Guy A. Rouleau

发表

Faculty Opinions recommendation of A machine-learning approach for accurate detection of copy number variants from exome sequencing.

Guy A. Rouleau, G. Rouleau, 2020 .

The Project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

Naomi R. Wray, Mamede de Carvalho, Blaz Koritnik, 2018, bioRxiv.

Comprehensive Research Synopsis and Systematic Meta-Analyses in ALS Genetics: The ALSGene Database (P01.095)

Lars Bertram, Christina M. Lill, Ammar Al-Chalabi, 2012 .

Genome-wide association study in essential tremor identifies three new loci

Dietrich Haubenberger, Mark Hallett, Günther Deuschl, 2016, Brain : a journal of neurology.

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

Wei-Yang Lu, Guy A. Rouleau, Lionel Carmant, 2002, Nature Genetics.

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

Laurent Mottron, Ann Marie Craig, Marie-Odile Krebs, 2011, Human Genetics.

SOD1 mutation is assosiated with accumulation of neurofilaments in amyotrophic lateral scelaries

Guy A. Rouleau, Jean-Pierre Julien, A. Clark, 1996 .

The case for locus-specific databases

Guy A. Rouleau, Mark E. Samuels, 2011, Nature Reviews Genetics.

Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report

Naomi R. Wray, Mark A. Frye, Alessio Squassina, 2013, PloS one.

Comparison of Sequencing Based CNV Discovery Methods Using Monozygotic Twin Quartets

Marie-Pierre Dubé, Marc-André Legault, Guy A. Rouleau, 2015, PloS one.

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2

Georg Auburger, Iscia Lopes-Cendes, Julie R. Korenberg, 1996, Nature Genetics.

Inhibition of the kinase WNK1/HSN2 ameliorates neuropathic pain by restoring GABA inhibition

Clifford J. Woolf, Guy A. Rouleau, G. Rouleau, 2016, Science Signaling.

A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing

Edouard Henrion, Julie Hussin, Carlos D. Bustamante, 2011, PLoS genetics.

De Novo Mutations in Moderate or Severe Intellectual Disability

Edouard Henrion, Guy A. Rouleau, Fadi F. Hamdan, 2014, PLoS genetics.

Human monogenic disorders — a source of novel drug targets

Marie-Pierre Dubé, Ryan R. Brinkman, Guy A. Rouleau, 2006, Nature Reviews Genetics.

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments

Elodie Ey, Thomas Bourgeron, Roberto Toro, 2014, PLoS genetics.

Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis

Jean-Pierre Bouchard, Mamede de Carvalho, Denis Brunet, 2016, Neurobiology of Aging.

Sequencing of the GBA coactivator, Saposin C, in Parkinson disease

Yves Dauvilliers, Edward A. Fon, Guy A. Rouleau, 2018, Neurobiology of Aging.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Probing the lithium-response pathway in hiPSCs implicates the phosphoregulatory set-point for a cytoskeletal modulator in bipolar pathogenesis

Dongmei Wu, Jeffrey H. Price, Guang Chen, 2017, Proceedings of the National Academy of Sciences.

Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture

Benjamin D. Greenberg, Ying Wang, Naomi R. Wray, 2013, PLoS genetics.