Patrick A. Dion

Montreal, QC, Canada

Last Updated: 09/26/2026

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Found 169 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

Oligogenic variants in NEK1 and ATXN2 in amyotrophic lateral sclerosis: report of two cases and review of the literature.

Oligogenic variants in NEK1 and ATXN2 in amyotrophic lateral sclerosis: report of two cases and review of the literature.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: June 10, 2026

Ancestry-specific and multi-ancestry genome-wide association studies of restless legs syndrome.

Ancestry-specific and multi-ancestry genome-wide association studies of restless legs syndrome.

Journal: medRxiv : the preprint server for health sciences

Published: May 18, 2026

Polygenic and spatial insights into the genetic uniqueness of essential tremor using common variants.

Polygenic and spatial insights into the genetic uniqueness of essential tremor using common variants.

Journal: Journal of the neurological sciences

Published: February 16, 2026

An Exploratory Analysis of Essential Tremor and Associated Phenotypes.

An Exploratory Analysis of Essential Tremor and Associated Phenotypes.

Journal: Tremor and other hyperkinetic movements (New York, N.Y.)

Published: January 19, 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

Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.

Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 24, 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

Lithium partially rescues gene expression and enhancer activity from heterozygous knockout of AKAP11 while inducing novel differential changes.

Lithium partially rescues gene expression and enhancer activity from heterozygous knockout of AKAP11 while inducing novel differential changes.

Journal: Scientific reports

Published: February 26, 2025

Tremor in the Age of Omics: An Overview of the Transcriptomic Landscape of Essential Tremor.

Tremor in the Age of Omics: An Overview of the Transcriptomic Landscape of Essential Tremor.

Journal: Cerebellum (London, England)

Published: January 19, 2025

Gold nanoclusters Au25AcCys18 normalize intracellular ROS without increasing cytoplasmic alarmin acHMGB1 abundance in human microglia and neurons.

Gold nanoclusters Au25AcCys18 normalize intracellular ROS without increasing cytoplasmic alarmin acHMGB1 abundance in human microglia and neurons.

Journal: Nanoscale

Published: November 28, 2024

C9orf72 expansion creates the unstable folate-sensitive fragile site FRA9A.

C9orf72 expansion creates the unstable folate-sensitive fragile site FRA9A.

Journal: bioRxiv : the preprint server for biology

Published: November 21, 2024

Showing 1-12 of 169

Last Updated: 09/26/2026