Morad Ansari
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Ocular Disorders and Treatments
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
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- Genomics and Chromatin Dynamics
- RNA Research and Splicing
- RNA modifications and cancer
Papers in
- Genetics 9
- Genomics and Rare Diseases 3
- Congenital Ear and Nasal Anomalies 2
- Ocular Disorders and Treatments 2
- Cleft Lip and Palate Research 2
- Craniofacial Disorders and Treatments 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
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- Genomics and Chromatin Dynamics 4
- Co-authors
- David Fitzpatrick (9 shared papers)Martin S. Taylor (2 shared papers)Alison Meynert (2 shared papers)Veronica van Heyningen (3 shared papers)Jacqueline K. Rainger (3 shared papers)Kathleen A. Williamson (3 shared papers)Wendy A. Bickmore (2 shared papers)Hemant Bengani (2 shared papers)
- Journals
- Human Molecular Genetics (2 papers)Genome Medicine (1 paper)BMC Bioinformatics (1 paper)European Journal of Medical Genetics (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United KingdomFranceUnited States
In The Last Decade
Morad Ansari
11 papers receiving 559 citations
Peers
Comparison fields: 5 of 66
- Genetics 285
- Molecular Biology 330
- Genetics 46
- Developmental Biology 10
- Cell Biology 47
Countries citing papers authored by Morad Ansari
This map shows the geographic impact of Morad Ansari'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 Morad Ansari with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Morad Ansari more than expected).
Fields of papers citing papers by Morad Ansari
This network shows the impact of papers produced by Morad Ansari. 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 Morad Ansari. The network helps show where Morad Ansari may publish in the future.
Co-authors
The 25 scholars most cited alongside Morad Ansari, 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 | 2014 | 142 | |
| 2 | 2018 | 90 | |
| 3 | 2014 | 79 | |
| 4 | 2014 | 67 | |
| 5 | 2013 | 64 | |
| 6 | 2013 | 46 | |
| 7 | 2013 | 29 | |
| 8 | 2019 | 22 | |
| 9 | 2017 | 18 | |
| 10 | 2014 | 16 | |
| 11 | 2024 | 2 | |
| 12 | 2024 | 0 |
About Morad Ansari
Morad Ansari is a scholar working on Genetics, Molecular Biology, Genetics, Pathology and Forensic Medicine and Surgery, having authored 12 papers that have together received 575 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (4 papers), Genomics and Rare Diseases (3 papers), Congenital Ear and Nasal Anomalies (2 papers), Ocular Disorders and Treatments (2 papers), Cleft Lip and Palate Research (2 papers), Tumors and Oncological Cases (2 papers), Craniofacial Disorders and Treatments (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Genetics (285 citations), Molecular Biology (330 citations), Genetics (46 citations), Developmental Biology (10 citations) and Cell Biology (47 citations). Morad Ansari has collaborated with scholars based in United Kingdom, France and United States. Frequent co-authors include David Fitzpatrick, Martin S. Taylor, Alison Meynert, Veronica van Heyningen, Jacqueline K. Rainger, Kathleen A. Williamson, Wendy A. Bickmore, Hemant Bengani, Joe Rainger and James Rhodes. Their work appears in journals such as Human Molecular Genetics, Genome Medicine, BMC Bioinformatics, European Journal of Medical Genetics and Journal of Medical 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.