| Clinical manifestations of the anti-IgLON5 disease C Gaig, F Graus, Y Compta, B Högl, L Bataller, N Brüggemann, ... Neurology 88 (18), 1736-1743, 2017 | 233 | 2017 |
| Mutations in PINK1 and Parkin impair ubiquitination of Mitofusins in human fibroblasts A Rakovic, A Grünewald, J Kottwitz, N Brüggemann, PP Pramstaller, ... PloS one 6 (3), e16746, 2011 | 225 | 2011 |
| 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 | 180 | 2009 |
| 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 | 156 | 2013 |
| Etiology of musician’s dystonia: familial or environmental? A Schmidt, HC Jabusch, E Altenmüller, J Hagenah, N Brüggemann, ... Neurology 72 (14), 1248-1254, 2009 | 135 | 2009 |
| Dopa-responsive dystonia revisited: diagnostic delay, residual signs, and nonmotor signs V Tadic, M Kasten, N Brüggemann, S Stiller, J Hagenah, C Klein Archives of neurology 69 (12), 1558-1562, 2012 | 122 | 2012 |
| Short-and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystonia N Brüggemann, A Kühn, SA Schneider, C Kamm, A Wolters, P Krause, ... Neurology 84 (9), 895-903, 2015 | 114 | 2015 |
| Clinical spectrum of Kufor‐Rakeb syndrome in the Chilean kindred with ATP13A2 mutations MI Behrens, N Brüggemann, P Chana, P Venegas, M Kägi, T Parrao, ... Movement Disorders 25 (12), 1929-1937, 2010 | 112 | 2010 |
| Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects E Seong, R Insolera, M Dulovic, EJ Kamsteeg, J Trinh, N Brüggemann, ... Annals of neurology 83 (6), 1075-1088, 2018 | 97 | 2018 |
| Gonadal steroids differentially regulate the messenger ribonucleic acid expression of pituitary orexin type 1 receptors and adrenal orexin type 2 receptors O Jöhren, N Brüggemann, A Dendorfer, P Dominiak Endocrinology 144 (4), 1219-1225, 2003 | 83 | 2003 |
| Nonmotor symptoms in genetic Parkinson disease M Kasten, L Kertelge, N Brüggemann, J van der Vegt, A Schmidt, V Tadic, ... Archives of neurology 67 (6), 670-676, 2010 | 82 | 2010 |
| Gaucher disease ascertained through a Parkinson's center: imaging and clinical characterization R Saunders‐Pullman, J Hagenah, V Dhawan, K Stanley, G Pastores, ... Movement disorders 25 (10), 1364-1372, 2010 | 81 | 2010 |
| Dominantly transmitted focal dystonia in families of patients with musician’s cramp A Schmidt, HC Jabusch, E Altenmüller, J Hagenah, N Brüggemann, ... Neurology 67 (4), 691-693, 2006 | 81 | 2006 |
| Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype N Brüggemann, J Hagenah, K Reetz, A Schmidt, M Kasten, I Buchmann, ... Archives of neurology 67 (11), 1357-1363, 2010 | 78 | 2010 |
| RAD51 haploinsufficiency causes congenital mirror movements in humans C Depienne, D Bouteiller, A Méneret, S Billot, S Groppa, S Klebe, ... The American Journal of Human Genetics 90 (2), 301-307, 2012 | 77 | 2012 |
| ATP13A2 variants in early‐onset Parkinson's disease patients and controls A Djarmati, J Hagenah, K Reetz, S Winkler, MI Behrens, H Pawlack, ... Movement disorders: official journal of the Movement Disorder Society 24 (14 …, 2009 | 73 | 2009 |
| A heterozygous frameshift mutation in PRKRA (DYT16) associated with generalised dystonia in a German patient. P Seibler, A Djarmati, B Langpap, J Hagenah, A Schmidt, N Brüggemann, ... The Lancet. Neurology 7 (5), 380-381, 2008 | 73 | 2008 |
| Mutations in GNAL: a novel cause of craniocervical dystonia KR Kumar, K Lohmann, I Masuho, R Miyamoto, A Ferbert, T Lohnau, ... JAMA neurology 71 (4), 490-494, 2014 | 72 | 2014 |
| Brain-derived neurotrophic factor–a major player in stimulation-induced homeostatic metaplasticity of human motor cortex? C Mastroeni, TO Bergmann, V Rizzo, C Ritter, C Klein, I Pohlmann, ... PloS one 8 (2), e57957, 2013 | 70 | 2013 |
| MDR1 variants and risk of Parkinson disease K Zschiedrich, IR König, N Brüggemann, N Kock, M Kasten, KL Leenders, ... Journal of neurology 256 (1), 115-120, 2009 | 67 | 2009 |
