P. Hince

发表

Exome sequencing identifies FUS mutations as a cause of essential tremor.

G. Rouleau, J. Rivière, M. Panisset, 2012, American journal of human genetics.

Mutations in DCC Cause Congenital Mirror Movements

F. Charron, M. Dubé, G. Rouleau, 2010, Science.

Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and Sweden

P. Andersen, V. Meininger, F. Salachas, 2008, Neurology.

RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population.

G. Rouleau, A. Dionne‐Laporte, D. Spiegelman, 2016, American journal of human genetics.

HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K 1 /Cl 2

G. Rouleau, M. Shekarabi, D. Rochefort, 2008 .

HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3.

G. Rouleau, M. Shekarabi, J. Laganière, 2008, Human molecular genetics.

KCC3 loss-of-function contributes to Andermann syndrome by inducing activity-dependent neuromuscular junction defects

M. Bowerman, J. Bouchard, G. Rouleau, 2017, Neurobiology of Disease.

Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum

M. Lassonde, G. Rouleau, A. Dionne‐Laporte, 2015, European Journal of Human Genetics.

Mutations in FUS cause FALS and SALS in French and French Canadian populations

V. Meininger, F. Salachas, J. Bouchard, 2009, Neurology.

KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2.

A. Mes-Masson, B. Brais, H. Van Esch, 2011, American journal of human genetics.

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.

J. Bouchard, Andrew W. Folkmann, G. Rouleau, 2015, Human molecular genetics.

Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II.

G. Rouleau, J. Rivière, L. Faivre, 2008, The Journal of clinical investigation.

A Mutation that Creates a Pseudoexon in SOD1 Causes Familial ALS

G. Rouleau, P. Couratier, B. Funalot, 2009, Annals of human 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.

Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors

C. Greenwood, M. Alda, G. Rouleau, 2018, Molecular Psychiatry.

Loss of Neuronal Potassium/Chloride Cotransporter 3 (KCC3) Is Responsible for the Degenerative Phenotype in a Conditional Mouse Model of Hereditary Motor and Sensory Neuropathy Associated with Agenesis of the Corpus Callosum

L. Richards, N. Kurniawan, G. Rouleau, 2012, The Journal of Neuroscience.

A polyalanine antibody for the diagnosis of oculopharyngeal muscular dystrophy and polyalanine-related diseases

P. McPherson, G. Rouleau, D. Rochefort, 2017 .

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.

J. Bouchard, Andrew W. Folkmann, G. Rouleau, 2015, Human Molecular Genetics.

Mutations in FUS cause FALS and SALS in French and French Canadian populations

V. Meininger, F. Salachas, J. Bouchard, 2009, Neurology.

Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II.

G. Rouleau, J. Rivière, L. Faivre, 2008, Journal of Clinical Investigation.

Exome sequencing identifies FUS mutations as a cause of essential tremor.

G. Rouleau, J. Rivière, M. Panisset, 2012, American journal of human genetics.