead of print) Methods in Molecular Biology. USA: Humana Press Inc., p. 179-188 10 p. (Methods in Molecular Biology; vol. 2964).Research output: Chapter in Book/Conference paper › Chapter › peer-review
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To splice or not to splice: pseudoexons in neurological disease and opportunities for intervention
Fletcher, S., Keegan, N. P., Mejzini, R. & Pitout, I. L., Jun 2025, In: Current Opinion in Genetics and Development. 92, 9 p., 102343.Research output: Contribution to journal › Review article › peer-review
Open Access4 Link opens in a new tab Citations (Web of Science) -
Is Exon Skipping a Viable Therapeutic Approach for Vascular Ehlers–Danlos Syndrome with Mutations in COL3A1 Exon 10 or 15?
Utama, S., Cale, J. M., Mitrpant, C., Fletcher, S., Wilton, S. D. & Aung-Htut, M. T., 13 Aug 2024, In: International Journal of Molecular Sciences. 25, 16, 17 p., 8816.Research output: Contribution to journal › Article › peer-review
Open Access -
Limb Girdle Muscular Dystrophy Type 2B (LGMD2B): Diagnosis and Therapeutic Possibilities
Poudel, B. H., Fletcher, S., Wilton, S. D. & Aung-Htut, M., Jun 2024, In: International Journal of Molecular Sciences. 25, 11, 19 p., 5572.Research output: Contribution to journal › Review article › peer-review
Open Access7 Link opens in a new tab Citations (Scopus)
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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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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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Definition of Dystrophin Functional Domains According to Exon Boundaries to Optimise Splice Switching Therapies for DMD
Wilton, S. (Investigator 01), Fletcher, S. (Investigator 02) & Pinniger, G. (Investigator 03)
NHMRC National Health and Medical Research Council
1/01/10 → 31/12/12
Project: Research
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Antisense Oligomer Induced Splice Switching Therapy In A Mouse Model Of Spinal Muscular Atrophy
Wilton, S. (Investigator 01), Fletcher, S. (Investigator 02), Burghes, A. (Investigator 03) & Mitrpant, C. (Investigator 04)
The University of Western Australia
1/01/10 → 31/12/10
Project: Research
Prizes
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HonDUniv, The University of Western Australia
Fletcher, S. (Recipient), 11 Dec 2024
Prize: Honorary award
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FAHMS
Fletcher, S. (Recipient), Dec 2022
Prize: Fellow of the Australian Academy of Health and Medical Sciences
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