E. Le Guern

943 citations

25 papers · 464 indexed · h-index 13

Cellular and Molecular Neuroscience top 5%
Molecular Biology
Neurology top 10%
Neurology top 10%
Genetics

Co-authors: Alexis Brice Ali Benomar Stéphanie Baulac N. Ravisé Michel Baulac Christel Depienne Jean Christophe Poncer Richard Miles
Topics: Hereditary Neurological Disorders (9 papers)Neurological diseases and metabolism (5 papers)RNA regulation and disease (5 papers)
Cited by: Cellular and Molecular Neuroscience Neurology
Journals: Journal of Neuroscience Neurology Annals of Neurology
Partner nations: France Italy United Kingdom

In The Last Decade

E. Le Guern

24 papers receiving 453 citations

Peers

Countries citing papers authored by E. Le Guern

Since Specialization

Citations

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

Fields of papers citing papers by E. Le Guern

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. Le Guern. 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 E. Le Guern. The network helps show where E. Le Guern may publish in the future.

Co-authorship network of co-authors of E. Le Guern

This figure shows the co-authorship network connecting the top 25 collaborators of E. Le Guern. A scholar is included among the top collaborators of E. Le Guern 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 E. Le Guern. E. Le Guern 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

#	Work	Indexed citations
1	Loss of function of ADNP by an intragenic inversion 2023 ·European Journal of Human Genetics ·(unknown),(unknown),Julien Buratti,(unknown),E. Le Guern,Delphine Héron,Boris Keren,Jean‐Madeleine de Sainte Agathe	5
2	Novel VCP mutations expand the mutational spectrum of frontotemporal dementia 2018 ·Neurobiology of Aging ·Dario Saracino,Fabienne Clot,Agnès Camuzat,Vincent Anquetil,Didier Hannequin,Lucie Guyant‐Maréchal,Mira Didic,Léna Guillot‐Noël,Daisy Rinaldi,Morwena Latouche,Sylvie Forlani,(unknown),Cinzia Coppola,Giuseppe Di Iorio,(unknown),E. Le Guern,Alexis Brice,(unknown)	21
3	GABA_AReceptor γ2 Subunit Mutations Linked to Human Epileptic Syndromes Differentially Affect Phasic and Tonic Inhibition 2007 ·Journal of Neuroscience ·Emmanuel Eugène,Christel Depienne,Stéphanie Baulac,Michel Baulac,Jean‐Marc Fritschy,E. Le Guern,Richard Miles,Jean Christophe Poncer	67
4	Hereditary Neuropathy with Liability to Pressure Palsies 2005 ·PubMed ·P. Bouché,(unknown),(unknown),(unknown),E. Le Guern,(unknown),Nadine Le Forestier	14
5	Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene 2003 ·Archives of Neurology ·Nazha Birouk,Hamid Azzedine,O. Dubourg,Marie‐Paule Muriel,Ali Benomar,Tarik Hamadouche,Thierry Maisonobe,Réda Ouazzani,Alexis Brice,Mohamed Yahyaoui,(unknown),E. Le Guern	45
6	The SOX10 transcription factor: evaluation as a candidate gene for central and peripheral hereditary myelin disorders 2001 ·Journal of Neurology ·Véronique Pingault,Nadège Bondurand,C. Le Caignec,Sandrine Tardieu,N Lemort,O. Dubourg,E. Le Guern,M. Goossens,Odile Boespflug‐Tanguy	21
7	Épilepsies, convulsions fébriles et canaux ioniques : le début d'une longue histoire. 2001 ·médecine/sciences ·Stéphanie Baulac,Isabelle An,Alexis Brice,E. Le Guern	1
8	Premières preuves génétiques de l'implication du récepteur GABAA dans l'épilepsie. 2001 ·médecine/sciences ·Stéphanie Baulac,Isabelle An-Gourfinkel,(unknown),Michel Baulac,Roberto Bruzzone,Alexis Brice,E. Le Guern	1
9	Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy 2000 ·Neuromuscular Disorders ·(unknown),Hamid Azzedine,Salima Assami,(unknown),Jean‐Michel Vallat,Thierry Maisonobe,Tarik Hamadouche,(unknown),(unknown),E. Le Guern,Djamel Grid,M. Tazir	33
