Mohammed E. El-Asrag
Mohammed E. El-Asrag
Institute of Cancer and Genomic Science, University of Birmingham, UK; Benha University EGY
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Biallelic mutations in the autophagy regulator DRAM2 cause retinal dystrophy with early macular involvement
ME El-Asrag, PI Sergouniotis, M McKibbin, V Plagnol, E Sheridan, ...
The American Journal of Human Genetics 96 (6), 948-954, 2015
Association between missense mutations in the BBS2 gene and nonsyndromic retinitis pigmentosa
E Shevach, M Ali, L Mizrahi-Meissonnier, M McKibbin, M El-Asrag, ...
JAMA ophthalmology 133 (3), 312-318, 2015
Specific alleles of CLN7/MFSD8, a protein that localizes to photoreceptor synaptic terminals, cause a spectrum of nonsyndromic retinal dystrophy
KN Khan, ME El-Asrag, CA Ku, GE Holder, M McKibbin, G Arno, ...
Investigative ophthalmology & visual science 58 (7), 2906-2914, 2017
Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility
N Bedoni, L Haer-Wigman, V Vaclavik, VH Tran, P Farinelli, S Balzano, ...
Human molecular genetics 25 (20), 4546-4555, 2016
Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencing
CM Watson, M El-Asrag, DA Parry, JE Morgan, CV Logan, IM Carr, ...
PLoS One 9 (8), e104281, 2014
Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family
A Al‐Amri, AA Saegh, W Al‐Mamari, ME El‐Asrag, JL Ivorra, AG Cardno, ...
American Journal of Medical Genetics Part A 170 (7), 1826-1831, 2016
Identification of inherited retinal disease-associated genetic variants in 11 candidate genes
GDN Astuti, LI Van den Born, MI Khan, CP Hamel, B Bocquet, G Manes, ...
Genes 9 (1), 21, 2018
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin
Z Ravesh, ME El Asrag, N Weisschuh, M McKibbin, P Reuter, CM Watson, ...
Molecular vision 21, 236, 2015
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5
ZA Abdelhamed, DI Abdelmottaleb, ME El-Asrag, S Natarajan, G Wheway, ...
Scientific reports 9 (1), 1-15, 2019
Disease expression in autosomal recessive retinal dystrophy associated with mutations in the DRAM2 gene
PI Sergouniotis, M McKibbin, AG Robson, HJ Bolz, E De Baere, PL Müller, ...
Investigative ophthalmology & visual science 56 (13), 8083-8090, 2015
New missense variants in RELT causing hypomineralised amelogenesis imperfecta
G Nikolopoulos, CEL Smith, SJ Brookes, ME El‐Asrag, CJ Brown, A Patel, ...
Clinical genetics 97 (5), 688-695, 2020
LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss
AH Al-Amri, A Al Saegh, W Al-Mamari, ME El-Asrag, MN Al-Kindi, ...
European journal of medical genetics 62 (12), 103592, 2019
PDZD8 Disruption Causes Cognitive Impairment in Humans, Mice, and Fruit Flies
AH Al-Amri, P Armstrong, M Amici, C Ligneul, J Rouse, ME El-Asrag, ...
Biological Psychiatry, 2022
Novel homozygous mutations in the transcription factor NRL cause non-syndromic retinitis pigmentosa
ME El-Asrag, M Corton, M McKibbin, A Avila-Fernandez, MD Mohamed, ...
Molecular Vision 28, 48, 2022
A recessively inherited risk locus on chromosome 13q22-31 conferring susceptibility to schizophrenia
T Mahmood, ME El-Asrag, JA Poulter, AG Cardno, A Tomlinson, S Ahmed, ...
Schizophrenia bulletin 47 (3), 796-802, 2021
Late-onset autosomal dominant macular degeneration caused by deletion of the CRX gene
S Yahya, CEL Smith, JA Poulter, M McKibbin, G Arno, J Ellingford, ...
Ophthalmology, 2022
Meta‐analysis of the demographic and prognostic significance of gastrointestinal symptoms in COVID‐19 patients
S Zaman, S Hajibandeh, S Hajibandeh, AYY Mohamedahmed, ...
JGH Open, 2021
Use of a gene-based case-control association approach in exome sequencing data to elucidate the molecular basis of a mendelian phenotype
PI Sergouniotis, AG Robson, ME El-Asrag, M Ali, GE Holder, GC Black, ...
The Lancet 389, S14, 2017
Protective effect of some medical plants against probable genotoxic effects of certain antibiotic on certain mammal
MEM Elasrag
Benha University, 2010
Patient Derived Organoids Confirm That PI3K/AKT Signalling Is an Escape Pathway for Radioresistance and a Target for Therapy in Rectal Cancer
K Wanigasooriya, JD Barros-Silva, L Tee, ME El-Asrag, A Stodolna, ...
Frontiers in oncology, 2875, 2022
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