Guy A Rouleau
Overview
Explore the profile of Guy A Rouleau including associated specialties, affiliations and a list of published articles.
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Articles
535
Citations
20382
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Recent Articles
1.
Medeiros M, Pastor-Bernier A, Azizi H, Schmilovich Z, Castonguay C, Savadjiev P, et al.
Mov Disord
. 2025 Mar;
PMID: 40088050
Essential tremor (ET) is a common movement disorder with a strong genetic basis. Magnetic resonance imaging (MRI), particularly diffusion-weighted MRI (dMRI) and T1 MRI, have been used to identify brain...
2.
Dilliott A, Costanzo M, Bandres-Ciga S, Blauwendraat C, Casey B, Hoang Q, et al.
Neurol Genet
. 2025 Feb;
11(2):e200246.
PMID: 39996130
Although large-scale genetic association studies have proven useful for the delineation of neurodegenerative disease processes, we still lack a full understanding of the pathologic mechanisms of these diseases, resulting in...
3.
Vilgalys T, Klunk J, Demeure C, Cheng X, Shiratori M, Madej J, et al.
Nature
. 2025 Feb;
638(8051):E23-E29.
PMID: 39972229
No abstract available.
4.
Demaegd K, Kernan A, Cooper-Knock J, van Vugt J, Harvey C, Moll T, et al.
Eur J Hum Genet
. 2025 Feb;
PMID: 39956874
Spinocerebellar ataxia type 2 (SCA2) and amyotrophic lateral sclerosis (ALS) are both associated with a CAG-repeat expansion in ATXN2 and with TDP-43-positive neuronal cytoplasmic inclusions. The two disorders have been...
5.
Iacoangeli A, Dilliott A, Al Khleifat A, Andersen P, Basak N, Cooper-Knock J, et al.
J Neurol Neurosurg Psychiatry
. 2025 Feb;
PMID: 39947885
Background: Despite several studies suggesting a potential oligogenic risk model in amyotrophic lateral sclerosis (ALS), case-control statistical evidence implicating oligogenicity with disease risk or clinical outcomes is limited. Considering its...
6.
Aboasali F, Castonguay C, Medeiros M, Dion P, Rouleau G
Cerebellum
. 2025 Jan;
24(2):35.
PMID: 39853640
Essential Tremor (ET) is the most common movement disorder and has a worldwide prevalence of 1%, including 5% of the population over 65 years old. It is characterized by an...
7.
OConnell K, Koromina M, van der Veen T, Boltz T, David F, Yang J, et al.
Nature
. 2025 Jan;
PMID: 39843750
Bipolar disorder is a leading contributor to the global burden of disease. Despite high heritability (60-80%), the majority of the underlying genetic determinants remain unknown. We analysed data from participants...
8.
Klunk J, Vilgalys T, Demeure C, Cheng X, Shiratori M, Madej J, et al.
Nature
. 2025 Jan;
637(8048):E30.
PMID: 39814901
No abstract available.
9.
Dy-Hollins M, Chibnik L, Tracy N, Osiecki L, Budman C, Cath D, et al.
Neurology
. 2025 Jan;
104(3):e210249.
PMID: 39813627
Objectives: To analyze sex differences in outcomes in Tourette syndrome (TS) and Persistent Motor or Vocal tic disorders (PMVT) in the Tourette Association of America International Consortium for Genetics (TAAICG)...
10.
Laugwitz L, Buchert R, Olguin P, Estiar M, Atanasova M, Marques Jr W, et al.
Am J Hum Genet
. 2025 Jan;
112(1):168-180.
PMID: 39753114
Inborn errors of selenoprotein expression arise from deleterious variants in genes encoding selenoproteins or selenoprotein biosynthetic factors, some of which are associated with neurodegenerative disorders. This study shows that bi-allelic...