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Alexander Münchau
Alexander Münchau
Institut für Systemische Motorikforschung
Verified email at neuro.uni-luebeck.de - Homepage
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Cited by
Year
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
10772019
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion
JM Lee, EM Ramos, JH Lee, T Gillis, JS Mysore, MR Hayden, SC Warby, ...
Neurology 78 (10), 690-695, 2012
4292012
Long-lasting increase in corticospinal excitability after 1800 pulses of subthreshold 5 Hz repetitive TMS to the primary motor cortex
A Peinemann, B Reimer, C Löer, A Quartarone, A Münchau, B Conrad, ...
Clinical neurophysiology 115 (7), 1519-1526, 2004
4062004
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
YG Weber, A Storch, TV Wuttke, K Brockmann, J Kempfle, S Maljevic, ...
The Journal of clinical investigation 118 (6), 2157-2168, 2008
3922008
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
DJH Moss, AF Pardiñas, D Langbehn, K Lo, BR Leavitt, R Roos, A Durr, ...
The Lancet Neurology 16 (9), 701-711, 2017
3062017
Functional connectivity of human premotor and motor cortex explored with repetitive transcranial magnetic stimulation
A Münchau, BR Bloem, K Irlbacher, MR Trimble, JC Rothwell
Journal of Neuroscience 22 (2), 554-561, 2002
3002002
Premotor transcranial direct current stimulation (tDCS) affects primary motor excitability in humans
K Boros, C Poreisz, A Münchau, W Paulus, MA Nitsche
European Journal of Neuroscience 27 (5), 1292-1300, 2008
2902008
The phenotypic spectrum of rapid-onset dystonia–parkinsonism (RDP) and mutations in the ATP1A3 gene
A Brashear, WB Dobyns, P de Carvalho Aguiar, M Borg, CJM Frijns, ...
Brain 130 (3), 828-835, 2007
2882007
Uses of botulinum toxin injection in medicine today
A Münchau, KP Bhatia
Bmj 320 (7228), 161-165, 2000
2802000
The functional anatomy of Gilles de la Tourette syndrome
C Ganos, V Roessner, A Münchau
Neuroscience & Biobehavioral Reviews 37 (6), 1050-1062, 2013
2152013
Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers
NE Mencacci, IU Isaias, MM Reich, C Ganos, V Plagnol, JM Polke, J Bras, ...
Brain 137 (9), 2480-2492, 2014
2122014
Neuromodulation in Tourette syndrome: dopamine and beyond
J Buse, K Schoenefeld, A Münchau, V Roessner
Neuroscience & Biobehavioral Reviews 37 (6), 1069-1084, 2013
1992013
Repeated premotor rTMS leads to cumulative plastic changes of motor cortex excitability in humans
T Bäumer, R Lange, J Liepert, C Weiller, HR Siebner, JC Rothwell, ...
Neuroimage 20 (1), 550-560, 2003
1982003
Shaping the excitability of human motor cortex with premotor rTMS
V Rizzo, HR Siebner, N Modugno, A Pesenti, A Münchau, W Gerschlager, ...
The Journal of physiology 554 (2), 483-495, 2004
1962004
Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study
A Djarmati, SA Schneider, K Lohmann, S Winkler, H Pawlack, J Hagenah, ...
The Lancet Neurology 8 (5), 447-452, 2009
1912009
Magnetic stimulation of human premotor or motor cortex produces interhemispheric facilitation through distinct pathways
T Bäumer, F Bock, G Koch, R Lange, JC Rothwell, HR Siebner, ...
The Journal of Physiology 572 (3), 857-868, 2006
1892006
Natural history and syndromic associations of orthostatic tremor: a review of 41 patients
W Gerschlager, A Münchau, R Katzenschlager, P Brown, JC Rothwell, ...
Movement Disorders 19 (7), 788-795, 2004
1842004
Generalised muscular weakness after botulinum toxin injections for dystonia: a report of three cases
KP Bhatia, A Münchau, PD Thompson, M Houser, VS Chauhan, ...
Journal of Neurology, Neurosurgery & Psychiatry 67 (1), 90-93, 1999
1831999
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene
K Lohmann, RA Wilcox, S Winkler, A Ramirez, A Rakovic, JS Park, B Arns, ...
Annals of neurology 73 (4), 537-545, 2013
1752013
De novo coding variants are strongly associated with Tourette disorder
AJ Willsey, TV Fernandez, D Yu, RA King, A Dietrich, J Xing, SJ Sanders, ...
Neuron 94 (3), 486-499. e9, 2017
1732017
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