Sandra B. Laurent
Montreal, QC H3T1C5, Canada
Last Updated: 09/26/2026
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Found 26 publications
Lack of epistatic interaction of SNCA with APOE in synucleinopathies.
Journal: Brain communications
Published: August 22, 2024
Novel germline and somatic variants in familial and sporadic meningioma genes.
Journal: NPJ genomic medicine
Published: November 27, 2023
Rare PSAP Variants and Possible Interaction with GBA in REM Sleep Behavior Disorder.
Journal: Journal of Parkinson's disease
Published: October 25, 2021
LRRK2 p.M1646T is associated with glucocerebrosidase activity and with Parkinson's disease.
Journal: Neurobiology of aging
Published: October 07, 2020
Novel Associations of BST1 and LAMP3 With REM Sleep Behavior Disorder.
Journal: Neurology
Published: July 23, 2020
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder.
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 16, 2020
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease.
Journal: Neurobiology of aging
Published: June 26, 2020
Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's disease.
Journal: Neurobiology of aging
Published: March 04, 2020
Oligogenicity, C9orf72 expansion, and variant severity in ALS.
Journal: Neurogenetics
Published: January 17, 2020
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies.
Journal: Annals of neurology
Published: September 03, 2019
Analysis of common and rare VPS13C variants in late-onset Parkinson disease.
Journal: Neurology. Genetics
Published: July 20, 2019
Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies.
Journal: Annals of neurology
Published: August 03, 2018
Last Updated: 09/26/2026