Guy A. Rouleau

Montreal Neurological Institute and Hospital

MedicineNeuroscienceBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 3%percentile

1.1Author DataRank

Indexed papers

5in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 5 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Sex Differences in Natural History and Health Outcomes Among Individuals With Tic Disorders

Neurology(2025)10.1212/wnl.0000000000210249

Top 39%

0.492DataRank

Top 39%11 citations

Lori B. Chibnik, Natasha Tracy, Lisa Osiecki, Cathy L. Budman, Daniëlle C. Cath +10 more

Papers

Driven by 64 papers — median percentile 56. Top paper: “Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets”.

Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

JAMA Neurology(2021)10.1001/jamaneurol.2020.5257

N/A

4.5DataRank · unranked

205 citations

David Zhang, Sebastian Guelfi, Claudia Manzoni, Leon Hubbard, Regina Hertfelder Reynolds +85 more

BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron disease

Genetics in Medicine(2022)10.1016/j.gim.2022.08.019

N/A

1.0DataRank · unranked

30 citations

Ariel Ruiz, Maike F. Dohrn, Melanie Wayand, Amjad Farooq, Matt C. Danzi +14 more

Evolution of immune genes is associated with the Black Death

Nature(2022)10.1038/s41586-022-05349-x

N/A

0.829DataRank · unranked

251 citations

Tauras P. Vilgalys, Christian E. Demeure, Xiaoheng Cheng, Mari Shiratori, Julien Madej +27 more

Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

Nature Communications(2021)10.1038/s41467-021-26280-1

N/A

0.808DataRank · unranked

217 citations

Demis A. Kia, Mona M. Almramhi, Sara Bandres-Ciga, Chris Finan, Alastair J. Noyce +170 more

Fine‐Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies

Annals of Neurology(2020)10.1002/ana.25687

N/A

0.628DataRank · unranked

65 citations

Richard Y. J. Wu, Karl Heilbron, Jennifer A. Ruskey, Sandra B. Laurent, Cornelis Blauwendraat +45 more

Lithium response in bipolar disorder is associated with focal adhesion and PI3K-Akt networks: a multi-omics replication study

Translational Psychiatry(2024)10.1038/s41398-024-02811-4

N/A

0.613DataRank · unranked

23 citations

Sara Brin Rosenthal, Mazda Adli, Kazufumi Akiyama, Nirmala Akula, Martin Alda +95 more

Synaptic processes and immune-related pathways implicated in Tourette syndrome

Translational Psychiatry(2021)10.1038/s41398-020-01082-z

N/A

0.612DataRank · unranked

58 citations

Dongmei Yu, Jae Hoon Sul, Alden Y. Huang, Cornelia Illmann, Lisa Osiecki +66 more

Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

Nature Genetics(2024)10.1038/s41588-024-01763-1

N/A

0.609DataRank · unranked

57 citations

Chen Zhao, Steven Bell, Maria Didriksen, Muhammad Sulaman Nawaz, Nathalie Schandra +65 more

Targeted sequencing of Parkinson’s disease loci genes highlights SYT11, FGF20 and other associations

Brain(2020)10.1093/brain/awaa401

N/A

0.606DataRank · unranked

56 citations

Eric Yu, Lynne Krohn, Jennifer A. Ruskey, Farnaz Asayesh, Yves Dauvilliers +11 more

Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease

Movement Disorders(2020)10.1002/mds.28299

N/A

0.587DataRank · unranked

49 citations

Uladzislau Rudakou, Lynne Krohn, Kheireddin Mufti, Jennifer A. Ruskey, Farnaz Asayesh +15 more

Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes

Neurology Genetics(2021)10.1212/nxg.0000000000000557

N/A

0.568DataRank · unranked

43 citations

Rami Al‐Ouran, Rainer von Coelln, Cornelis Blauwendraat, Emily J. Hill, Lan Luo +17 more

HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders

Scientific Reports(2021)10.1038/s41598-021-97140-7

N/A

0.556DataRank · unranked

25 citations

Laura Lombardi, Bernhard T. Baune, Azmeraw T. Amare, Klaus Oliver Schubert, Liping Hou +95 more

Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

Biological Psychiatry(2023)10.1016/j.biopsych.2023.01.023

N/A

0.520DataRank · unranked

31 citations

Apostolia Topaloudi, Pritesh Jain, Zhiyu Yang, Dongmei Yu, Petros Kolovos +94 more

C9orf72 repeat expansion creates the unstable folate-sensitive fragile site FRA9A

NAR Molecular Medicine(2024)10.1093/narmme/ugae019

N/A

0.499DataRank · unranked

15 citations

Monika H.M. Schmidt, Natalie Shum, Tanya Prasolava, Bryanna Meikle, Stella Lanni +30 more

Polygenic Scores and Onset of Major Mood or Psychotic Disorders Among Offspring of Affected Parents

American Journal of Psychiatry(2023)10.1176/appi.ajp.20220476

N/A

0.494DataRank · unranked

26 citations

Janice M. Fullerton, Niamh Mullins, Frances Rice, Danella Hafeman, Neeltje E.M. van Haren +29 more

Sex Differences in Natural History and Health Outcomes Among Individuals With Tic Disorders

Neurology(2025)10.1212/wnl.0000000000210249

Top 39%

0.492DataRank

Top 39%11 citations

Lori B. Chibnik, Natasha Tracy, Lisa Osiecki, Cathy L. Budman, Daniëlle C. Cath +10 more

Variants in the Niemann–Pick type C gene NPC1 are not associated with Parkinson's disease

Neurobiology of Aging(2020)10.1016/j.neurobiolaging.2020.03.021

N/A

0.464DataRank · unranked

21 citations

Konstantin Senkevich, Uladzislau Rudakou, Eric Yu, Kheireddin Mufti, Jennifer A. Ruskey +16 more

Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders

Biological Psychiatry(2024)10.1016/j.biopsych.2024.07.025

Top 44%

0.421DataRank

Top 44%13 citations

Matthew Halvorsen, Jakob Grove, Bergrún Ásbjörnsdóttir, Pétur Lúðvígsson, Ólafur Thorarensen +93 more

Immunogenetics of lithium response and psychiatric phenotypes in patients with bipolar disorder

Translational Psychiatry(2024)10.1038/s41398-024-02865-4

N/A

0.406DataRank · unranked

14 citations

Karina Gutiérrez-Fragoso, Anbupalam Thalamuthu, Azmeraw T. Amare, Mazda Adli, Kazufumi Akiyama +95 more

Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome

Annals of Neurology(2024)10.1002/ana.27040

N/A

0.385DataRank · unranked

12 citations

Ruth Chia, Sara Sáez-Atiénzar, Paola Ruffo, Memoona Rasheed, Jay P. Ross +7 more

HLA in isolated REM sleep behavior disorder and Lewy body dementia

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51841

N/A

0.345DataRank · unranked

9 citations

Lynne Krohn, Jennifer A. Ruskey, Farnaz Asayesh, Dan Spiegelman, Zalak Shah +38 more

Progress in the genetics of restless legs syndrome: the path ahead in the era of whole-genome sequencing

Sleep(2022)10.1093/sleep/zsac136

N/A

0.208DataRank · unranked

3 citations

Patrick A Dion, Guy A. Rouleau, Fulya Akçimen

A comprehensive analysis of dominant and recessive parkinsonism genes in REM sleep behavior disorder

medRxiv(2020)10.1101/2020.03.17.20032664

N/A

0.208DataRank · unranked

3 citations

Uladzislau Rudakou, Eric Yu, Jennifer A. Ruskey, Farnaz Asayesh, Sandra B. Laurent +36 more

Association study of DNAJC13, UCHL1, HTRA2, GIGYF2 and EIF4G1 with Parkinson’s disease

medRxiv(2020)10.1101/2020.06.26.20141176

N/A

0.165DataRank · unranked

2 citations

Uladzislau Rudakou, Eric Yu, Jennifer A. Ruskey, Farnaz Asayesh, Sandra B. Laurent +15 more

A multi-ancestry genetic reference for the Quebec population

Nature Communications(2026)10.1038/s41467-026-68820-7

Top 70%

0.165DataRank

Top 70%2 citations

Georgette Femerling, Rose Laflamme, Alejandro Mejia-Garcia, Mohadese Sayahian Dehkordi, Hongyu Xiao +34 more

