M. Chaouch
Impact in
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- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Cell Biology top 10%
Papers in
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- Hereditary Neurological Disorders 4
- Genetic Neurodegenerative Diseases 3
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- Muscle Physiology and Disorders 4
- Nuclear Structure and Function 3
- RNA Research and Splicing 3
- RNA modifications and cancer 1
- Co-authors
- Kevin P. Campbell (2 shared papers)France Leturcq (3 shared papers)Michel Fardeau (3 shared papers)Fernando M. S. Tomé (3 shared papers)Nicolas Lévy (4 shared papers)Djamel Grid (4 shared papers)Annachiara De Sandre‐Giovannoli (3 shared papers)M. Tazir (3 shared papers)
- Journals
- Neuromuscular Disorders (3 papers)Nature Genetics (1 paper)Journal of Neurology (1 paper)Neurology (1 paper)Annals of Human Genetics (1 paper)
- Partner nations
- FranceAlgeriaUnited States
In The Last Decade
M. Chaouch
10 papers receiving 483 citations
Peers
Comparison fields: 5 of 37
- Cellular and Molecular Neuroscience 224
- Cell Biology 119
- Molecular Biology 432
- Genetics 55
- Cardiology and Cardiovascular Medicine 103
Countries citing papers authored by M. Chaouch
This map shows the geographic impact of M. Chaouch'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 M. Chaouch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Chaouch more than expected).
Fields of papers citing papers by M. Chaouch
This network shows the impact of papers produced by M. Chaouch. 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 M. Chaouch. The network helps show where M. Chaouch may publish in the future.
Co-authors
The 25 scholars most cited alongside M. Chaouch, 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 | 169 | |
| 2 | 1997 | 109 | |
| 3 | 1993 | 89 | |
| 4 | 2002 | 78 | |
| 5 | 2008 | 22 | |
| 6 | Laminin abnormality in severe childhood autosomal recessive muscular dystrophy. | 1995 | 19 |
| 7 | 2002 | 14 | |
| 8 | 2010 | 13 | |
| 9 | 2007 | 3 | |
| 10 | 1996 | 1 |
About M. Chaouch
M. Chaouch is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Cell Biology, Dermatology and Immunology, having authored 10 papers that have together received 517 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (4 papers), Muscle Physiology and Disorders (4 papers), Genetic Neurodegenerative Diseases (3 papers), Nuclear Structure and Function (3 papers), RNA Research and Splicing (3 papers), RNA modifications and cancer (1 paper), Immunodeficiency and Autoimmune Disorders (1 paper) and Adipose Tissue and Metabolism (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (224 citations), Cell Biology (119 citations), Molecular Biology (432 citations), Genetics (55 citations) and Cardiology and Cardiovascular Medicine (103 citations). M. Chaouch has collaborated with scholars based in France, Algeria and United States. Frequent co-authors include Kevin P. Campbell, France Leturcq, Michel Fardeau, Fernando M. S. Tomé, Nicolas Lévy, Djamel Grid, Annachiara De Sandre‐Giovannoli, M. Tazir, T. Hammadouche and Kemal Azibi. Their work appears in journals such as Neuromuscular Disorders, Nature Genetics, Journal of Neurology, Neurology and Annals 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.