Christine Klein, Hauke Baumann, Luisa Olschewski, Henrike Hanssen, Alexander Münchau, Andreas Ferbert, Norbert Brüggemann, and Katja Lohmann,
De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient, Parkinsonism Relat Disord , vol. 64, pp. 337–339, 2019.

DOI:	10.1016/j.parkreldis.2019.03.018

Shu-Chen Li, Roxane Dilcher, and Alexander Münchau,
Developmental Trajectories of Sensorimotor and Cognitive Control in Gilles de la Tourette Syndrome, Z Neuropsych , vol. 30, no. 4, pp. 231–237, 2019.

DOI:	10.1024/1016-264X/a000271

Alexander Münchau,
Einige Leute simulieren Tourette nur, Frankfurter Allgemeine Sonntagszeitung , 2019.

Anette Schrag, Davide Martino, Alan Apter, Juliane Ball, Erika Bartolini, Noa Benaroya-Milshtein, Maura Buttiglione, Francesco Cardona, Roberta Creti, Androulla Efstratiou, Maria Gariup, Marianthi Georgitsi, Tammy Hedderly, Isobel Heyman, Immaculada Margarit, Pablo Mir, Natalie Moll, Astrid Morer, Norbert Müller, Kirsten Müller-Vahl, Alexander Münchau, Graziella Orefici, Kerstin J. Plessen, Cesare Porcelli, Peristera Paschou, Renata Rizzo, Veit Roessner, Markus J. Schwarz, Tamar Steinberg, Friederike Tagwerker Gloor, Zsanett Tarnok, Susanne Walitza, Andrea Dietrich, Pieter J. Hoekstra, and [GROUP] EMTICS Collaborative Group,
European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents, Eur Child Adolesc Psychiatry , vol. 28, no. 1, pp. 91–109, 2019.

DOI:	10.1007/s00787-018-1190-4

Tim W. Rattay, Tobias Lindig, Jonathan Baets, Katrien Smets, Tine Deconinck, Anne S. Söhn, Konstanze Hörtnagel, Kathrin N. Eckstein, Sarah Wiethoff, Jennifer Reichbauer, Marion Döbler-Neumann, Ingeborg Krägeloh-Mann, Michaela Auer-Grumbach, Barbara Plecko, Alexander Münchau, Bernd Wilken, Marc Janauschek, Anne-Katrin Giese, Jan L. De Bleecker, Els Ortibus, Martine Debyser, Adolfo Lopez de Munain, Aurora Pujol, Maria Teresa Bassi, Maria Grazia D’Angelo, Peter De Jonghe, Stephan Züchner, Peter Bauer, Ludger Schöls, and Rebecca Schüle,
FAHN/SPG35: a narrow phenotypic spectrum across disease classifications, Brain , vol. 142, no. 6, pp. 1561–1572, 2019.

DOI:	10.1093/brain/awz102

[GROUP] Cross-Disorder Group of the Psychiatric Genomics Consortium,
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders, Cell , vol. 179, no. 7, pp. 1469-1482.e11, 2019.

DOI:	10.1016/j.cell.2019.11.020

Maximilian Kleimaker, Alexander Kleimaker, Christian Beste, Soyoung Q. Park, and Alexander Münchau,
Gilles de la Tourette Syndrome, Z Neuropsych , vol. 30, no. 4, pp. 215–221, 2019.

DOI:	10.1024/1016-264X/a000274

J. Prasuhn, K. Lohmann, H. Hanßen, Alexander Münchau, and N. Brüggemann,
Grenzen der Exomsequenzierung in der Diagnostik genetischer Erkrankungen, DGNeurologie , vol. 2, no. 2, pp. 109–112, 2019.

DOI:	10.1007/s42451-018-0046-y

Katja Herrmann, Andreas Sprenger, Leoni Baumung, Daniel Alvarez-Fischer, Alexander Münchau, and Valerie Brandt,
Help or hurt? How attention modulates tics under different conditions, Cortex , vol. 120, pp. 471–482, 2019.

