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Investigative Ophthalmology & Visual Science|December 2, 2011
A single-base substitution in the seed region of miR-184 causes EDICT syndromeBenjamin W Iliff, S Amer Riazuddin, John D GottschExpert Review of Ophthalmology|April 16, 2013
The genetics of Fuchs' corneal dystrophyBenjamin W Iliff, S Amer Riazuddin, John D GottschCornea|March 19, 2016
Distinct Clinical Phenotype of Corneal Dystrophy Predicts the p.(Leu450Trp) Substitution in COL8A2Allen O Eghrari, S Amer Riazuddin, John D GottschProgress in Molecular Biology and Translational Science|August 28, 2015
Overview of the Cornea: Structure, Function, and DevelopmentAllen O Eghrari, S Amer Riazuddin, John D GottschAmerican Journal of Ophthalmology|February 11, 2012
Prevalence and severity of fuchs corneal dystrophy in Tangier IslandAllen O Eghrari, Elyse J McGlumphy, Benjamin W Iliff, et al.Progress in Molecular Biology and Translational Science|August 28, 2015
Fuchs Corneal DystrophyAllen O Eghrari, S Amer Riazuddin, John D GottschAmerican Journal of Human Genetics|October 8, 2013
Mutations in AGBL1 cause dominant late-onset Fuchs corneal dystrophy and alter protein-protein interaction with TCF4S Amer Riazuddin, Shivakumar Vasanth, Nicholas Katsanis, et al.American Journal of Human Genetics|February 21, 2012
Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophyS Amer Riazuddin, David S Parker, Elyse J McGlumphy, et al.Experimental Eye Research|September 10, 2018
Comparative transcriptome analysis of hESC- and iPSC-derived corneal endothelial cellsMuhammad Ali, Shahid Y Khan, Firoz Kabir, et al.Investigative Ophthalmology & Visual Science|December 3, 2017
CTG18.1 Expansion in TCF4 Among African Americans With Fuchs' Corneal DystrophyAllen O Eghrari, Sina Vahedi, Natalie A Afshari, et al.Pageof 16