Lang D. Liu

Montreal, QC, Canada

Last Updated: 09/26/2026

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Found 39 publications

Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.

Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.

Journal: Journal of Parkinson's disease

Published: August 06, 2026

Genome-wide association studies identify genetic determinants of synucleinopathy biomarkers.

Genome-wide association studies identify genetic determinants of synucleinopathy biomarkers.

Journal: Research square

Published: July 17, 2026

Rare-Variant Burden Analysis of Dystonia Genes in Parkinson's Disease.

Rare-Variant Burden Analysis of Dystonia Genes in Parkinson's Disease.

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

Published: April 04, 2026

The GBA1 p.E427K (p.E388K) Variant is a Risk Factor for Synucleinopathies: A Meta-Analysis.

The GBA1 p.E427K (p.E388K) Variant is a Risk Factor for Synucleinopathies: A Meta-Analysis.

Journal: medRxiv : the preprint server for health sciences

Published: March 27, 2026

The GBA1 p.E427K (p.E388K) Variant Is a Risk Factor for Synucleinopathies: A Meta-Analysis.

The GBA1 p.E427K (p.E388K) Variant Is a Risk Factor for Synucleinopathies: A Meta-Analysis.

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

Published: March 18, 2026

Episode-state-associated and shared intrinsic functional network patterns in bipolar disorder.

Episode-state-associated and shared intrinsic functional network patterns in bipolar disorder.

Journal: Journal of affective disorders

Published: March 16, 2026

Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's Disease.

Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's Disease.

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

Published: March 10, 2026

Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's disease.

Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's disease.

Journal: medRxiv : the preprint server for health sciences

Published: February 27, 2026

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.

Journal: medRxiv : the preprint server for health sciences

Published: February 12, 2026

Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.

Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.

Journal: medRxiv : the preprint server for health sciences

Published: February 06, 2026

Genome-wide association studies identify genetic determinants of synucleinopathy biomarkers.

Genome-wide association studies identify genetic determinants of synucleinopathy biomarkers.

Journal: medRxiv : the preprint server for health sciences

Published: January 08, 2026

Genetic associations between post-traumatic stress disorder and REM-sleep behavior disorder.

Genetic associations between post-traumatic stress disorder and REM-sleep behavior disorder.

Journal: NPJ Parkinson's disease

Published: November 20, 2025

Showing 1-12 of 39

Last Updated: 09/26/2026