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Valerie Drouet
Valerie Drouet
ICM - Brain and Spine Institute
Verified email at icm-institute.org
Title
Cited by
Cited by
Year
Trans-synaptic spread of tau pathology in vivo
L Liu, V Drouet, JW Wu, MP Witter, SA Small, C Clelland, K Duff
PloS one 7 (2), e31302, 2012
12572012
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
5002016
Sustained effects of nonallele‐specific Huntingtin silencing
V Drouet, V Perrin, R Hassig, N Dufour, G Auregan, S Alves, G Bonvento, ...
Annals of neurology 65 (3), 276-285, 2009
2692009
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing
IE Jansen, H Ye, S Heetveld, MC Lechler, H Michels, RI Seinstra, ...
Genome biology 18 (1), 1-26, 2017
1312017
Unconscious associative memory affects visual processing before 100 ms
M Chaumon, V Drouet, C Tallon-Baudry
Journal of vision 8 (3), 10-10, 2008
1132008
Haemophore‐mediated signalling in Serratia marcescens: a new mode of regulation for an extra cytoplasmic function (ECF) sigma factor involved in haem acquisition
F Biville, H Cwerman, S Létoffé, MS Rossi, V Drouet, JM Ghigo, ...
Molecular microbiology 53 (4), 1267-1277, 2004
992004
A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal‐Recessive Juvenile‐Onset Parkinson's Disease
LEO Elsayed, V Drouet, T Usenko, IN Mohammed, AAAA Hamed, ...
Annals of neurology 79 (2), 335-337, 2016
892016
Allele-specific silencing of mutant huntingtin in rodent brain and human stem cells
V Drouet, M Ruiz, D Zala, M Feyeux, G Auregan, K Cambon, L Troquier, ...
PloS one 9 (6), e99341, 2014
822014
A new F‐box protein 7 gene mutation causing typical Parkinson's disease
E Lohmann, AS Coquel, A Honoré, H Gurvit, H Hanagasi, M Emre, ...
Movement Disorders 30 (8), 1130-1133, 2015
812015
Synaptojanin 1 mutation in Parkinson’s disease brings further insight into the neuropathological mechanisms
V Drouet, S Lesage
BioMed research international 2014, 2014
782014
Evidence that COMT genotype and proline interact on negative-symptom outcomes in schizophrenia and bipolar disorder
CL Clelland, V Drouet, KC Rilett, JA Smeed, RH Nadrich, A Rajparia, ...
Translational psychiatry 6 (9), e891-e891, 2016
512016
Vitamin D insufficiency and schizophrenia risk: evaluation of hyperprolinemia as a mediator of association
JD Clelland, LL Read, V Drouet, A Kelly, KE Duff, RH Nadrich, A Rajparia, ...
Schizophrenia research 156 (1), 15-22, 2014
492014
International Parkinson’s Disease Genomics Consortium (IPDGC) 2016
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
Loss of VPS13C function in autosomal‐recessive Parkinsonism causes …, 0
49*
Mutation analysis of consanguineous Moroccan Patients with Parkinson’s Disease combining Microarray and gene Panel
A Bouhouche, C Tesson, W Regragui, M Rahmani, V Drouet, H Tibar, ...
Frontiers in neurology 8, 567, 2017
282017
Identification of potential new genes involved in autosomal recessive forms of Parkinson's disease: 1113
C Tesson, A Honoré, V Drouet, H Bertrand, S Lesage, A Brice
Movement Disorders 34, 2019
2019
Identification of new genes involved in autosomal dominant forms of Parkinson's disease
C Tesson, C Condroyer, L Ruaud, V Drouet, S Lesage, A Brice
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 295-295, 2019
2019
Gene discovery and prioritization in recessive Parkinson's disease
V Drouet, S Ben Romdhan, J Guegan, J Taeger, E Lohmann, P Heutink, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 26, 409-409, 2018
2018
Allele-Specific Silencing of Mutant Huntingtin in HD Neural Stem Cells and In Vivo
N Deglon, M Ruiz, V Drouet, D Zala, M Feyeux, G Auregan, R Hassig, ...
MOLECULAR THERAPY 20, S30-S30, 2012
2012
Poster# 125 ASSOCIATION OF HYPERPROLINEMIA WITH SCHIZOPHRENIA: IMPLICATIONS FOR THE ETIOLOGY, CLINICAL MANAGEMENT AND TREATMENT OF SCHIZOPHRENIA PATIENTS
CL Clelland, V Drouet, I Orozco, A Kelly, L Liu, R Suckow, LL Read, ...
Schizophrenia Research, S136-S137, 2012
2012
Toward the treatment of Huntington's disease with RNAi
V Drouet, M Ruiz, D Zala, M Feyeux, G Auregan, K Cambon, S Aubert, ...
Collaborative Congress of the European Society of Gene and Cell Therapy …, 2012
2012
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Articles 1–20