Thomas Wirth

26PUBLICATIONS
101CO-AUTHORS
Epidemiological modellingNeurogeneticsNeurology and neuromuscular diseasesGenomicsGene expression (incl. microarray and other genome-wide approaches)
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Publications (26)

|Mar 12, 2026
Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal Dyskinesia.

Cyril Mignot, Matthildi Athina Papathanasiou Terzi, Claudia Ravelli

|Sep 22, 2025
Progress and challenges in sporadic late-onset cerebellar ataxias.

Thomas Wirth, Jennifer Faber, Christel Depienne

|Jun 28, 2025
Neuropathy in GAA-FGF14 Late-Onset Cerebellar Ataxia (SCA27B): Prevalence and Characteristics.

Julian Theuriet, Lukas Paulet, Blandine Acket

|Apr 23, 2025
Long-Read Sequencing: The Third Generation of Diagnostic Testing for Dystonia.

Thomas Wirth, Kishore R Kumar, Michael Zech

|Sep 03, 2024
Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions.

Lars Mohren, Friedrich Erdlenbruch, Elsa Leitão

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