Author

Renske T.W. Schellens

Radboud University Medical CenterORCID 0000-0002-3575-1301Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Renske T.W. Schellens1 paper · 2. Department of Otorhinolaryngology, Radboud University Medical Center, Nijmegen, the Netherlands;

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Amanda M. LaueriD· 1 shared Barbara VonaiD· 1 shared Cordula Neuner· 1 shared Daniel Bengl· 1 shared Daniel LiedtkeiD· 1 shared Erik de VriezeiD· 1 shared Erwin van WijkiD· 1 shared Eva KlopockiiD· 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 paperGenetic & Genomic Medicine

Amanda M. LauerORCID

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1 paper

Recent·Most cited

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, Philip Hehlert, Niloofar Chamanrou, Daniel Bengl, Radoslaw Katana, Soganad Heydaran, Julia Doll, Mei Han, Indrajit Nanda, Pingkalai R. Senthilan, Lukas Juergens, Linda Bieniussa, Johannes Voelker, , 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.

medRxiv · Mar 30, 2026 · PreprintGenetic & Genomic Medicine