Review 2: Probe the relationship between BTBD9 and MEIS1 in C. elegans and mouse

(2020)10.1017/exp.2020.12.pr2

N/A

0DataRank · unranked

0 citations

Guy A. Rouleau

Novel Associations of BST1 and LAMP3 With REM Sleep Behavior Disorder

Neurology(2021)10.1212/wnl.0000000000011464

N/A

0DataRank · unranked

18 citations

Eric Yu, Uladzislau Rudakou, Lynne Krohn, Jennifer A. Ruskey, Farnaz Asayesh +39 more

Lack of Causal Effects or Genetic Correlation between Restless Legs Syndrome and Parkinson's Disease

Movement Disorders(2021)10.1002/mds.28640

N/A

0DataRank · unranked

13 citations

Konstantin Senkevich, Eric Yu, Parizad Varghaei, Lynne Krohn, Sara Bandrés‐Ciga +4 more

Genome-wide association study of REM sleep behavior disorder identifies novel loci with distinct polygenic and brain expression effects

medRxiv(2021)10.1101/2021.09.08.21254232

N/A

0DataRank · unranked

8 citations

Karl Heilbron, Cornelis Blauwendraat, Regina Hertfelder Reynolds, Eric Yu, Konstantin Senkevich +53 more

Copy-Number Variants in The Contactin-5 Gene Are a Potential Risk Factor for Autism Spectrum Disorder

Research Square(2021)10.21203/rs.3.rs-660740/v1

N/A

0DataRank · unranked

0 citations

Guillaume Huguet, Qin He, Amélie Musa-Johnson, Élise Douard, Mor Absa Loum +16 more

Novel associations of BST1 and LAMP3 with rapid eye movement sleep behavior disorder

medRxiv(2020)10.1101/2020.06.27.20140350

N/A

0DataRank · unranked

0 citations

Eric Yu, Uladzislau Rudakou, Lynne Krohn, Jennifer A. Ruskey, Farnaz Asayesh +39 more

Genome-Wide Association Study Meta-Analysis for Parkinson’s Disease Motor Subtypes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.26.174276

N/A

0DataRank · unranked

0 citations

Rami Al‐Ouran, Rainer von Coelln, Cornelis Blauwendraat, Emily J. Hill, Lan Luo +16 more

TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.10.007

N/A

0DataRank · unranked

26 citations

Linda M. Reis, Davut Pehli̇van, Jonathan A. Bernstein, Michael Muriello, Erin Syverson +33 more

Copy-number variants in the contactin-5 gene are a potential risk factor for autism spectrum disorder

Research in autism spectrum disorders(2022)10.1016/j.rasd.2022.102055

N/A

0DataRank · unranked

3 citations

Guillaume Huguet, Qin He, Amélie Musa-Johnson, Élise Douard, Mor Absa Loum +18 more

Convergent coexpression of autism associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies

medRxiv(2022)10.1101/2022.02.28.22271620

N/A

0DataRank · unranked

0 citations

Mariana Moysés‐Oliveira, Celine E. de Esch, Riya Bhavsar, Xander Nuttle, Aiqun Li +14 more

Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson’s disease

medRxiv(2020)10.1101/2020.03.06.20030734

N/A

0DataRank · unranked

0 citations

Konstantin Senkevich, Uladzislau Rudakou, Eric Yu, Kheireddin Mufti, Jennifer A. Ruskey +16 more

Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies

Cell Genomics(2023)10.1016/j.xgen.2023.100277

N/A

0DataRank · unranked

24 citations

Mariana Moysés‐Oliveira, Celine E.F. De Esch, Riya Bhavsar, Xander Nuttle, Aiqun Li +14 more

Genetics of mirror movements identifies a multifunctional complex required for Netrin-1 guidance and lateralization of motor control

Science Advances(2023)10.1126/sciadv.add5501

N/A

0DataRank · unranked

21 citations

Patricia T. Yam, Nursen Balekoglu, Hugo Ducuing, J. Michaud, Shirin Makihara +9 more

Clinical testing panels for ALS: global distribution, consistency, and challenges

