Jay Self

University of Southampton

United Kingdom

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Articles (14)

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2025

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2025

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2025

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2024

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2021

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2021

Collaborators (10)

Roly Megaw

Clinical Lecturer

University of Edinburgh

UNITED KINGDOM

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Eloise Keeling

University of Southampton

UNITED KINGDOM

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Helena Lee

Associate Professor & Consultant Ophthalmologist

University of Southampton

UNITED KINGDOM

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Samantha De Silva

University of Oxford

UNITED KINGDOM

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Richard P. Gale

Professor of Ophthalmology

University of York

UNITED KINGDOM

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Rose Gilbert

Cambridge University Hospitals NHS Foundation Trust

UNITED KINGDOM

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Nicholas Beare

Senior Lecturer

University of Liverpool

UNITED KINGDOM

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Steffen Bayer

University of Southampton

UNITED KINGDOM

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Daniel Osborne

University of Bristol

UNITED KINGDOM

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Sally Brailsford

University of Southampton

UNITED KINGDOM

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Jay Self

Research Interests

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Articles (14)

Can a Portable Flash Visual Evoked Potential (VEP) Device Identify Chiasmal Decussation Anomalies in Albinism?

Could a hand-held, visual electrophysiology device theoretically reduce diagnostic waiting times for complex eye conditions in the NHS? A Discrete Event Simulation (DES) modelling study

Real-World Views of Patching Differ to Health Professionals’: An Online Survey of Professionals, Patients, Teachers, Parents and Carers

The UK clinical eye research strategy: refreshing research priorities for clinical eye research in the UK

Impact of the COVID-19 pandemic on the research activities of UK ophthalmologists

Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxia

Four cases of acute comitant esotropia associated with diffuse intrinsic pontine glioma in children

Aetiologies of acquired pediatric sixth nerve palsies in a U.K. based population

Impact of the COVID-19 pandemic on individuals with nystagmus and an exploration of public assumptions about the condition: an electronic questionnaire study

An OTX2 Gene Mutation Causing a More Severe Retinal Phenotype in a Female RPGR Mutation Carrier

Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B)

A severe case of Bosch-Boonstra-Schaaf optic atrophy syndrome with a novel description of coloboma and septo-optic dysplasia, owing to a start codon variant in the NR2F1 gene

Correction: Comparison of the handheld RETeval ERG system with a routine ERG system in healthy adults and in paediatric patients

Comparison of the handheld RETeval ERG system with a routine ERG system in healthy adults and in paediatric patients (October, 10.1038/s41433-020-01221-2, 2020)

Collaborators (10)

Roly Megaw

Eloise Keeling

Helena Lee

Samantha De Silva

Richard P. Gale

Rose Gilbert

Nicholas Beare

Steffen Bayer

Daniel Osborne

Sally Brailsford

Make your next move.

Jay Self

Research Interests

Explore related searches

Contact this professor

Articles (14)

Can a Portable Flash Visual Evoked Potential (VEP) Device Identify Chiasmal Decussation Anomalies in Albinism?

Could a hand-held, visual electrophysiology device theoretically reduce diagnostic waiting times for complex eye conditions in the NHS? A Discrete Event Simulation (DES) modelling study

Real-World Views of Patching Differ to Health Professionals&rsquo;: An Online Survey of Professionals, Patients, Teachers, Parents and Carers

The UK clinical eye research strategy: refreshing research priorities for clinical eye research in the UK

Impact of the COVID-19 pandemic on the research activities of UK ophthalmologists

Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxia

Four cases of acute comitant esotropia associated with diffuse intrinsic pontine glioma in children

Aetiologies of acquired pediatric sixth nerve palsies in a U.K. based population

Impact of the COVID-19 pandemic on individuals with nystagmus and an exploration of public assumptions about the condition: an electronic questionnaire study

An OTX2 Gene Mutation Causing a More Severe Retinal Phenotype in a Female RPGR Mutation Carrier

Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B)

A severe case of Bosch-Boonstra-Schaaf optic atrophy syndrome with a novel description of coloboma and septo-optic dysplasia, owing to a start codon variant in the NR2F1 gene

Correction: Comparison of the handheld RETeval ERG system with a routine ERG system in healthy adults and in paediatric patients

Comparison of the handheld RETeval ERG system with a routine ERG system in healthy adults and in paediatric patients (October, 10.1038/s41433-020-01221-2, 2020)

Collaborators (10)

Roly Megaw

Eloise Keeling

Helena Lee

Samantha De Silva

Richard P. Gale

Rose Gilbert

Nicholas Beare

Steffen Bayer

Daniel Osborne

Sally Brailsford

Make your next move.

Real-World Views of Patching Differ to Health Professionals’: An Online Survey of Professionals, Patients, Teachers, Parents and Carers