DOI:	10.1016/j.cortex.2019.06.016

Armin Steffen, Wolfgang Jost, Tobias Bäumer, Dirk Beutner, Sabine Degenkolb-Weyers, Martin Groß, Maria Grosheva, Samer Hakim, Kai G. Kahl, Rainer Laskawi, Rebekka Lencer, Jan Löhler, Thekla Meyners, Saskia Rohrbach-Volland, Rainer Schönweiler, Sara-Christina Schröder, Sebastian Schröder, Heidrun Schröter-Morasch, Maria Schuster, Susanne Steinlechner, Roland Urban, and Orlando Guntinas-Lichius,
Hypersalivation: update of the German S2k guideline (AWMF) in short form, J Neural Transm (Vienna) , vol. 126, no. 7, pp. 853–862, 2019.

DOI:	10.1007/s00702-019-02000-4

Valerie Cathérine Brandt, Agnes Moczydlowski, Melanie Jonas, Kai Boelmans, Tobias Bäumer, Marcel Brass, and Alexander Münchau,
Imitation inhibition in children with Tourette syndrome, J Neuropsychol , vol. 13, no. 1, pp. 82–95, 2019.

DOI:	10.1111/jnp.12132

Sebastian Löns,
KMT2B-Dystonie im Kindesalter – Häufigkeit und phänotypisches Spektrum, DGNeurologie , vol. 2, no. 6, pp. 510–512, 2019.

DOI:	10.1007/s42451-019-00124-1

Darius Ebrahimi-Fakhari, Clara Van Karnebeek, and Alexander Münchau,
Movement Disorders in Treatable Inborn Errors of Metabolism, Mov Disord , vol. 34, no. 5, pp. 598–613, 2019.

DOI:	10.1002/mds.27568

Adam Takacs, Annet Bluschke, Alexander Münchau, and Christian Beste,
Neuropharmacological Interventions and Event File Coding in Gilles de la Tourette Syndrome, Z Neuropsych , vol. 30, no. 4, pp. 223–229, 2019.

DOI:	10.1024/1016-264X/a000270

Sinem Tunc, Nastasja Baginski, Juliane Lubs, Julien F. Bally, Anne Weissbach, Magdalena Khira Baaske, Vera Tadic, Norbert Brüggemann, Tobias Bäumer, Christian Beste, and Alexander Münchau,
Predictive coding and adaptive behavior in patients with genetically determined cerebellar ataxia--A neurophysiology study, Neuroimage Clin , vol. 24, pp. 102043, 2019.

DOI:	10.1016/j.nicl.2019.102043

Meike Dieringer, Christian Beck, Julius Verrel, Alexander Münchau, Bartosz Zurowski, and Valerie Brandt,
Quality and temporal properties of premonitory urges in patients with skin picking disorder, Cortex , vol. 121, pp. 125–134, 2019.

DOI:	10.1016/j.cortex.2019.08.015

Luisa Olschewski, Silvia Jesús, Han-Joon Kim, Sinem Tunc, Sebastian Löns, Johanna Junker, Kirsten E. Zeuner, Andrea A. Kühn, Gregor Kuhlenbäumer, Eva Schäffer, Daniela Berg, Meike Kasten, Andreas Ferbert, Eckart Altenmüller, Norbert Brüggemann, Peter Bauer, Arndt Rolfs, Beomseok Jeon, Tobias Bäumer, Pablo Mir, Christine Klein, and Katja Lohmann,
Role of ANO3 mutations in dystonia: A large-scale mutational screening study, Parkinsonism Relat Disord , vol. 62, pp. 196–200, 2019.

