Naomi Chadderton

7PUBLICATIONS
159CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesVision scienceMedical devices
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Publications (7)

|Jun 26, 2026
First Exonic Cryptic Branchpoint Variant in an Inherited Retinal Degeneration Detected in an Irish RPGR Pedigree with X-Linked Retinitis Pigmentosa.

|Jan 25, 2025
Novel Splice-Altering Variants in the CHM and CACNA1F Genes Causative of X-Linked Choroideremia and Cone Dystrophy.

Anna R Ridgeway, Ciara Shortall, Laura K Finnegan

|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Aug 29, 2024
AAV-NDI1 Therapy Provides Significant Benefit to Murine and Cellular Models of Glaucoma.

Sophia Millington-Ward, Arpad Palfi, Ciara Shortall

|Feb 25, 2023
Optimisation of AAV-NDI1 Significantly Enhances Its Therapeutic Value for Correcting Retinal Mitochondrial Dysfunction.

Naomi Chadderton, Arpad Palfi, Daniel M Maloney

|Feb 25, 2023
RPE-Directed Gene Therapy Improves Mitochondrial Function in Murine Dry AMD Models.

Sophia Millington-Ward, Naomi Chadderton, Laura K Finnegan

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Frequent Collaborators

6 joint publications

Laura K Finnegan

4 joint publications

Sophia Millington-Ward

2 joint publications

Ella Kopčić

2 joint publications

Adrian Dockery