Samira Ismail
Impact in
- Developmental Biology top 10%
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 5
- Craniofacial Disorders and Treatments 3
- Genomics and Rare Diseases 3
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- RNA modifications and cancer 4
- Co-authors
- Samia A. Temtamy (15 shared papers)Mohamed S. Abdel‐Hamid (10 shared papers)Ghada M. H. Abdel‐Salam (7 shared papers)Maha S. Zaki (15 shared papers)Hanan H. Afifi (3 shared papers)Ranad Shaheen (1 shared paper)Fowzan S. Alkuraya (1 shared paper)Michael P. Guy (1 shared paper)
- Journals
- The American Journal of Human Genetics (1 paper)Gene (1 paper)Neurological Sciences (1 paper)Sexual Development (1 paper)Human Genetics (1 paper)
- Partner nations
- EgyptUnited StatesFrance
In The Last Decade
Samira Ismail
43 papers receiving 604 citations
Peers
Comparison fields: 5 of 71
- Developmental Biology 25
- Genetics 217
- Pediatrics, Perinatology and Child Health 88
- Molecular Biology 339
- Cancer Research 59
Countries citing papers authored by Samira Ismail
This map shows the geographic impact of Samira Ismail'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 Samira Ismail with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Samira Ismail more than expected).
Fields of papers citing papers by Samira Ismail
This network shows the impact of papers produced by Samira Ismail. 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 Samira Ismail. The network helps show where Samira Ismail may publish in the future.
Co-authors
The 25 scholars most cited alongside Samira Ismail, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 46 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 139 | |
| 2 | 2002 | 63 | |
| 3 | 2016 | 61 | |
| 4 | 2016 | 42 | |
| 5 | 2007 | 39 | |
| 6 | 1998 | 25 | |
| 7 | 2019 | 25 | |
| 8 | 2003 | 18 | |
| 9 | 2013 | 17 | |
| 10 | 2010 | 16 | |
| 11 | Predominance of G to A codon 12 mutation K-ras gene in Dukes' B colorectal cancer. | 2012 | 16 |
| 12 | 2019 | 15 | |
| 13 | 2013 | 14 | |
| 14 | 2019 | 9 | |
| 15 | 2018 | 9 | |
| 16 | 2005 | 8 | |
| 17 | 2020 | 8 | |
| 18 | 2018 | 8 | |
| 19 | 2018 | 7 | |
| 20 | Roberts syndrome: study of 4 new Rgyptian cases with comparison of clinical and cytogenetic findings. | 2006 | 7 |
About Samira Ismail
Samira Ismail is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience and Rheumatology, having authored 46 papers that have together received 617 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (5 papers), Autism Spectrum Disorder Research (4 papers), Prenatal Screening and Diagnostics (4 papers), RNA modifications and cancer (4 papers), Craniofacial Disorders and Treatments (3 papers), Genomics and Rare Diseases (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Developmental Biology (25 citations), Genetics (217 citations), Pediatrics, Perinatology and Child Health (88 citations), Molecular Biology (339 citations) and Cancer Research (59 citations). Samira Ismail has collaborated with scholars based in Egypt, United States and France. Frequent co-authors include Samia A. Temtamy, Mohamed S. Abdel‐Hamid, Ghada M. H. Abdel‐Salam, Maha S. Zaki, Hanan H. Afifi, Ranad Shaheen, Fowzan S. Alkuraya, Michael P. Guy, Rana Alomar and Eric M. Phizicky. Their work appears in journals such as The American Journal of Human Genetics, Gene, Neurological Sciences, Sexual Development and Human Genetics.
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.