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration(2023)10.1080/21678421.2023.2173015

N/A

0DataRank · unranked

17 citations

Ahmad Al Nasser, Marwa Elnagheeb, Jennifer A. Fifita, Lyndal Henden, Ingrid M. Keseler +33 more

Analysis of heterozygous PRKN variants and copy number variations in Parkinson’s disease

medRxiv(2020)10.1101/2020.05.07.20072728

N/A

0DataRank · unranked

2 citations

Uladzislau Rudakou, Lynne Krohn, Kheireddin Mufti, Jennifer A. Ruskey, Farnaz Asayesh +15 more

Reply to Barton et al: signatures of natural selection during the Black Death

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.06.535944

N/A

0DataRank · unranked

3 citations

Jennifer Klunk, Christian E. Demeure, Xiaoheng Cheng, Mari Shiratori, Julien Madej +27 more

Genomic analysis identifies risk factors in restless legs syndrome

medRxiv(2023)10.1101/2023.12.19.23300211

N/A

0DataRank · unranked

3 citations

Ruth Chia, Sara Sáez-Atiénzar, Paola Ruffo, Memoona Rasheed, Jay P. Ross +7 more

HLA in isolated REM sleep behavior disorder and Lewy body dementia

medRxiv(2023)10.1101/2023.01.31.23284682

N/A

0DataRank · unranked

1 citations

Lynne Krohn, Jennifer A. Ruskey, Farnaz Asayesh, Dan Spiegelman, Zalak Shah +38 more

Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability

medRxiv(2023)10.1101/2023.11.29.23299190

N/A

0DataRank · unranked

0 citations

Vincent-Raphaël Bourque, Élise Douard, Guillaume Huguet, Cécile Poulain, Jay P. Ross +19 more

Synaptic processes and immune-related pathways implicated in Tourette Syndrome

medRxiv(2020)10.1101/2020.04.24.20047845

N/A

0DataRank · unranked

7 citations

Dongmei Yu, Jae Hoon Sul, Alden Y. Huang, Cornelia Illmann, Lisa Osiecki +59 more

Autism-associated CHD8 controls reactive gliosis and neuroinflammation via remodeling chromatin in astrocytes

Cell Reports(2024)10.1016/j.celrep.2024.114637

N/A

0DataRank · unranked

22 citations

Mei Yuan, Rachel Yan, Lin Yuan, Jonathan J. Wilde, Hailey Eckersberg +23 more

Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease

Neurobiology of Aging(2020)10.1016/j.neurobiolaging.2020.10.019

N/A

0DataRank · unranked

44 citations

Uladzislau Rudakou, Eric Yu, Jennifer A. Ruskey, Farnaz Asayesh, Sandra B. Laurent +15 more

Exome-wide rare variant analysis in familial essential tremor

Parkinsonism & Related Disorders(2020)10.1016/j.parkreldis.2020.11.021

N/A

0DataRank · unranked

15 citations

Gabrielle Houle, Sara Ortega‐Cubero, Sara Bandrés‐Ciga, Ignacio Álvarez, María Cárcel +28 more

Machine learning analysis of exome trios to contrast the genomic architecture of autism and schizophrenia

BMC Psychiatry(2020)10.1186/s12888-020-02503-5

N/A

0DataRank · unranked

17 citations

Bill Qi, Alexandre Dionne‐Laporte, Guy A. Rouleau, Reihaneh Rabbany, Yannis Trakadis +1 more

A Physiological Instability Displayed in Hippocampal Neurons Derived From Lithium-Nonresponsive Bipolar Disorder Patients

Biological Psychiatry(2020)10.1016/j.biopsych.2020.01.020

N/A

0DataRank · unranked

52 citations

Anindita Sarkar, Dekel Galor, Tchelet Stern, Arianna Mei, Yam Stern +9 more

Evolution of a Human-Specific Tandem Repeat Associated with ALS

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.07.004

N/A

0DataRank · unranked

60 citations

Kathryn Gudsnuk, Samuel N. Smukowski, Kosuke Winston, Nitin Desai, Jay P. Ross +15 more

The Challenge of Examining Social Determinants of Health in People Living With Tourette Syndrome

