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G. Rouleau · SciRah

Researcher profile · Semantic Scholar

G. Rouleau

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G. Rouleau — researcher profile on SciRah

h-index: 128
Works: 847
Citations: 65K

Most-cited papers

Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology
N. Mullins, A. Forstner, K. O’Connell, B. Coombes +313 more
2021Nature Genetics1,030 citations Open access
Semantic Scholar
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
W. van Rheenen, R. V. D. van der Spek, M. Bakker, L. H. van den Berg +188 more
2021Nature Genetics446 citations Open access
Semantic Scholar
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS
P. Hop, R. Zwamborn, E. Hannon, Gemma Shireby +79 more
2022Science Translational Medicine90 citations Open access
Semantic Scholar
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
L. Krohn, K. Heilbron, C. Blauwendraat, R. Reynolds +102 more
2022Nature Communications84 citations Open access
Semantic Scholar
Identification of sixteen novel candidate genes for late onset Parkinson’s disease
A. Gialluisi, M. G. Reccia, N. Modugno, T. Nutile +173 more
2021Molecular Neurodegeneration80 citations Open access
Semantic Scholar
Association of polygenic score for major depression with response to lithium in patients with bipolar disorder
A. Amare, K. Schubert, L. Hou, S. Clark +110 more
2020Molecular Psychiatry78 citations Open access
Semantic Scholar
Life-threatening viral disease in a novel form of autosomal recessive IFNAR2 deficiency in the Arctic
C. J. Duncan, M. K. Skouboe, Sophie Howarth, A. Hollensen +33 more
2022Journal of Experimental Medicine76 citations Open access
Semantic Scholar
Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders
J. Gilley, O. Jackson, M. Pipis, M. Estiar +18 more
2021medRxiv66 citations Open access
Semantic Scholar
Moyamoya Disease Susceptibility Gene RNF213 Regulates Endothelial Barrier Function
Vincent Roy, J. Ross, Rémy Pépin, Sergio Cortez Ghio +13 more
2022Stroke60 citations
Semantic Scholar
Fine-mapping of SNCA in REM sleep behavior disorder and overt synucleinopathies
L. Krohn, R. Y. Wu, K. Heilbron, J. Ruskey +46 more
2020Annals of Neurology57 citations Open access
Semantic Scholar
Evolution of a Human-Specific Tandem Repeat Associated with ALS.
Meredith M. Course, Kathryn Gudsnuk, Samuel N. Smukowski, Kosuke Winston +16 more
2020American Journal of Human Genetics57 citations Open access
Semantic Scholar
Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids
Yoshitaka Tamaki, J. Ross, Paria Alipour, Charles-Etienne Castonguay +9 more
2022bioRxiv51 citations Open access
Semantic Scholar
Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations
Uladzislau Rudakou, E. Yu, L. Krohn, J. Ruskey +12 more
2020medRxiv49 citations Open access
Semantic Scholar
Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease
E. Yu, Uladzislau Rudakou, L. Krohn, K. Mufti +16 more
2020medRxiv46 citations Open access
Semantic Scholar
Exome sequencing in genetic disease: recent advances and considerations
J. Ross, P. Dion, G. Rouleau
2020F1000Research46 citations Open access
Semantic Scholar
Association of Essential Tremor With Novel Risk Loci
C. Liao, Charles-Etienne Castonguay, K. Heilbron, Veikko Vuokila +44 more
2022JAMA Neurology38 citations Open access
Semantic Scholar
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes
Isabel Alfradique-Dunham, Rami Al-ouran, R. von Coelln, C. Blauwendraat +18 more
2021Neurology: Genetics36 citations Open access
Semantic Scholar
Is Persistent Motor or Vocal Tic Disorder a Milder Form of Tourette Syndrome?
K. Claudio-Campos, D. Stevens, S. Koo, A. Valko +27 more
2021Movement Disorders35 citations Open access
Semantic Scholar
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2 and EIF4G1 with Parkinson’s disease
P. Saini, Uladzislau Rudakou, E. Yu, J. Ruskey +16 more
2020medRxiv34 citations Open access
Semantic Scholar
Chronic lithium treatment alters the excitatory/inhibitory balance of synaptic networks and reduces mGluR5–PKC signalling in mouse cortical neurons
A. Khayachi, A. Ase, C. Liao, A. Kamesh +8 more
2021Journal of Psychiatry & Neuroscience27 citations Open access
Semantic Scholar
Characterization of the phenotype with cognitive impairment and protein mislocalization in SCA34
M. Beaudin, L. Sellami, Christian Martel, Lydia Touzel-Deschênes +9 more
2020Neurology: Genetics27 citations Open access
Semantic Scholar
Genetic, structural and clinical analysis of spastic paraplegia 4
P. Varghaei, M. Estiar, S. Ashtiani, S. Veyron +13 more
2021medRxiv25 citations Open access
Semantic Scholar
Assessing non-Mendelian Inheritance in Inherited Axonopathies
Dana M. Bis-Brewer, Z. Gan-or, P. Sleiman, Aixa Rodriguez +62 more
2020Genetics in Medicine24 citations Open access
Semantic Scholar
Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective
Felipe Franco da Graça, T. Peluzzo, L. Bonadia, A. Martinez +9 more
2021Cerebellum21 citations
Semantic Scholar
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies.
C. Liao, M. Moyses-Oliveira, C. de Esch, Riya Bhavsar +15 more
2023Cell Genomics19 citations Open access
Semantic Scholar
TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions.
