Steve D Wilton
6PUBLICATIONS
77CO-AUTHORS
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Publications (6)
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|Apr 08, 2024
The recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy.A Reghan Foley, Véronique Bolduc, Fady Guirguis
|Aug 30, 2021
Stargardt disease and progress in therapeutic strategies.Di Huang, Rachael C Heath Jeffery, May Thandar Aung-Htut
|Sep 11, 2020
NEAT1 polyA-modulating antisense oligonucleotides reveal opposing functions for both long non-coding RNA isoforms in neuroblastoma.Alina Naveed, Jack A Cooper, Ruohan Li
|Aug 09, 2020
Progress in the molecular pathogenesis and nucleic acid therapeutics for Parkinson's disease in the precision medicine era.Dunhui Li, Frank L Mastaglia, Sue Fletcher
|Jul 07, 2020
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defect.Di Huang, Jennifer A Thompson, Jason Charng
|Dec 21, 2018
YAPping about and not forgetting TAZ.Bernard A Callus, Megan L Finch-Edmondson, Sue Fletcher
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Frequent Collaborators
4 joint publications
Sue Fletcher
2 joint publications
Samuel McLenachan
2 joint publications
Fred K Chen
2 joint publications
May Thandar Aung-Htut
1 joint publications
Carsten G Bönnemann
1 joint publications
Jennifer A Thompson
1 joint publications
Jason Charng
1 joint publications
Enid Chelva
1 joint publications
Shang-Chih Chen
1 joint publications
Terri L McLaren
