E. Le Guern - Concepedia

Author

E. Le Guern

Inserm

Also Known As

A. Vidaller, E Le Guern, E. Le Guern, Eric Le Guern, Eric le Guern, Le Guern, E, Y. Bahou, É Le Guern, Éric Le Guern

Publications

927

Citations

H-Index

Concepts

All Affiliations

Inserm Sorbonne Université Pitié-Salpêtrière Hospital Centre National de la Recherche Scientifique Assistance Publique – Hôpitaux de Paris

About

E. Le Guern is an author at Inserm specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	290
2	Molecular Genetics	3	3	115
3	Biology	2	2	37
4	Natural Sciences	1	1	23
5	Public Health	1	1	24

E. Le Guern

Publications

684

Citations

H-Index

Page 1

	Year	Citations
GABA<sub>A</sub>Receptor γ2 Subunit Mutations Linked to Human Epileptic Syndromes Differentially Affect Phasic and Tonic Inhibition Emmanuel Eugène, Christel Depienne, Stéphanie Baulac, Journal of Neuroscience	2007	83
Characterization of Recessive Parkinson Disease in a Large Multicenter Study Suzanne Lesage, Ariane Lunati, Marion Houot, Annals of Neurology	2020	77
Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene Nazha Birouk, Hamid Azzedine, O. Dubourg, Archives of Neurology	2003	76
New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease L.J. Bone, Niklas Dahl, M. William Lensch, Neurology Molecular Diagnostic TechniquesMendelian DisorderGenetic DisorderMedicineGenetics	1995	69
Autosomal‐dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I Ali Benomar, E. Le Guern, Alexandra Dürr, Annals of Neurology	1994	65
Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP) E. Le Guern, F. Sturtz, Michel Gugenheim, Cytogenetic and Genome Research	1994	52
Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy R. Zemmouri, Hamid Azzedine, Salima Assami, Neuromuscular Disorders Peripheral NervesCharcot–marie–tooth 2-Like PresentationGiant Axonal NeuropathyNeuroanatomyMedicine	2000	37
The SOX10 transcription factor: evaluation as a candidate gene for central and peripheral hereditary myelin disorders Véronique Pingault, Nadège Bondurand, C. Le Caignec, Journal of Neurology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisSox10 Transcription FactorGenetic DisorderGenetics	2001	29
Novel VCP mutations expand the mutational spectrum of frontotemporal dementia Dario Saracino, Fabienne Clot, Agnès Camuzat, Neurobiology of Aging Neurodegenerative DiseasesNovel Vcp MutationsGenetic DisorderGeneticsFrontotemporal Dementia	2018	28
Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP) Vincent Timmerman, Ann Löfgren, E. Le Guern, Human Genetics Hereditary NeuropathyPeripheral NervesMendelian DisorderGenetic DisorderMedicine	1996	26

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