Samir Belal
Impact in
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- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Neurology top 2%
- Neurological diseases and metabolism
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
Papers in
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- Genetic Neurodegenerative Diseases 23
- Hereditary Neurological Disorders 10
-
- Mitochondrial Function and Pathology 17
- DNA Repair Mechanisms 5
- Co-authors
- Fayçal Hentati (22 shared papers)M. Ben Hamida (16 shared papers)Christiane Ben Hamida (9 shared papers)F. Hentati (5 shared papers)M. Kœnig (3 shared papers)L Cavalier (3 shared papers)Ilhem Turki (5 shared papers)Alexis Brice (8 shared papers)
- Journals
- Neurology (7 papers)Human Molecular Genetics (3 papers)Cytokine (3 papers)Journal of Neural Transmission (2 papers)Neuromuscular Disorders (2 papers)
- Partner nations
- TunisiaFranceUnited States
In The Last Decade
Samir Belal
61 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 89
- Cellular and Molecular Neuroscience 1.0k
- Neurology 369
- Biochemistry 167
- Neurology 416
- Cell Biology 299
Countries citing papers authored by Samir Belal
This map shows the geographic impact of Samir Belal'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 Samir Belal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Samir Belal more than expected).
Fields of papers citing papers by Samir Belal
This network shows the impact of papers produced by Samir Belal. 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 Samir Belal. The network helps show where Samir Belal may publish in the future.
Co-authors
The 25 scholars most cited alongside Samir Belal, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 313 | |
| 2 | 1993 | 163 | |
| 3 | 1995 | 112 | |
| 4 | 2001 | 96 | |
| 5 | 1993 | 96 | |
| 6 | 1994 | 92 | |
| 7 | 1998 | 76 | |
| 8 | 2003 | 75 | |
| 9 | 2003 | 69 | |
| 10 | 2000 | 52 | |
| 11 | 1998 | 44 | |
| 12 | 1997 | 42 | |
| 13 | 1994 | 42 | |
| 14 | Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families. | 1995 | 42 |
| 15 | 2009 | 41 | |
| 16 | Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval. | 1994 | 41 |
| 17 | 1997 | 39 | |
| 18 | 2008 | 38 | |
| 19 | 1995 | 36 | |
| 20 | 1994 | 32 |
About Samir Belal
Samir Belal is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Neurology and Cell Biology, having authored 61 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (23 papers), Mitochondrial Function and Pathology (17 papers), Neurological diseases and metabolism (11 papers), Hereditary Neurological Disorders (10 papers), Alzheimer's disease research and treatments (6 papers), DNA Repair Mechanisms (5 papers), Cholinesterase and Neurodegenerative Diseases (5 papers) and Multiple Sclerosis Research Studies (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.0k citations), Neurology (369 citations), Biochemistry (167 citations), Neurology (416 citations) and Cell Biology (299 citations). Samir Belal has collaborated with scholars based in Tunisia, France and United States. Frequent co-authors include Fayçal Hentati, M. Ben Hamida, Christiane Ben Hamida, F. Hentati, M. Kœnig, L Cavalier, Ilhem Turki, Alexis Brice, Rim Amouri and A. Larnaout. Their work appears in journals such as Neurology, Human Molecular Genetics, Cytokine, Journal of Neural Transmission and Neuromuscular Disorders.
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.