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Mohammed E. El-Asrag

University of Leeds

15

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135

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Myocilin mutations account for 5% of POAG in a West Yorkshire clinic

2021 Investigative Ophthalmology & Visual Science
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A Recessively Inherited Risk Locus on Chromosome 13q22-31 Conferring Susceptibility to Schizophrenia.

2020 Schizophrenia Bulletin
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The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5

2019 Scientific Reports
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LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss

2018 European Journal of Medical Genetics
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Use of a gene-based case-control association approach in exome sequencing data to elucidate the molecular basis of a mendelian phenotype

2017 The Lancet
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Determining the causes of recessive retinal dystrophy

2016
- Mohammed E. El-Asrag
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Association between missense mutations in the BBS2 gene and nonsyndromic retinitis pigmentosa.

2015 JAMA Ophthalmology
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Biallelic Mutations in the Autophagy Regulator DRAM2 Cause Retinal Dystrophy with Early Macular Involvement

2015 American Journal of Human Genetics
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Biallelic mutations in the autophagy regulator DRAM2 cause retinal dystrophy with early macular involvement.

2015 Investigative Ophthalmology & Visual Science
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Mutation Screening of Retinal Dystrophy Patients by Targeted Capture from Tagged Pooled DNAs and Next Generation Sequencing

2014 PLOS ONE
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Citations (13)