Andrew Webster

18PUBLICATIONS
258CO-AUTHORS
Neurology and neuromuscular diseasesSensory systemsOptical technologyGenetic immunologyGene expression (incl. microarray and other genome-wide approaches)
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Publications (18)

|Jul 17, 2026
Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy.

|Jan 09, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Jul 09, 2025
Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.

William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei

|Jun 26, 2025
Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene.

Nikolas Pontikos, William A Woof, Siying Lin

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

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Apr 08, 2024
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom.

William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei

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Frequent Collaborators

7 joint publications

Omar Mahroo

7 joint publications

Siying Lin

6 joint publications

Michel Michaelides

6 joint publications

Juliana Sallum