DOI:	10.1016/j.parkreldis.2018.12.030

Johannes Levin, Sylvia Maaß, Madeleine Schuberth, Armin Giese, Wolfgang H. Oertel, Werner Poewe, Claudia Trenkwalder, Gregor K. Wenning, Ulrich Mansmann, Martin Südmeyer, Karla Eggert, Brit Mollenhauer, Axel Lipp, Matthias Löhle, Joseph Claßen, Alexander Münchau, Jan Kassubek, Florin Gandor, Daniela Berg, Silvia Egert-Schwender, Cornelia Eberhardt, Friedemann Paul, Kai Bötzel, Birgit Ertl-Wagner, Hans-Jürgen Huppertz, Ingrid Ricard, Günter U. Höglinger, and [GROUP] PROMESA study group,
Safety and efficacy of epigallocatechin gallate in multiple system atrophy (PROMESA): a randomised, double-blind, placebo-controlled trial, Lancet Neurol , vol. 18, no. 8, pp. 724–735, 2019.

DOI:	10.1016/S1474-4422(19)30141-3

Max Borsche, Stefanie Hahn, Henrike Hanssen, Alexander Münchau, Klaus-Peter Wandinger, and Norbert Brüggemann,
Sez6l2-antibody-associated progressive cerebellar ataxia: a differential diagnosis of atypical parkinsonism, J Neurol , vol. 266, no. 2, pp. 522–524, 2019.

DOI:	10.1007/s00415-018-9115-1

Anne Weissbach, Kaviraja Udupa, Zhen Ni, Carolyn Gunraj, Cricia Rinchon, Julianne Baarbe, Alfonso Fasano, Renato P. Munhoz, Anthony Lang, Vera Tadic, Norbert Brüggemann, Alexander Münchau, Tobias Bäumer, and Robert Chen,
Single-pulse subthalamic deep brain stimulation reduces premotor-motor facilitation in Parkinson’s disease, Parkinsonism Relat Disord , vol. 66, pp. 224–227, 2019.

DOI:	10.1016/j.parkreldis.2019.08.003

Alexander Kleimaker, Maximilian Kleimaker, Christian Beste, Tobias Bäumer, and Alexander Münchau,
Somatosensory Processing in Gilles de la Tourette Syndrome, Z Neuropsych , vol. 30, no. 4, pp. 238–242, 2019.

DOI:	10.1024/1016-264X/a000273

Matt J. N. Brown, Anne Weissbach, Martje G. Pauly, Michael Vesia, Carolyn Gunraj, Julianne Baarbe, Alexander Münchau, Tobias Bäumer, and Robert Chen,
Somatosensory-motor cortex interactions measured using dual-site transcranial magnetic stimulation, Brain Stimul , vol. 12, no. 5, pp. 1229–1243, 2019.

DOI:	10.1016/j.brs.2019.04.009

Alexander Münchau, and Christian Beste,
Sonderheft – Gilles de la Tourette Syndrom, Z Neuropsych , vol. 30, no. 4, pp. 213–214, 2019.

DOI:	10.1024/1016-264X/a000269

Sinem Tunc, Marija Dulovic-Mahlow, Hauke Baumann, Magdalena Khira Baaske, Magdalena Jahn, Johanna Junker, Alexander Münchau, Norbert Brüggemann, and Katja Lohmann,
Spinocerebellar Ataxia Type 28-Phenotypic and Molecular Characterization of a Family with Heterozygous and Compound-Heterozygous Mutations in AFG3L2, Cerebellum , vol. 18, no. 4, pp. 817–822, 2019.

DOI:	10.1007/s12311-019-01036-2

Stefan Hess, Petroula Mousikou, Julius Verrel, and Sascha Schroeder,
Syllabic processing in handwritten word production in German children and adults, Hum Mov Sci , vol. 65, pp. 5–14, 2019.

DOI:	10.1016/j.humov.2018.07.003

Johanna Junker, Theresa Paulus, Valerie Brandt, Anne Weissbach, Sinem Tunc, Sebastian Löns, Richard B. Reilly, Michael Hutchinson, and Tobias Bäumer,
Temporal discrimination threshold and blink reflex recovery cycle in cervical dystonia - two sides of the same coin?, Parkinsonism Relat Disord , vol. 68, pp. 4–7, 2019.

