Eric Leguern

5.9k citations

33 papers · 2.6k indexed · 1 hit paper · h-index 20

Psychiatry and Mental health top 1%
- Epilepsy research and treatment 15
Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders 6
- Neuroscience and Neuropharmacology Research 5
Genetics top 2%
- Genetics and Neurodevelopmental Disorders 12
- Genomics and Rare Diseases 3
Cell Biology top 5%
- Cellular transport and secretion 4
Molecular Biology top 10%
Neurology
- Autoimmune Neurological Disorders and Treatments 4
Rheumatology
- Glycogen Storage Diseases and Myoclonus 4

Co-authors: Stéphanie Baulac Christel Depienne Alexis Brice Gilles Huberfeld Isabelle Gourfinkel‐An Miriam H. Meisler Bruno Moulard Isabelle An-Gourfinkel
Cited by: Psychiatry and Mental health Cellular and Molecular Neuroscience Genetics
Journals: Nature Genetics (2 papers)PLoS ONE (1 paper)The Journal of Clinical Endocrinology & Metabolism (1 paper)
Partner nations: France Switzerland United States

In The Last Decade

Eric Leguern

32 papers receiving 2.6k citations

Hit Papers

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Peers

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

The 25 scholars most cited alongside Eric 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 Eric Leguern Line = papers co-authored together Eric Leguern links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	SCN1A-related epilepsy with recessive inheritance: Two further families European Journal of Paediatric Neurology ·Raffaella Moretti,Lionel Arnaud,Delphine Bouteiller,Oriane Trouillard,Patricia Moreau,Julien Buratti,Agnès Rastetter,Boris Keren,Vincent des Portes,Joseph Toulouse,Isabelle Gourfinkel‐An,Eric Leguern,Christel Depienne,Cyril Mignot,Caroline Nava	2021	4
2	Evidence of mosaicism in SPAST variant carriers in four French families European Journal of Human Genetics ·Chloé Angelini,Cyril Goizet,Samia Ait Said,William Camu,Christel Depienne,Bénédicte Héron,Bophara Kol,Marine Guillaud-Bataille,Perrine Pennamen,Caroline Rooryck,Clarisse Scherer‐Gagou,Laurène Tissier,Giovanni Stévanin,Eric Leguern,Guillaume Banneau	2021	2
3	Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations Epilepsy Research ·Lynette G. Sadleir,Dahbia Agher,E Chabrol,Léa Elkouby,Eric Leguern,Sarah Paterson,Rosie Harty,Susannah T. Bellows,Samuel F. Berkovic,Ingrid E. Scheffer,Stéphanie Baulac	2013	11
4	STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients Epilepsia ·Cyril Mignot,Marie‐Laure Moutard,Oriane Trouillard,Isabelle Gourfinkel‐An,Aurélia Jacquette,Benoı̂t Arveiler,Fanny Morice‐Picard,Didier Lacombe,Catherine Chiron,Dorothée Ville,Perrine Charles,Eric Leguern,Christel Depienne,Delphine Héron	2011	76
5	Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism Journal of Molecular Medicine ·Philippe Couarch,Santiago Vernia,Isabelle Gourfinkel‐An,Gaëtan Lesca,Svetlana Gataullina,Estelle Fédirko,Oriane Trouillard,Christel Depienne,Olivier Dulac,Dominique Steschenko,Eric Leguern,Pascual Sanz,Stéphanie Baulac	2011	19
6	Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome Journal of Medical Genetics ·Christel Depienne,Oriane Trouillard,Isabelle Gourfinkel‐An,Cécile Saint‐Martin,Delphine Bouteiller,Denis Graber,Marie‐Anne Barthez‐Carpentier,Agnès Gautier,Nathalie Villeneuve,Charlotte Dravet,Marie-Odile Livet,Clotilde Rivier-Ringenbach,Claude Adam,Sabrina Dupont,Stéphanie Baulac,Delphine Héron,Rima Nabbout,Eric Leguern	2010	117
7	Elicited repetitive daily blindness Neurology ·Katayoun Vahedi,Christel Depienne,D. Fort,Florence Riant,P. Chaine,Oriane Trouillard,Alain Gaudric,Michael A. Morris,Eric Leguern,Elisabeth Tournier‐Lasserve,M-G Bousser	2009	66
8	Two novelCLCN2mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy Human Mutation ·C��cile Saint-Martin,Grégory Gauvain,Georgeta Teodorescu,Isabelle Gourfinkel‐An,Estelle Fédirko,Yvonne Weber,Snezana Maljevic,Jan‐Peter Ernst,Jennie García‐Olivares,Christoph Fahlke,Rima Nabbout,Eric Leguern,Holger Lerche,Jean Christophe Poncer,Christel Depienne	2009	46
9	CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy Epilepsy Research ·Rima Nabbout,Christel Depienne,Mathilde Chipaux,Benôıt Girard,Isabelle Souville,Oriane Trouillard,Olivier Dulac,Jamel Chelly,Alexandra Afenjar,Delphine Héron,Eric Leguern,Chérif Beldjord,Thierry Bienvenu,Nadia Bahi‐Buisson	2009	3
