Emeritus Prof. Dr. Ulrich Müller
Publikationen
2026
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Donlon TA and Müller U (2026) Risk genes in progressive supranuclear palsy (PSP) affect integrity and function of microtubules. Front. Aging 7:1769377. doi: 10.3389/fragi.2026.1769377
2025
- Müller U, Höglinger G, Dickson DW. Multifactorial etiology of progressive supranuclear palsy (PSP): the genetic component. Acta Neuropathol. 2025 Jun 4;149(1):58. doi: 10.1007/s00401-025-02898-z.
- Wang H, Chang TS, Dombroski BA, … Müller U, … Geschwind DH, Schellenberg GD, Lee WP. Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells. Mov Disord. 2025 May;40(5):950-961. doi: 10.1002/mds.30150. Epub 2025 Mar 8. PMID: 40055946; PMCID: PMC12089919.
2024
- Farrell K, Humphrey J, Chang T, … Müller U, … Goate A, Schellenberg G, Geschwind DH; PSP Genetics Study Group; Crary JF, Naj A. Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes. Nat Commun. 2024 Sep 9;15(1):7880. doi: 10.1038/s41467-024-52025-x. Erratum in: Nat Commun. 2024 Nov 13;15(1):9828. doi: 10.1038/s41467-024-53617-3.
- Wang H, Chang TS, Dombroski BA, … Müller U, … Schellenberg GD, Geschwind DH, Lee WP. Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy. Mol Neurodegener. 2024 Aug 16;19(1):61. doi: 10.1186/s13024-024-00747-3. Erratum in: Mol Neurodegener. 2024 Oct 14;19(1):73. doi: 10.1186/s13024-024-00763-3.
2022
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Hopfner F, Tietz AK, Ruf VC, … Müller U, … Herms J, Kuhlenbäumer G, Höglinger G. Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy. Mov Disord. 2022 Oct;37(10):2110-2121. doi: 10.1002/mds.29164. Epub 2022 Aug 23.
2021
- Müller U. Spinocerebellar ataxias (SCAs) caused by common mutations. Neurogenetics. 2021 Oct;22(4):235-250. doi: 10.1007/s10048-021-00662-5.
- Laabs BH, Klein C, Pozojevic J, … Müller U, … Kaiser FJ, König IR, Westenberger A. Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism. Nat Commun. 2021 May 28;12(1):3216. doi: 10.1038/s41467-021-23491-4.
2019
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Rösler TW, Tayaranian Marvian A, Brendel M, …Müller U, … Meissner WG, Kovacs GG, Höglinger GU. Four-repeat tauopathies. Prog Neurobiol. 2019 Sep;180:101644. doi: 10.1016/j.pneurobio.2019.101644.