Edor Kabashi

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Sorana CiuraImagine InstituteAdresse e-mail validée de institutimagine.org
Guy RouleauMontreal Neurological Institute-Hospital, McGill UniversityAdresse e-mail validée de mcgill.ca
Patrick A. DionMcGill UniversityAdresse e-mail validée de mcgill.ca
Paul ValdmanisAssociate Professor, University of WashingtonAdresse e-mail validée de uw.edu
Nicolas DupreUniversité LavalAdresse e-mail validée de fmed.ulaval.ca
william camuchu montpellierAdresse e-mail validée de chu-montpellier.fr
Pradat Pierre-francoisSorbonne University. UPMC. INSERM. CNRSAdresse e-mail validée de psl.aphp.fr
Jeffrey AgarAssociate Professor of Chemistry and Pharm. Sci., NortheasternAdresse e-mail validée de neu.edu
Dr Hussein DaoudScientist - Genomics Specialist, Genetics Diagnostic Laboratory - Children's Hospital of EasternAdresse e-mail validée de cheo.on.ca
Chantal SellierChargé de recherche INSERMAdresse e-mail validée de igbmc.fr
Hervé TostivintMuséum National d'Histoire Naturelle. ParisAdresse e-mail validée de mnhn.fr
Jose BrasRegeneron Genetics Center, Regeneron PharmaceuticalsAdresse e-mail validée de regeneron.com
Rita GuerreiroVan Andel Research InstituteAdresse e-mail validée de vai.org
Raul C. MuresanTransylvanian Institute of NeuroscienceAdresse e-mail validée de tins.ro
Peter De JongheVIB Department of Molecular Genetics, Neurogenetics Group, University of Antwerp, Institute BornAdresse e-mail validée de molgen.vib-ua.be
Luc DupuisDirecteur de recherches InsermAdresse e-mail validée de unistra.fr
JAVIER SAEZ VALEROInstituto de Neurociencias, Universidad Miguel Hernández & CIBERNED & ISABIALAdresse e-mail validée de umh.es
Peter HeutinkAlectorAdresse e-mail validée de alector.com
Andrew SingletonNational Institute on AgingAdresse e-mail validée de mail.nih.gov

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Edor Kabashi

ICM - Institut du Cerveau et de la Moelle épinière

Adresse e-mail validée de icm-institute.org - Page d'accueil

Neuroscience neurological disorders genetics ALS zebrafish


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis E Kabashi, PN Valdmanis, P Dion, D Spiegelman, BJ McConkey, ... Nature genetics 40 (5), 572-574, 2008	1784	2008
Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo E Kabashi, L Lin, ML Tradewell, PA Dion, V Bercier, P Bourgouin, ... Human molecular genetics 19 (4), 671-683, 2010	477	2010
Loss of C9 ORF 72 impairs autophagy and synergizes with polyQ Ataxin‐2 to induce motor neuron dysfunction and cell death C Sellier, ML Campanari, C Julie Corbier, A Gaucherot, I Kolb‐Cheynel, ... The EMBO journal 35 (12), 1276-1297, 2016	421	2016
Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis S Ciura, S Lattante, I Le Ber, M Latouche, H Tostivint, A Brice, E Kabashi Annals of neurology 74 (2), 180-187, 2013	419	2013
Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... The American Journal of Human Genetics 98 (3), 500-513, 2016	412	2016
TARDBP and FUS Mutations Associated with Amyotrophic Lateral Sclerosis: Summary and Update S Lattante, GA Rouleau, E Kabashi Human mutation 34 (6), 812-826, 2013	321	2013
FUS and TARDBP but Not SOD1 Interact in Genetic Models of Amyotrophic Lateral Sclerosis E Kabashi, V Bercier, A Lissouba, M Liao, E Brustein, GA Rouleau, ... PLoS genetics 7 (8), e1002214, 2011	237	2011
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis H Daoud, PN Valdmanis, E Kabashi, P Dion, N Dupre, W Camu, ... Journal of medical genetics 46 (2), 112-114, 2009	232	2009
Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia E Martin, R Schüle, K Smets, A Rastetter, A Boukhris, JL Loureiro, ... The American Journal of Human Genetics 92 (2), 238-244, 2013	197	2013
SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis I Le Ber, A Camuzat, R Guerreiro, K Bouya-Ahmed, J Bras, G Nicolas, ... JAMA neurology 70 (11), 1403-1410, 2013	189	2013
Focal dysfunction of the proteasome: a pathogenic factor in a mouse model of amyotrophic lateral sclerosis E Kabashi, JN Agar, DM Taylor, S Minotti, HD Durham Journal of neurochemistry 89 (6), 1325-1335, 2004	183	2004
Mutations in FUS cause FALS and SALS in French and French Canadian populations VV Belzil, PN Valdmanis, PA Dion, H Daoud, E Kabashi, A Noreau, ... Neurology 73 (15), 1176-1179, 2009	178	2009
Oxidized/misfolded superoxide dismutase‐1: the cause of all amyotrophic lateral sclerosis? E Kabashi, PN Valdmanis, P Dion, GA Rouleau Annals of Neurology: Official Journal of the American Neurological …, 2007	178	2007
Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD) S Lattante, S Ciura, GA Rouleau, E Kabashi Trends in Genetics 31 (5), 263-273, 2015	148	2015
Zebrafish models for the functional genomics of neurogenetic disorders E Kabashi, E Brustein, N Champagne, P Drapeau Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1812 (3), 335-345, 2011	143	2011
Pharmacological reduction of ER stress protects against TDP-43 neuronal toxicity in vivo A Vaccaro, SA Patten, D Aggad, C Julien, C Maios, E Kabashi, P Drapeau, ... Neurobiology of disease 55, 64-75, 2013	142	2013
ATXN2 trinucleotide repeat length correlates with risk of ALS W Sproviero, A Shatunov, D Stahl, M Shoai, W van Rheenen, AR Jones, ... Neurobiology of aging 51, 178. e1-178. e9, 2017	113	2017
Methylene Blue Protects against TDP-43 and FUS Neuronal Toxicity in C. elegans and D. rerio A Vaccaro, SA Patten, S Ciura, C Maios, M Therrien, P Drapeau, ... Public Library of Science 7 (7), e42117, 2012	112	2012
Failure of protein quality control in amyotrophic lateral sclerosis E Kabashi, HD Durham Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1762 (11-12 …, 2006	112	2006
Homozygous TREM2 mutation in a family with atypical frontotemporal dementia I Le Ber, A De Septenville, R Guerreiro, J Bras, A Camuzat, P Caroppo, ... Neurobiology of aging 35 (10), 2419. e23-2419. e25, 2014	107	2014

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