Patrick A. Dion

Patrick A. Dion

McGill University

H-index: 62

North America-Canada

About Patrick A. Dion

Patrick A. Dion, With an exceptional h-index of 62 and a recent h-index of 43 (since 2020), a distinguished researcher at McGill University, specializes in the field of patrick.a.dion@mcgill.ca.

His recent articles reflect a diverse array of research interests and contributions to the field:

Convergence of bipolar disorder treatments and gene knockdown on the transcriptome

De novo variant analysis of childhood-onset obsessive-compulsive disorder in the French-Canadian population

Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome

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

Transcriptomic and epigenomic consequences of heterozygous loss of function mutations in AKAP11, the first large-effect shared risk gene for bipolar disorder and schizophrenia

Rare copy number variation in TMEM50A implicated in essential tremor

Huntington's disease in an African family

Exploring the common genetic architecture of autism spectrum disorder using a novel multi-polygenic risk score approach

Patrick A. Dion Information

University

Position

___

Citations(all)

15800

Citations(since 2020)

7344

Cited By

11626

hIndex(all)

62

hIndex(since 2020)

43

i10Index(all)

168

i10Index(since 2020)

140

Email

University Profile Page

McGill University

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Patrick A. Dion Skills & Research Interests

patrick.a.dion@mcgill.ca

Top articles of Patrick A. Dion

Title

Journal

Author(s)

Publication Date

Convergence of bipolar disorder treatments and gene knockdown on the transcriptome

Journal of the Neurological Sciences

Veikko Vuokila

Charles-Etienne Castonguay

Nargess Farhangdoost

Anouar Khayachi

Calwing Liao

...

2023/12/1

De novo variant analysis of childhood-onset obsessive-compulsive disorder in the French-Canadian population

Journal of the Neurological Sciences

Kathleen Bornais

Jay Ross

Zoe Schmilovich

Miranda Medeiros

Dan Spiegelman

...

2023/12/1

Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome

Genetics in Medicine

Jay P Ross

Fulya Akçimen

Calwing Liao

Karina Kwan

Daniel E Phillips

...

2024/1/1

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

Frontiers in Psychiatry

Zoe Schmilovich

Vincent-Raphaël Bourque

Elise Douard

Guillaume Huguet

Cécile Poulain

...

2023/11/29

Transcriptomic and epigenomic consequences of heterozygous loss of function mutations in AKAP11, the first large-effect shared risk gene for bipolar disorder and schizophrenia

bioRxiv

Nargess Farhangdoost

Calwing Liao

Yumin Liu

Martin Alda

Patrick A Dion

...

2024

Rare copy number variation in TMEM50A implicated in essential tremor

Journal of the Neurological Sciences

Miranda Medeiros

Calwing Liao

Allison Dilliott

Jay Ross

Dan Spiegelman

...

2023/12/1

Huntington's disease in an African family

Journal of the Neurological Sciences

Damelan Kombate

Daniel Rochefort

Adadé Ephoévi-Ga

Helene Catoire

Panabalo Waklatsi

...

2023/12/1

Exploring the common genetic architecture of autism spectrum disorder using a novel multi-polygenic risk score approach

Journal of the Neurological Sciences

Zoe Schmilovich

Raphael Bourque

Guillaume Huguet

Jay Ross

Patrick Dion

...

2023/12/1

Cerebellar oligodendrocytes as key initial players in essential tremor pathophysiology

Journal of the Neurological Sciences

Charles-Etienne Castonguay

Farah Aboasali

Theodore Becret

Miranda Medeiros

Daniel Rochefort

...

2023/12/1

Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids

PLoS Genetics

Yoshitaka Tamaki

Jay P Ross

Paria Alipour

Charles-Étienne Castonguay

Boting Li

...

2023/2/6

Restless legs syndrome drug discovery using A C. elegans model

Journal of the Neurological Sciences

Rachel De Barros Oliveira

Patrick Dion

Alex Parker

Guy Rouleau

2023/12/1

CRISPR/CAS9 system corrects PABPN1 mutation in oculopharyngeal muscular dystrophy

Journal of the Neurological Sciences

Aida Abu-Baker

Daniel Rochefort

Patrick Dion

Guy Rouleau

2023/12/1

Genomic analysis identifies risk factors in restless legs syndrome

medRxiv

Fulya Akçimen

Ruth Chia

Sara Saez-Atienzar

Paola Ruffo

Memoona Rasheed

...

2023/12/20

CACNA1A mutations in essential tremor lead to dysregulation of neuron exocytosis machinery

Journal of the Neurological Sciences

Farah Aboasali

Charles-Etienne Castonguay

Gabrielle Houle

Daniel Rochefort

Patrick Dion

...

2023/12/1

Exploring ALS differential vulnerability using single-cell transcriptomic analysis

Journal of the Neurological Sciences

Paria Alipour

Patrick Dion

Guy Rouleau

Jay Ross

2023/12/1

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific …

Nature genetics

Wouter van Rheenen

Rick AA van der Spek

Mark K Bakker

Joke JFA van Vugt

Paul J Hop

...

2022/3

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

Fulya Akçimen

Patrick A Dion

Guy A Rouleau

2022/8/1

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

Research in Autism Spectrum Disorders

Zoe Schmilovich

Guillaume Huguet

Qin He

Amélie Musa-Johnson

Elise Douard

...

2022/11/1

Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS

Science translational medicine

Paul J Hop

Ramona AJ Zwamborn

Eilis Hannon

Gemma L Shireby

Marta F Nabais

...

2022/2/23

Questioning the Association of the STMN2 Dinucleotide Repeat With Amyotrophic Lateral Sclerosis

Neurology: Genetics

Jay P Ross

Fulya Akçimen

Calwing Liao

Dan Spiegelman

Ben Weisburd

...

2022/7/13

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