H. Hijazi, Linda M. Reis, D. Pehlivan, Jonathan A. Bernstein +34 more
2022American Journal of Human Genetics17 citations Open access
Semantic Scholar
Genetics of primary lateral sclerosis
V. Silani, P. Corcia, M. Harms, G. Rouleau +2 more
2020Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration17 citations Open access
Semantic Scholar
Oligogenicity, C9orf72 expansion, and variant severity in ALS
J. Ross, C. Leblond, S. Laurent, D. Spiegelman +5 more
2020Neurogenetics17 citations
Semantic Scholar
The C-BIG Repository: an Institution-Level Open Science Platform
Samir Das, R. Abou-Haidar, Henri Rabalais, Sonia Lai Wing Sun +19 more
2021Neuroinformatics16 citations Open access
Semantic Scholar
Prediction of lithium response using genomic data
William Stone, Abraham Nunes, Kazufumi Akiyama, N. Akula +49 more
2021Scientific Reports16 citations Open access
Semantic Scholar
Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette’s syndrome
C. Liao, Veikko Vuokila, Hélène Catoire, F. Akçimen +5 more
2022Communications Biology15 citations Open access
Semantic Scholar
SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndrome
Faezeh Sarayloo, D. Spiegelman, D. Rochefort, F. Akçimen +3 more
2020European Journal of Human Genetics15 citations Open access
Semantic Scholar
Novel Associations of BST1 and LAMP3 With REM Sleep Behavior Disorder
K. Mufti, E. Yu, Uladzislau Rudakou, L. Krohn +40 more
2021Neurology14 citations Open access
Semantic Scholar
Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar Ataxia
A. Accogli, J. St‐Onge, Nassima Addour-Boudrahem, Joël Lafond-Lapalme +4 more
2020Journal of Child Neurology14 citations
Semantic Scholar
Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases
W. M. Alenezi, Caitlin T. Fierheller, C. Serruya, T. Revil +15 more
2023Frontiers in Oncology13 citations Open access
Semantic Scholar
Hereditary spastic paraplegia initially diagnosed as cerebral palsy
O. Suchowersky, S. Ashtiani, P. Au, Scott A McLeod +3 more
2021Clinical Parkinsonism & Related Disorders13 citations Open access
Semantic Scholar
Polygenic scores differentially predict developmental trajectories of subtypes of social withdrawal in childhood.
G. Morneau-Vaillancourt, T. Andlauer, I. Ouellet-Morin, S. Paquin +13 more
2021Journal of Child Psychology and Psychiatry and Allied Disciplines13 citations
Semantic Scholar
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid‐Eye‐Movement Sleep Behavior Disorder
K. Mufti, Uladzislau Rudakou, E. Yu, L. Krohn +38 more
2020Movement Disorders13 citations Open access
Semantic Scholar
GCH1 mutations in hereditary spastic paraplegia
P. Varghaei, G. Yoon, M. Estiar, S. Veyron +5 more
2021medRxiv12 citations Open access
Semantic Scholar
Genome-wide association study of intracranial aneurysms 1 reveals 17 risk loci , polygenic architecture , genetic overlap 2 with clinical risk factors , and opportunities for prevention
M. Bakker, R. V. D. van der Spek, W. van Rheenen, S. Morel +56 more
202112 citations
Semantic Scholar
Machine learning analysis of exome trios to contrast the genomic architecture of autism and schizophrenia
Sameer Sardaar, B. Qi, A. Dionne-Laporte, G. Rouleau +2 more
2020BMC Psychiatry12 citations Open access
Semantic Scholar
A potential role for Zinc in Restless Legs Syndrome.
Pan Chen, J. Bornhorst, S. Patton, K. Bagai +12 more
2020Sleep12 citations Open access
Semantic Scholar
Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project
F. Akçimen, J. Ross, C. Liao, D. Spiegelman +2 more
2020Movement Disorders12 citations
Semantic Scholar
Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor
C. Liao, Faezeh Sarayloo, Veikko Vuokila, D. Rochefort +9 more
2020Frontiers in Genetics12 citations Open access
Semantic Scholar
Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor
Charles-Etienne Castonguay, C. Liao, A. Khayachi, Yu-Min Liu +5 more
2022npj Genomic Medicine11 citations Open access
Semantic Scholar
Intracranial Aneurysm Classifier Using Phenotypic Factors: An International Pooled Analysis
S. Morel, I. Hostettler, Georg R. Spinner, R. Bourcier +54 more
2022Journal of Personalized Medicine11 citations Open access
Semantic Scholar
The Genetic and Molecular Analyses of RAD51C and RAD51D Identifies Rare Variants Implicated in Hereditary Ovarian Cancer from a Genetically Unique Population
W. M. Alenezi, L. Milano, Caitlin T. Fierheller, C. Serruya +17 more
2022Cancers11 citations Open access
Semantic Scholar
Reversibility and Therapeutic Development for Neurodevelopmental Disorders, Insights from Genetic Animal Models.
P. Megagiannis, Rahul Suresh, G. Rouleau, Yang Zhou
2022Advanced Drug Delivery Reviews11 citations
Semantic Scholar
Rapid Generation of Ventral Spinal Cord-like Astrocytes from Human iPSCs for Modeling Non-Cell Autonomous Mechanisms of Lower Motor Neuron Disease
Vincent Soubannier, M. Chaineau, Lale Gursu, Ghazal Haghi +4 more
2021bioRxiv11 citations Open access
Semantic Scholar
Lack of Causal Effects or Genetic Correlation between Restless Legs Syndrome and Parkinson’s Disease
M. Estiar, K. Senkevich, E. Yu, P. Varghaei +5 more
2021medRxiv11 citations Open access
Semantic Scholar

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