Mohammed E. El‐Asrag

478 total citations
17 papers, 211 citations indexed

About

Mohammed E. El‐Asrag is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Mohammed E. El‐Asrag has authored 17 papers receiving a total of 211 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Oncology. Recurrent topics in Mohammed E. El‐Asrag's work include Retinal Development and Disorders (7 papers), Advanced biosensing and bioanalysis techniques (3 papers) and Photoreceptor and optogenetics research (2 papers). Mohammed E. El‐Asrag is often cited by papers focused on Retinal Development and Disorders (7 papers), Advanced biosensing and bioanalysis techniques (3 papers) and Photoreceptor and optogenetics research (2 papers). Mohammed E. El‐Asrag collaborates with scholars based in United Kingdom, Egypt and United States. Mohammed E. El‐Asrag's co-authors include Chris F. Inglehearn, Manir Ali, Martin McKibbin, Carmel Toomes, Christopher M. Watson, Dror Sharon, Tamar Ben‐Yosef, Graham E. Holder, Anat Blumenfeld and Andrew D. Beggs and has published in prestigious journals such as The Lancet, PLoS ONE and Scientific Reports.

In The Last Decade

Mohammed E. El‐Asrag

17 papers receiving 209 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Mohammed E. El‐Asrag United Kingdom 10 153 58 51 32 28 17 211
Virginie G. Peter Switzerland 10 198 1.3× 121 2.1× 65 1.3× 41 1.3× 22 0.8× 17 325
Samuel Koller Switzerland 10 191 1.2× 76 1.3× 65 1.3× 11 0.3× 13 0.5× 26 266
Saoud Tahsin Swafiri Spain 11 175 1.1× 98 1.7× 61 1.2× 21 0.7× 7 0.3× 15 252
Lama AlAbdi Saudi Arabia 12 203 1.3× 64 1.1× 61 1.2× 32 1.0× 7 0.3× 26 318
Pooja Biswas United States 11 190 1.2× 69 1.2× 111 2.2× 30 0.9× 11 0.4× 25 232
Bala Bharathi Burugula United States 6 115 0.8× 45 0.8× 13 0.3× 29 0.9× 25 0.9× 8 220
Briana L. Winer United States 6 123 0.8× 31 0.5× 38 0.7× 11 0.3× 10 0.4× 7 221
Sara D. Ragi United States 8 173 1.1× 39 0.7× 72 1.4× 28 0.9× 6 0.2× 33 246
Diana Freas‐Lutz United States 7 239 1.6× 228 3.9× 45 0.9× 15 0.5× 26 0.9× 8 435
Natsue Omi Japan 8 143 0.9× 38 0.7× 187 3.7× 32 1.0× 9 0.3× 12 295

Countries citing papers authored by Mohammed E. El‐Asrag

Since Specialization
Citations

This map shows the geographic impact of Mohammed E. El‐Asrag's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mohammed E. El‐Asrag with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mohammed E. El‐Asrag more than expected).

Fields of papers citing papers by Mohammed E. El‐Asrag

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mohammed E. El‐Asrag. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mohammed E. El‐Asrag. The network helps show where Mohammed E. El‐Asrag may publish in the future.

