Ajoy Vincent
University of Toronto
H-index: 25
North America-Canada
Top articles of Ajoy Vincent
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
The validation of inherited retinal disease-specific patient-reported outcome measures in adolescent patients | Ophthalmic genetics | Kavin Selvan Rebhi Abuzaitoun Maria Fernanda Abalem Ajoy Vincent Chris A Andrews | 2023/5/4 |
KCNV2-associated retinopathy: genotype–phenotype correlations–KCNV2 study group report 3 | British Journal of Ophthalmology | Thales AC de Guimaraes Michalis Georgiou Anthony G Robson Kaoru Fujinami Ajoy Vincent | 2023/10/18 |
Bilateral compressive optic neuropathy and outer retinopathy due to optic canal hyperostosis in a child with isolated vitamin a deficiency | Documenta Ophthalmologica | Austin Pereira Birgit Ertl-Wagner Anupreet Tumber Ajoy Vincent Michael J Wan | 2023/4 |
Validating Patient-Reported Outcome Measures for Adolescents with Inherited Retinal Diseases | Investigative Ophthalmology & Visual Science | Kavin Selvan Rebhi Abuzaitoun Maria Fernanda Abalem Ajoy Vincent Chris A Andrews | 2023/6/1 |
Retinal Phenotyping of a Murine Model of Lafora Disease | Genes | Ajoy Vincent Kashif Ahmed Rowaida Hussein Zorana Berberovic Anupreet Tumber | 2023/3/31 |
SLC24A1 mutations are a cause of autosomal recessive retinitis pigmentosa | Investigative Ophthalmology & Visual Science | Imran H Yusuf Richard Caswell Parveen Sen Maria Vadala Patrik Schatz | 2023/6/1 |
Shedding light on myopia by studying complete congenital stationary night blindness | Christina Zeitz Jérome E Roger Isabelle Audo Christelle Michiels Nuria Sánchez-Farías | 2023/3/1 | |
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 | Ajoy Vincent | 2023/6/1 |
Treatment Strategy With Gene Editing for Late-Onset Retinal Degeneration Caused by a Founder Variant in C1QTNF5 | Investigative Ophthalmology & Visual Science | Randa TH Li Alejandro J Roman Alexander Sumaroka Chloe M Stanton Malgorzata Swider | 2023/12/1 |
Genetics of retinal degeneration in 2023 | Canadian Eye Care Today | Elise Héon Ajoy Vincent Alaa Tayyib | 2023/2/1 |
Characterization of the Retinal Phenotype in PYGM-related McArdle Disease | Investigative Ophthalmology & Visual Science | Alaa Tayyib Rowaida Hussein Anupreet Tumber Kashif Ahmed Erika Tavares | 2023/6/1 |
Deep phenotypic characterization of the retinal dystrophy in patients with RNU4ATAC-associated Roifman syndrome | Eye | Brian G Ballios Amarilla Mandola Alaa Tayyib Anupreet Tumber Jenny Garkaby | 2023/12 |
Baseline microperimetry and OCT in the RUSH2A study: structure− function association and correlation with disease severity | American journal of ophthalmology | Eleonora M Lad Jacque L Duncan Wendi Liang Maureen G Maguire Allison R Ayala | 2022/12/1 |
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 | Ajoy Vincent Eleonora M Lad | 2022/6/1 |
Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non‐syndromic retinitis pigmentosa | Clinical Genetics | Anna Dvaladze Erika Tavares Matteo Di Scipio Graeme Nimmo Monika K Grudzinska‐Pechhacker | 2022/12 |
The state of patient-reported outcome measures for pediatric patients with inherited retinal disease | Kavin Selvan Maria F Abalem Gabrielle D Lacy Ajoy Vincent Elise Héon | 2022/6 | |
Unilateral cataract and congenital stationary night blindness in a child with novel variants in TRPM1 | Journal of American Association for Pediatric Ophthalmology and Strabismus | Eman Saleh Monika Grudzinska Pechhacker Anjali Vig Maanik Mehta Jason Maynes | 2022/8/1 |
Values of Retinoblastoma Survivors and Parents Regarding Treatment Outcomes: A Qualitative Study | JCO Oncology Practice | Ana Janic Ajoy Vincent Jennifer Stinson Helen Dimaras | 2022/6 |
Ocular phenotype and electroretinogram abnormalities in Lafora disease and correlation with disease stage | Neurology | Ajoy Vincent Angelo Macrì Anupreet Tumber Nikolas Koukas Saija Ahonen | 2018/7/17 |
A large animal model of RDH5-associated retinopathy recapitulates important features of the human phenotype | Human Molecular Genetics | Laurence M Occelli Anahita Daruwalla Samantha R De Silva Paige A Winkler Kelian Sun | 2022/4/15 |
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