Author

Carles Vilariño‐Güell

University of British ColumbiaORCID 0000-0002-5612-5940Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Organism:human· 2 Research Focus:benchmarking· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1

Frequent Co-Authors

Alex H. RajputiD· 2 shared Ali H. Rajput· 1 shared Allison Ann DilliottiD· 1 shared Andrew A. HicksiD· 1 shared Anne GrünewaldiD· 1 shared Anthony Edward LangiD· 1 shared Calwing LiaoiD· 1 shared Cecily Q. BernalesiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Alex H. RajputORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicineTremor and Other Hyperkinetic MovementsPeer-reviewedFeb 10, 2026

Copy Number Variant Duplications Associated with Essential Tremor

Miranda Medeiros, Calwing Liao, Allison Ann Dilliott…·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.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicineBrainPeer-reviewedDec 7, 2022

Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1- and PRKN-linked Parkinson's disease

Joanne Trinh, Andrew A. Hicks, Inke Regina König…·Anne Grünewald

The paper identifies mitochondrial DNA heteroplasmy as a marker distinguishing disease manifestation in PINK1/PRKN mutation carriers.

28 citations

humanDNA methylation

𝕏 PostBluesky

Molecular BiologybioRxivPreprintMar 17, 2021

Transcriptome analysis of the NR1H3 mouse model of multiple sclerosis reveals a pro-inflammatory phenotype with dysregulation of lipid metabolism and immune response genes

Carles Vilariño‐Güell, Mary Joy Encarnacion, Cecily Q. Bernales…·Jacqueline A. Quandt

The paper analyzes the transcriptome of an NR1H3 mouse model of multiple sclerosis, identifying dysregulated genes and pathways associated with pro-inflammatory and immune response changes.

DOI 10.1101/2021.03.17.435678

mousebulk RNA-seq

𝕏 PostBluesky