Eva Klopocki
6PUBLICATIONS
19CO-AUTHORS
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Publications (6)
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|Apr 10, 2026
FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss.Daniel Liedtke, Kristen Rak, Katrina M Schrode
|Apr 10, 2026
Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signatures.Asuman Koparir, Jennifer Kerkhof, Jessica Rzasa
|Apr 26, 2025
Functional analyses of splice site variants in TCF12.Angela Borst, Tilmann Schweitzer, Denise Horn
|Aug 10, 2020
Investigation of alpl expression and Tnap-activity in zebrafish implies conserved functions during skeletal and neuronal development.Barbara Ohlebusch, Angela Borst, Tina Frankenbach
|Sep 19, 2019
ECM alterations in Fndc3a (Fibronectin Domain Containing Protein 3A) deficient zebrafish cause temporal fin development and regeneration defects.Daniel Liedtke, Melanie Orth, Michelle Meissler
|Jun 13, 2019
On the traces of tcf12: Investigation of the gene expression pattern during development and cranial suture patterning in zebrafish (Danio rerio).Rabea Blümel, Miriam Zink, Eva Klopocki
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Frequent Collaborators
4 joint publications
Daniel Liedtke
1 joint publications
Franz Jakob
1 joint publications
Stephanie Graser
1 joint publications
Angela Borst
1 joint publications
Tilmann Schweitzer
1 joint publications
Denise Horn
1 joint publications
Erdmute Kunstmann
1 joint publications
Kristen Rak
1 joint publications
Philip Hehlert
1 joint publications
Julia Doll
