Univ.-Prof. Dr. med. Alexander Münchau

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

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

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

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

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

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

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

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

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

Katja Lohmann, Ikuo Masuho, Dipak N. Patil, Hauke Baumann, Eva Hebert, Sofia Steinrücke, Daniel Trujillano, Nickolas K. Skamangas, Valerija Dobricic, Irina Hüning, Gabriele Gillessen-Kaesbach, Ana Westenberger, Dusanka Savic-Pavicevic, Alexander Münchau, Gabriela Oprea, Christine Klein, Arndt Rolfs, and Kirill A. Martemyanov,
Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans, Hum Mol Genet , vol. 26, no. 6, pp. 1078–1086, 2017.

DOI:	10.1093/hmg/ddx018