DOI:	10.1016/j.parkreldis.2019.09.028

Wolfgang H. Jost, Tobias Bäumer, Rainer Laskawi, Jaroslaw Slawek, Björn Spittau, Armin Steffen, Martin Winterholler, and Ganesh Bavikatte,
Therapy of Sialorrhea with Botulinum Neurotoxin, Neurol Ther , vol. 8, no. 2, pp. 273–288, 2019.

DOI:	10.1007/s40120-019-00155-6

Joanne Trinh, Katja Lohmann, Hauke Baumann, Alexander Balck, Max Borsche, Norbert Brüggemann, Leon Dure, Marissa Dean, Jens Volkmann, Sinem Tunc, Jannik Prasuhn, Heike Pawlack, Sophie Imhoff, Christina M. Lill, Meike Kasten, Peter Bauer, Arndt Rolfs, [GROUP] International Parkinson’s Disease Genomics Consortium (IPDGC), and Christine Klein,
Utility and implications of exome sequencing in early-onset Parkinson’s disease, Mov Disord , vol. 34, no. 1, pp. 133–137, 2019.

DOI:	10.1002/mds.27559

N. H. Jung, Alexander Münchau, and V. Mall,
[Neuronal plasticity and neuromodulation in pediatric neurology], Nervenarzt , vol. 89, no. 10, pp. 1131–1139, 2018.

DOI:	10.1007/s00115-018-0586-1

Alexander Balck, Sinem Tunc, Johanna Schmitz, Ronja Hollstein, Frank J. Kaiser, and Norbert Brüggemann,
A Novel Frameshift CACNA1A Mutation Causing Episodic Ataxia Type 2, Cerebellum , vol. 17, no. 4, pp. 504–506, 2018.

DOI:	10.1007/s12311-018-0931-8

Martje G. Pauly, Victor Krajka, Felix Stengel, Philip Seibler, Christine Klein, and Philipp Capetian,
Adherent vs. Free-Floating Neural Induction by Dual SMAD Inhibition for Neurosphere Cultures Derived from Human Induced Pluripotent Stem Cells, Front Cell Dev Biol , vol. 6, pp. 3, 2018.

DOI:	10.3389/fcell.2018.00003

Jennifer Tübing, Bettina Gigla, Valerie Cathérine Brandt, Julius Verrel, Anne Weissbach, Christian Beste, Alexander Münchau, and Tobias Bäumer,
Associative plasticity in supplementary motor area - motor cortex pathways in Tourette syndrome, Sci Rep , vol. 8, no. 1, pp. 11984, 2018.

DOI:	10.1038/s41598-018-30504-8

L. Schöls, T. Gasser, I. Krägeloh-Mann, H. Graessner, T. Klockgether, and Alexander Münchau,
Centers for Rare Neurological Diseases, Aktuel Neurol , vol. 45, no. 3, pp. 178–186, 2018.

DOI:	10.1055/s-0043-114000

Sheng Wang, Jeffrey D. Mandell, Yogesh Kumar, Nawei Sun, Montana T. Morris, Juan Arbelaez, Cara Nasello, Shan Dong, Clif Duhn, Xin Zhao, Zhiyu Yang, Shanmukha S. Padmanabhuni, Dongmei Yu, Robert A. King, Andrea Dietrich, Najah Khalifa, Niklas Dahl, Alden Y. Huang, Benjamin M. Neale, Giovanni Coppola, Carol A. Mathews, Jeremiah M. Scharf, [GROUP] Tourette International Collaborative Genetics Study (TIC Genetics), [GROUP] Tourette Syndrome Genetics Southern and Eastern Europe Initiative (TSGENESEE), [GROUP] Tourette Association of America International Consortium for Genetics (TAAICG), Thomas V. Fernandez, Joseph D. Buxbaum, Silvia De Rubeis, Dorothy E. Grice, Jinchuan Xing, Gary A. Heiman, Jay A. Tischfield, Peristera Paschou, A. Jeremy Willsey, and Matthew W. State,
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis, Cell Rep , vol. 24, no. 13, pp. 3441-3454.e12, 2018.

