Ajoy Vincent
University of Toronto
H-index: 25
North America-Canada
Top articles of Ajoy Vincent
SLC24A1 mutations are a cause of autosomal recessive retinitis pigmentosa
Investigative Ophthalmology & Visual Science
2023/6/1
The Pro-EYS Study: Visual Acuity, Electroretinography, Contrast Sensitivity, and Full-Field Stimulus Thresholds in Patients With Retinal Degeneration Associated With Biallelic …
Investigative Ophthalmology & Visual Science
2023/6/1
Ajoy Vincent
H-Index: 15
Characterization of the Retinal Phenotype in PYGM-related McArdle Disease
Investigative Ophthalmology & Visual Science
2023/6/1
The validation of inherited retinal disease-specific patient-reported outcome measures in adolescent patients
Ophthalmic genetics
2023/5/4
Bilateral compressive optic neuropathy and outer retinopathy due to optic canal hyperostosis in a child with isolated vitamin a deficiency
Documenta Ophthalmologica
2023/4
Retinal Phenotyping of a Murine Model of Lafora Disease
Genes
2023/3/31
Shedding light on myopia by studying complete congenital stationary night blindness
2023/3/1
Ajoy Vincent
H-Index: 15
Genetics of retinal degeneration in 2023
Canadian Eye Care Today
2023/2/1
Ajoy Vincent
H-Index: 15
Treatment Strategy With Gene Editing for Late-Onset Retinal Degeneration Caused by a Founder Variant in C1QTNF5
Investigative Ophthalmology & Visual Science
2023/12/1
Ajoy Vincent
H-Index: 15
Deep phenotypic characterization of the retinal dystrophy in patients with RNU4ATAC-associated Roifman syndrome
Eye
2023/12
Anupreet Tumber
H-Index: 6
Ajoy Vincent
H-Index: 15
KCNV2-associated retinopathy: genotype–phenotype correlations–KCNV2 study group report 3
British Journal of Ophthalmology
2023/10/18
Validating Patient-Reported Outcome Measures for Adolescents with Inherited Retinal Diseases
Investigative Ophthalmology & Visual Science
2023/6/1
Baseline microperimetry and OCT in the RUSH2A study: structure− function association and correlation with disease severity
American journal of ophthalmology
2022/12/1
Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non‐syndromic retinitis pigmentosa
Clinical Genetics
2022/12
Unilateral cataract and congenital stationary night blindness in a child with novel variants in TRPM1
Journal of American Association for Pediatric Ophthalmology and Strabismus
2022/8/1
Ocular phenotype and electroretinogram abnormalities in Lafora disease and correlation with disease stage
Neurology
2018/7/17
Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction
International journal of molecular sciences
2022/6/20
Ajoy Vincent
H-Index: 15
Mario Teruo Sato
H-Index: 4
Visual acuity and full-field stimulus thresholds (FST) over 2 years in the RUSH2A study: annual rates of change from mixed effects modeling
Investigative Ophthalmology & Visual Science
2022/6/1
Michel Michaelides
H-Index: 46
Ajoy Vincent
H-Index: 15
Microperimetry and optical coherence tomography measures over 2 years in the RUSH2A study: annual rates of change from mixed effects modeling
Investigative Ophthalmology & Visual Science
2022/6/1
Ajoy Vincent
H-Index: 15
The state of patient-reported outcome measures for pediatric patients with inherited retinal disease
2022/6
Ajoy Vincent
H-Index: 15
Co-Authors
