Thomas R W Nixon

7PUBLICATIONS
6CO-AUTHORS
NeonatologyVision scienceDevelopmental genetics (incl. sex determination)Gene mappingGene expression (incl. microarray and other genome-wide approaches)
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Publications (7)

|Jul 31, 2026
A simple questionnaire to prevent blindness-a cross-sectional study screening for Stickler syndrome in children.

|Oct 29, 2024
Ultrastructural investigation of the posterior hyaloid membrane in posterior vitreous detachment.

Thomas R W Nixon, Matthew J Hayes, David Snead

|Oct 05, 2023
Posterior vitreous detachment and retinal tear - a prospective study of community referrals.

Thomas R W Nixon, Rebecca L Davie, Martin P Snead

|Jul 27, 2022
Autosomal Recessive Stickler Syndrome.

Thomas R W Nixon, Allan J Richards, Howard Martin

|Jun 25, 2020
Inherited and de novo biallelic pathogenic variants in COL11A1 result in type 2 Stickler syndrome with severe hearing loss.

Thomas Nixon, Allan J Richards, Adrian Lomas

|May 16, 2019
Homozygous Type IX collagen variants (COL9A1, COL9A2, and COL9A3) causing recessive Stickler syndrome-Expanding the phenotype.

Thomas R W Nixon, Philip Alexander, Allan Richards

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Frequent Collaborators

5 joint publications

Martin P Snead

2 joint publications

Philip Alexander

1 joint publications

Allan J Richards

1 joint publications

Robert Smyth