Author

Katalin Komlósi

University Medical Center FreiburgORCID 0000-0002-6076-9992Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Katalin Komlósi1 paper · University of Freiburg

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:genome assembly· 1 Assay:Hi-C· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Azza Soliman· 1 shared Daniel PiehiD· 1 shared Jannik Foerster· 1 shared Jennifer WinteriD· 1 shared Lea ZografidouiD· 1 shared Malin DewenteriD· 1 shared Marcel Misak· 1 shared Marco Bertin· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperPathology

Azza Soliman

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1 paper

Recent·Most cited

16p11.2 Copy Number Variation Alters Genome Architecture and Transcriptional Regulation During Neurodevelopment

Marco Bertin, Marcel Misak, Mohit Navandar, Azza Soliman, Ruxandra A. Lambuta, Roshan Tumdam, Jennifer Winter, Matthias Linke, Stephan Käseberg, Malin Dewenter, Katalin Komlósi, Lea Zografidou, Oliver Tuescher, Sergiy Davydenko, Daniel Pieh, , Susann Schweiger

This study investigates how 16p11.2 copy number variations affect genome architecture and transcription during neurodevelopment, finding both local dosage effects and broader chromatin changes.

bioRxiv · May 8, 2026 · PreprintPathology