Adel M. Ashour

459 total citations
16 papers, 322 citations indexed

About

Adel M. Ashour is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Adel M. Ashour has authored 16 papers receiving a total of 322 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Adel M. Ashour's work include Connective tissue disorders research (3 papers), Skin and Cellular Biology Research (2 papers) and Congenital limb and hand anomalies (2 papers). Adel M. Ashour is often cited by papers focused on Connective tissue disorders research (3 papers), Skin and Cellular Biology Research (2 papers) and Congenital limb and hand anomalies (2 papers). Adel M. Ashour collaborates with scholars based in Egypt, United States and Spain. Adel M. Ashour's co-authors include Samia A. Temtamy, Mona Aglan, Maha S. Zaki, Khalda Amr, Pablo Lapunzina, Víctor L. Ruiz‐Pérez, Eulalia Valencia, Ranad Shaheen, Ghada M. H. Abdel‐Salam and Shinu Ansari and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Human Mutation.

In The Last Decade

Adel M. Ashour

15 papers receiving 309 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adel M. Ashour Egypt 9 196 168 61 36 35 16 322
Valentina Citro Italy 14 346 1.8× 184 1.1× 50 0.8× 21 0.6× 27 0.8× 25 494
Takeshi Ishimaru Japan 5 276 1.4× 170 1.0× 170 2.8× 29 0.8× 21 0.6× 5 419
Ka Sin Mak Australia 11 245 1.3× 65 0.4× 33 0.5× 27 0.8× 22 0.6× 11 348
Anja Brehm Germany 7 333 1.7× 159 0.9× 55 0.9× 42 1.2× 33 0.9× 9 429
Takaya Tohma Japan 11 203 1.0× 175 1.0× 25 0.4× 19 0.5× 7 0.2× 19 354
Daniah Beleford United States 9 154 0.8× 57 0.3× 34 0.6× 11 0.3× 33 0.9× 11 249
Nina Reichert Germany 9 514 2.6× 79 0.5× 47 0.8× 7 0.2× 103 2.9× 11 569
Glenda M. Beaman United Kingdom 9 129 0.7× 86 0.5× 18 0.3× 34 0.9× 12 0.3× 20 278
Gerdy ten Dam Netherlands 7 269 1.4× 59 0.4× 234 3.8× 17 0.5× 14 0.4× 8 393
Amy Duguay United States 4 234 1.2× 40 0.2× 28 0.5× 7 0.2× 41 1.2× 4 323

Countries citing papers authored by Adel M. Ashour

Since Specialization
Citations

This map shows the geographic impact of Adel M. Ashour'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 Adel M. Ashour with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Adel M. Ashour more than expected).

Fields of papers citing papers by Adel M. Ashour

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adel M. Ashour. 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 Adel M. Ashour. The network helps show where Adel M. Ashour may publish in the future.

Co-authorship network of co-authors of Adel M. Ashour

This figure shows the co-authorship network connecting the top 25 collaborators of Adel M. Ashour. A scholar is included among the top collaborators of Adel M. Ashour 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 Adel M. Ashour. Adel M. Ashour is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Murshed, Khaled, Mohammed Akhtar, Abdullah Hamad, et al.. (2022). Kidney Biopsy in Patients With Markedly Reduced Kidney Function. Kidney International Reports. 7(11). 2505–2508.
2.
3.
Aglan, Mona, Khalda Amr, Samira Ismail, et al.. (2015). Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations. American Journal of Medical Genetics Part A. 167(12). 3054–3061. 6 indexed citations
4.
Ashour, Adel M., et al.. (2014). Environmental risk factors in isolated limb reduction defects. 3(2). 53–64. 1 indexed citations
5.
Shaheen, Ranad, Mona Aglan, Kim M. Keppler‐Noreuil, et al.. (2013). Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome. The American Journal of Human Genetics. 92(4). 598–604. 86 indexed citations
6.
Temtamy, Samia A., Mona Aglan, Eulalia Valencia, et al.. (2012). Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum. Human Mutation. 33(10). 1444–1449. 72 indexed citations
7.
Temtamy, Samia A., Mona Aglan, Adel M. Ashour, et al.. (2012). A report of three patients with MMP2 associated hereditary osteolysis.. PubMed. 23(2). 175–84. 12 indexed citations
8.
Afifi, Hanan H., Hala T. El‐Bassyouni, Mona Aglan, et al.. (2010). The most encountered groups of genetic disorders in Giza Governorate, Egypt.. PubMed. 111(2). 62–9. 16 indexed citations
9.
Abo‐Shosha, M.H., et al.. (2009). Tetracycline Hydrate and Gentamicine Sulfate Containing Carboxymethylated Cotton Fabric Suitable for Moist Wound Healing Dressings: Properties and Evaluation. Journal of Industrial Textiles. 38(4). 341–360. 12 indexed citations
10.
11.
Aglan, Mona, et al.. (2009). Dyggve–Melchior–Clausen syndrome: Clinical, genetic, and radiological study of 15 Egyptian patients from nine unrelated families. Journal of Children s Orthopaedics. 3(6). 451–458. 16 indexed citations
12.
Temtamy, Samia A., Mona Aglan, Eulalia Valencia, et al.. (2008). Long interspersed nuclear element-1 (LINE1)-mediated deletion ofEVC,EVC2,C4orf6, andSTK32B in Ellis–van Creveld syndrome with borderline intelligence. Human Mutation. 29(7). 931–938. 39 indexed citations
13.
Temtamy, Samia A., Mona Aglan, Adel M. Ashour, & Maha S. Zaki. (2007). Adams–Oliver syndrome: further evidence of an autosomal recessive variant. Clinical Dysmorphology. 16(3). 141–149. 23 indexed citations
14.
Temtamy, Samia A., et al.. (2006). 3-M syndrome: a report of three Egyptian cases with review of the literature. Clinical Dysmorphology. 15(2). 55–64. 22 indexed citations
15.
El‐Bassyouni, Hala T., et al.. (2006). The Effect of Diet on Antioxidant Status in Patients with Galactosemia. Journal of Medical Sciences(Faisalabad). 6(3). 452–457. 2 indexed citations
16.
Meguid, Nagwa A. & Adel M. Ashour. (2001). Holoprosencephaly and split hand/foot: an additional case with this rare association. Clinical Dysmorphology. 10(4). 277–279. 7 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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