Prof. Dr. med. Anne Weissbach

Mark S. LeDoux, Satya R. Vemula, Jianfeng Xiao, Misty M. Thompson, Joel S. Perlmutter, Laura J. Wright, H. A. Jinnah, Ami R. Rosen, Peter Hedera, Cynthia L. Comella, Anne Weissbach, Johanna Junker, Joseph Jankovic, Richard L. Barbano, Stephen G. Reich, Ramon L. Rodriguez, Brian D. Berman, Sylvain Chouinard, Lawrence Severt, Pinky Agarwal, and Natividad P. Stover,
Clinical and genetic features of cervical dystonia in a large multicenter cohort, Neurol Genet , vol. 2, no. 3, pp. e69, 2016.

DOI:	10.1212/NXG.0000000000000069

Niccolò E. Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, Friedrich Asmus, Marthe H. R. Ludtmann, Mina Ryten, Vincent Plagnol, Ann-Kathrin Hauser, Sara Bandres-Ciga, Conceição Bettencourt, Paola Forabosco, Deborah Hughes, Marc M. P. Soutar, Kathryn Peall, Huw R. Morris, Daniah Trabzuni, Mehmet Tekman, Horia C. Stanescu, Robert Kleta, Miryam Carecchio, Giovanna Zorzi, Nardo Nardocci, Barbara Garavaglia, Ebba Lohmann, Anne Weissbach, Christine Klein, John Hardy, Alan M. Pittman, Thomas Foltynie, Andrey Y. Abramov, Thomas Gasser, Kailash P. Bhatia, and Nicholas W. Wood,
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia, Am J Hum Genet , vol. 96, no. 6, pp. 938–947, 2015.

DOI:	10.1016/j.ajhg.2015.04.008

Anne Weissbach, Tobias Bäumer, Raymond Rosales, Lillian V. Lee, Norbert Brüggemann, Aloysius Domingo, Ana Westenberger, Roland D. Jamora, Cid C. Diesta, Valerie Brandt, Vera Tadic, Simone Zittel, Christine Klein, and Alexander Münchau,
Neurophysiological fingerprints of X-linked dystonia-parkinsonism: A model basal ganglia disease, Mov Disord , vol. 30, no. 6, pp. 873–875, 2015.

DOI:	10.1002/mds.26224

Anne Weissbach, Tobias Bäumer, Norbert Brüggemann, Vera Tadic, Simone Zittel, Bastian Cheng, Götz Thomalla, Christine Klein, and Alexander Münchau,
Premotor-motor excitability is altered in dopa-responsive dystonia, Mov Disord , vol. 30, no. 12, pp. 1705–1709, 2015.

DOI:	10.1002/mds.26365

Niccolò E. Mencacci, Léa R’bibo, Sara Bandres-Ciga, Miryam Carecchio, Giovanna Zorzi, Nardo Nardocci, Barbara Garavaglia, Amit Batla, Kailash P. Bhatia, Alan M. Pittman, John Hardy, Anne Weissbach, Christine Klein, Thomas Gasser, Ebba Lohmann, and Nicholas W. Wood,
The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort, Hum Mol Genet , vol. 24, no. 18, pp. 5326–5329, 2015.

DOI:	10.1093/hmg/ddv255

Anne Weissbach, and Christine Klein,
Hereditary dystonia and parkinsonism: two sides of the same coin?, Brain , vol. 137, no. Pt 9, pp. 2402–2404, 2014.

DOI:	10.1093/brain/awu181

Franca Vulinovic, Katja Lohmann, Aleksandar Raković, Philipp Capetian, Daniel Alvarez-Fischer, Alexander Schmidt, Anne Weissbach, Alev Erogullari, Frank J. Kaiser, Karin Wiegers, Andreas Ferbert, Arndt Rolfs, Christine Klein, and Philip Seibler,
Unraveling cellular phenotypes of novel TorsinA/TOR1A mutations, Hum Mutat , vol. 35, no. 9, pp. 1114–1122, 2014.

DOI:	10.1002/humu.22604

Anne Weissbach, Meike Kasten, Anne Grünewald, Norbert Brüggemann, Peter Trillenberg, Christine Klein, and Johann Hagenah,
Prominent psychiatric comorbidity in the dominantly inherited movement disorder myoclonus-dystonia, Parkinsonism Relat Disord , vol. 19, no. 4, pp. 422–425, 2013.

DOI:	10.1016/j.parkreldis.2012.12.004

Anne Weissbach, Katharina Siegesmund, Norbert Brüggemann, Alexander Schmidt, Meike Kasten, Irene Pichler, Hiltrud Muhle, Ebba Lohmann, Thora Lohnau, Eberhard Schwinger, Johann Hagenah, Ulrich Stephani, Peter P. Pramstaller, Christine Klein, and Katja Lohmann,
Exome sequencing in a family with restless legs syndrome, Mov Disord , vol. 27, no. 13, pp. 1686–1689, 2012.

DOI:	10.1002/mds.25191

Kishore R. Kumar, Anne Weissbach, Marcus Heldmann, Meike Kasten, Sinem Tunc, Carolyn M. Sue, Marina Svetel, Vladimir S. Kostić, Juan Segura-Aguilar, Alfredo Ramirez, David K. Simon, Peter Vieregge, Thomas F. Münte, Johann Hagenah, Christine Klein, and Katja Lohmann,
Frequency of the D620N mutation in VPS35 in Parkinson disease, Arch Neurol , vol. 69, no. 10, pp. 1360–1364, 2012.

DOI:	10.1001/archneurol.2011.3367