Author

Joanna Widomska

Radboud University Medical Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Barbara FrankeiD· 2 shared Geert PoelmansiD· 2 shared Ágota ApátiiD· 1 shared Baran E. GüleriD· 1 shared Carol A. MathewsiD· 1 shared Chang LiuiD· 1 shared Christie L. BurtoniD· 1 shared Claudio AcunaiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

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10 top collaborators · 30 mutual co-author links

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2 shared papersMolecular Biology

Barbara FrankeORCID

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2 papers

Recent·Most cited

KCNQ1 regulates human neuronal development through mitochondrial and insulin signalling pathways

Dorothea Schall, Baran E. Güler, Siamand Alibrahim, Md. Mahmudul Hasan, Joanna Widomska, Claudio Acuna, Mairéad Sullivan, Ralph Röth, Chang Liu, Linda Blaier, Katalin Vincze, Karin Burau, Daniela Mauceri, Marcin Luzarowski, Ágota Apáti, , Simone Berkel

This study shows KCNQ1 regulates human neuronal development by affecting cell adhesion, mitochondrial function, and insulin signalling pathways.

bioRxiv · Dec 5, 2025 · PreprintMolecular Biology

Shared genetic etiology between obsessive-compulsive disorder, obsessive-compulsive symptoms in the population, and insulin signaling

Janita Bralten, Joanna Widomska, Ward De Witte, Dongmei Yu, Carol A. Mathews, Jeremiah M. Scharf, Jan K. Buitelaar, Jennifer Crosbie, Russell James Schachar, Paul Daniel Arnold, Mathieu Lemire, Christie L. Burton, Barbara Franke, Geert Poelmans

The paper identifies shared genetic risk factors between OCD, population-based OCS, and insulin signaling traits, suggesting a common etiological mechanism.

Translational Psychiatry · Apr 27, 2020Peer-reviewedGenetics