Author

Mikko Marttila

Orion Corporation (Finland)

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· 2

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1 Assay:GWAS summary statistics· 1 Organism:human· 1 Research Focus:software / tool· 1

Frequent Co-Authors

Edward J. HolloxiD· 2 shared Louise V. WainiD· 2 shared Martin D. TobiniD· 2 shared Nick R. G. ShrineiD· 2 shared Richard J. PackeriD· 2 shared William HennahiD· 2 shared Abril G. IzquierdoiD· 1 shared Ahmed EdrisiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Edward J. HolloxORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genomics of chronic cough unravels neurological pathways

Kayesha Coley, Catherine John, Jonas Ghouse, David J. Shepherd, Nick R. G. Shrine, Abril G. Izquierdo, Stavroula Kanoni, Emma Forton Magavern, Richard J. Packer, Lorcan P. McGarvey, John A. Smith, Henning Bundgaard, Sisse Rye Ostrowski, Christian Erikstrup, Ole Birger Pedersen, , Chiara Batini

This study identifies seven novel genetic loci associated with chronic dry cough and ACEi-induced cough, implicating neurological genes and highlighting potential therapeutic targets.

medRxiv · Jul 23, 2024 · PreprintGenetic & Genomic Medicine

DeepPheWAS: an R package for phenotype generation and association analysis for phenome-wide association studies.

Richard J. Packer, Alex Williams, William Hennah, Micaela Eisenberg, Nick R. G. Shrine, Katherine A. Fawcett, Willow Pearson, Anna L. Guyatt, Ahmed Edris, Edward J. Hollox, Mikko Marttila, Balasubramanya Seetharama Rao, John Raymond Bratty, Louise V. Wain, Frank Dudbridge, Martin D. Tobin

DeepPheWAS creates composite phenotypes and performs association analysis for phenome-wide studies using genetic inputs and various models.

Bioinformatics · Feb 4, 2023Peer-reviewedGenetic & Genomic Medicine