Author

Berten Ceulemans

Antwerp University HospitalORCID 0000-0001-7818-0679Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2

Frequent Co-Authors

Peter De Jonghe· 2 shared Sarah WeckhuyseniD· 2 shared Adam FrankishiD· 1 shared Alba Sanchis‐JuaniD· 1 shared Anne Fabienne LepineiD· 1 shared Anthony S. RogersiD· 1 shared Barbara Uszczyńska-RatajczakiD· 1 shared Berge Arakel MinassianiD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersNeuroscience

Peter De Jonghe

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintJul 22, 2025

Kv7.2 Loss-of-Function Causes Early Hyperexcitability and Network Remodeling

Nina Dirkx, Mark D. Kaji, Els De Vriendt…·Sarah Weckhuysen

This study shows that KCNQ2 loss-of-function causes early hyperexcitability and network remodeling in human neurons, with biphasic changes in function, gene expression, and structure.

DOI 10.1101/2025.07.22.664856

humanbulk RNA-seq

𝕏 PostBluesky

GenomicsbioRxivPreprintMay 30, 2019

Systematic re-annotation of 191 genes associated with early-onset epilepsy unmasks de novo variants linked to Dravet syndrome in novel SCN1A exons

Charles A. Steward, Jolien Roovers, Marie‐Marthe Suner…·Adam Frankish

The paper updates gene annotations for 191 epilepsy genes, reclassifying variants and identifying new de novo SCN1A variants in Dravet syndrome patients.

DOI 10.1101/648576

humanbulk RNA-seq

𝕏 PostBluesky