Mohammed E. El‐Asrag

Association Between Missense Mutations in the<i>BBS2</i>Gene and Nonsyndromic Retinitis Pigmentosa

Elia Shevach, Manir Ali, Liliana Mizrahi‐Meissonnier et al. · JAMA Ophthalmology · 2014 · 52 citations

Life Sciences, Genetics, Molecular Genetics +17

Specific Alleles of <i>CLN7</i> / <i>MFSD8</i> , a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy

Kamron N. Khan, Mohammed E. El‐Asrag, Cristy A. Ku et al. · Investigative Ophthalmology & Visual Science · 2017 · 52 citations · Full text

Medicine, Genetics, Ophthalmology +17

Biallelic Mutations in the Autophagy Regulator DRAM2 Cause Retinal Dystrophy with Early Macular Involvement

Mohammed E. El‐Asrag, Panagiotis I. Sergouniotis, Martin McKibbin et al. · The American Journal of Human Genetics · 2015 · 49 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Mutations in the polyglutamylase gene<i>TTLL5</i>, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility

Nicola Bedoni, Lonneke Haer‐Wigman, Veronika Vaclavik et al. · Human Molecular Genetics · 2016 · 37 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes

Galuh Astuti, L. van den Born, Muhammad Imran Khan et al. · Genes · 2018 · 31 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16