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Meeting Abstract (4)
Journal Articles (2)

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Investigative Ophthalmology & Visual Science (6)

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ARVO Annual Meeting Abstract (4)
Retina (2)

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Eye Anatomy and Disorders (2)
Genetics (2)
Retina (2)
Low Vision (1)
Visual Neuroscience (1)

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autosomal recessive inheritance (2)
family (1)
genome (1)
homozygote (1)
mutation (1)
night blindness, congenital stationary (1)
phenotype (1)
progressive cone-rod dystrophy (1)
proteins (1)
retinitis pigmentosa (1)

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Retina November 2019

Homozygous Variant in ARL3 Causes Autosomal Recessive Cone Rod Dystrophy

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Shakeel A. Sheikh; Robert A. Sisk; Cara R. Schiavon; Yar M. Waryah; Muhammad A. Usmani; David H. Steel; John A. Sayer; Ashok K. Narsani; Robert B. Hufnagel; Saima Riazuddin; Richard A. Kahn; Ali M. Waryah; Zubair M. Ahmed
TAGS: autosomal recessive inheritance, family, homozygote, mutation, phenotype, progressive cone-rod dystrophy, proteins, retinitis pigmentosa
Invest. Ophthalmol. Vis. Sci.. 2019; 60(14):4811-4819. doi: https://doi.org/10.1167/iovs.19-27263

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2019

CIB2 is essential for autophagy in the retinal pigment epithelium and visual function

Zubair Ahmed; Saumil Sethna; Patrick A. Scott; Arnaud P. Giese; Todd Duncan; Sheikh Riazuddin; T Michael Redmond; Steven L Bernstein; Saima Riazuddin

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):3868. doi:

ARVO Annual Meeting Abstract June 2017

Usher Syndrome protein, CIB2, is essential for murine retinal sensory cells maintenance and function

Saumil Sethna; Patrick A Scott; Arnaud Giese; Mary A Johnson; Saima Riazuddin; Steven L Bernstein; Maureen A McCall; Zubair Ahmed

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):270. doi:

ARVO Annual Meeting Abstract June 2017

Variable penetrance of Fraser syndrome-associated FREM2 allele and candidate genetic modifier

Sairah Yousaf; Rehan Sadiq Shaikh; Rehana Iqbal; Saima Riazuddin; Zubair Ahmed

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4527. doi:

Retina March 2012

GNAT1 Associated with Autosomal Recessive Congenital Stationary Night Blindness

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Muhammad Asif Naeem; Venkata R. M. Chavali; Shahbaz Ali; Muhammad Iqbal; Saima Riazuddin; Shaheen N. Khan; Tayyab Husnain; Paul A. Sieving; Radha Ayyagari; Sheikh Riazuddin; J. Fielding Hejtmancik; S. Amer Riazuddin
TAGS: autosomal recessive inheritance, night blindness, congenital stationary, genome
Invest. Ophthalmol. Vis. Sci.. 2012; 53(3):1353-1361. doi: https://doi.org/10.1167/iovs.11-8026

ARVO Annual Meeting Abstract April 2011

Blue Cone Monochromatism: Phenotype And Genotype Assessment In Three U.S. Families

Robert B. Hufnagel; Robert A. Sisk; Saima Riazuddin; Zubair M. Ahmed

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):6663. doi:

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Online ISSN: 1552-5783

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

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Copyright © 2015 Association for Research in Vision and Ophthalmology.

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