Morad Ansari
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Ocular Disorders and Treatments
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
- Congenital Ear and Nasal Anomalies
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- Genomics and Chromatin Dynamics
- RNA Research and Splicing
Papers in
-
- Genomics and Chromatin Dynamics 4
- Genetics 9
- Genomics and Rare Diseases 3
- Cleft Lip and Palate Research 2
- Craniofacial Disorders and Treatments 2
- Genomic variations and chromosomal abnormalities 2
- Ocular Disorders and Treatments 2
- Congenital Ear and Nasal Anomalies 2
- Co-authors
- David Fitzpatrick (9 shared papers)Martin S. Taylor (2 shared papers)Alison Meynert (2 shared papers)Veronica van Heyningen (3 shared papers)Kathleen A. Williamson (3 shared papers)Jacqueline K. Rainger (3 shared papers)Wendy A. Bickmore (2 shared papers)Hemant Bengani (2 shared papers)
- Journals
- Human Molecular Genetics (2 papers)Human Mutation (1 paper)Nature Genetics (1 paper)The American Journal of Human Genetics (1 paper)BMC Bioinformatics (1 paper)
- Partner nations
- United KingdomFranceUnited States
In The Last Decade
Morad Ansari
11 papers receiving 552 citations
Peers
Comparison fields: 5 of 69
- Genetics 303
- Molecular Biology 365
- Genetics 54
- Developmental Biology 10
- Cancer Research 46
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 | 138 | |
| 2 | 2018 | 89 | |
| 3 | 2014 | 77 | |
| 4 | 2014 | 67 | |
| 5 | 2013 | 63 | |
| 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 Molecular Biology, Genetics, Genetics, Pathology and Forensic Medicine and Surgery, having authored 12 papers that have together received 567 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (4 papers), Genomics and Rare Diseases (3 papers), Cleft Lip and Palate Research (2 papers), Craniofacial Disorders and Treatments (2 papers), Tumors and Oncological Cases (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Ocular Disorders and Treatments (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Genetics (303 citations), Molecular Biology (365 citations), Genetics (54 citations), Developmental Biology (10 citations) and Cancer Research (46 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, Kathleen A. Williamson, Jacqueline K. Rainger, Wendy A. Bickmore, Hemant Bengani, Joe Rainger and Shelagh Boyle. Their work appears in journals such as Human Molecular Genetics, Human Mutation, Nature Genetics, The American Journal of Human Genetics and BMC Bioinformatics.
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.