Author

Liisa Metsähonkala

Helsinki University HospitalORCID 0009-0006-2067-256XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:proteomics· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Aaron Kleinman· 1 shared Adam AutoniD· 1 shared Adele A. Mitchell· 1 shared Alfons MacayaiD· 1 shared Alina MalyutinaiD· 1 shared Andrea Carmine BeliniD· 1 shared Andrés IngasoniD· 1 shared Ann-Louise EsserlindiD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

Aaron Kleinman

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintSep 4, 2026

A novel method for obtaining epileptic brain tissue for omic analyses using electrodes from a clinical stereoelectroencephalography study

Ninja Ehrnrooth, Salla M. Kangas, Alina Malyutina…·Erika Ignatius

This paper describes a method to obtain brain tissue for omic analyses using SEEG electrodes, showing concordant transcriptomic and proteomic findings across different epileptic zones.

DOI 10.64898/2026.09.01.747265

humanbulk RNA-seq

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GeneticsNeuronPeer-reviewedMay 1, 2018

Common variant burden contributes significantly to the familial aggregation of migraine in 1,589 families

Padhraig Gormley, Mitja Kurki, Marjo Eveliina Hiekkala…·George McMahon

This study shows common genetic variants significantly contribute to migraine family clustering, with higher burden in familial cases compared to population-based cases.

101 citationstop 1%

humanwhole-exome sequencing

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