| Gut microbiota in Parkinson disease in a northern German cohort F Hopfner, A Künstner, SH Müller, S Künzel, KE Zeuner, NG Margraf, ... Brain research 1667, 41-45, 2017 | 89 | 2017 |
| Genetics of essential tremor: meta-analysis and review G Kuhlenbäumer, F Hopfner, G Deuschl Neurology 82 (11), 1000-1007, 2014 | 69 | 2014 |
| Co-aggregate formation of CADASIL-mutant NOTCH3: a single-particle analysis M Duering, A Karpinska, S Rosner, F Hopfner, M Zechmeister, N Peters, ... Human molecular genetics 20 (16), 3256-3265, 2011 | 63 | 2011 |
| Genome-wide association study in essential tremor identifies three new loci SH Müller, SL Girard, F Hopfner, ND Merner, CV Bourassa, D Lorenz, ... Brain 139 (12), 3163-3169, 2016 | 49 | 2016 |
| Knowledge gaps and research recommendations for essential tremor F Hopfner, D Haubenberger, WR Galpern, K Gwinn, A Van't Veer, S White, ... Parkinsonism & related disorders 33, 27-35, 2016 | 33 | 2016 |
| Early‐and late‐onset essential tremor patients represent clinically distinct subgroups F Hopfner, A Ahlf, D Lorenz, S Klebe, KE Zeuner, G Kuhlenbäumer, ... Movement Disorders 31 (10), 1560-1566, 2016 | 30 | 2016 |
| Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features F Hopfner, B Schormair, F Knauf, A Berthele, TR Tölle, R Baron, C Maier, ... BMC neurology 11 (1), 134, 2011 | 30 | 2011 |
| The role of SCARB2 as susceptibility factor in Parkinson's disease F Hopfner, EC Schulte, B Mollenhauer, B Bereznai, F Knauf, P Lichtner, ... Movement Disorders 28 (4), 538-540, 2013 | 29 | 2013 |
| The etiology of essential tremor: genes versus environment F Hopfner, RC Helmich Parkinsonism & related disorders 46, S92-S96, 2018 | 24 | 2018 |
| Testing for alcohol sensitivity of tremor amplitude in a large cohort with essential tremor F Hopfner, T Erhart, K Knudsen, D Lorenz, SA Schneider, KE Zeuner, ... Parkinsonism & related disorders 21 (8), 848-851, 2015 | 23 | 2015 |
| Is essential tremor a single entity? F Hopfner, G Deuschl European journal of neurology 25 (1), 71-82, 2018 | 22 | 2018 |
| Four-repeat tauopathies TW Rösler, AT Marvian, M Brendel, NP Nykänen, M Höllerhage, ... Progress in neurobiology, 101644, 2019 | 21 | 2019 |
| Rest tremor revisited: Parkinson’s disease and other disorders W Chen, F Hopfner, JS Becktepe, G Deuschl Translational neurodegeneration 6 (1), 16, 2017 | 17 | 2017 |
| ALS2 mutations: juvenile amyotrophic lateral sclerosis and generalized dystonia UM Sheerin, SA Schneider, L Carr, G Deuschl, F Hopfner, M Stamelou, ... Neurology 82 (12), 1065-1067, 2014 | 17 | 2014 |
| Progress of pharmacological approaches in Parkinson's disease KE Zeuner, E Schäffer, F Hopfner, N Brüggemann, D Berg Clinical Pharmacology & Therapeutics 105 (5), 1106-1120, 2019 | 13 | 2019 |
| Topography of essential tremor W Chen, F Hopfner, S Szymczak, O Granert, SH Müller, G Kuhlenbäumer, ... Parkinsonism & related disorders 40, 58-63, 2017 | 12 | 2017 |
| The impact of rare variants in FUS in essential tremor F Hopfner, G Stevanin, SH Müller, E Mundwiller, M Bungeroth, A Durr, ... Movement Disorders 30 (5), 721-724, 2015 | 11 | 2015 |
| HTLV-1 associated myelopathy after renal transplantation. F Gövert, A Krumbholz, K Witt, F Hopfner, T Feldkamp, K Korn, A Knöll, ... Journal of clinical virology: the official publication of the Pan American …, 2015 | 9 | 2015 |
| RAB39B mutations are a rare finding in Parkinson disease patients T Löchte, N Brüggemann, EJ Vollstedt, P Krause, A Domingo, R Rosales, ... Parkinsonism & related disorders 23, 116-117, 2016 | 7 | 2016 |
| c. 207C> G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia AS Shalash, TW Rösler, SH Müller, M Salama, G Deuschl, U Müller, ... Neurology Genetics 3 (6), e197, 2017 | 5 | 2017 |
Günther DeuschlDepartment of Neurology, UKSH, Christian-Albrechts University KielGeverifieerd e-mailadres voor neurologie.uni-kiel.de
