Mohamed F. El-Ashry

EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa

Mai M. Abd El-Aziz, Isabel Barragán, C. O'Driscoll et al. · Nature Genetics · 2008 · 209 citations · Full text

Biology, Developmental Biology, Developmental Genetics +10

Identification of novel mutations in the carbohydrate sulfotransferase gene (CHST6) causing macular corneal dystrophy.

Mohamed F. El-Ashry, Mai M. Abd El-Aziz, Simon Wilkins et al. · PubMed · 2002 · 100 citations

The Effect of Phacoemulsification Cataract Surgery on the Measurement of Retinal Nerve Fiber Layer Thickness Using Optical Coherence Tomography

Mohamed F. El-Ashry, Shivashankar Appaswamy, Sunil Deokule et al. · Current Eye Research · 2006 · 77 citations

Novel<i>SLC4A11</i>mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2)

Vedam L. Ramprasad, Neil D. Ebenezer, Tin Aung et al. · Human Mutation · 2007 · 72 citations · Full text

Allelic Variant, Genetic Disorder, Genetics +12

Novel CHST6 nonsense and missense mutations responsible for macular corneal dystrophy

Mohamed F. El-Ashry, Mai M. Abd El-Aziz, Osama E. Shalaby et al. · American Journal of Ophthalmology · 2005 · 67 citations

Missense Mutations, Ocular Disease, Ophthalmology +8