Ajoy Vincent

Associate Professor

University of Toronto Faculty of Medicine

Canada

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Articles (15)

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2024

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2024

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2023

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2023

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2023

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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

Collaborators (9)

Gislin Dagnelie

professor

Johns Hopkins University

UNITED STATES

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Roly Megaw

Clinical Lecturer

University of Edinburgh

UNITED KINGDOM

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Chris Andrews

University of Michigan

UNITED STATES

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Danial Roshandel

University of Western Australia

AUSTRALIA

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Elfride De Baere

BELGIUM

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Samuel McLenachan

University of Western Australia

AUSTRALIA

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Joseph Carroll

Medical College of Wisconsin

UNITED STATES

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Susanne Kohl

University of Tübingen

GERMANY

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Jenny Garkaby

McMaster University

CANADA

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Ajoy Vincent

Research Interests

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Articles (15)

Retinal Dystrophies Associated With Peripherin-2

Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study

Deep phenotypic characterization of the retinal dystrophy in patients with RNU4ATAC-associated Roifman syndrome

The validation of inherited retinal disease-specific patient-reported outcome measures in adolescent patients

Retinal Phenotyping of a Murine Model of Lafora Disease

Shedding light on myopia by studying complete congenital stationary night blindness

Bilateral compressive optic neuropathy and outer retinopathy due to optic canal hyperostosis in a child with isolated vitamin a deficiency

Treatment Strategy With Gene Editing for Late-Onset Retinal Degeneration Caused by a Founder Variant in C1QTNF5.

Virtual reality headsets for perimetry testing: a systematic review.

<i>KCNV2</i>-associated retinopathy: genotype-phenotype correlations - <i>KCNV2</i> study group report 3.

Baseline Microperimetry and OCT in the RUSH2A Study: Structure−Function Association and Correlation With Disease Severity

Deep intronic variant in <i>MVK</i> as a cause for mevalonic aciduria initially presenting as non‐syndromic retinitis pigmentosa

Unilateral cataract and congenital stationary night blindness in a child with novel variants in TRPM1

Ocular phenotype and electroretinogram abnormalities in Lafora disease and correlation with disease stage

Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction

Collaborators (9)

Gislin Dagnelie

Roly Megaw

Chris Andrews

Danial Roshandel

Elfride De Baere

Samuel McLenachan

Joseph Carroll

Susanne Kohl

Jenny Garkaby

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