Patrick A. Dion

Montreal Neurological Institute and Hospital

ORCID: 0000-0002-2099-954X

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 14 papers. Top paper: “Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome”.

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

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

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

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

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

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

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

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

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

NAR Molecular Medicine(2024)10.1093/narmme/ugae019

N/A

0DataRank · unranked

15 citations

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

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

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

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