Author

Thomas M. Werge

University of Copenhagen

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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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Agnete KirkebyiD· 1 shared Árni J. Geirsson· 1 shared Arnór VíkingssoniD· 1 shared Ástrós SkúladóttiriD· 1 shared August Benjamin SmitiD· 1 shared Bente GlintborgiD· 1 shared Bitten AagaardiD· 1 shared Caleb JiiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Agnete KirkebyORCID

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2 papers

Recent·Most cited

The genetic architecture of fibromyalgia across 2.5 million individuals

Isabel Kerrebijn, Gyða Björnsdóttir, Keon Arbabi, Lea Urpa, Hele Haapaniemi, Guðmar Þorleifsson, Lilja Stefánsdóttir, Stephan G. Frangakis, Jesse Tyler Valliere, Lovemore Kunorozva, Erik Abner, Caleb Ji, Markus Kangur, Bitten Aagaard, Henning Bliddal, , Michael Wainberg

This study identifies 26 risk loci for fibromyalgia through a genome-wide association analysis of 2.5 million individuals, revealing genetic links to neural functions and chronic pain disorders.

Nature Medicine · Jul 28, 2026Peer-reviewedGenetic & Genomic Medicine

A foundational neuronal protein network model unifying multimodal genetic, transcriptional, and proteomic perturbations in schizophrenia.

Greta Pintacuda, Yu-Han H. Hsu, Petra Páleníková, Ugne Dubonyte, Nadine Fornelos, Miao Chen, Daya Mena, Julia C. Biagini, Travis Botts, Makayla Martorana, Danzel Rebelo, Joshua Ching, Ethan Crouse, Hilena Gebre, Xian Adiconis, , Kasper Lage

The paper identifies three neuron-specific schizophrenia protein networks enriched for genetic and transcriptional perturbations and validates their disruption in 22q11.2 deletion carriers.

medRxiv · May 2, 2025 · PreprintGenetic & Genomic Medicine