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Patrick A Dion

Showing results (41-50 of 188) with videos related to

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Nature Communications|October 3, 2019
Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypesCalwing Liao, Alexandre D Laporte, Dan Spiegelman, et al.
Neurobiology of Disease|April 10, 2007
Soluble expanded PABPN1 promotes cell death in oculopharyngeal muscular dystrophyChristiane Messaed, Patrick A Dion, Aida Abu-Baker, et al.
BMC Medicine|November 2, 2022
Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization studyParia Alipour, Konstantin Senkevich, Jay P Ross, et al.
Neurology. Genetics|April 29, 2016
De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopiaClaire S Leblond, Alina Webber, Ziv Gan-Or, et al.
European Journal of Human Genetics : EJHG|November 22, 2012
Analysis of the effects of rare variants on splicing identifies alterations in GABAA receptor genes in autism spectrum disorder individualsAmélie Piton, Loubna Jouan, Daniel Rochefort, et al.
Plos One|March 2, 2013
Comparative analysis of the expression profile of Wnk1 and Wnk1/Hsn2 splice variants in developing and adult mouse tissuesMasoud Shekarabi, Ron G Lafrenière, Rébecca Gaudet, et al.
Parkinsonism & Related Disorders|October 28, 2018
Investigating the association and causal relationship between restless legs syndrome and essential tremorCalwing Liao, Gabrielle Houle, Qin He, et al.
European Journal of Human Genetics : EJHG|June 24, 2020
SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndromeFaezeh Sarayloo, Dan Spiegelman, Daniel Rochefort, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|May 28, 2016
KCC3 axonopathy: neuropathological features in the central and peripheral nervous systemRoland N Auer, Janet L Laganière, Yves O Robitaille, et al.
Communications Biology|July 12, 2020
Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genesFulya Akçimen, Faezeh Sarayloo, Calwing Liao, et al.
Pageof 19

Showing results (41-50 of 188) with videos related to

Sort By:
Pageof 19
Nature Communications|October 3, 2019
Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypesCalwing Liao, Alexandre D Laporte, Dan Spiegelman, et al.
Neurobiology of Disease|April 10, 2007
Soluble expanded PABPN1 promotes cell death in oculopharyngeal muscular dystrophyChristiane Messaed, Patrick A Dion, Aida Abu-Baker, et al.
BMC Medicine|November 2, 2022
Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization studyParia Alipour, Konstantin Senkevich, Jay P Ross, et al.
Neurology. Genetics|April 29, 2016
De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopiaClaire S Leblond, Alina Webber, Ziv Gan-Or, et al.
European Journal of Human Genetics : EJHG|November 22, 2012
Analysis of the effects of rare variants on splicing identifies alterations in GABAA receptor genes in autism spectrum disorder individualsAmélie Piton, Loubna Jouan, Daniel Rochefort, et al.
Plos One|March 2, 2013
Comparative analysis of the expression profile of Wnk1 and Wnk1/Hsn2 splice variants in developing and adult mouse tissuesMasoud Shekarabi, Ron G Lafrenière, Rébecca Gaudet, et al.
Parkinsonism & Related Disorders|October 28, 2018
Investigating the association and causal relationship between restless legs syndrome and essential tremorCalwing Liao, Gabrielle Houle, Qin He, et al.
European Journal of Human Genetics : EJHG|June 24, 2020
SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndromeFaezeh Sarayloo, Dan Spiegelman, Daniel Rochefort, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|May 28, 2016
KCC3 axonopathy: neuropathological features in the central and peripheral nervous systemRoland N Auer, Janet L Laganière, Yves O Robitaille, et al.
Communications Biology|July 12, 2020
Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genesFulya Akçimen, Faezeh Sarayloo, Calwing Liao, et al.
Pageof 19