Eric Leguern

5.9k total citations · 1 hit paper
33 papers, 2.6k citations indexed

About

Eric Leguern is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Eric Leguern has authored 33 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 15 papers in Psychiatry and Mental health and 12 papers in Molecular Biology. Recurrent topics in Eric Leguern's work include Epilepsy research and treatment (15 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Hereditary Neurological Disorders (6 papers). Eric Leguern is often cited by papers focused on Epilepsy research and treatment (15 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Hereditary Neurological Disorders (6 papers). Eric Leguern collaborates with scholars based in France, Switzerland and United States. Eric Leguern's co-authors include Stéphanie Baulac, Christel Depienne, Alexis Brice, Gilles Huberfeld, Isabelle Gourfinkel‐An, Miriam H. Meisler, Bruno Moulard, Isabelle An-Gourfinkel, Denys Chaigne and Catherine Burési and has published in prestigious journals such as Nature Genetics, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Eric Leguern

32 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

2000 739 citations Andrew Escayg, Bryan T. MacDonald et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Eric Leguern France	20	1.2k	1.2k	993	943	330	33	2.6k
Gabrielle Rudolf France	24	698 0.6×	658 0.6×	708 0.7×	592 0.6×	138 0.4×	69	2.1k
Davide Mei Italy	30	888 0.7×	1.0k 0.9×	482 0.5×	1.2k 1.2×	226 0.7×	81	2.4k
Agathe Roubertie France	28	769 0.6×	424 0.4×	618 0.6×	359 0.4×	230 0.7×	114	2.1k
Elena Parrini Italy	22	899 0.7×	598 0.5×	549 0.6×	1.0k 1.1×	227 0.7×	61	2.2k
Raffaella Cusmai Italy	30	553 0.4×	1.1k 0.9×	512 0.5×	618 0.7×	107 0.3×	69	2.5k
Teruyuki Tanaka Japan	20	1.0k 0.8×	261 0.2×	634 0.6×	450 0.5×	663 2.0×	35	2.1k
Michael C. Kruer United States	25	746 0.6×	342 0.3×	449 0.5×	412 0.4×	133 0.4×	74	2.2k
Laura Canafoglia Italy	26	523 0.4×	407 0.3×	388 0.4×	475 0.5×	188 0.6×	106	2.0k
László Sztriha United Arab Emirates	23	817 0.7×	355 0.3×	301 0.3×	672 0.7×	232 0.7×	66	1.8k
Roberta Biancheri Italy	31	1.3k 1.0×	136 0.1×	350 0.4×	377 0.4×	339 1.0×	100	2.5k

Countries citing papers authored by Eric Leguern

Since Specialization

Citations

This map shows the geographic impact of Eric 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 Eric Leguern with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric Leguern more than expected).

Fields of papers citing papers by Eric Leguern

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric 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 Eric Leguern. The network helps show where Eric Leguern may publish in the future.

Co-authorship network of co-authors of Eric Leguern

This figure shows the co-authorship network connecting the top 25 collaborators of Eric Leguern. A scholar is included among the top collaborators of Eric Leguern based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Eric Leguern. Eric Leguern is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Moretti, Raffaella, Lionel Arnaud, Delphine Bouteiller, et al.. (2021). SCN1A-related epilepsy with recessive inheritance: Two further families. European Journal of Paediatric Neurology. 33. 121–124. 4 indexed citations

Goizet, Cyril, William Camu, Christel Depienne, et al.. (2021). Evidence of mosaicism in SPAST variant carriers in four French families. European Journal of Human Genetics. 29(7). 1158–1163. 2 indexed citations

Sadleir, Lynette G., E Chabrol, Eric Leguern, et al.. (2013). Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations. Epilepsy Research. 107(3). 311–317. 11 indexed citations

Mignot, Cyril, Marie‐Laure Moutard, Oriane Trouillard, et al.. (2011). STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients. Epilepsia. 52(10). 1820–1827. 76 indexed citations

Couarch, Philippe, Santiago Vernia, Isabelle Gourfinkel‐An, et al.. (2011). Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism. Journal of Molecular Medicine. 89(9). 915–925. 19 indexed citations

Depienne, Christel, Oriane Trouillard, Isabelle Gourfinkel‐An, et al.. (2010). Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome. Journal of Medical Genetics. 47(6). 404–410. 117 indexed citations

Vahedi, Katayoun, Christel Depienne, Florence Riant, et al.. (2009). Elicited repetitive daily blindness. Neurology. 72(13). 1178–1183. 66 indexed citations

Gauvain, Grégory, Isabelle Gourfinkel‐An, Estelle Fédirko, et al.. (2009). Two novelCLCN2mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy. Human Mutation. 30(3). 397–405. 46 indexed citations

Nabbout, Rima, Christel Depienne, Mathilde Chipaux, et al.. (2009). CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy. Epilepsy Research. 87(1). 25–30. 3 indexed citations

10.

Depienne, Christel, Delphine Héron, Catalina Betancur, et al.. (2009). Autism, language delay and mental retardation in a patient with 7q11 duplication. BMJ Case Reports. 2009. bcr0520091911–bcr0520091911. 5 indexed citations

11.

Baulac, Stéphanie, Isabelle Gourfinkel‐An, Philippe Couarch, et al.. (2008). A Novel Locus for Generalized Epilepsy With Febrile Seizures Plus in French Families. Archives of Neurology. 65(7). 943–51. 33 indexed citations

12.

Navarro, Vincent, Christel Depienne, Estelle Fédirko, et al.. (2008). K-complex-induced seizures in autosomal dominant nocturnal frontal lobe epilepsy. Clinical Neurophysiology. 119(10). 2201–2204. 21 indexed citations

13.

Chojnowski, Alexandre, N. Ravisé, Corinne Bachelin, et al.. (2007). Silencing of the Charcot–Marie–Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells. Neurobiology of Disease. 26(2). 323–331. 10 indexed citations

14.

Baulac, Stéphanie, Isabelle Gourfinkel‐An, Rima Nabbout, et al.. (2004). Fever, genes, and epilepsy. The Lancet Neurology. 3(7). 421–430. 129 indexed citations

15.

Dejager, S., Hélène Bry‐Gauillard, Éric Bruckert, et al.. (2002). A Comprehensive Endocrine Description of Kennedy’s Disease Revealing Androgen Insensitivity Linked to CAG Repeat Length. The Journal of Clinical Endocrinology & Metabolism. 87(8). 3893–3901. 124 indexed citations

16.

Moore, Tom, Dorothée Ville, Djamel Grid, et al.. (2001). Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME. Epilepsy Research. 46(2). 157–167. 30 indexed citations

17.

Bolino, Alessandra, M. Muglia, F. L. Conforti, et al.. (2000). Genetic Refinement and Physical Mapping of the CMT4B Gene on Chromosome 11q22. Genomics. 63(2). 271–278. 14 indexed citations

18.

Bolino, Alessandra, M. Muglia, F. L. Conforti, et al.. (2000). Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2. Nature Genetics. 25(1). 17–19. 360 indexed citations

19.

Escayg, Andrew, Bryan T. MacDonald, Miriam H. Meisler, et al.. (2000). Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2. Nature Genetics. 24(4). 343–345. 739 indexed citations breakdown →

20.

Baulac, Stéphanie, Isabelle Gourfinkel‐An, Fabienne Picard, et al.. (1999). A Second Locus for Familial Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2q21-q33. The American Journal of Human Genetics. 65(4). 1078–1085. 155 indexed citations

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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