Nour Ewida
Impact in
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- Genetic and Kidney Cyst Diseases
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- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- RNA Research and Splicing
- Hedgehog Signaling Pathway Studies
- Renal and related cancers
Papers in
- Genetics 6
- Genetic and Kidney Cyst Diseases 3
- Genetics and Neurodevelopmental Disorders 1
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
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- RNA modifications and cancer 2
- Ubiquitin and proteasome pathways 1
- Epigenetics and DNA Methylation 1
- Co-authors
- Fowzan S. Alkuraya (9 shared papers)Ranad Shaheen (6 shared papers)Eman Alobeid (3 shared papers)Eissa Faqeih (2 shared papers)Lu Han (1 shared paper)Eric M. Phizicky (1 shared paper)Ghada M. H. Abdel‐Salam (2 shared papers)Sateesh Maddirevula (2 shared papers)
- Journals
- Human Genetics (3 papers)The American Journal of Human Genetics (2 papers)Genetics in Medicine (1 paper)Hepatology (1 paper)American Journal of Medical Genetics Part A (2 papers)
- Partner nations
- Saudi ArabiaUnited StatesEgypt
In The Last Decade
Nour Ewida
9 papers receiving 341 citations
Peers
Comparison fields: 5 of 52
- Genetics 126
- Molecular Biology 241
- Reproductive Medicine 23
- Cancer Research 33
- Cell Biology 37
Countries citing papers authored by Nour Ewida
This map shows the geographic impact of Nour Ewida'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 Nour Ewida with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nour Ewida more than expected).
Fields of papers citing papers by Nour Ewida
This network shows the impact of papers produced by Nour Ewida. 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 Nour Ewida. The network helps show where Nour Ewida may publish in the future.
Co-authors
The 25 scholars most cited alongside Nour Ewida, 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 | 118 | |
| 2 | 2018 | 62 | |
| 3 | 2020 | 55 | |
| 4 | 2016 | 26 | |
| 5 | 2019 | 23 | |
| 6 | 2019 | 21 | |
| 7 | 2019 | 14 | |
| 8 | 2021 | 13 | |
| 9 | 2021 | 9 |
About Nour Ewida
Nour Ewida is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Oncology, having authored 9 papers that have together received 341 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (3 papers), Fetal and Pediatric Neurological Disorders (2 papers), RNA modifications and cancer (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Ubiquitin and proteasome pathways (1 paper), Epigenetics and DNA Methylation (1 paper), Genomics and Rare Diseases (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (126 citations), Molecular Biology (241 citations), Reproductive Medicine (23 citations), Cancer Research (33 citations) and Cell Biology (37 citations). Nour Ewida has collaborated with scholars based in Saudi Arabia, United States and Egypt. Frequent co-authors include Fowzan S. Alkuraya, Ranad Shaheen, Eman Alobeid, Eissa Faqeih, Lu Han, Eric M. Phizicky, Ghada M. H. Abdel‐Salam, Sateesh Maddirevula, Firdous Abdulwahab and Amal Hashem. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Genetics in Medicine, Hepatology and American Journal of Medical Genetics Part A.
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.