Author

Martin James O'Donnell

Ollscoil na Gaillimhe – University of GalwayORCID 0000-0002-7347-7761Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:fine-mapping· 1 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Guillaume ParéiD· 2 shared Michael ChongiD· 2 shared Abdonas Tamosiunas· 1 shared Adelaida Sánchez-Gálvez· 1 shared Albert HenryiD· 1 shared Albert Hofman DiD· 1 shared Allan LinnebergiD· 1 shared Amand Floriaan SchmidtiD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Guillaume ParéORCID

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2 papers

Recent·Most cited

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, Walter Nelson, Robert W. Morton, Sukrit Narula, Ricky Lali, Irfan I. Khan, Mohammad Daud Khan, Conor S. Judge, Tafadzwa Machipisa, Nathan Cawte, Martin James O'Donnell, Marie Pigeyre, Loubna Akhabir, 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.

eLife · Jan 12, 2022Peer-reviewedGenetic & Genomic Medicine

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

Amand Floriaan Schmidt, Michael Vaclav Holmes, David Preiss, Daniel I. Swerdlow, Spiros Denaxas, Ghazaleh Fatemifar, Rupert Faraway, Chris Finan, R Thomas Lumbers, Albert Henry, Dennis Valentine, Zammy Fairhurst-Hunter, Fernando Pires Hartwig, Bernardo Lessa Horta, Elina Hyppönen, , Albert Hofman D

The paper analyzes genetic variants at the PCSK9 locus to assess their phenotypic effects on lipid levels and disease outcomes, finding concordance with PCSK9 inhibitor trials for myocardial infarction but discordance for type 2 diabetes.

BMC Cardiovascular Disorders · Oct 29, 2019Peer-reviewedGenetics