Adel M. Ashour
Impact in
- Genetics top 10%
- Connective tissue disorders research
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 7
- Connective tissue disorders research 3
- Genomic variations and chromosomal abnormalities 2
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- Glycosylation and Glycoproteins Research 1
- Co-authors
- Mona Aglan (11 shared papers)Samia A. Temtamy (11 shared papers)Maha S. Zaki (3 shared papers)Khalda Amr (4 shared papers)Pablo Lapunzina (2 shared papers)Ghada M. H. Abdel‐Salam (2 shared papers)Víctor L. Ruiz‐Pérez (2 shared papers)Fatema Alzahrani (1 shared paper)
- Journals
- Human Mutation (2 papers)The American Journal of Human Genetics (1 paper)Journal of Industrial Textiles (1 paper)Kidney International Reports (1 paper)Clinical Dysmorphology (4 papers)
- Partner nations
- EgyptUnited StatesSpain
In The Last Decade
Adel M. Ashour
16 papers receiving 313 citations
Peers
Comparison fields: 5 of 56
- Genetics 161
- Developmental Biology 10
- Cell Biology 61
- Molecular Biology 180
- Genetics 25
Countries citing papers authored by Adel M. Ashour
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
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-authors
The 25 scholars most cited alongside Adel M. Ashour, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 87 | |
| 2 | 2012 | 73 | |
| 3 | 2008 | 40 | |
| 4 | 2007 | 23 | |
| 5 | 2006 | 22 | |
| 6 | 2009 | 16 | |
| 7 | The most encountered groups of genetic disorders in Giza Governorate, Egypt. | 2010 | 16 |
| 8 | 2009 | 12 | |
| 9 | A report of three patients with MMP2 associated hereditary osteolysis. | 2012 | 12 |
| 10 | 2001 | 7 | |
| 11 | 2015 | 6 | |
| 12 | 2009 | 6 | |
| 13 | 2021 | 2 | |
| 14 | 2006 | 2 | |
| 15 | 2022 | 1 | |
| 16 | 2014 | 1 | |
| 17 | 2022 | 0 |
About Adel M. Ashour
Adel M. Ashour is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Developmental Biology, having authored 17 papers that have together received 326 indexed citations. Recurring topics across this work include Connective tissue disorders research (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Skin and Cellular Biology Research (2 papers), Prenatal Screening and Diagnostics (2 papers), Congenital limb and hand anomalies (2 papers), Biomarkers in Disease Mechanisms (1 paper), Glycosylation and Glycoproteins Research (1 paper) and Global Health and Surgery (1 paper). The work is most often cited by research in Genetics (161 citations), Developmental Biology (10 citations), Cell Biology (61 citations), Molecular Biology (180 citations) and Genetics (25 citations). Adel M. Ashour has collaborated with scholars based in Egypt, United States and Spain. Frequent co-authors include Mona Aglan, Samia A. Temtamy, Maha S. Zaki, Khalda Amr, Pablo Lapunzina, Ghada M. H. Abdel‐Salam, Víctor L. Ruiz‐Pérez, Fatema Alzahrani, Shinu Ansari and Ranad Shaheen. Their work appears in journals such as Human Mutation, The American Journal of Human Genetics, Journal of Industrial Textiles, Kidney International Reports and Clinical Dysmorphology.
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.