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Ajoy Vincent

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2015-2023
Publications (10 Years): 16

Top Venues

Genes

Documenta ophthalmologica. Advances in ophthalmology

JCO oncology practice

Ophthalmic genetics

University of Toronto Faculty of Medicine

Saint John's Medical College (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Toronto Faculty of Medicine Jul 1o 2019

Canada

Associate Professor :: Ophthalmology and Vision Sciences

Education History

Saint John's Medical College

India

MSC :: Ophthalmology Residency

Publications

Brian G Ballios, Amarilla Mandola, Alaa Tayyib, Anupreet Tumber, Jenny Garkaby, Linda Vong, Elise Heon, Chaim M Roifman, Ajoy Vincent
Deep phenotypic characterization of the retinal dystrophy in patients with RNU4ATAC-associated Roifman syndrome. Eye (London, England) (2023)
Ajoy Vincent, Kashif Ahmed, Rowaida Hussein, Zorana Berberovic, Anupreet Tumber, Xiaochu Zhao, Berge A Minassian
Retinal Phenotyping of a Murine Model of Lafora Disease. Genes 14 (4) (2023)
Ajoy Vincent, Kashif Ahmed, Rowaida Hussein, Zorana Berberovic, Anupreet Tumber, Xiaochu Zhao, Berge A Minassian
Retinal Phenotyping of a Murine Model of Lafora Disease. Genes 14 (4) (2023)
Kavin Selvan, Rebhi Abuzaitoun, Maria Fernanda Abalem, Ajoy Vincent, Christopher A Andrews, Gabrielle Davis Lacy, Rafid Farjo, Karissa Kao, Krystal Kao, Gislin Dagnelie, David C Musch, Kanishka T Jayasundera, Elise Heon
The validation of inherited retinal disease-specific patient-reported outcome measures in adolescent patients. Ophthalmic genetics (2023)
Ajoy Vincent, Kashif Ahmed, Rowaida Hussein, Zorana Berberovic, Anupreet Tumber, Xiaochu Zhao, Berge A Minassian
Retinal Phenotyping of a Murine Model of Lafora Disease. Genes 14 (4) (2023)
Ajoy Vincent, Kashif Ahmed, Rowaida Hussein, Zorana Berberovic, Anupreet Tumber, Xiaochu Zhao, Berge A Minassian
Retinal Phenotyping of a Murine Model of Lafora Disease. Genes 14 (4) (2023)
Katarina Stingl, Britta Baumann, Pietro De Angeli, Ajoy Vincent, Elise Héon, Monique Cordonnier, Elfriede De Baere, Salmo Raskin, Mario Teruo Sato, Naoye Shiokawa, Susanne Kohl, Bernd Wissinger
Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction. International journal of molecular sciences 23 (12) (2022)
Ana Janic, Ajoy Vincent, Jennifer Nan Stinson, Helen Dimaras
Values of Retinoblastoma Survivors and Parents Regarding Treatment Outcomes: A Qualitative Study. JCO oncology practice 18 (6) (2022)
Kate Elspeth Leahy, Tom Wright, Monika K Grudzinska Pechhacker, Isabelle Audo, Anupreet Tumber, Erika Tavares, Heather MacDonald, Jeff Locke, Cynthia VandenHoven, Christina Zeitz, Elise Heon, J Raymond Buncic, Ajoy Vincent
Optic Atrophy and Inner Retinal Thinning in CACNA1F-related Congenital Stationary Night Blindness. Genes 12 (3) (2021)
Zhuo Shao, Ikuo Masuho, Anupreet Tumber, Jason T Maynes, Erika Tavares, Asim Ali, Stacy Hewson, Andreas Schulze, Peter Kannu, Kirill A Martemyanov, Ajoy Vincent
Extended Phenotyping and Functional Validation Facilitate Diagnosis of a Complex Patient Harboring Genetic Variants in MCCC1 and GNB5 Causing Overlapping Phenotypes. Genes 12 (9) (2021)
Kit Green Sanderson, Eoghan Millar, Anupreet Tumber, Regan Klatt, Neal Sondheimer, Ajoy Vincent
Rod bipolar cell dysfunction in POLG retinopathy. Documenta ophthalmologica. Advances in ophthalmology 142 (1) (2020)
Zhuo Shao, Anupreet Tumber, Jason Maynes, Erika Tavares, Peter Kannu, Elise Heon, Ajoy Vincent
Unique retinal signaling defect in GNB5-related disease. Documenta ophthalmologica. Advances in ophthalmology 140 (3) (2019)
Henry Liu, Xiang Ji, Sabrina Dhaliwal, Syeda Naima Rahman, Michelle McFarlane, Anupreet Tumber, Jeff Locke, Tom Wright, Ajoy Vincent, Carol Westall
Evaluation of light- and dark-adapted ERGs using a mydriasis-free, portable system: clinical classifications and normative data. Documenta ophthalmologica. Advances in ophthalmology 137 (3) (2018)
Santhosh Dhanraj, Anna Matveev, Hongbing Li, Supanun Lauhasurayotin, Lawrence Jardine, Michaela Cada, Bozana Zlateska, Chetankumar S Tailor, Joseph Zhou, Roberto Mendoza-Londono, Ajoy Vincent, Peter R Durie, Stephen W Scherer, Johanna M Rommens, Elise Heon, Yigal Dror
Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome. Blood 129 (11) (2017)
Eva Lenassi, Ajoy Vincent, Zheng Li, Zubin Saihan, Alison J Coffey, Heather B Steele-Stallard, Anthony T Moore, Karen P Steel, Linda M Luxon, Elise Héon, Maria Bitner-Glindzicz, Andrew R Webster
A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants. European journal of human genetics : EJHG 23 (10) (2015)
Susanne Kohl, Ditta Zobor, Wei-Chieh Chiang, Nicole Weisschuh, Jennifer Staller, Irene Gonzalez Menendez, Stanley Chang, Susanne C Beck, Marina Garcia Garrido, Vithiyanjali Sothilingam, Mathias W Seeliger, Franco Stanzial, Francesco Benedicenti, Francesca Inzana, Elise Héon, Ajoy Vincent, Jill Beis, Tim M Strom, Günther Rudolph, Susanne Roosing, Anneke I den Hollander, Frans P M Cremers, Irma Lopez, Huanan Ren, Anthony T Moore, Andrew R Webster, Michel Michaelides, Robert K Koenekoop, Eberhart Zrenner, Randal J Kaufman, Stephen H Tsang, Bernd Wissinger, Jonathan H Lin
Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia. Nature genetics 47 (7) (2015)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ajoy Vincent