Priv. doz. Dr. med. Anne Weissbach

Ana Westenberger, Christoph Max, Norbert Brüggemann, Aloysius Domingo, Karen Grütz, Heike Pawlack, Anne Weissbach, Andrea A. Kühn, Juliane Spiegler, Anthony E. Lang, Jürgen Sperner, Victor S. C. Fung, Jens Schallner, Gabriele Gillessen-Kaesbach, Alexander Münchau, and Christine Klein,
Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases, J Pediatr , vol. 181, pp. 306-308.e1, 2017.

DOI:	10.1016/j.jpeds.2016.10.079

Karen Grütz, Philip Seibler, Anne Weissbach, Katja Lohmann, Francesca A. Carlisle, Derek J. Blake, Ana Westenberger, Christine Klein, and Anne Grünewald,
Faithful SGCE imprinting in iPSC-derived cortical neurons: an endogenous cellular model of myoclonus-dystonia, Sci Rep , vol. 7, pp. 41156, 2017.

DOI:	10.1038/srep41156

Anne Weissbach, Elisa Werner, Julien F. Bally, Sinem Tunc, Sebastian Löns, Dagmar Timmann, Kirsten E. Zeuner, Vera Tadic, Norbert Brüggemann, Anthony Lang, Christine Klein, Alexander Münchau, and Tobias Bäumer,
Alcohol improves cerebellar learning deficit in myoclonus-dystonia: A clinical and electrophysiological investigation, Ann Neurol , vol. 82, no. 4, pp. 543–553, 2017.

DOI:	10.1002/ana.25035

Anne Weissbach, Tobias Bäumer, Peter P. Pramstaller, Norbert Brüggemann, Vera Tadic, Robert Chen, Christine Klein, and Alexander Münchau,
Abnormal premotor-motor interaction in heterozygous Parkin- and Pink1 mutation carriers, Clin Neurophysiol , vol. 128, no. 1, pp. 275–280, 2017.

DOI:	10.1016/j.clinph.2016.10.007

Eva Koschmidder, Anne Weissbach, Norbert Brüggemann, Meike Kasten, Christine Klein, and Katja Lohmann,
A nonsense mutation in CHCHD2 in a patient with Parkinson disease, Neurology , vol. 86, no. 6, pp. 577–579, 2016.

DOI:	10.1212/WNL.0000000000002361

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