MEIS1 and Restless Legs Syndrome: A Comprehensive Review

by Faezeh Sarayloo, Faezeh Sarayloo, Patrick A. Dion, Patrick A. Dion, Guy A. Rouleau, Guy A. Rouleau
Published 2019-08-01

Exome sequencing in genetic disease: recent advances and considerations [version 1; peer review: 2 approved]

by Jay P. Ross, Patrick A. Dion, Guy A. Rouleau
Published 2020-05-01

Synapsin II is involved in the molecular pathway of lithium treatment in bipolar disorder.

by Cristiana Cruceanu, Martin Alda, Paul Grof, Guy A Rouleau, Gustavo Turecki
Published 2012-01-01

Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C. elegans.

by Martine Therrien, Guy A Rouleau, Patrick A Dion, J Alex Parker
Published 2013-01-01

Reliability and correlation of mixture cell correction in methylomic and transcriptomic blood data

by Boris Chaumette, Oussama Kebir, Patrick A. Dion, Guy A. Rouleau, Marie-Odile Krebs
Published 2020-02-01

The impact of phenotypic and genetic heterogeneity on results of genome wide association studies of complex diseases.

by Mirko Manchia, Jeffrey Cullis, Gustavo Turecki, Guy A Rouleau, Rudolf Uher, Martin Alda
Published 2013-01-01

Increased Prevalence of Non-Motor Symptoms in Essential Tremor

by Annie Lacerte, Sylvain Chouinard, Nicolas Jodoin, Genevieve Bernard, Guy A. Rouleau, Michel Panisset
Published 2014-09-01

Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor

by Calwing Liao, Calwing Liao, Faezeh Sarayloo, Faezeh Sarayloo, Veikko Vuokila, Daniel Rochefort, Fulya Akçimen, Fulya Akçimen, Simone Diamond, Gabrielle Houle, Gabrielle Houle, Alexandre D. Laporte, Dan Spiegelman, Qin He, Hélène Catoire, Patrick A. Dion, Patrick A. Dion, Guy A. Rouleau, Guy A. Rouleau, Guy A. Rouleau
Published 2020-07-01

Machine learning analysis of exome trios to contrast the genomic architecture of autism and schizophrenia

by Sameer Sardaar, Bill Qi, Alexandre Dionne-Laporte, Guy. A. Rouleau, Reihaneh Rabbany, Yannis J. Trakadis
Published 2020-02-01

FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis.

by Edor Kabashi, Valérie Bercier, Alexandra Lissouba, Meijiang Liao, Edna Brustein, Guy A Rouleau, Pierre Drapeau
Published 2011-08-01

Comparison of sequencing based CNV discovery methods using monozygotic twin quartets.

by Marc-André Legault, Simon Girard, Louis-Philippe Lemieux Perreault, Guy A Rouleau, Marie-Pierre Dubé
Published 2015-01-01

Cross-talk between canonical Wnt signaling and the sirtuin-FoxO longevity pathway to protect against muscular pathology induced by mutant PABPN1 expression in C. elegans

by Matthieu Y. Pasco, Hélène Catoire, J. Alex Parker, Bernard Brais, Guy A. Rouleau, Christian Néri
Published 2010-06-01

Investigation of the RFC1 Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations

by Fulya Akçimen, Fulya Akçimen, Jay P. Ross, Jay P. Ross, Cynthia V. Bourassa, Calwing Liao, Calwing Liao, Daniel Rochefort, Maria Thereza Drumond Gama, Marie-Josée Dicaire, Orlando G. Barsottini, Bernard Brais, Bernard Brais, Bernard Brais, José Luiz Pedroso, Patrick A. Dion, Patrick A. Dion, Guy A. Rouleau, Guy A. Rouleau, Guy A. Rouleau
Published 2019-11-01

Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes

by Calwing Liao, Alexandre D. Laporte, Dan Spiegelman, Fulya Akçimen, Ridha Joober, Patrick A. Dion, Guy A. Rouleau
Published 2019-10-01

Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype

by Mehrdad A. Estiar, Etienne Leveille, Dan Spiegelman, Nicolas Dupre, Jean-François Trempe, Guy A. Rouleau, Ziv Gan‐Or
Published 2020-03-01

Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1 Características clínicas e moleculares de uma família Brasileira com ataxia espinoce...

by Iscia Lopes-Cendes, Carlos E. Steiner, Isabel Silveira, Walter Pinto-Junior, Jayme A. Maciel, Guy A. Rouleau
Published 1996-09-01

WNK1/HSN2 mutation in human peripheral neuropathy deregulates KCC2 expression and posterior lateral line development in zebrafish (Danio rerio).

by Valérie Bercier, Edna Brustein, Meijiang Liao, Patrick A Dion, Ronald G Lafrenière, Guy A Rouleau, Pierre Drapeau
Published 2013-01-01

Soluble expanded PABPN1 promotes cell death in oculopharyngeal muscular dystrophy

by Christiane Messaed, Patrick A. Dion, Aida Abu-Baker, Daniel Rochefort, Janet Laganiere, Bernard Brais, Guy A. Rouleau
Published 2007-06-01

Comparative analysis of the expression profile of Wnk1 and Wnk1/Hsn2 splice variants in developing and adult mouse tissues.

by Masoud Shekarabi, Ron G Lafrenière, Rébecca Gaudet, Janet Laganière, Martin M Marcinkiewicz, Patrick A Dion, Guy A Rouleau
Published 2013-01-01

Potassium-chloride cotransporter 3 interacts with Vav2 to synchronize the cell volume decrease response with cell protrusion dynamics.

by Adèle Salin-Cantegrel, Masoud Shekarabi, Sarah Rasheed, François M Charron, Janet Laganière, Rebecca Gaudet, Patrick A Dion, Jean-Yves Lapointe, Guy A Rouleau
Published 2013-01-01