Author

Eva Klopocki

University of WürzburgORCID 0000-0003-1438-2081Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Organism:zebrafish· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Organism:mouse· 1

Frequent Co-Authors

Daniel LiedtkeiD· 2 shared Alexandra M. KleiniD· 1 shared Amanda M. LaueriD· 1 shared Barbara VonaiD· 1 shared Bettina Vignolo· 1 shared Christoph ErbacheriD· 1 shared Christoph MaackiD· 1 shared Cordula Neuner· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Daniel LiedtkeORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMar 30, 2026

FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss

Daniel Liedtke, K Rak, Katrina M. Schrode…·Barbara Vona

The paper identifies FRMPD4 as a causal gene for X-linked non-syndromic hearing loss through genetic analysis and cross-species functional studies.

DOI 10.64898/2026.03.27.26349271

𝕏 PostBluesky

NeurosciencebioRxivPreprintAug 9, 2023

Small fibre neuropathy in Fabry disease: a human-derived neuronal in vitro disease model

Thomas C. Klein, Julia Grüner, Maximilian Breyer…·Nurcan Üçeyler

This study creates a neuronal in vitro model of Fabry disease to investigate small fibre neuropathy mechanisms, finding Gb3 accumulation, altered ion channel function, and mitochondrial trafficking issues.

4 citations

humanexperimental assay

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Developmental BiologyScientific ReportsPeer-reviewedSep 16, 2019

Fndc3a (Fibronectin Domain Containing Protein 3A) influences median fin fold development and caudal fin regeneration in zebrafish by ECM alteration.

Daniel Liedtke, Melanie Orth, Michelle Meissler…·Eva Klopocki

This study shows Fndc3a affects fin fold development and regeneration in zebrafish by altering the extracellular matrix, with temporary effects during development and impaired regeneration in adults.

21 citations

zebrafishexperimental assay

𝕏 PostBluesky