Payman Jamali
- Co-authors
- Akbar FotouhiAlireza JafariHassan HashemiKimia KahriziHossein NajmabadiMasoud GarshasbiAndreas W. KußAndreas Tzschach
- Topics
- Genetics and Neurodevelopmental Disorders (4 papers)Genomics and Rare Diseases (3 papers)Hearing, Cochlea, Tinnitus, Genetics (3 papers)
- Journals
- SHILAP Revista de lepidopterologíaHuman MutationEuropean Journal of Human Genetics
- Partner nations
- IranUnited StatesGermany
In The Last Decade
Payman Jamali
17 papers receiving 276 citations
Peers
Comparison fields: 5 of 52
- Molecular Biology 131
- Epidemiology 79
- Ophthalmology 70
- Sensory Systems 62
- Genetics 47
Countries citing papers authored by Payman Jamali
This map shows the geographic impact of Payman Jamali'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 Payman Jamali with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Payman Jamali more than expected).
Fields of papers citing papers by Payman Jamali
This network shows the impact of papers produced by Payman Jamali. 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 Payman Jamali. The network helps show where Payman Jamali may publish in the future.
Co-authorship network of co-authors of Payman Jamali
This figure shows the co-authorship network connecting the top 25 collaborators of Payman Jamali. A scholar is included among the top collaborators of Payman Jamali based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Payman Jamali. Payman Jamali is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 3 | |
| 3 | 1 | |
| 4 | 2 | |
| 5 | 2 | |
| 6 | 2 | |
| 7 | 6 | |
| 8 | 6 | |
| 9 | 20 | |
| 10 | 47 | |
| 11 | 17 | |
| 12 | 6 | |
| 13 | 9 | |
| 14 | 81 | |
| 15 | 16 | |
| 16 | 26 | |
| 17 | SCREENING OF DFNB4 LOCUS IN IRANIAN FAMILIES WITH HEREDITARY HEARING IMPAIRMENT | 0 |
| 18 | 38 | |
| 19 | HIGH RECALL RATE IN THE SCREENING PROGRAM FOR CONGENITAL HYPOTHYROIDISM IN RAFSANJAN | 3 |
About Payman Jamali
Payman Jamali is a scholar working on Sensory Systems, Genetics and Neurology, having authored 19 papers that have together received 285 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). The work is most often cited by research in Sensory Systems (62 citations), Ophthalmology (70 citations) and Otorhinolaryngology (20 citations). Payman Jamali has collaborated with scholars based in Iran, United States and Germany. Frequent co-authors include Akbar Fotouhi, Alireza Jafari, Hassan Hashemi, Kimia Kahrizi, Hossein Najmabadi, Masoud Garshasbi, Andreas W. Kuß, Andreas Tzschach, Hao Hu and Richard J. Smith. Their work appears in journals such as SHILAP Revista de lepidopterología, Human Mutation and European Journal of 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.