Author

Denis Lajkó

Humboldt-Universität zu Berlin

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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Neuroscience· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1

Frequent Co-Authors

Kathrin Textoris‐TaubeiD· 2 shared Marta RosárioiD· 2 shared Theres SchaubiD· 2 shared Andrew G. NewmaniD· 1 shared Ekaterina A. EpifanovaiD· 1 shared Elisa PederseniD· 1 shared Emanuel KemmleriD· 1 shared Ethiraj RavindraniD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersNeuroscience

Kathrin Textoris‐TaubeORCID

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2 papers

Recent·Most cited

DTX4 regulates neural progenitor transitions during cortical development

Elisa Pedersen, Sicheng Zhang, Xushuai Dong, Valeria Beatriz Fernández Vallone, Ekaterina A. Epifanova, Paul Moritz Willecke, Denis Lajkó, Theres Schaub, Mateusz C. Ambrozkiewicz, Kathrin Textoris‐Taube, Harald Stachelscheid, Marta Rosário

This study identifies DTX4 as a regulator of neural progenitor transitions during cortical development, showing its role in maintaining radial glia identity and preventing intermediate progenitor generation.

bioRxiv · Apr 10, 2025 · PreprintNeuroscience

Sema7A and Sema4D Heterodimerization is Essential for Membrane Targeting and Neocortical Wiring

Paraskevi Bessa, Andrew G. Newman, Kuo Yan, Theres Schaub, Rike Dannenberg, Denis Lajkó, Julia Eilenberger, Theresa Brunet, Kathrin Textoris‐Taube, Emanuel Kemmler, Priyanka Banerjee, Ethiraj Ravindran, Michael Mülleder, Robert Preißner, Rudolf Grosschedl, , Victor S. Tarabykin

The paper shows that Sema7A and Sema4D heterodimerization is essential for membrane targeting and neocortical wiring, with a mutation in Sema4D causing epilepsy.

bioRxiv · Feb 10, 2023 · PreprintNeuroscience