Guy A Rouleau

发表

A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family

Jean-Baptiste Rivière, Dominique J Verlaan, Masoud Shekarabi, 2004, Annals of neurology.

Dopamine Beta‐Hydroxylase (DBH) gene and schizophrenia phenotypic variability: A genetic association study

Kenji Yamamoto, Pierre Lalonde, Joel Gelernter, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetics of Intracranial Aneurysms.

Guy A Rouleau, G. Rouleau, P. Dion, 2018, Stroke.

Genetics of familial and sporadic amyotrophic lateral sclerosis.

Guy A Rouleau, G. Rouleau, C. Gaspar, 2006, Biochimica et biophysica acta.

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

Laurent Mottron, Guy A Rouleau, Eric Fombonne, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura

Marie-Pierre Dubé, Olaf Ansorge, Namrata Gupta, 2010, Nature Medicine.

Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients.

Guy A Rouleau, Ute Woehlbier, Robert H. Brown, 2015, Gene.

Disruption at the Ptchd1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability Nih Public Access

Chi-Chung Hui, Andre Franke, Geraldine Dawson, 2010 .

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

Marie-Pierre Dubé, Christian Néri, Marie-Odile Krebs, 2010, Proceedings of the National Academy of Sciences.

High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.

François Dubeau, Guillaume Bourque, Ange-Line Bruel, 2017, American journal of human genetics.

Integrative gene-tissue microarray-based approach for identification of human disease biomarkers: application to amyotrophic lateral sclerosis.

Martina Wiedau-Pazos, Stanislav L Karsten, Guy A Rouleau, 2010, Human molecular genetics.

The emerging role of SMPD1 mutations in Parkinson's disease: Implications for future studies.

Nir Giladi, Guy A Rouleau, Nir Giladi, 2015, Parkinsonism & related disorders.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Jakob Grove, Esben Agerbo, Andres Metspalu, 2017, bioRxiv.

SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function.

Laurent Mottron, Fabio Benfenati, Flavia Valtorta, 2011, Human molecular genetics.

Common variants in P2RY11 are associated with narcolepsy

Christian Gieger, Poul Jennum, Thomas Meitinger, 2010, Nature Genetics.

Loss-of-function de novo mutations play an important role in severe human neural tube defects

Guy A Rouleau, Dan Spiegelman, G. Rouleau, 2015, Journal of Medical Genetics.