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Rochefort, Daniel
123
results:
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Format
Online (122)
Print (1)
Mediatypes
Articles (Online) (69)
OpenAccess-fulltext (53)
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french (2)
english (115)
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1
CACNA1A mutations in essential tremor lead to dysregulation..:
Aboasali, Farah
;
Castonguay, Charles-Etienne
;
Houle, Gabrielle
...
Journal of the Neurological Sciences. 455 (2023) - p. 121727 , 2023
Link:
https://doi.org/10.1016/..
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2
Spinal cord extracts of amyotrophic lateral sclerosis sprea..:
Tamaki, Yoshitaka
;
Ross, Jay P.
;
Alipour, Paria
...
PLOS Genetics. 19 (2023) 2 - p. e1010606 , 2023
Link:
https://doi.org/10.1371/..
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3
Cerebellar oligodendrocytes as key initial players in essen..:
Castonguay, Charles-Etienne
;
Aboasali, Farah
;
Becret, Theodore
...
Journal of the Neurological Sciences. 455 (2023) - p. 121142 , 2023
Link:
https://doi.org/10.1016/..
?
4
Huntington's disease in an African family:
Kombate, Damelan
;
Rochefort, Daniel
;
Ephoévi-Ga, Adadé
...
Journal of the Neurological Sciences. 455 (2023) - p. 121937 , 2023
Link:
https://doi.org/10.1016/..
?
5
CRISPR/CAS9 system corrects PABPN1 mutation in oculopharyng..:
Abu-Baker, Aida
;
Rochefort, Daniel
;
Dion, Patrick
.
Journal of the Neurological Sciences. 455 (2023) - p. 121728 , 2023
Link:
https://doi.org/10.1016/..
?
6
Transcriptomic Changes Resulting From STK32B Overexpression..:
Liao, Calwing
;
Sarayloo, Faezeh
;
Vuokila, Veikko
...
Frontiers in Genetics. 11 (2020) - p. , 2020
Link:
https://doi.org/10.3389/..
?
7
Multiomics Analyses Identify Genes and Pathways Relevant to..:
Liao, Calwing
;
Sarayloo, Faezeh
;
Rochefort, Daniel
...
Movement Disorders. 35 (2020) 7 - p. 1153-1162 , 2020
Link:
https://doi.org/10.1002/..
?
8
SKOR1 has a transcriptional regulatory role on genes involv..:
Sarayloo, Faezeh
;
Spiegelman, Dan
;
Rochefort, Daniel
...
European Journal of Human Genetics. 28 (2020) 11 - p. 1520-1528 , 2020
Link:
https://doi.org/10.1038/..
?
9
Mineral absorption is an enriched pathway in a brain region..:
Sarayloo, Faezeh
;
Dionne-Laporte, Alexandre
;
Catoire, Helene
...
PLOS ONE. 14 (2019) 11 - p. e0225186 , 2019
Link:
https://doi.org/10.1371/..
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10
Investigation of the RFC1 Repeat Expansion in a Canadian an..:
Akçimen, Fulya
;
Ross, Jay P.
;
Bourassa, Cynthia V.
...
Frontiers in Genetics. 10 (2019) - p. , 2019
Link:
https://doi.org/10.3389/..
?
11
A direct interaction between two Restless Legs Syndrome pre..:
Catoire, Helene
;
Sarayloo, Faezeh
;
Mourabit Amari, Karim
...
Scientific Reports. 8 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1038/..
?
12
Exome sequencing of sporadic childhood‐onset schizophrenia ..:
Ambalavanan, Amirthagowri
;
Chaumette, Boris
;
Zhou, Sirui
...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 180 (2018) 6 - p. 335-340 , 2018
Link:
https://doi.org/10.1002/..
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13
A polyalanine antibody for the diagnosis of oculopharyngeal..:
Stochmanski, Shawn J.
;
Blondeau, François
;
Girard, Martine
...
MNI Open Research. 1 (2017) - p. 1 , 2017
Link:
https://doi.org/10.12688..
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14
Deleterious mutations in the essential mRNA metabolism fact..:
Kaneb, Hannah M.
;
Folkmann, Andrew W.
;
Belzil, Véronique V.
...
Human Molecular Genetics. 24 (2014) 5 - p. 1363-1373 , 2014
Link:
https://doi.org/10.1093/..
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15
C9orf72 Repeat Expansions in Rapid Eye Movement Sleep Behav..:
Daoud, Hussein
;
Postuma, Ronald B.
;
Bourassa, Cynthia V.
...
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 41 (2014) 6 - p. 759-762 , 2014
Link:
https://doi.org/10.1017/..
1-15
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