Author

Farah Aboasali

Montreal Neurological Institute and Hospital

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Assay:scRNA-seq· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alex H. RajputiD· 2 shared Charles-Etienne CastonguayiD· 2 shared Guy Armand RouleauiD· 2 shared Miranda MedeirosiD· 2 shared Patrick A. DioniD· 2 shared Ali H. Rajput· 1 shared Allison Ann DilliottiD· 1 shared Anouar KhayachiiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alex H. RajputORCID

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2 papers

Recent·Most cited

Copy Number Variant Duplications Associated with Essential Tremor

Miranda Medeiros, Calwing Liao, Allison Ann Dilliott, Jay P. Ross, Veikko Vuokila, Farah Aboasali, Charles-Etienne Castonguay, Dan Spiegelman, Franziska Hopfner, Carles Vilariño‐Güell, Elena García‐Martín, Hortensia Alonso‐Navarro, José A. G. Agúndez, Félix Javier Jiménez‐Jiménez, Pau Pástor, , Guy Armand Rouleau

This study identifies rare copy number duplications in protein coding regions as risk factors for essential tremor, but does not reliably identify specific susceptibility genes.

Tremor and Other Hyperkinetic Movements · Feb 10, 2026Peer-reviewedGenetic & Genomic Medicine

A single-cell eQTL atlas of the human cerebellum reveals vulnerability of oligodendrocytes in essential tremor

Charles-Etienne Castonguay, Farah Aboasali, Miranda Medeiros, Théodore Becret, Zoe Schmilovich, Anouar Khayachi, Alex H. Rajput, Patrick A. Dion, Guy Armand Rouleau

The paper constructs a single-cell eQTL atlas of the human cerebellum and identifies ET-associated variants linked to BACE2 downregulation in oligodendrocytes, suggesting demyelination and dysfunctional interactions.

bioRxiv · May 22, 2024 · PreprintGenomics