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Andrew R Webster

17PUBLICATIONS

255CO-AUTHORS

Sensory systemsOptical technologyGenetic immunologyNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)

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Publications (17)

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|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

|Mar 20, 2023

Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene).

Quang Nguyen, William Woof, Nathaniel Kabiri

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Frequent Collaborators

6 joint publications

Omar Mahroo

6 joint publications

Michel Michaelides

6 joint publications

Juliana Sallum

6 joint publications

Siying Lin

5 joint publications

Nikolas Pontikos

5 joint publications

Dayyanah Sumodhee

4 joint publications

Thales Antonio Cabral De Guimaraes

4 joint publications

William Woof

4 joint publications

Quang Nguyen

4 joint publications

Gavin Arno

Frequent Collaborators

6 joint publications

Omar Mahroo

6 joint publications

Michel Michaelides

6 joint publications

Juliana Sallum

6 joint publications

Siying Lin

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