Jay P. Ross

Montreal, QC, Canada

Last Updated: 09/26/2026

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Found 63 publications

Erratum: Consequences of the Novel ALS-Associated KIF5A Variant c.2993-6C>A for Exon 27 Splicing and Axonal Transport of SFPQ.

Erratum: Consequences of the Novel ALS-Associated KIF5A Variant c.2993-6C>A for Exon 27 Splicing and Axonal Transport of SFPQ.

Journal: Neurology. Genetics
Published: July 24, 2026

Generation of two iPSC lines from ALS patients harboring C9orf72 hexanucleotide repeat expansions.

Generation of two iPSC lines from ALS patients harboring C9orf72 hexanucleotide repeat expansions.

Journal: Stem cell research
Published: June 05, 2026

Copy Number Variant Duplications Associated with Essential Tremor.

Copy Number Variant Duplications Associated with Essential Tremor.

Journal: Tremor and other hyperkinetic movements (New York, N.Y.)
Published: November 11, 2025

Polyserine likes the tau and not the label.

Polyserine likes the tau and not the label.

Journal: Neuron
Published: September 10, 2025

Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disorders.

Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disorders.

Journal: BMC medicine
Published: July 29, 2025

KIF5A downregulation in spinal muscular atrophy links axonal regeneration defects with ALS.

KIF5A downregulation in spinal muscular atrophy links axonal regeneration defects with ALS.

Journal: bioRxiv : the preprint server for biology
Published: July 17, 2025

KIF5A downregulation in spinal muscular atrophy links axonal regeneration defects with ALS.

KIF5A downregulation in spinal muscular atrophy links axonal regeneration defects with ALS.

Journal: JCI insight
Published: July 14, 2025

Consequences of the Novel ALS-Associated KIF5A Variant c.2993-6C > A for Exon 27 Splicing and Axonal Transport of SFPQ.

Consequences of the Novel ALS-Associated KIF5A Variant c.2993-6C > A for Exon 27 Splicing and Axonal Transport of SFPQ.

Journal: Neurology. Genetics
Published: May 16, 2025

TARDBP (TDP-43) Knock-in Zebrafish Display a Late-Onset Motor Phenotype and Loss of Large Spinal Cord Motor Neurons.

TARDBP (TDP-43) Knock-in Zebrafish Display a Late-Onset Motor Phenotype and Loss of Large Spinal Cord Motor Neurons.

Journal: Annals of neurology
Published: April 10, 2025

De novo variant analysis of childhood-onset obsessive-compulsive disorder in the French-Canadian population.

De novo variant analysis of childhood-onset obsessive-compulsive disorder in the French-Canadian population.

Journal: Translational psychiatry
Published: September 30, 2024

Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome.

Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome.

Journal: Annals of neurology
Published: February 09, 2024

Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.

Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.

Journal: Frontiers in psychiatry
Published: January 12, 2024
Showing 1-12 of 63

Last Updated: 09/26/2026