Éric Leguern

10.6k citations
101 papers · 4.8k · 1 hit paper · h-index 39

Impact in

    • Hereditary Neurological Disorders
    • Genetic Neurodegenerative Diseases
    • Neuroscience and Neuropharmacology Research
  • Neurology top 0.5%
    • Neurological diseases and metabolism
    • Amyotrophic Lateral Sclerosis Research

Papers in

Éric Leguern

99 papers receiving 4.7k citations

Hit Papers

First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene 2001 · 574 citations
5740+8+16Years since publication100200300400500

Peers

Éric Leguern
Comparison fields: 5 of 96
  • Cellular and Molecular Neuroscience 2.7k
  • Neurology 936
  • Neurology 1.4k
  • Psychiatry and Mental health 827
  • Cell Biology 684
Replace Albena Jordanova with:
Albena Jordanova Belgium
A E Harding United Kingdom
Alan Pittman United Kingdom
E. R. Brunt Netherlands
Giovanni Stévanin France
Katja Lohmann Germany
Luís Bataller Spain
Eric Leguern France
G. Jackson Snipes United States
Paymaan Jafar‐Nejad United States
Éric Leguern relative to Albena Jordanova Belgium Albena Jordanova's profile →
Citations per field
00.5×2.7×
Albena Jordanova · 1×
Citations per year

Countries citing papers authored by Éric Leguern

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Éric Leguern Line = papers co-authored together Éric Leguern links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 101 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 →
2001574
2 2001262
3 2003226
4 2013185
5 2013167
6 2018155
7 1998133
8 2012129
9 1995126
10 2016126
11 1999120
12 1996105
13 201095
14 201495
15 199692
16 199584
17 200676
18 201673
19 200171
20 199968

About Éric Leguern

Éric Leguern is a scholar working on Cellular and Molecular Neuroscience, Neurology, Molecular Biology, Neurology and Genetics, having authored 101 papers that have together received 4.8k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (47 papers), Neurological diseases and metabolism (25 papers), Epilepsy research and treatment (20 papers), Genetics and Neurodevelopmental Disorders (16 papers), Genetic Neurodegenerative Diseases (15 papers), Neurogenetic and Muscular Disorders Research (11 papers), Cellular transport and secretion (11 papers) and Amyotrophic Lateral Sclerosis Research (10 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.7k citations), Neurology (936 citations), Neurology (1.4k citations), Psychiatry and Mental health (827 citations) and Cell Biology (684 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 Neurogenetics.

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.

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