DOI:	10.1016/j.celrep.2018.08.082

L. Schöls, H. Graessner, and Alexander Münchau,
Deutsche Akademie für Seltene Neurologische Erkrankungen, Nervenheilkunde , vol. 37, no. 03, pp. 136–141, 2018.

DOI:	10.1055/s-0038-1642087

Hauke Baumann, Magdalena Jahn, Alexander Münchau, Michaela Trilck-Winkler, Katja Lohmann, and Philip Seibler,
Generation and characterization of eight human-derived iPSC lines from affected and unaffected THAP1 mutation carriers, Stem Cell Res , vol. 33, pp. 60–64, 2018.

DOI:	10.1016/j.scr.2018.09.018

Anne Weissbach, and Katja Lohmann,
Genetische Ursachen bei Dystonien, Aktuel Neurol , vol. 45, no. 10, pp. 726–736, 2018.

DOI:	10.1055/a-0740-3212

Joanne Trinh, Vera Tadic, and Christine Klein,
How Do I Confirm that a New Mutation is Pathogenic?, Mov Disord Clin Pract , vol. 5, no. 2, pp. 229, 2018.

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Mohamed Abdulkadir, Douglas Londono, Derek Gordon, Thomas V. Fernandez, Lawrence W. Brown, Keun-Ah Cheon, Barbara J. Coffey, Lonneke Elzerman, Carolin Fremer, Odette Fründt, Blanca Garcia-Delgar, Donald L. Gilbert, Dorothy E. Grice, Tammy Hedderly, Isobel Heyman, Hyun Ju Hong, Chaim Huyser, Laura Ibanez-Gomez, Ewgeni Jakubovski, Young Key Kim, Young Shin Kim, Yun-Joo Koh, Sodahm Kook, Samuel Kuperman, Bennett Leventhal, Andrea G. Ludolph, Marcos Madruga-Garrido, Athanasios Maras, Pablo Mir, Astrid Morer, Kirsten Müller-Vahl, Alexander Münchau, Tara L. Murphy, Kerstin J. Plessen, Veit Roessner, Eun-Young Shin, Dong-Ho Song, Jungeun Song, Jennifer Tübing, Els van den Ban, Frank Visscher, Sina Wanderer, Martin Woods, Samuel H. Zinner, Robert A. King, Jay A. Tischfield, Gary A. Heiman, Pieter J. Hoekstra, and Andrea Dietrich,
Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach, Eur Arch Psychiatry Clin Neurosci , vol. 268, no. 3, pp. 301–316, 2018.

DOI:	10.1007/s00406-017-0808-8

Philip Seibler, Lena F. Burbulla, Marija Dulovic, Simone Zittel, Johanne Heine, Thomas Schmidt, Franziska Rudolph, Ana Westenberger, Aleksandar Raković, Alexander Münchau, Dimitri Krainc, and Christine Klein,
Iron overload is accompanied by mitochondrial and lysosomal dysfunction in WDR45 mutant cells, Brain , vol. 141, no. 10, pp. 3052–3064, 2018.

DOI:	10.1093/brain/awy230

J. Tübing, J. Bohnenpoll, J. Spiegler, G. Gillessen-Kaesbach, Tobias Bäumer, C. Max, J. Sperner, C. Klein, and Alexander Münchau,
Methylphenidate Can Improve Chorea in NKX2.1 and ADCY5 Mutation-positive Patients-A Report of Two Children, Mov Disord Clin Pract , vol. 5, no. 3, pp. 343–345, 2018.

