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Patrick A. Dion
Patrick A. Dion
Verified email at mcgill.ca
Title
Cited by
Year
A single-cell eQTL atlas of the human cerebellum reveals vulnerability of oligodendrocytes in essential tremor
G Rouleau, CE Castonguay, F Aboasali, M Medeiros, T Becret, ...
2024
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability
Z Schmilovich, VR Bourque, E Douard, G Huguet, C Poulain, JP Ross, ...
Frontiers in Psychiatry 15, 1369767, 2024
2024
Brain Imaging Phenotypes Associated With Polygenic Risk For Essential Tremor
M Medeiros, A Pastor-Bernier, H Azizi, Z Schmilovich, CE Castonguay, ...
medRxiv, 2024.07. 16.24310501, 2024
2024
A single-cell eQTL atlas of the human cerebellum reveals vulnerability of oligodendrocytes in essential tremor
CE Castonguay, F Aboasali, M Medeiros, T Becret, Z Schmilovich, ...
bioRxiv, 2024.05. 22.595233, 2024
2024
Transcriptomic and epigenomic consequences of heterozygous loss of function mutations in AKAP11, the first large-effect shared risk gene for bipolar disorder and schizophrenia
N Farhangdoost, C Liao, Y Liu, M Alda, PA Dion, G Rouleau, A Khayachi, ...
bioRxiv, 2024.03. 14.584883, 2024
2024
Single-nucleus RNA-sequencing of the cerebellar cortex reveals oligodendrocytes as underlying disease risk in essential tremor
CE Castonguay, F Aboasali, T Becret, M Medeiros, A Rajput, P Dion, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 502-503, 2024
2024
Convergence of bipolar disorder treatments and gene knockdown on the transcriptome
V Vuokila, CE Castonguay, N Farhangdoost, A Khayachi, C Liao, P Dion, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 215-216, 2024
2024
Exploring the utility of a multi-polygenic risk score to capture the common genetic architecture of autism spectrum disorder
Z Schmilovich, R Bourque, G Huguet, J Ross, S Jacquemont, P Dion, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 501-502, 2024
2024
rare copy number variants in CACNA1H implicated in essential tremor
M Medeiros, C Liao, D Spiegelman, A Dilliott, J Ross, S Farhan, P Dion, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 202-203, 2024
2024
De novo variant analysis of childhood-onset obsessive-compulsive disorder in the French-Canadian population
K Bornais, J Ross, Z Schmilovich, M Medeiros, D Spiegelman, P Dion, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 196-196, 2024
2024
Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome
JP Ross, F Akçimen, C Liao, K Kwan, DE Phillips, Z Schmilovich, ...
Genetics in Medicine 26 (1), 100967, 2024
2024
Genomic analysis identifies risk factors in restless legs syndrome
F Akçimen, R Chia, S Saez‐Atienzar, P Ruffo, M Rasheed, JP Ross, ...
Annals of Neurology, 2023
2023
Exploring ALS differential vulnerability using single-cell transcriptomic analysis
P Alipour, P Dion, G Rouleau, J Ross
Journal of the Neurological Sciences 455, 2023
2023
Huntington's disease in an African family
D Kombate, D Rochefort, A Ephoévi-Ga, H Catoire, P Waklatsi, P Dion, ...
Journal of the Neurological Sciences 455, 2023
2023
Cerebellar oligodendrocytes as key initial players in essential tremor pathophysiology
CE Castonguay, F Aboasali, T Becret, M Medeiros, D Rochefort, A Rajput, ...
Journal of the Neurological Sciences 455, 2023
2023
De novo variant analysis of childhood-onset obsessive-compulsive disorder in the French-Canadian population
K Bornais, J Ross, Z Schmilovich, M Medeiros, D Spiegelman, P Dion, ...
Journal of the Neurological Sciences 455, 2023
2023
Restless legs syndrome drug discovery using A C. elegans model
RDB Oliveira, P Dion, A Parker, G Rouleau
Journal of the Neurological Sciences 455, 2023
2023
CRISPR/CAS9 system corrects PABPN1 mutation in oculopharyngeal muscular dystrophy
A Abu-Baker, D Rochefort, P Dion, G Rouleau
Journal of the Neurological Sciences 455, 2023
2023
CACNA1A mutations in essential tremor lead to dysregulation of neuron exocytosis machinery
F Aboasali, CE Castonguay, G Houle, D Rochefort, P Dion, G Rouleau
Journal of the Neurological Sciences 455, 2023
2023
Convergence of bipolar disorder treatments and gene knockdown on the transcriptome
V Vuokila, CE Castonguay, N Farhangdoost, A Khayachi, C Liao, P Dion, ...
Journal of the Neurological Sciences 455, 2023
2023
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