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2019
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Westenberger A, Reyes CJ, Saranza G, Dobricic V, Hanssen H, Domingo A, Laabs B-H, Schaake S, Pozojevic J, Rakovic A, Grütz K, Begemann K, Walter U, Dressler D, Bauer P, Rolfs A, Münchau A, Kaiser FJ, Ozelius LJ, Jamora RDG, Rosales RL, Diesta CCE, Lohmann K, König IR, Brüggemann N, Klein C. A hexanucleotide repeat modifies expressivity of X-linked dystonia-parkinsonism. Annals of Neurology 85(6):812-822
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2020
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Krause C, Schaake S, Grütz K, Sievert H, Reyes CJ, König IR, Laabs B-H, Jamora RDG, Rosales RL, Diesta CCE, Pozojevic J, Gemoll T, Westenberger A, Kaiser FJ, Klein C, Kirchner H. DNA Methylation as a Potential Molecular Mechanism in X-Linked Dystonia-Parkinsonism. Movement Disorders 35(12):2220-2229
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2021
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Laabs B-H, Klein C, Pozojevic J, Domingo A, Brüggemann N, Grütz K, Rosales RL, Jamora RDG, Saranza G, Diesta CCE, Wittig M, Schaake S, Mahlow MD, Quismundo J, Otto P, Acuna P, Go CL, Sharma N, Multhaupt-Buell TJ, Müller U, Hanssen H, Kilpert F, Franke A, Rolfs A, Bauer P, Dobricic V, Lohmann K, Ozelius LJ, Kaiser FJ, König IR, Westenberger A. Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism. Nature Communications 12(1):3216
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2021
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Reyes CJ, Laabs B-H, Schaake S, Lüth T, Ardicoglu R, Rakovic A, Grütz K, Alvarez-Fischer D, Jamora RDG, Rosales RL, Weyers I, König IR, Brüggemann N, Klein C, Dobricic V, Westenberger A, Trinh J. Brain Regional Differences in Hexanucleotide Repeat Length in X-linked Dystonia-Parkinsonism Using Nanopore Sequencing. Neurology Genetics 7(4):1
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2021
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Balck A, Schaake S, Kuhnke NS, Domingo A, Madoev H, Margolesky J, Dobricic V, Alvarez-Fischer D, Laabs B-H, Kasten M, Luo W, Nicolas G, Marras C, Lohmann K, Klein C, Westenberger A. Genotype-Phenotype Relations in Primary Familial Brain Calcification: Systematic MDSGene Review. Movement Disorders 36(11):2468-2480
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2021
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Koch S, Laabs B-H, Kasten M, Vollstedt E-J, Becktepe JS, Brüggeman N, Franke A, Krämer U, Kuhlenbäumer G, Lieb W, Mollenhauer B, Neis M, Trenkwalder C, Schaeffer E, Usnich T, Wittig M, Klein C, König IR, Lohmann K, Krawczak M, Caliebe A. Validity and Prognostic Value of a Polygenic Risk Score for Parkinson’s Disease. Genes 12(12):1859
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2022
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Trinh J, Lüth T, Schaake S, Laabs B-H, Schlüter K, Laß J, Pozojevic J, Tse R, König IR, Jamora RDG, Rosales Rl, Brüggemann N, Saranza G, Diesta CCE, Kaiser FJ, Depienne C, Pearson CE, Westenberger A, Klein C. Mosaic divergent repeat interruptions in XDP influence repeat stability and disease onset. Brain awac160
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2022
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Steinhardt J, Hanßen H, Heldmann M, Sprenger A, Laabs B-H, Domingo A, Reyes CJ, Prasuhn J, Brand M, Rosales RL, Münte TF, Klein C, Westenberger A, Oropilla JQ, Diesta CCE, Brüggeman N. Prodromal X-Linked Dystonia-Parkinsonism is Characterized by a Subclinical Motor Phenotype. Movement Disorders 37(7):1474-1482
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2022
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Pozojevic J, Laabs B-H, Westenberger A. Factors influencing reduced penetrance and variable expressivity in X-linked dystonia-parkinsonism. Medizinische Genetik 34(2):97-102
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