Georges Imbert - Concepedia

Concepedia

Author

Georges Imbert

Centre National de la Recherche Scientifique

Also Known As

Georges Imbert, Imbert, Georges

24

Publications

3.5K

Citations

11

H-Index

43

Concepts

All Affiliations

Centre National de la Recherche Scientifique Inserm Institut de génétique et de biologie moléculaire et cellulaire Pitié-Salpêtrière Hospital Sorbonne Université

GI

About

Georges Imbert is an author at Centre National de la Recherche Scientifique specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	3.1K
2	Natural Sciences	2	2	861
3	Social Sciences	2	2	887
4	Health Sciences	1	1	301
5	Biochemistry	1	1	92

Georges Imbert

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11

Publications

3.5K

Citations

11

H-Index

	Year	Citations
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats Georges Imbert, Frédéric Saudou, Gaël Yvert, Nature Genetics Molecular NeuroscienceSpinocerebellar Ataxia 2High SensitivityGenetic DisorderMendelian Disorder	1996	846
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion Gilles David, Nacer Abbas, Giovanni Stévanin, Nature Genetics Sca7 GeneMolecular ResearchNatural SciencesGeneticsMolecular Biology	1997	769
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias Yvon Trottier, Yves Lutz, Giovanni Stévanin, Nature Pathological EpitopeDegenerative DiseaseDominant Cerebellar AtaxiasNeurochemical BiomarkersNeurology	1995	653
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form Yvon Trottier, Didier Devys, Georges Imbert, Nature Genetics Knockout MouseDisease ProteinGeneticsCellular LocalizationMolecular Neurobiology	1995	445
Safety, tolerability, and antibody response of active Aβ immunotherapy with CAD106 in patients with Alzheimer's disease: randomised, double-blind, placebo-controlled, first-in-human study Bengt Winblad, Niels Andreasen, Lennart Minthon, The Lancet Neurology Neurodegenerative DiseasesGeriatric NeurologyAlzheimer's DiseaseImmunologyClinical Trials	2012	301
Origin of the expansion mutation in myotonic dystrophy Georges Imbert, Christine Kretz, Keith Johnson, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsDegenerative DiseaseMyotonic Dystrophy	1993	212
Controlled Protein Precipitation in Combination with Chip-Based Nanospray Infusion Mass Spectrometry. An Approach for Metabolomics Profiling of Plasma K. Olaf Boernsen, Stephan Gatzek, Georges Imbert Analytical Chemistry Liquid Chromatography-mass SpectrometryBiological Mass SpectrometryMetabolomic ProfilingMetabolomics ProfilingBioanalysis	2005	92
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream region Yvon Trottier, Georges Imbert, Annemarie Poustka, American Journal of Medical Genetics	1994	57
Differential distribution of the normal and mutated forms of huntingtin in the human brain Isabelle Gourfinkel‐An, Géraldine Cancel‐Tassin, Yvon Trottier, Annals of Neurology	1997	54
The human small conductance calcium-regulated potassium channel gene ( hSKCa3 ) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia Oliver H. Wittekindt, Anna Jauch, E. Omer Burgert, Neurogenetics ChannelopathiesMolecular NeuroscienceCag RepeatsExon 1Genetic Disorder	1998	41

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