Fatemeh Alasti
- Sensory Systems top 2%
- Molecular Biology
- Surgery
- Otorhinolaryngology top 5%
- Neurology top 10%
- Co-authors
- Guy Van CampMohammad Hossein SanatiRichard J. SmithMohammad FarhadiThomas SomersMorteza Hashemzadeh ChaleshtoriCarla NishimuraKimia Kahrizi
- Topics
- Hearing, Cochlea, Tinnitus, Genetics (9 papers)Hearing Loss and Rehabilitation (4 papers)Vestibular and auditory disorders (3 papers)
- Partner nations
- IranBelgiumUnited States
In The Last Decade
Fatemeh Alasti
16 papers receiving 448 citations
Peers
Comparison fields: 5 of 54
- Sensory Systems 221
- Molecular Biology 176
- Surgery 142
- Otorhinolaryngology 107
- Neurology 98
Countries citing papers authored by Fatemeh Alasti
This map shows the geographic impact of Fatemeh Alasti'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 Fatemeh Alasti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fatemeh Alasti more than expected).
Fields of papers citing papers by Fatemeh Alasti
This network shows the impact of papers produced by Fatemeh Alasti. 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 Fatemeh Alasti. The network helps show where Fatemeh Alasti may publish in the future.
Co-authorship network of co-authors of Fatemeh Alasti
This figure shows the co-authorship network connecting the top 25 collaborators of Fatemeh Alasti. A scholar is included among the top collaborators of Fatemeh Alasti 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 Fatemeh Alasti. Fatemeh Alasti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | Pendred Syndrome/DFNB4 | 2 |
| 2 | 27 | |
| 3 | 9 | |
| 4 | Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss. | 33 |
| 5 | Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive. | 1 |
| 6 | Contribution of GJB2 mutations and Four common DFNB loci in autosomal recessive non-syndromic hearing impairment in Markazi and Qom provinces of Iran | 17 |
| 7 | 107 | |
| 8 | SHORT COMMUNICATION: CONTRIBUTION OF GJB2 MUTATIONS AND FOUR COMMON DFNB LOCI IN AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING IMPAIRMENT IN MARKAZI AND QOM PROVINCES OF IRAN | 2 |
| 9 | 77 | |
| 10 | 55 | |
| 11 | 6 | |
| 12 | 39 | |
| 13 | 23 | |
| 14 | 38 | |
| 15 | Mutation analysis of connexin 26 gene and del(GJB6- D13S1830) in patients with hereditary deafness from two provinces in Iran | 12 |
| 16 | Cloning and expression of human gamma-interferon cDNA in E. coli | 3 |
About Fatemeh Alasti
Fatemeh Alasti is a scholar working on Sensory Systems, Neurology and Endocrine and Autonomic Systems, having authored 16 papers that have together received 451 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Hearing Loss and Rehabilitation (4 papers) and Vestibular and auditory disorders (3 papers). The work is most often cited by research in Sensory Systems (221 citations), Otorhinolaryngology (107 citations) and Neurology (98 citations). Fatemeh Alasti has collaborated with scholars based in Iran, Belgium and United States. Frequent co-authors include Guy Van Camp, Mohammad Hossein Sanati, Richard J. Smith, Mohammad Farhadi, Thomas Somers, Morteza Hashemzadeh Chaleshtori, Carla Nishimura, Kimia Kahrizi, Yasser Riazalhosseini and Mahdi Malekpour. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics and 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.