Stefan Hauser

13PUBLICATIONS
84CO-AUTHORS
Neurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)NeonatologyCellular nervous systemInfant and child health
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Publications (13)

|Oct 22, 2026
Single-nucleotide polymorphism-directed design of allele-specific antisense oligonucleotides for spinocerebellar ataxia type 3.

|Aug 22, 2024
Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy.

Emily Banks, Vincent Francis, Sheng-Jia Lin

|Jul 22, 2024
Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences.

Theresa Kagermeier, Stefan Hauser, Kseniia Sarieva

|Apr 08, 2024
Unraveling Axonal Transcriptional Landscapes: Insights from iPSC-Derived Cortical Neurons and Implications for Motor Neuron Degeneration.

Jishu Xu, Michaela Hörner, Maike Nagel

|Feb 14, 2024
Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy.

Emily Banks, Vincent Francis, Sheng-Jia Lin

|Mar 09, 2023
TR-FRET-Based Immunoassay to Measure Ataxin-2 as a Target Engagement Marker in Spinocerebellar Ataxia Type 2.

Jessica Bux, Nesli Ece Sen, Isa-Maria Klink

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Frequent Collaborators

4 joint publications

Ludger Schöls

4 joint publications

Jeannette Hübener-Schmid

3 joint publications

Olaf Riess

2 joint publications

Vladimir Fonov