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Movement Disorders Clinical Practice|October 27, 2018
Ataxia Telangiectasia Gene Mutation in Isolated Segmental Dystonia Without Ataxia and TelangiectasiaJán Necpál, Michael Zech, Matej Škorvánek, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|September 30, 2024
Tremor-Dominant Movement Disorder in ANKRD11- Associated KBG SyndromeAntonia M Stehr, Thomas Koeglsperger, Maureen Jacob, et al.Neurogenetics|March 7, 2021
Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variantIvana Dzinovic, Tereza Serranová, Clement Prouteau, et al.Current Neurology and Neuroscience Reports|June 11, 2008
Genetics of restless legs syndromeJuliane WinkelmannCase Reports in Genetics|December 8, 2017
SOX5-Null Heterozygous Mutation in a Family with Adult-Onset Hyperkinesia and Behavioral AbnormalitiesMichael Zech, Katharina Poustka, Sylvia Boesch, et al.Human Molecular Genetics|December 10, 2021
Intronic elements associated with insomnia and restless legs syndrome exhibit cell-type-specific epigenetic features contributing to MEIS1 regulationDaniel D Lam, Ana Antic Nikolic, Chen Zhao, et al.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.American Journal of Human Genetics|May 26, 2015
Recessive mutations in the α3 (VI) collagen gene COL6A3 cause early-onset isolated dystoniaMichael Zech, Daniel D Lam, Ludmila Francescatto, et al.Parkinsonism & Related Disorders|October 26, 2017
Microstructural white matter abnormalities in patients with COL6A3 mutations (DYT27 dystonia)Angela Jochim, Yong Li, Michael Zech, et al.Journal of Neurology|March 5, 2024
CHD8-related disorders redefined: an expanding spectrum of dystonic phenotypesUgo Sorrentino, Sylvia Boesch, Diane Doummar, et al.Pageof 35