Publications by authors named "Patrick A Dion"

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Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.
Rui Zhu, Lang Liu, Mehrdad A Estiar, Farnaz Asayesh, Jamil Ahmad, Patrick A Dion

Mov Disord· November 2025

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Transcriptomic and epigenomic consequences of heterozygous loss-of-function mutations in AKAP11, a shared risk gene for bipolar disorder and schizophrenia.
Nargess Farhangdoost, Calwing Liao, Yumin Liu, Daniel Rochefort, Farah Aboasali, Patrick A Dion

Mol Psychiatry· October 2025

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Lithium partially rescues gene expression and enhancer activity from heterozygous knockout of AKAP11 while inducing novel differential changes.
Nargess Farhangdoost, Alessia Pietrantonio, Yumin Liu, Calwing Liao, Daniel Rochefort, Patrick A Dion

Sci Rep· October 2025

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De novo variant analysis of childhood-onset obsessive-compulsive disorder in the French-Canadian population.
Kate Bornais, Jay P Ross, Zoe Schmilovich, Miranda Medeiros, Charles-Étienne Castonguay, Patrick A Dion

Transl Psychiatry· October 2025

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An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2.
Koen C Demaegd, Aoife Kernan, Johnathan Cooper-Knock, Joke J F A van Vugt, Calum Harvey, Patrick A Dion

Eur J Hum Genet· September 2025

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Brain Imaging Phenotypes Associated with Polygenic Risk for Essential Tremor.
Miranda Medeiros, Alexandre Pastor-Bernier, Houman Azizi, Zoe Schmilovich, Charles-Etienne Castonguay, Patrick A Dion

Mov Disord· June 2025

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Novel germline and somatic variants in familial and sporadic meningioma genes.
Bouchra Ouled Amar Bencheikh, Allison A Dilliott, Julie Gauthier, Sandra Beatrice Laurent, Amirthagowri Ambalavanan, Alexandre Dionne-Laporte, Patrick A Dion

NPJ Genom Med· May 2025

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Gold nanoclusters AuAcCys normalize intracellular ROS without increasing cytoplasmic alarmin acHMGB1 abundance in human microglia and neurons.
Issan Zhang, Dusica Maysinger, Maja Beus, Antonija Mravak, Ziqi Yu, Patrick A Dion

Nanoscale· January 2025

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Tremor in the Age of Omics: An Overview of the Transcriptomic Landscape of Essential Tremor.
Farah Aboasali, Charles-Etienne Castonguay, Miranda Medeiros, Patrick A Dion, Guy A Rouleau

Cerebellum· January 2025

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Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome.
Fulya Akçimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Patrick A Dion

Ann Neurol· November 2024

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expansion creates the unstable folate-sensitive fragile site FRA9A.
Mila Mirceta, Monika H M Schmidt, Natalie Shum, Tanya K Prasolava, Bryanna Meikle, Patrick A Dion

bioRxiv· October 2024

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repeat expansion creates the unstable folate-sensitive fragile site FRA9A.
Mila Mirceta, Monika H M Schmidt, Natalie Shum, Tanya K Prasolava, Bryanna Meikle, Patrick A Dion

NAR Mol Med· October 2024

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Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.
Zoe Schmilovich, Vincent-Raphaël Bourque, Elise Douard, Guillaume Huguet, Cécile Poulain, Patrick A Dion

Front Psychiatry· May 2024

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Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome.
Jay P Ross, Fulya Akçimen, Calwing Liao, Karina Kwan, Daniel E Phillips, Patrick A Dion

Genet Med· January 2024

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Genomic analysis identifies risk factors in restless legs syndrome.
Fulya Akçimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Patrick A Dion

medRxiv· December 2023

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Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.
Zoe Schmilovich, Vincent-Raphaël Bourque, Elise Douard, Guillaume Huguet, Cécile Poulain, Patrick A Dion

medRxiv· November 2023

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Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies.
Calwing Liao, Mariana Moyses-Oliveira, Celine E F De Esch, Riya Bhavsar, Xander Nuttle, Patrick A Dion

Cell Genom· April 2023

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Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids.
Yoshitaka Tamaki, Jay P Ross, Paria Alipour, Charles-Étienne Castonguay, Boting Li, Patrick A Dion

PLoS Genet· February 2023

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The value of testing for ATXN2 intermediate repeat expansions in routine clinical practice for amyotrophic lateral sclerosis.
Kristiana Salmon, Jay P Ross, Vanessa Bertone, Maria Gobbo, Nancy Anoja, Patrick A Dion

Eur J Hum Genet· November 2022

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Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia?
Isabelle Peretz, Jay Ross, Cynthia V Bourassa, Louis-Philippe Lemieux Perreault, Patrick A Dion

Ann N Y Acad Sci· November 2022

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Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study.
Paria Alipour, Konstantin Senkevich, Jay P Ross, Dan Spiegelman, Despoina Manousaki, Patrick A Dion

BMC Med· November 2022

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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

Sleep· August 2022

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Questioning the Association of the Dinucleotide Repeat With Amyotrophic Lateral Sclerosis.
Jay P Ross, Fulya Akçimen, Calwing Liao, Dan Spiegelman, Ben Weisburd, Patrick A Dion

Neurol Genet· August 2022

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Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor.
Charles-Etienne Castonguay, Calwing Liao, Anouar Khayachi, Yumin Liu, Miranda Medeiros, Patrick A Dion

NPJ Genom Med· August 2022

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Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome.
Calwing Liao, Veikko Vuokila, Hélène Catoire, Fulya Akçimen, Jay P Ross, Patrick A Dion

Commun Biol· March 2022

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