Kamel Ben Othmane
Impact in
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- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Neurology top 5%
- Neurological diseases and metabolism
Papers in
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- Hereditary Neurological Disorders 6
- Genetic Neurodegenerative Diseases 2
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- Muscle Physiology and Disorders 3
- Co-authors
- Jeffery M. Vance (9 shared papers)Fayçal Hentati (6 shared papers)Mongi Ben Hamida (5 shared papers)Margaret A. Pericak‐Vance (4 shared papers)Carsten G. Bönnemann (2 shared papers)Elizabeth M. McNally (2 shared papers)Louis M. Kunkel (2 shared papers)Peter H. Denton (2 shared papers)
- Journals
- Genomics (3 papers)Nature Genetics (2 papers)Science (1 paper)Human Molecular Genetics (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United StatesTunisiaCyprus
In The Last Decade
Kamel Ben Othmane
10 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 51
- Cellular and Molecular Neuroscience 799
- Neurology 224
- Cell Biology 254
- Molecular Biology 832
- Genetics 115
Countries citing papers authored by Kamel Ben Othmane
This map shows the geographic impact of Kamel Ben Othmane'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 Kamel Ben Othmane with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kamel Ben Othmane more than expected).
Fields of papers citing papers by Kamel Ben Othmane
This network shows the impact of papers produced by Kamel Ben Othmane. 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 Kamel Ben Othmane. The network helps show where Kamel Ben Othmane may publish in the future.
Co-authors
The 25 scholars most cited alongside Kamel Ben Othmane, 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 | 1995 | 415 | |
| 2 | 2001 | 271 | |
| 3 | 1992 | 143 | |
| 4 | 1993 | 136 | |
| 5 | Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. | 1996 | 126 |
| 6 | 1993 | 120 | |
| 7 | 1999 | 59 | |
| 8 | 1995 | 21 | |
| 9 | 1998 | 8 | |
| 10 | 1992 | 5 |
About Kamel Ben Othmane
Kamel Ben Othmane is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Cell Biology, Immunology and Genetics, having authored 10 papers that have together received 1.3k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (6 papers), Muscle Physiology and Disorders (3 papers), Genetic Neurodegenerative Diseases (2 papers), Hippo pathway signaling and YAP/TAZ (2 papers), Genomics and Rare Diseases (1 paper), Muscle metabolism and nutrition (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and Toxin Mechanisms and Immunotoxins (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (799 citations), Neurology (224 citations), Cell Biology (254 citations), Molecular Biology (832 citations) and Genetics (115 citations). Kamel Ben Othmane has collaborated with scholars based in United States, Tunisia and Cyprus. Frequent co-authors include Jeffery M. Vance, Fayçal Hentati, Mongi Ben Hamida, Margaret A. Pericak‐Vance, Carsten G. Bönnemann, Elizabeth M. McNally, Louis M. Kunkel, Peter H. Denton, Lefkos Middleton and Christiane Ben Hamida. Their work appears in journals such as Genomics, Nature Genetics, Science, Human Molecular 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.