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Meeting Abstract (4)
Journal Articles (1)

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Investigative Ophthalmology & Visual Science (5)

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ARVO Annual Meeting Abstract (4)
Genetics (1)

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Eye Anatomy and Disorders (1)
Genetics (1)
Retina (1)

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autosomal recessive inheritance (1)
de novo mutation (1)
genes (1)
language morphology (1)
macular disorders (1)
morphology (1)
mutation (1)
phenotype (1)
retinitis pigmentosa (1)

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ARVO Annual Meeting Abstract June 2020

Discovery of novel disease-causing mutations in inherited retinal dystrophies – an application to retinitis pigmentosa

Caberry W. Yu; Erika Tavares; Vaishnavi Batmanabane; Ajoy Vincent; Elise Heon

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):4475.

ARVO Annual Meeting Abstract July 2019

The yield of "clinical" genetic testing in inherited retinal disease: experience at the Hospital for Sick Children, Toronto, Canada

Vaishnavi Batmanabane; Alexander Liam Pearson; Caberry Yu; Ajoy Vincent; Elise Heon

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):3976.

Genetics August 2017

C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations

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Christina Gerth-Kahlert; Amit Tiwari; James V. M. Hanson; Vaishnavi Batmanabane; Elias Traboulsi; Mark E. Pennesi; Abdullah A. Al-Qahtani; Byron L. Lam; John Heckenlively; Sandrine A. Zweifel; Ajoy Vincent; Fabienne Fierz; Daniel Barthelmes; Kari Branham; Naheed Khan; Angela Bahr; Luzy Baehr; István Magyar; Samuel Koller; Silvia Azzarello-Burri; Dunja Niedrist; Elise Heon; Wolfgang Berger
TAGS: autosomal recessive inheritance, de novo mutation, genes, mutation, phenotype, retinitis pigmentosa, language morphology, morphology, macular disorders
Invest. Ophthalmol. Vis. Sci.. 2017; 58(10):3840-3850. https://doi.org/10.1167/iovs.17-21597

ARVO Annual Meeting Abstract June 2017

Retinal sensitivity and fixation stability as surrogate markers of visual function in molecularly confirmed choroideremia patients.

Vaishnavi Batmanabane; Ajoy Vincent; Elise Heon

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3283.

ARVO Annual Meeting Abstract September 2016

Screening for vestibular impairment in congenital neurosensory hearing loss identifies a population at high risk of ocular anomalies, including Usher syndrome

Vaishnavi Batmanabane; Tianyang Dai; Stephanie Kletke; Ajoy Vincent; Blake C Papsin; Sharon L. Cushing; Jeff Locke; Elise Heon

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):1563.

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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