10	Autism, language delay and mental retardation in a patient with 7q11 duplication BMJ Case Reports ·Christel Depienne,Delphine Héron,Catalina Betancur,B Benyahia,Oriane Trouillard,Delphine Bouteiller,Alain Verloès,Eric Leguern,Marion Leboyer,Alexis Brice	2009	5
11	A Novel Locus for Generalized Epilepsy With Febrile Seizures Plus in French Families Archives of Neurology ·Stéphanie Baulac,Isabelle Gourfinkel‐An,Philippe Couarch,Christel Depienne,Anna Kamińska,Olivier Dulac,Michel Baulac,Eric Leguern,Rima Nabbout	2008	33
12	K-complex-induced seizures in autosomal dominant nocturnal frontal lobe epilepsy Clinical Neurophysiology ·Jeanine El Helou,Vincent Navarro,Christel Depienne,Estelle Fédirko,Eric Leguern,Michel Baulac,Isabelle An-Gourfinkel,Claude Adam	2008	21
13	Silencing of the Charcot–Marie–Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells Neurobiology of Disease ·Alexandre Chojnowski,N. Ravisé,Corinne Bachelin,Christel Depienne,Merle Ruberg,Bernard Brugg,Jocelyn Laporte,Anne Baron‐Van Evercooren,Eric Leguern	2007	10
14	Fever, genes, and epilepsy The Lancet Neurology ·Stéphanie Baulac,Isabelle Gourfinkel‐An,Rima Nabbout,Gilles Huberfeld,José M. Serratosa,Eric Leguern,Michel Baulac	2004	129
15	A Comprehensive Endocrine Description of Kennedy’s Disease Revealing Androgen Insensitivity Linked to CAG Repeat Length The Journal of Clinical Endocrinology & Metabolism ·S. Dejager,Hélène Bry‐Gauillard,Éric Bruckert,B. Eymard,François Salachas,Eric Leguern,Sandrine Tardieu,Rita Chadarévian,P. Giral,G Turpin	2002	124
16	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 ·Tom Moore,Stéphane Hecquet,Andrew McLellann,Dorothée Ville,Djamel Grid,Fabienne Picard,Bruno Moulard,Philip Asherson,Andrew J Makoff,David McCormick,Lina Nashef,Philippe Froguel,Alexis Arzimanoglou,Eric Leguern,Bernard Bailleul	2001	30
17	Genetic Refinement and Physical Mapping of the CMT4B Gene on Chromosome 11q22 Genomics ·Alessandra Bolino,Elaine R. Levy,M. Muglia,F. L. Conforti,Eric Leguern,Mustafa A. Salih,Domna-Maria Georgiou,Kyproula Christodoulou,I Hausmanowa-Pétrusewicz,Paola Mandich,Antonio Gambardella,Aldo Quattrone,Marcella Devoto,Anthony P. Monaco	2000	14
18	Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 Nature Genetics ·Alessandra Bolino,M. Muglia,F. L. Conforti,Eric Leguern,Mustafa A. Salih,Domna-Maria Georgiou,Kyproula Christodoulou,I Hausmanowa-Pétrusewicz,Paola Mandich,Angelo Schenone,Antonio Gambardella,Francesco Bono,Aldo Quattrone,Marcella Devoto,Anthony P. Monaco	2000	360
19	Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2breakdown → Nature Genetics ·Andrew Escayg,Bryan T. MacDonald,Miriam H. Meisler,Stéphanie Baulac,Gilles Huberfeld,Isabelle An-Gourfinkel,Alexis Brice,Eric Leguern,Bruno Moulard,Denys Chaigne,Catherine Burési,Alain Malafosse	2000	739
20	A Second Locus for Familial Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2q21-q33 The American Journal of Human Genetics ·Stéphanie Baulac,Isabelle Gourfinkel‐An,Fabienne Picard,Myriam Rosenberg‐Bourgin,Jean‐François Prud'homme,Michel Baulac,Alexis Brice,Eric Leguern	1999	155

About Eric Leguern

Eric Leguern is a scholar working on Psychiatry and Mental health, Cellular and Molecular Neuroscience and Genetics, having authored 33 papers that have together received 2.6k indexed citations. Recurring topics across this work include Epilepsy research and treatment (15 papers), Genetics and Neurodevelopmental Disorders (12 papers), Hereditary Neurological Disorders (6 papers), Neuroscience and Neuropharmacology Research (5 papers), Autoimmune Neurological Disorders and Treatments (4 papers), Glycogen Storage Diseases and Myoclonus (4 papers), Cellular transport and secretion (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Psychiatry and Mental health (1.2k citations), Cellular and Molecular Neuroscience (993 citations) and Genetics (943 citations). Eric Leguern has collaborated with scholars based in France, Switzerland and United States. Frequent 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. Their work appears in journals such as Nature Genetics, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

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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