E. Le Guern

966 citations

25 papers · 433 · h-index 12

Impact in

Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
Neurology top 10%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders

Papers in

Molecular Biology 14
- RNA regulation and disease 5
Cellular and Molecular Neuroscience 13
- Hereditary Neurological Disorders 9
- Genetic Neurodegenerative Diseases 4
- Neuroscience and Neuropharmacology Research 2

Co-authors: Alexis Brice (10 shared papers)Ali Benomar (3 shared papers)Michel Baulac (2 shared papers)Stéphanie Baulac (3 shared papers)Richard Miles (1 shared paper)Thierry Maisonobe (3 shared papers)Jean‐Marc Fritschy (1 shared paper)Emmanuel Eugène (1 shared paper)
Journals: Neuromuscular Disorders (3 papers)Genomics (3 papers)Acta Oncologica (1 paper)Prenatal Diagnosis (1 paper)Human Genetics (1 paper)
Partner nations: France Italy Switzerland

In The Last Decade

E. Le Guern

24 papers receiving 422 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-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	GABA_AReceptor γ2 Subunit Mutations Linked to Human Epileptic Syndromes Differentially Affect Phasic and Tonic Inhibition Journal of Neuroscience ·Emmanuel Eugène, Christel Depienne, Stéphanie Baulac, Michel Baulac, Jean‐Marc Fritschy, E. Le Guern, Richard Miles, Jean Christophe Poncer	2007	67
2	New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease Neurology ·L.J. Bone, Niklas Dahl, M. William Lensch, P. F. Chance, Thaddeus E. Kelly, E. Le Guern, S. Magi, Gordon Parry, Howard K. Shapiro, S. Wang, Kenneth H. Fischbeck	1995	60
3	Autosomal‐dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I Annals of Neurology ·Ali Benomar, E. Le Guern, Alexandra Dürr, H. Ouhabi, Giovanni Stévanin, M. Yahyaoui, T. Chkili, Yves Agid, Alexis Brice	1994	47
4	Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene Archives of Neurology ·Nazha Birouk, Hamid Azzedine, O. Dubourg, Marie‐Paule Muriel, Ali Benomar, Tarik Hamadouche, Thierry Maisonobe, Réda Ouazzani, Alexis Brice, Mohamed Yahyaoui, T Chkili, E. Le Guern	2003	45
5	Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy Neuromuscular Disorders ·R. Zemmouri, Hamid Azzedine, Salima Assami, N. Kitouni, Jean‐Michel Vallat, Thierry Maisonobe, Tarik Hamadouche, M. Kessaci, B. Mansouri, E. Le Guern, Djamel Grid, M. Tazir	2000	33
6	Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP) Human Genetics ·Vincent Timmerman, Ann Löfgren, E. Le Guern, Ping Liang, Peter De Jonghe, Jean-Jacques Martin, Damienne Verhalle, Wim Robberecht, Riadh Gouider, Alexis Brice, Christine Van Broeckhoven	1996	23
7	Novel VCP mutations expand the mutational spectrum of frontotemporal dementia 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, Yassaman Ghassab, Cinzia Coppola, Giuseppe Di Iorio, Isabelle David, E. Le Guern, Alexis Brice, Isabelle Le Ber	2018	21
8	The SOX10 transcription factor: evaluation as a candidate gene for central and peripheral hereditary myelin disorders Journal of Neurology ·Véronique Pingault, Nadège Bondurand, C. Le Caignec, Sandrine Tardieu, N Lemort, O. Dubourg, E. Le Guern, M. Goossens, Odile Boespflug‐Tanguy	2001	21
9	Assignment of 112 Microsatellite Markers to 23 Chromosome 11 Subregions Delineated by Somatic Hybrids: Comparison with the Genetic Map Genomics ·P Couillin, E. Le Guern, Alain Vignal, Cécile Fizames, N. Ravisé, D. Delportes, I. Reguigne, Marie-Françoise Rosier, Claudine Junien, Veronica van Heyningen, J. Weissenbach	1994	19
10	Antineoplastic agents exacerbating Charcot Marie Tooth disease: red flags to avoid permanent disability Acta Oncologica ·María-José Ibáñez-Juliá, Giulia Berzero, G. Reyes-Botero, Thierry Maisonobe, Timothée Lenglet, Michel Slim, Sarah Louis, (unknown), Marc Sanson, E. Le Guern, Philippe Latour, Damien Ricard, Tanya Stojkovic, Dimitri Psimaras	2017	19