Pediatric Neurology(2024)10.1016/j.pediatrneurol.2024.02.008

N/A

0DataRank · unranked

9 citations

Samuel J. Carr, Angela Essa, Lisa Osiecki, Daniel T. Lackland, Jenifer H. Voeks +14 more

From spastic paraplegia to infantile neurodegenerative disorder: Expanding the phenotypic spectrum associated with biallelic SPAST variants

European Journal of Neurology(2024)10.1111/ene.70025

N/A

0DataRank · unranked

6 citations

Chloé Angelini, Claire Bar, Wahiba Amer El Khedoud, Christine Barnérias, Razika Boulariah‐Hadjou +15 more

Sex Differences in People with Tourette Syndrome and Persistent Motor or Vocal Tic Disorder in the Tourette Association of America International Consortium for Genetics Database

medRxiv(2024)10.1101/2024.01.07.24300816

N/A

0DataRank · unranked

10 citations

Lori B. Chibnik, Natasha Tracy, Lisa Osiecki, Cathy L. Budman, Daniëlle C. Cath +10 more

An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2

Research Square(2024)10.21203/rs.3.rs-5419198/v1

N/A

0DataRank · unranked

0 citations

Koen C. Demaegd, Aoife Kernan, Joke J.F.A. van Vugt, Calum Harvey, Tobias Moll +25 more

GBA variants in REM sleep behavior disorder

Neurology(2020)10.1212/wnl.0000000000010042

N/A

0DataRank · unranked

77 citations

Jennifer A. Ruskey, Uladzislau Rudakou, Etienne Léveillé, Farnaz Asayesh, Joshua Shulman +33 more

An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2

European Journal of Human Genetics(2025)10.1038/s41431-025-01811-2

N/A

0DataRank · unranked

8 citations

Aoife Kernan, Johnathan Cooper‐Knock, Joke J.F.A. van Vugt, Calum Harvey, Tobias Moll +25 more

Is Persistent Motor or Vocal Tic Disorder a Milder Form of Tourette Syndrome?

Movement Disorders(2021)10.1002/mds.28593

N/A

0DataRank · unranked

45 citations

Daniel A. Stevens, Sang‐Wahn Koo, Alexa Valko, O. Joseph Bienvenu, Cathy B. Budman +26 more

Post-traumatic stress disorder and REM-sleep behavior disorder: exploring genetic associations and causal links

medRxiv(2025)10.1101/2025.09.05.25335205

N/A

0DataRank · unranked

0 citations

Lang Liu, Mohammad H. Ghamgosar Shahkhali, Eric Yu, Farnaz Asayesh, Jamil Ahmad +58 more

Insights into Essential Tremor and Essential Tremor-Plus from Common Variants

medRxiv(2025)10.64898/2025.12.02.25341457

N/A

0DataRank · unranked

0 citations

Dylan Gharibian, Patrick A. Dion, Guy A. Rouleau, Miranda Medeiros

Genome-wide association study of REM-sleep behaviour disorder identifies new risk loci

medRxiv(2025)10.64898/2025.12.01.25339623

N/A

0DataRank · unranked

0 citations

Lang Liu, Lynne Krohn, Farnaz Asayesh, Jamil Ahmad, Dan Spiegelman +70 more

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Neuron(2020)10.1016/j.neuron.2020.11.005

N/A

0DataRank · unranked

83 citations

Ruth Chia, Jinhui Ding, Richard A. Hickman, Thor D. Stein, Yevgeniya Abramzon +95 more

Polygenic Scores and Mood Disorder Onsets in the Context of Family History and Early Psychopathology

JAMA Network Open(2025)10.1001/jamanetworkopen.2025.5331

N/A

0DataRank · unranked

5 citations

Alyson Zwicker, Janice M. Fullerton, Danella Hafeman, Neeltje E.M. van Haren, John Merranko +25 more

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

JAMA Neurology(2021)10.1001/jamaneurol.2021.2598

N/A

0DataRank · unranked

85 citations

Ruth Chia, Danny E. Miller, Rachel Li, Ravindran Kumaran, Yevgeniya Abramzon +87 more

Guy A. Rouleau

Indexed papers

Top data-sharing exemplar

Papers