Annie Levert

Montreal, QC, Canada

Last Updated: 09/26/2026

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Found 10 publications

Peripheral blood age-sensitive immune markers in multiple sclerosis: relation to sex, cytomegalovirus status, and treatment.

Peripheral blood age-sensitive immune markers in multiple sclerosis: relation to sex, cytomegalovirus status, and treatment.

Journal: EBioMedicine

Published: August 14, 2024

GM-CSF distinctly impacts human monocytes and macrophages via ERK1/2-dependent pathways.

GM-CSF distinctly impacts human monocytes and macrophages via ERK1/2-dependent pathways.

Journal: Immunology letters

Published: April 27, 2023

Stress Signal ULBP4, an NKG2D Ligand, Is Upregulated in Multiple Sclerosis and Shapes CD8+ T-Cell Behaviors.

Stress Signal ULBP4, an NKG2D Ligand, Is Upregulated in Multiple Sclerosis and Shapes CD8+ T-Cell Behaviors.

Journal: Neurology(R) neuroimmunology & neuroinflammation

Published: August 17, 2021

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.

Journal: Nature communications

Published: August 10, 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

Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy.

Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy.

Journal: EMBO reports

Published: June 15, 2014

Congenital Mirror Movements in a New Italian Family.

Congenital Mirror Movements in a New Italian Family.

Journal: Movement disorders clinical practice

Published: February 15, 2014

SYNE1 mutations in autosomal recessive cerebellar ataxia.

SYNE1 mutations in autosomal recessive cerebellar ataxia.

Journal: JAMA neurology

Published: August 21, 2013

CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjects.

CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjects.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Published: March 06, 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 1-10 of 10

Last Updated: 09/26/2026