Co-authorship network of co-authors of Mohammed E. El‐Asrag

This figure shows the co-authorship network connecting the top 25 collaborators of Mohammed E. El‐Asrag. A scholar is included among the top collaborators of Mohammed E. El‐Asrag based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mohammed E. El‐Asrag. Mohammed E. El‐Asrag is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Watson, Christopher M., Ian Carr, Martin McKibbin, et al.. (2023). Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells. Molecular Diagnosis & Therapy. 27(4). 525–535. 4 indexed citations
2.
Zaman, Shafquat, Akinfemi Akingboye, Ali Yasen Mohamedahmed, et al.. (2023). Faecal Microbiota Transplantation [FMT] in the Treatment of Chronic Refractory Pouchitis: A Systematic Review and Meta-analysis. Journal of Crohn s and Colitis. 18(1). 144–161. 14 indexed citations
3.
Kumar, Aditi, Mohammed Nabil Quraishi, Hafid O. Al‐Hassi, et al.. (2023). The analysis of gut microbiota in patients with bile acid diarrhoea treated with colesevelam. Frontiers in Microbiology. 14. 1134105–1134105. 6 indexed citations
4.
Payne, Karl, Jill Brooks, Nikolaos Batis, et al.. (2023). Feasibility of mass cytometry proteomic characterisation of circulating tumour cells in head and neck squamous cell carcinoma for deep phenotyping. British Journal of Cancer. 129(10). 1590–1598. 9 indexed citations
5.
Wanigasooriya, Kasun, João D. Barros‐Silva, Louise Tee, et al.. (2022). Patient Derived Organoids Confirm That PI3K/AKT Signalling Is an Escape Pathway for Radioresistance and a Target for Therapy in Rectal Cancer. Frontiers in Oncology. 12. 920444–920444. 11 indexed citations
6.
El‐Asrag, Mohammed E., Marta Cortón, Martin McKibbin, et al.. (2022). Novel homozygous mutations in the transcription factor NRL cause non-syndromic retinitis pigmentosa. PubMed Central. 8 indexed citations
7.
Zaman, Shafquat, Shahin Hajibandeh, Shahab Hajibandeh, et al.. (2022). Meta‐analysis of the demographic and prognostic significance of gastrointestinal symptoms in COVID‐19 patients. JGH Open. 6(10). 711–722. 2 indexed citations
8.
Smith, Claire E. L., Steven J. Brookes, Mohammed E. El‐Asrag, et al.. (2020). New missense variants in RELT causing hypomineralised amelogenesis imperfecta. Clinical Genetics. 97(5). 688–695. 10 indexed citations
9.
Abdelhamed, Zakia A., Mohammed E. El‐Asrag, Subaashini Natarajan, et al.. (2019). The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5. Scientific Reports. 9(1). 5446–5446. 13 indexed citations
10.
Al‐Mamari, Watfa, et al.. (2018). LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. European Journal of Medical Genetics. 62(12). 103592–103592. 5 indexed citations
11.
Astuti, Galuh, Muhammad Imran Khan, Christian Hamel, et al.. (2018). Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes. Genes. 9(1). 21–21. 19 indexed citations
12.
Khan, Kamron N., Mohammed E. El‐Asrag, Cristy A. Ku, et al.. (2017). Specific Alleles of CLN7 / MFSD8 , a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy. Investigative Ophthalmology & Visual Science. 58(7). 2906–2906. 38 indexed citations
13.
Sergouniotis, Panagiotis I., Anthony G. Robson, Mohammed E. El‐Asrag, et al.. (2017). Use of a gene-based case-control association approach in exome sequencing data to elucidate the molecular basis of a mendelian phenotype. The Lancet. 389. S14–S14. 2 indexed citations
14.
Al‐Mamari, Watfa, Mohammed E. El‐Asrag, José Luis Ivorra, et al.. (2016). Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. American Journal of Medical Genetics Part A. 170(7). 1826–1831. 10 indexed citations
15.
Sergouniotis, Panagiotis I., Martin McKibbin, Anthony G. Robson, et al.. (2015). Disease Expression in Autosomal Recessive Retinal Dystrophy Associated With Mutations in theDRAM2Gene. Investigative Ophthalmology & Visual Science. 56(13). 8083–8083. 12 indexed citations
16.
Watson, Christopher M., Mohammed E. El‐Asrag, David Parry, et al.. (2014). Mutation Screening of Retinal Dystrophy Patients by Targeted Capture from Tagged Pooled DNAs and Next Generation Sequencing. PLoS ONE. 9(8). e104281–e104281. 17 indexed citations
17.
Ali, Manir, Liliana Mizrahi‐Meissonnier, Martin McKibbin, et al.. (2014). Association Between Missense Mutations in theBBS2Gene and Nonsyndromic Retinitis Pigmentosa. JAMA Ophthalmology. 133(3). 312–312. 31 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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