Author

Mikael Skorpil

Karolinska InstitutetORCID 0000-0002-2759-4692Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:imaging· 1 Approach:simulation· 1 Research Focus:software / tool· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Per SvenningssoniD· 2 shared Andrea VarroneiD· 1 shared Anna WedelliD· 1 shared Christer HalldiniD· 1 shared Christoffer OlssoniD· 1 shared Cilla SöderhälliD· 1 shared Daniel NilssoniD· 1 shared Göran Solders· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersNeuroscience

Per SvenningssonORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintAug 20, 2026

✦ In-depth digest

Anisotropic conductivity modeling for tDCS in Parkinsons disease using multidimensional diffusion MRI

Santiago Osorio Jurado, Mikael Skorpil, Per Svenningsson…·Christoffer Olsson

tDCS fields from a multidimensional diffusion MRI conductivity model stayed within a few percent of DTI and isotropic predictions in 29 participants; whole-brain field instead tracked CSF fraction.

DOI 10.64898/2026.08.02.742293

humanimaging

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Genetic & Genomic MedicineJournal of Internal MedicinePeer-reviewedJul 7, 2024

Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs

Martin Paucar, Daniel Nilsson, Martin Engvall…·Per Svenningsson

This study identifies a GGC expansion in the ZFHX3 gene as the cause of SCA4, associated with dysautonomia and motor neuron signs.

26 citationstop 4%

humanwhole-genome sequencing

𝕏 PostBluesky