Éric Leguern
Impact in
- Cellular and Molecular Neuroscience top 0.5%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
- Neurology top 0.5%
- Neurological diseases and metabolism
- Amyotrophic Lateral Sclerosis Research
Papers in
-
- Hereditary Neurological Disorders 46
- Genetic Neurodegenerative Diseases 15
- Neuroscience and Neuropharmacology Research 10
- Neurology 30
- Neurological diseases and metabolism 22
- Amyotrophic Lateral Sclerosis Research 10
- Co-authors
- Alexis Brice (57 shared papers)Stéphanie Baulac (28 shared papers)Michel Baulac (12 shared papers)Nazha Birouk (16 shared papers)Riadh Gouider (18 shared papers)Isabelle Gourfinkel‐An (9 shared papers)P. Bouché (15 shared papers)Sandrine Tardieu (15 shared papers)
- Journals
- Neurology (13 papers)Neuromuscular Disorders (8 papers)Nature Genetics (5 papers)Neurobiology of Aging (5 papers)Journal of Medical Genetics (4 papers)
- Partner nations
- FranceUnited StatesTunisia
In The Last Decade
Éric Leguern
99 papers receiving 4.9k citations
Éric Leguern's Hit Papers
Peers
Comparison fields: 5 of 96
- Cellular and Molecular Neuroscience 2.8k
- Neurology 882
- Neurology 1.3k
- Psychiatry and Mental health 807
- Genetics 398
Countries citing papers authored by Éric Leguern
This map shows the geographic impact of Éric Leguern'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 Éric Leguern with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Éric Leguern more than expected).
Fields of papers citing papers by Éric Leguern
This network shows the impact of papers produced by Éric Leguern. 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 Éric Leguern. The network helps show where Éric Leguern may publish in the future.
Co-authors
The 25 scholars most cited alongside Éric Leguern, 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 103 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene Hit paper breakdown → | 2001 | 618 |
| 2 | 2001 | 280 | |
| 3 | 2003 | 239 | |
| 4 | 2013 | 194 | |
| 5 | 2013 | 183 | |
| 6 | 2018 | 163 | |
| 7 | 1998 | 148 | |
| 8 | 2012 | 139 | |
| 9 | 1999 | 137 | |
| 10 | 1995 | 136 | |
| 11 | 2016 | 132 | |
| 12 | 1996 | 118 | |
| 13 | 2010 | 99 | |
| 14 | 1996 | 98 | |
| 15 | 2014 | 98 | |
| 16 | 1995 | 93 | |
| 17 | 2006 | 83 | |
| 18 | 2016 | 77 | |
| 19 | 1999 | 76 | |
| 20 | 2001 | 74 |
About Éric Leguern
Éric Leguern is a scholar working on Cellular and Molecular Neuroscience, Neurology, Molecular Biology, Neurology and Cell Biology, having authored 103 papers that have together received 5.1k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (46 papers), Neurological diseases and metabolism (22 papers), Epilepsy research and treatment (18 papers), Genetics and Neurodevelopmental Disorders (15 papers), Genetic Neurodegenerative Diseases (15 papers), Cellular transport and secretion (12 papers), Amyotrophic Lateral Sclerosis Research (10 papers) and Neuroscience and Neuropharmacology Research (10 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.8k citations), Neurology (882 citations), Neurology (1.3k citations), Psychiatry and Mental health (807 citations) and Genetics (398 citations). Éric Leguern has collaborated with scholars based in France, United States and Tunisia. Frequent co-authors include Alexis Brice, Stéphanie Baulac, Michel Baulac, Nazha Birouk, Riadh Gouider, Isabelle Gourfinkel‐An, P. Bouché, Sandrine Tardieu, Gilles Huberfeld and Roberto Bruzzone. Their work appears in journals such as Neurology, Neuromuscular Disorders, Nature Genetics, Neurobiology of Aging 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.