Pascale Hince

Montreal, QC H3A2B4, Canada

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 8 publications

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

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

Journal: Molecular psychiatry

Published: June 02, 2017

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

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

Journal: Neurobiology of disease

Published: March 21, 2017

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

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

Journal: American journal of human genetics

Published: April 22, 2016

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

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

Journal: Science signaling

Published: March 31, 2016

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

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

Journal: European journal of human genetics : EJHG

Published: January 26, 2015

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

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

Journal: Human molecular genetics

Published: October 26, 2014

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.

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.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience

Published: March 17, 2012

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

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

Journal: American journal of human genetics

Published: February 06, 2012

Showing 1-8 of 8

Last Updated: 09/26/2026