Author

Arndt-Peter Schulz

Friedrich-Alexander-Universität Erlangen-NürnbergORCID 0009-0009-2605-4350Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1

Signature Assays, Organisms & Methods

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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 Organism:human· 1

Frequent Co-Authors

Arif B. EkiciiD· 1 shared Christian Thomas ThieliD· 1 shared Emily M BrockmanniD· 1 shared Steffen UebeiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

4 top collaborators · 6 mutual co-author links

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1 shared paperGenetics

Arif B. EkiciORCID

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1 paper

Recent·Most cited

GeneticsiSciencePeer-reviewedJul 10, 2026

LAMA5 deficiency disrupts ECM-WNT crosstalk in chondrogenesis and contributes to idiopathic short stature

Arndt-Peter Schulz, Emily M Brockmann, Steffen Uebe…·Christian Thomas Thiel

The paper identifies LAMA5 as a candidate gene for idiopathic short stature, showing its role in ECM-WNT signaling during chondrogenesis and demonstrating partial rescue via WNT activation.

DOI 10.1016/j.isci.2026.116687

humanbulk RNA-seq

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