Mohammed E. El-Asrag

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Chris InglehearnProfessor of Molecular Ophthalmology, University of LeedsVerified email at leeds.ac.uk
Christopher M. WatsonThe Leeds Teaching Hospitals NHS Trust & The University of LeedsVerified email at leeds.ac.uk
James A PoulterUKRI Future Leaders Fellow, University of LeedsVerified email at leeds.ac.uk
Andrew WebsterUCL Institute of OphthalmologyVerified email at ucl.ac.uk
Prof. Graham E HolderSingapore, UCL, Moorfields, Sydney, Kings, Brook, AstonVerified email at moorfields.nhs.uk
Black G, Black GC, Black GCMManchester UniversityVerified email at manchester.ac.uk
Chaim JalasDirector of Genetic Resources and Services, Center for Rare Jewish Genetic DisordersVerified email at feclabs.org
Dror SharonHadassah-Hebrew University Medical CenterVerified email at mail.huji.ac.il
Vincent PlagnolDirector, Precision Health, Genomics plcVerified email at genomicsplc.com
Gavin ArnoUCL Institute of OphthalmologyVerified email at ucl.ac.uk
Hendrik Peter Nicolas SchollDirector of the Institute of Molecular and Clinical Ophthalmology Basel (IOB) and Professor and Chairman of the Department of Ophthalmology, University of Basel, SwitzerlandVerified email at iob.ch
Dr Keren CarssAstraZenecaVerified email at astrazeneca.com
Mark PennesiProfessor of Ophthalmology, Oregon Health & Science UniversityVerified email at ohsu.edu
Saghar Bagheri, MD, PhDHarvardVerified email at meei.harvard.edu
Anthony MooreUCL Institute of OphthalmologyVerified email at ucsf.edu
Michel MichaelidesUCL Institute of Ophthalmology and Moorfields Eye HospitalVerified email at ucl.ac.uk
Panagiotis SergouniotisSenior Lecturer & Honorary Consultant, University of Manchester, Manchester, UKVerified email at manchester.ac.uk
Anthony G. RobsonConsultant Electrophysiologist and Head of Electrophysiology, Moorfields Eye HospitalVerified email at nhs.net
Graham TaylorViapath, Guy's Hospital & King's College, LondonVerified email at kcl.ac.uk
Carr IMSchool of Medicine, University of LeedsVerified email at leeds.ac.uk

Mohammed E. El-Asrag

Institute of Cancer and Genomic Science, University of Birmingham, UK; Benha University EGY

Verified email at bham.ac.uk

Genetics and Molecular Biology


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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	43	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	42	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	41	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	29	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	24	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	22	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	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	18	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	16	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	16	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	12	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	6	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	4	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	3	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	3	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	1	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	1	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	1	2017
Protective effect of some medical plants against probable genotoxic effects of certain antibiotic on certain mammal MEM Elasrag Benha University, 2010	1	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		2022

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