Alexandre Dionne-Laporte
Alexandre Dionne-Laporte
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The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus)
R Ming, S Hou, Y Feng, Q Yu, A Dionne-Laporte, JH Saw, P Senin, ...
Nature 452 (7190), 991-996, 2008
Increased exonic de novo mutation rate in individuals with schizophrenia
SL Girard, J Gauthier, A Noreau, L Xiong, S Zhou, L Jouan, ...
Nature genetics 43 (9), 860-863, 2011
De novo mutations in moderate or severe intellectual disability
FF Hamdan, M Srour, JM Capo-Chichi, H Daoud, C Nassif, L Patry, ...
PLoS Genet 10 (10), e1004772, 2014
Draft genome sequence of the rubber tree Hevea brasiliensis
AYA Rahman, AO Usharraj, BB Misra, GP Thottathil, K Jayasekaran, ...
BMC genomics 14 (1), 1-15, 2013
Exome sequencing identifies FUS mutations as a cause of essential tremor
ND Merner, SL Girard, H Catoire, CV Bourassa, VV Belzil, JB Rivière, ...
The American Journal of Human Genetics 91 (2), 313-319, 2012
Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia
A Boukhris, R Schule, JL Loureiro, CM Lourenço, E Mundwiller, ...
The American Journal of Human Genetics 93 (1), 118-123, 2013
Genetically encoded impairment of neuronal KCC 2 cotransporter function in human idiopathic generalized epilepsy
KT Kahle, ND Merner, P Friedel, L Silayeva, B Liang, A Khanna, Y Shang, ...
EMBO reports 15 (7), 766-774, 2014
Exome sequencing reveals SPG11 mutations causing juvenile ALS
H Daoud, S Zhou, A Noreau, M Sabbagh, V Belzil, A Dionne-Laporte, ...
Neurobiology of aging 33 (4), 839. e5-839. e9, 2012
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
Z Gan-Or, N Bouslam, N Birouk, A Lissouba, DB Chambers, J Vérièpe, ...
The American Journal of Human Genetics 98 (5), 1038-1046, 2016
Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia
T Esteves, A Durr, E Mundwiller, JL Loureiro, M Boutry, MA Gonzalez, ...
The American Journal of Human Genetics 94 (2), 268-277, 2014
De novo variants in sporadic cases of childhood onset schizophrenia
A Ambalavanan, SL Girard, K Ahn, S Zhou, A Dionne-Laporte, ...
European Journal of Human Genetics 24 (6), 944-948, 2016
Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia
M Coutelier, C Goizet, A Durr, F Habarou, S Morais, A Dionne-Laporte, ...
Brain 138 (8), 2191-2205, 2015
Loss-of-function de novo mutations play an important role in severe human neural tube defects
P Lemay, MC Guyot, É Tremblay, A Dionne-Laporte, D Spiegelman, ...
Journal of Medical Genetics 52 (7), 493-497, 2015
Joubert syndrome in French Canadians and identification of mutations in CEP104
M Srour, FF Hamdan, D McKnight, E Davis, H Mandel, J Schwartzentruber, ...
The American Journal of Human Genetics 97 (5), 744-753, 2015
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis
CS Leblond, Z Gan-Or, D Spiegelman, SB Laurent, A Szuto, ...
Neurobiology of aging 37, 209. e17-209. e21, 2016
Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease
JP Ross, N Dupre, Y Dauvilliers, S Strong, A Ambalavanan, ...
Neurobiology of aging 45, 212. e13-212. e17, 2016
RNF213 is associated with intracranial aneurysms in the French-Canadian population
S Zhou, A Ambalavanan, D Rochefort, P Xie, CV Bourassa, P Hince, ...
The American Journal of Human Genetics 99 (5), 1072-1085, 2016
The draft genome of the transgenic tropical fruit tree papaya
R Ming, S Hou, Y Feng, Q Yu, A Dionne-Laporte, JH Saw, P Senin, ...
Carica papaya, 991-996, 0
SMPD1 mutations, activity, and α‐synuclein accumulation in Parkinson's disease
RN Alcalay, V Mallett, B Vanderperre, O Tavassoly, Y Dauvilliers, RYJ Wu, ...
Movement Disorders 34 (4), 526-535, 2019
Global characterization of copy number variants in epilepsy patients from whole genome sequencing
J Monlong, SL Girard, C Meloche, M Cadieux-Dion, DM Andrade, ...
PLoS genetics 14 (4), e1007285, 2018
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