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F1000Research
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May 21, 2020
Exome sequencing in genetic disease: recent advances and considerations
Jay P Ross, Patrick A Dion, Guy A Rouleau
F1000 Biology Reports
|
September 24, 2011
Amyotrophic lateral sclerosis: new genes, new models, and new mechanisms
Christine Vande Velde, Patrick A Dion, Guy A Rouleau
Autophagy
|
July 25, 2015
Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson disease
Ziv Gan-Or, Patrick A Dion, Guy A Rouleau
Human Heredity
|
April 19, 2013
Rare variants in complex traits: novel identification strategies and the role of de novo mutations
Loubna Jouan, Julie Gauthier, Patrick A Dion, et al.
Journal of the Neurological Sciences
|
April 2, 2026
Polygenic and spatial insights into the genetic uniqueness of essential tremor using common variants
Miranda Medeiros, Dylan Gharibian, Patrick A Dion, et al.
The Lancet. Neurology
|
August 31, 2010
Chromosome 9p21 in amyotrophic lateral sclerosis: the plot thickens
Hussein Daoud, Véronique Belzil, Patrick A Dion, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)
|
May 4, 2026
An Exploratory Analysis of Essential Tremor and Associated Phenotypes
Dylan Gharibian, Miranda Medeiros, Patrick A Dion, et al.
Scientific Reports
|
April 28, 2016
FET proteins regulate lifespan and neuronal integrity
Martine Therrien, Guy A Rouleau, Patrick A Dion, et al.
European Journal of Human Genetics : EJHG
|
November 29, 2007
ALS predisposition modifiers: knock NOX, who's there? SOD1 mice still are
Paul N Valdmanis, Edor Kabashi, Patrick A Dion, et al.
Archives of Neurology
|
March 16, 2011
No effect on SOD1 splicing by TARDP or FUS mutations
Véronique V Belzil, Hussein Daoud, Patrick A Dion, et al.
Page
of 19
Search research articles
Search
Showing results (11-20 of 188) with videos related to
Sort By:
Page
of 19
F1000Research
|
May 21, 2020
Exome sequencing in genetic disease: recent advances and considerations
Jay P Ross, Patrick A Dion, Guy A Rouleau
F1000 Biology Reports
|
September 24, 2011
Amyotrophic lateral sclerosis: new genes, new models, and new mechanisms
Christine Vande Velde, Patrick A Dion, Guy A Rouleau
Autophagy
|
July 25, 2015
Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson disease
Ziv Gan-Or, Patrick A Dion, Guy A Rouleau
Human Heredity
|
April 19, 2013
Rare variants in complex traits: novel identification strategies and the role of de novo mutations
Loubna Jouan, Julie Gauthier, Patrick A Dion, et al.
Journal of the Neurological Sciences
|
April 2, 2026
Polygenic and spatial insights into the genetic uniqueness of essential tremor using common variants
Miranda Medeiros, Dylan Gharibian, Patrick A Dion, et al.
The Lancet. Neurology
|
August 31, 2010
Chromosome 9p21 in amyotrophic lateral sclerosis: the plot thickens
Hussein Daoud, Véronique Belzil, Patrick A Dion, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)
|
May 4, 2026
An Exploratory Analysis of Essential Tremor and Associated Phenotypes
Dylan Gharibian, Miranda Medeiros, Patrick A Dion, et al.
Scientific Reports
|
April 28, 2016
FET proteins regulate lifespan and neuronal integrity
Martine Therrien, Guy A Rouleau, Patrick A Dion, et al.
European Journal of Human Genetics : EJHG
|
November 29, 2007
ALS predisposition modifiers: knock NOX, who's there? SOD1 mice still are
Paul N Valdmanis, Edor Kabashi, Patrick A Dion, et al.
Archives of Neurology
|
March 16, 2011
No effect on SOD1 splicing by TARDP or FUS mutations
Véronique V Belzil, Hussein Daoud, Patrick A Dion, et al.
Page
of 19