De novo mutations in neurological and psychiatric disorders: effects, diagnosis and prevention

por Gauthier, Julie, Rouleau, Guy A
Publicado 2012

The ongoing dissection of the genetic architecture of autistic spectrum disorder

por Gillis, Rob F, Rouleau, Guy A
Publicado 2011

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

por Julie, Gauthier, Hamdan, Fadi F., Rouleau, Guy A.
Publicado 2011

MEIS1 and Restless Legs Syndrome: A Comprehensive Review

por Sarayloo, Faezeh, Dion, Patrick A., Rouleau, Guy A.
Publicado 2019

Progress in the genetics of restless legs syndrome: the path ahead in the era of whole-genome sequencing

por Akçimen, Fulya, Dion, Patrick A, Rouleau, Guy A
Publicado 2022

Amyotrophic lateral sclerosis: new genes, new models, and new mechanisms

por Vande Velde, Christine, Dion, Patrick A., Rouleau, Guy A.
Publicado 2011

Exome sequencing in genetic disease: recent advances and considerations

por Ross, Jay P., Dion, Patrick A., Rouleau, Guy A.
Publicado 2020

Systematic review of autosomal recessive ataxias and proposal for a classification

por Beaudin, Marie, Klein, Christopher J., Rouleau, Guy A., Dupré, Nicolas
Publicado 2017

Synapsin II Is Involved in the Molecular Pathway of Lithium Treatment in Bipolar Disorder

por Cruceanu, Cristiana, Alda, Martin, Grof, Paul, Rouleau, Guy A., Turecki, Gustavo
Publicado 2012

Deletion of C9ORF72 Results in Motor Neuron Degeneration and Stress Sensitivity in C. elegans

por Therrien, Martine, Rouleau, Guy A., Dion, Patrick A., Parker, J. Alex
Publicado 2013

FET proteins regulate lifespan and neuronal integrity

por Therrien, Martine, Rouleau, Guy A., Dion, Patrick A., Parker, J. Alex
Publicado 2016

Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1–LGI1 signaling

por Thomas, Rhalena A., Ambalavanan, Amirthagowri, Rouleau, Guy A., Barker, Philip A.
Publicado 2016

The Impact of Phenotypic and Genetic Heterogeneity on Results of Genome Wide Association Studies of Complex Diseases

por Manchia, Mirko, Cullis, Jeffrey, Turecki, Gustavo, Rouleau, Guy A., Uher, Rudolf, Alda, Martin
Publicado 2013

Increased Prevalence of Non-motor Symptoms in Essential Tremor

por Lacerte, Annie, Chouinard, Sylvain, Jodoin, Nicolas, Bernard, Geneviève, Rouleau, Guy A., Panisset, Michel
Publicado 2014

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

por Chaumette, Boris, Kebir, Oussama, Dion, Patrick A., Rouleau, Guy A., Krebs, Marie-Odile
Publicado 2020

Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes

por Dilliott, Allison A, Kwon, Seulki, Rouleau, Guy A, Iqbal, Sumaiya, Farhan, Sali M K
Publicado 2023

FUS and TARDBP but Not SOD1 Interact in Genetic Models of Amyotrophic Lateral Sclerosis

por Kabashi, Edor, Bercier, Valérie, Lissouba, Alexandra, Liao, Meijiang, Brustein, Edna, Rouleau, Guy A., Drapeau, Pierre
Publicado 2011

Comparison of Sequencing Based CNV Discovery Methods Using Monozygotic Twin Quartets

por Legault, Marc-André, Girard, Simon, Lemieux Perreault, Louis-Philippe, Rouleau, Guy A., Dubé, Marie-Pierre
Publicado 2015

Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellum

por Noreau, Anne, Beauchemin, Philippe, Dionne-Laporte, Alexandre, Dion, Patrick A, Rouleau, Guy A, Dupré, Nicolas
Publicado 2014

Screening of novel restless legs syndrome–associated genes in French-Canadian families

por Akçimen, Fulya, Spiegelman, Dan, Dionne-Laporte, Alexandre, Gan-Or, Ziv, Dion, Patrick A., Rouleau, Guy A.
Publicado 2018