Tzung-Chien Hsieh
19PUBLICATIONS
304CO-AUTHORS

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Publications (19)
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|Apr 09, 2026
Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome.Amber S E van Oirsouw, Tzung-Chien Hsieh, Martijn Koetsier
|Nov 26, 2025
Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies.Sébastien Küry, Janelle E Stanton, Geeske M van Woerden
|Jun 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.Axel Schmidt, Magdalena Danyel, Kathrin Grundmann
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Peter M Krawitz
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Shahida Moosa
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Alexej Knaus
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Theresa Brunet
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Sébastien Küry
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Stéphane Bézieau
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Jean Tori Pantel
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Markus Nöthen