Author

Robert W. Morton

McMaster UniversityORCID 0000-0003-0099-4167Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:fine-mapping· 1 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Guillaume ParéiD· 2 shared Marie PigeyreiD· 2 shared Michael ChongiD· 2 shared Pedrum Mohammadi‐ShemiraniiD· 2 shared Alysha C. D’SouzaiD· 1 shared Cameron J. MitchelliD· 1 shared Changhyun LimiD· 1 shared Chris McGloryiD· 1 shared

Activity by Year

2020-2024 · 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

Guillaume ParéORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BioinformaticsNAR Molecular MedicinePeer-reviewedOct 1, 2024

Network-based modelling reveals cell-type enriched patterns of non-coding RNA regulation during human skeletal muscle remodelling

Jonathan C. Mcleod, Changhyun Lim, Tanner Stokes…·Stuart M. Phillips

The paper identifies ncRNA genes regulated during skeletal muscle hypertrophy in 144 individuals using transcriptomic analysis and network modelling.

12 citations

humanbulk RNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicineeLifePeer-reviewedJan 12, 2022

GWAS and ExWAS of blood Mitochondrial DNA copy number identifies 73 loci and highlights a potential causal role in dementia

Michael Chong, Pedrum Mohammadi‐Shemirani, Nicolas Perrot…·Guillaume Paré

This study identifies 73 genetic loci associated with blood mitochondrial DNA copy number and suggests a causal link between low mtDNA-CN and dementia risk.

128 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicineeLifePeer-reviewedOct 16, 2020

Clinical benefits and adverse effects of genetically-elevated free testosterone levels: a Mendelian randomization analysis

Pedrum Mohammadi‐Shemirani, Michael Chong, Marie Pigeyre…·Guillaume Paré

This study uses Mendelian randomization to assess the effects of genetically elevated free testosterone on 23 health outcomes, finding both clinical benefits and adverse effects.

68 citationstop 3%

humanGWAS summary statistics

𝕏 PostBluesky