Amira Nabil
Impact in
-
- Amino Acid Enzymes and Metabolism
-
- Metabolism and Genetic Disorders
Papers in
- Genetics 4
- Genomics and Rare Diseases 2
- Connective tissue disorders research 1
- Neurogenetic and Muscular Disorders Research 1
-
- Epigenetics and DNA Methylation 1
- Ubiquitin and proteasome pathways 1
- Co-authors
- Fowzan S. Alkuraya (3 shared papers)Ranad Shaheen (1 shared paper)Jozef Hertecant (1 shared paper)Hassan Galadari (1 shared paper)Ayman W. El‐Hattab (1 shared paper)Ebtesam Abdalla (4 shared papers)Isabelle Jéru (1 shared paper)Olivier Lascols (1 shared paper)
- Journals
- European Journal of Pediatrics (1 paper)Clinical Genetics (1 paper)European Journal of Medical Genetics (1 paper)Journal of Assisted Reproduction and Genetics (1 paper)Frontiers in Immunology (1 paper)
- Partner nations
- EgyptSaudi ArabiaUnited Arab Emirates
In The Last Decade
Amira Nabil
8 papers receiving 96 citations
Peers
Comparison fields: 5 of 38
- Biochemistry 27
- Clinical Biochemistry 12
- Genetics 28
- Molecular Biology 51
- Cancer Research 9
Countries citing papers authored by Amira Nabil
This map shows the geographic impact of Amira Nabil'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 Amira Nabil with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amira Nabil more than expected).
Fields of papers citing papers by Amira Nabil
This network shows the impact of papers produced by Amira Nabil. 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 Amira Nabil. The network helps show where Amira Nabil may publish in the future.
Co-authors
The 25 scholars most cited alongside Amira Nabil, 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 | 2016 | 37 | |
| 2 | 2014 | 17 | |
| 3 | 2022 | 14 | |
| 4 | 2020 | 14 | |
| 5 | 2021 | 9 | |
| 6 | 2022 | 4 | |
| 7 | 2021 | 2 | |
| 8 | 2024 | 1 | |
| 9 | 2023 | 0 | |
| 10 | 2025 | 0 |
About Amira Nabil
Amira Nabil is a scholar working on Genetics, Molecular Biology, Surgery, Nephrology and Genetics, having authored 10 papers that have together received 98 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (2 papers), Connective tissue disorders research (1 paper), Epigenetics and DNA Methylation (1 paper), Ubiquitin and proteasome pathways (1 paper), Cancer Genomics and Diagnostics (1 paper), Neurogenetic and Muscular Disorders Research (1 paper), Amino Acid Enzymes and Metabolism (1 paper) and Urological Disorders and Treatments (1 paper). The work is most often cited by research in Biochemistry (27 citations), Clinical Biochemistry (12 citations), Genetics (28 citations), Molecular Biology (51 citations) and Cancer Research (9 citations). Amira Nabil has collaborated with scholars based in Egypt, Saudi Arabia and United Arab Emirates. Frequent co-authors include Fowzan S. Alkuraya, Ranad Shaheen, Jozef Hertecant, Hassan Galadari, Ayman W. El‐Hattab, Ebtesam Abdalla, Isabelle Jéru, Olivier Lascols, Ahmed Habib and Marius Kraenzlin. Their work appears in journals such as European Journal of Pediatrics, Clinical Genetics, European Journal of Medical Genetics, Journal of Assisted Reproduction and Genetics and Frontiers in Immunology.
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.