Naomi Chadderton
Dublin, L, Ireland
Last Updated: 09/26/2026
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Found 31 publications
First Exonic Cryptic Branchpoint Variant in an Inherited Retinal Degeneration Detected in an Irish RPGR Pedigree with X-Linked Retinitis Pigmentosa.
Journal: Genes
Published: May 14, 2026
The landscape of variants in pre-mRNA-processing factor genes in an Irish cohort.
Journal: Genetics in medicine open
Published: September 11, 2025
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.
Journal: Nature genetics
Published: June 02, 2025
The Challenge of VUS in Inherited Retinal Degeneration: Insight from Functional Studies.
Journal: Advances in experimental medicine and biology
Published: February 10, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.
Journal: medRxiv : the preprint server for health sciences
Published: January 20, 2025
AAV-NDI1 Therapy Provides Significant Benefit to Murine and Cellular Models of Glaucoma.
Journal: International journal of molecular sciences
Published: July 09, 2024
RPE-Directed Gene Therapy Improves Mitochondrial Function in Murine Dry AMD Models.
Journal: International journal of molecular sciences
Published: November 01, 2022
AAV-mediated gene therapy improving mitochondrial function provides benefit in age-related macular degeneration models.
Journal: Clinical and translational medicine
Published: April 25, 2022
AAV-PHP.eB transduces both the inner and outer retina with high efficacy in mice.
Journal: Molecular therapy. Methods & clinical development
Published: December 07, 2021
SARM1 Ablation Is Protective and Preserves Spatial Vision in an In Vivo Mouse Model of Retinal Ganglion Cell Degeneration.
Journal: International journal of molecular sciences
Published: October 27, 2021
Last Updated: 09/26/2026