DOI:	10.1002/mdc3.12608

Eunju Seong, Ryan Insolera, Marija Dulovic, Erik-Jan Kamsteeg, Joanne Trinh, Norbert Brüggemann, Erin Sandford, Sheng Li, Ayse Bilge Ozel, Jun Z. Li, Tamison Jewett, Anneke J. A. Kievit, Alexander Münchau, Vikram Shakkottai, Christine Klein, Catherine A. Collins, Katja Lohmann, Bart P. van de Warrenburg, and Margit Burmeister,
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects, Ann Neurol , vol. 83, no. 6, pp. 1075–1088, 2018.

DOI:	10.1002/ana.25220

Humera Manzoor, Norbert Brüggemann, Hafiz Muhammad Jafar Hussain, Tobias Bäumer, Frauke Hinrichs, Muhammad Wajid, Alexander Münchau, Sadaf Naz, and Katja Lohmann,
Novel homozygous variants in ATCAY, MCOLN1, and SACS in complex neurological disorders, Parkinsonism Relat Disord , vol. 51, pp. 91–95, 2018.

DOI:	10.1016/j.parkreldis.2018.02.005

Sinem Tunc, Vera Tadic, Christine Zühlke, Yorck Hellenbroich, and Norbert Brüggemann,
Pearls & Oy-sters: Family history of Huntington disease disguised a case of dentatorubral-pallidoluysian atrophy, Neurology , vol. 90, no. 3, pp. 142–143, 2018.

DOI:	10.1212/WNL.0000000000004833

Johanna Junker, Valerie Brandt, Brian D. Berman, Marie Vidailhet, Emmanuel Roze, Anne Weissbach, Cynthia Comella, Irene A. Malaty, Joseph Jankovic, Mark S. LeDoux, Alfredo Berardelli, Richard Barbano, Stephen G. Reich, Joel S. Perlmutter, H. A. Jinnah, and Norbert Brüggemann,
Predictors of alcohol responsiveness in dystonia, Neurology , vol. 91, no. 21, pp. e2020–e2026, 2018.

DOI:	10.1212/WNL.0000000000006551

O. Kuseyri, Anne Weissbach, N. Brüggemann, C. Klein, M. Giżewska, D. Karall, S. Scholl-Bürgi, H. Romanowska, E. Krzywińska-Zdeb, A. A. Monavari, I. Knerr, Z. Yapıcı, V. Leuzzi, and T. Opladen,
Pregnancy management and outcome in patients with four different tetrahydrobiopterin disorders, J Inherit Metab Dis , vol. 41, no. 5, pp. 849–863, 2018.

DOI:	10.1007/s10545-018-0169-0

S. Zittel, Vera Tadic, C. K. E. Moll, Tobias Bäumer, A. Fellbrich, A. Gulberti, D. Rasche, N. Brüggemann, V. Tronnier, and Alexander Münchau,
Prospective evaluation of Globus pallidus internus deep brain stimulation in Huntington’s disease, Parkinsonism Relat Disord , vol. 51, pp. 96–100, 2018.

DOI:	10.1016/j.parkreldis.2018.02.030

M. Blankenburg, J. Junker, G. Hirschfeld, E. Michel, F. Aksu, J. Wager, and B. Zernikow,
Quantitative sensory testing profiles in children, adolescents and young adults (6-20 years) with cerebral palsy: Hints for a neuropathic genesis of pain syndromes, Eur J Paediatr Neurol , vol. 22, no. 3, pp. 470–481, 2018.

DOI:	10.1016/j.ejpn.2017.12.015

Paul McNulty, Richard Pilcher, Raviram Ramesh, Renata Necuiniate, Alis Hughes, Daniel Farewell, Peter Holmans, Lesley Jones, and [GROUP] REGISTRY Investigators of the European Huntington’s Disease Network,
Reduced cancer incidence in Huntington’s disease: analysis in the Registry study, J Huntington Disease , vol. 7, no. 3, pp. 209–222, 2018.

Alexander Münchau,
Seltene neurologische Erkrankungen, Nervenheilkunde , vol. 37, no. 03, pp. 119–121, 2018.

DOI:	10.1055/s-0038-1642085