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Scientific Reports|November 23, 2024
RLS-associated MEIS transcription factors control distinct processes in human neural stem cellsVolker Kittke, Chen Zhao, Daniel D Lam, et al.Nature Neuroscience|March 26, 2024
Spatial enhancer activation influences inhibitory neuron identity during mouse embryonic developmentElena Dvoretskova, May C Ho, Volker Kittke, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 25, 2025
Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate SynthasePhilip Harrer, Magdalena Krygier, Martin Krenn, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 10, 2026
Neurodevelopmental Disorder with Dystonia and Chorea Linked to De Novo Variants in the Splicing Regulator SRRM4Philip Harrer, Volker Kittke, Alice Saparov, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Dystonia Linked to EIF4A2 Haploinsufficiency: A Disorder of Protein Translation DysfunctionPhilip Harrer, Matej Škorvánek, Volker Kittke, et al.Nature Genetics|June 5, 2024
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk predictionBarbara Schormair, Chen Zhao, Steven Bell, et al.Brain : a Journal of Neurology|February 12, 2025
Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystoniaMichael Zech, Ivana Dzinovic, Matej Skorvanek, et al.Pageof 1