10	Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP) 1996 ·Human Genetics ·Vincent Timmerman,Ann Löfgren,E. Le Guern,Ping Liang,Peter De Jonghe,(unknown),(unknown),Wim Robberecht,Riadh Gouider,Alexis Brice,Christine Van Broeckhoven	23
11	New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease 1995 ·Neurology ·(unknown),Niklas Dahl,M. William Lensch,P. F. Chance,Thaddeus E. Kelly,E. Le Guern,(unknown),Gordon Parry,(unknown),S. Wang,Kenneth H. Fischbeck	61
12	Allelic association at the D14S43 locus in early onset Alzheimer's disease 1995 ·American Journal of Medical Genetics ·Alexis Brice,Sandrine Tardieu,Dominique Campion,E. Le Guern,María Martínez,Alexandre Carpentier,Christiane Penet,Bruno Dubois,(unknown),Jacques Mallet,Didier Hannequin,Françoise Clerget‐Darpoux,Yves Agid	3
13	Prenatal diagnosis of X‐linked retinitis pigmentosa (RP) in five pregnancies at risk 1994 ·Prenatal Diagnosis ·(unknown),Rita Mingarelli,E. Le Guern,Giuseppe Novelli,Bruno Dallapiccola	1
14	Autosomal‐dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I 1994 ·Annals of Neurology ·Ali Benomar,E. Le Guern,Alexandra Dürr,H. Ouhabi,Giovanni Stévanin,M. Yahyaoui,T. Chkili,Yves Agid,Alexis Brice	47
15	Assignment of 112 Microsatellite Markers to 23 Chromosome 11 Subregions Delineated by Somatic Hybrids: Comparison with the Genetic Map 1994 ·Genomics ·(unknown),E. Le Guern,Alain Vignal,Cécile Fizames,N. Ravisé,(unknown),(unknown),(unknown),Claudine Junien,Veronica van Heyningen,J. Weissenbach	19
16	Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP) 1994 ·Cytogenetic and Genome Research ·E. Le Guern,(unknown),Michel Gugenheim,Riadh Gouider,(unknown),N. Ravisé,Pierre‐Marie Gonnaud,(unknown),P. Bouché,G Chazot,Y. Agid,A. Vandenberghe,Alexis Brice	37
17	Genetic heterogeneity of autosomal dominant cerebellar ataxia type I: evidence for the existence of a third locus 1993 ·Human Molecular Genetics ·Giovanni Stévanin,(unknown),E. Le Guern,(unknown),(unknown),(unknown),Yves Agid,Alexis Brice	7
18	Mapping around the Xq13.1 breakpoints of two X/A translocations in hypohidrotic ectodermal dysplasia (EDA) female patients 1992 ·Genomics ·Béatrice Plougastel-Douglas,P. Couillin,Véronique Blanquet,E. Le Guern,Egbert Bakker,C Turleau,J. de Grouchy,N. Créau-Goldberg	7
19	Molecular studies of a translocated (X;22) DiGeorge patient using somatic cell hybridization. 1992 ·PubMed ·P. Couillin,Jessica Zucman‐Rossi,E. Le Guern,(unknown),(unknown),Olivier Delattre,Giuseppe Novelli,Bruno Dallapiccola,A Boué	2
20	More precise localization of the gene for Hunter syndrome 1990 ·Genomics ·E. Le Guern,P. Couillin,I. Oberlé,N. Ravisé,J Boué	16

About E. Le Guern

E. Le Guern is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 25 papers that have together received 464 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (5 papers) and RNA regulation and disease (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (322 citations), Neurology (106 citations) and Neurology (109 citations). E. Le Guern has collaborated with scholars based in France, Italy and United Kingdom. Frequent co-authors include Alexis Brice, Ali Benomar, Stéphanie Baulac, N. Ravisé, Michel Baulac, Christel Depienne, Jean Christophe Poncer, Richard Miles, Jean‐Marc Fritschy and Emmanuel Eugène. Their work appears in journals such as Journal of Neuroscience, Neurology and Annals of Neurology.

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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