11	More precise localization of the gene for Hunter syndrome Genomics ·E. Le Guern, P. Couillin, I. Oberlé, N. Ravisé, J Boué	1990	16
12	Hereditary Neuropathy with Liability to Pressure Palsies PubMed ·P. Bouché, Philippe Mouton, R Gouider, O Dubourg, E. Le Guern, T Maisonobe, Nadine Le Forestier	2005	14
13	Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11–Xq21 microsatellites in a new large family: Three new markers are closely linked to the gene Neuromuscular Disorders ·E. Le Guern, N. Ravisé, Michel Gugenheim, Alain Vignal, Christiane Penet, P. Bouché, Jean Weissenbach, Yves Agid, Alexis Brice	1994	8
14	Mapping around the Xq13.1 breakpoints of two X/A translocations in hypohidrotic ectodermal dysplasia (EDA) female patients Genomics ·Béatrice Plougastel-Douglas, P. Couillin, Véronique Blanquet, E. Le Guern, Egbert Bakker, C Turleau, J. de Grouchy, N. Créau-Goldberg	1992	7
15	Genetic heterogeneity of autosomal dominant cerebellar ataxia type I: evidence for the existence of a third locus Human Molecular Genetics ·(unknown), Hervé Chnelweiss, E. Le Guern, Nicola Ravise, Alexandra Dürr, Christlane Penet, Yves Agid, Alexis Brice	1993	7
16	Loss of function of ADNP by an intragenic inversion European Journal of Human Genetics ·Mathieu Georget, Élodie Lejeune, Julien Buratti, Euphrasie Servant, E. Le Guern, Delphine Héron, Boris Keren, Jean‐Madeleine de Sainte Agathe	2023	6
17	Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP) Cytogenetics and Cell Genetics ·E. Le Guern, F. Sturtz, Michel Gugenheim, Riadh Gouider, C. Bonnebouche, N. Ravisé, Pierre‐Marie Gonnaud, S. Tardieu, P. Bouché, G Chazot, Y. Agid, A. Vandenberghe, Alexis Brice	2008	6
18	Strategy for constructing somatic hybrids isolating the two derivative chromosomes in X;autosome translocations. Application to a female patient t(X;5) with Hunter syndrome. PubMed ·P. Couillin, E. Le Guern, N. Ravisé, M Grisard, Ben A. Oostra, A Boué	1990	4
19	Allelic association at the D14S43 locus in early onset Alzheimer's disease American Journal of Medical Genetics ·Alexis Brice, Sandrine Tardieu, Dominique Campion, E. Le Guern, María Martínez, Alexandre Carpentier, Christiane Penet, Bruno Dubois, Michel Bellis, Jacques Mallet, Didier Hannequin, Françoise Clerget‐Darpoux, Yves Agid	1995	3
20	Molecular studies of a translocated (X;22) DiGeorge patient using somatic cell hybridization. PubMed ·P. Couillin, Jessica Zucman‐Rossi, E. Le Guern, I. Reguigne, M Grisard, Olivier Delattre, Giuseppe Novelli, Bruno Dallapiccola, A Boué	1992	2

About E. Le Guern

E. Le Guern is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Genetics and Physiology, having authored 25 papers that have together received 433 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (5 papers), RNA regulation and disease (5 papers), Genetic Neurodegenerative Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Alzheimer's disease research and treatments (2 papers), Neuroscience and Neuropharmacology Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (283 citations), Neurology (78 citations), Neurology (81 citations), Molecular Biology (209 citations) and Cell Biology (46 citations). E. Le Guern has collaborated with scholars based in France, Italy and Switzerland. Frequent co-authors include Alexis Brice, Ali Benomar, Michel Baulac, Stéphanie Baulac, Richard Miles, Thierry Maisonobe, Jean‐Marc Fritschy, Emmanuel Eugène, Jean Christophe Poncer and Christel Depienne. Their work appears in journals such as Neuromuscular Disorders, Genomics, Acta Oncologica, Prenatal Diagnosis and Human 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.

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E. Le Guern

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