Publications by authors named "Sandra B Laurent"

Claim this Profile
L
Lack of epistatic interaction of with in synucleinopathies.
Prabhjyot Saini, Eric Yu, Mehrdad A Estiar, Lynne Krohn, Kheireddin Mufti, Sandra B Laurent

Brain Commun· December 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel germline and somatic variants in familial and sporadic meningioma genes.
Bouchra Ouled Amar Bencheikh, Allison A Dilliott, Julie Gauthier, Sandra Beatrice Laurent, Amirthagowri Ambalavanan

NPJ Genom Med· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rare PSAP Variants and Possible Interaction with GBA in REM Sleep Behavior Disorder.
Yuri L Sosero, Eric Yu, Mehrdad A Estiar, Lynne Krohn, Kheireddin Mufti, Sandra B Laurent

J Parkinsons Dis· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
LRRK2 p.M1646T is associated with glucocerebrosidase activity and with Parkinson's disease.
Yuri L Sosero, Eric Yu, Lynne Krohn, Uladzislau Rudakou, Kheireddin Mufti, Sandra B Laurent

Neurobiol Aging· July 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease.
Prabhjyot Saini, Uladzislau Rudakou, Eric Yu, Jennifer A Ruskey, Farnaz Asayesh, Sandra B Laurent

Neurobiol Aging· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel Associations of and With REM Sleep Behavior Disorder.
Kheireddin Mufti, Eric Yu, Uladzislau Rudakou, Lynne Krohn, Jennifer A Ruskey, Sandra B Laurent

Neurology· March 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder.
Kheireddin Mufti, Uladzislau Rudakou, Eric Yu, Lynne Krohn, Jennifer A Ruskey, Sandra B Laurent

Mov Disord· January 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's disease.
Bouchra Ouled Amar Bencheikh, Konstantin Senkevich, Uladzislau Rudakou, Eric Yu, Kheireddin Mufti, Sandra B Laurent

Neurobiol Aging· September 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Oligogenicity, C9orf72 expansion, and variant severity in ALS.
Jay P Ross, Claire S Leblond, Sandra B Laurent, Dan Spiegelman, Alexandre Dionne-Laporte

Neurogenetics· July 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies.
Lynne Krohn, Richard Y J Wu, Karl Heilbron, Jennifer A Ruskey, Sandra B Laurent

Ann Neurol· April 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Analysis of common and rare variants in late-onset Parkinson disease.
Uladzislau Rudakou, Jennifer A Ruskey, Lynne Krohn, Sandra B Laurent, Dan Spiegelman

Neurol Genet· February 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies.
Lynne Krohn, Tuğba Nur Öztürk, Benoît Vanderperre, Bouchra Ouled Amar Bencheikh, Jennifer A Ruskey, Sandra B Laurent

Ann Neurol· January 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor Cases.
Jean-François Schmouth, Gabrielle Houle, Amirthagowri Ambalavanan, Claire S Leblond, Dan Spiegelman, Sandra B Laurent

Mol Neurobiol· June 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease.
Roy N Alcalay, Victoria Mallett, Benoît Vanderperre, Omid Tavassoly, Yves Dauvilliers, Sandra B Laurent

Mov Disord· April 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Common and rare GCH1 variants are associated with Parkinson's disease.
Uladzislau Rudakou, Bouchra Ouled Amar Bencheikh, Jennifer A Ruskey, Lynne Krohn, Sandra B Laurent

Neurobiol Aging· January 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder.
Jiao Li, Jennifer A Ruskey, Isabelle Arnulf, Yves Dauvilliers, Michele T M Hu, Sandra B Laurent

Mov Disord· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
No rare deleterious variants from , , and are associated with essential tremor.
Gabrielle Houle, Amirthagowri Ambalavanan, Jean-François Schmouth, Claire S Leblond, Dan Spiegelman, Sandra B Laurent

Neurol Genet· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population.
Gabrielle Houle, Jean-François Schmouth, Claire S Leblond, Amirthagowri Ambalavanan, Dan Spiegelman, Sandra B Laurent

Mov Disord· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder.
Ziv Gan-Or, Noreen Mohsin, Simon L Girard, Jacques Y Montplaisir, Amirthagowri Ambalavanan, Sandra B Laurent

Neurobiol Aging· July 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Ziv Gan-Or, Naima Bouslam, Nazha Birouk, Alexandra Lissouba, Daniel B Chambers, Sandra B Laurent

Am J Hum Genet· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Ziv Gan-Or, Naima Bouslam, Nazha Birouk, Alexandra Lissouba, Daniel B Chambers, Sandra B Laurent

Am J Hum Genet· May 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis.
Claire S Leblond, Ziv Gan-Or, Dan Spiegelman, Sandra B Laurent, Anna Szuto

Neurobiol Aging· January 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations.
Dominique J Verlaan, Sandra B Laurent, Daniel L Rochefort, Christina L Liquori, Douglas A Marchuk

Ann Neurol· May 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation.
Nicolas Dupré, Dominique J Verlaan, Collette K Hand, Sandra B Laurent, Gustavo Turecki

Can J Neurol Sci· May 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis