| Beyond the comparator model: a multifactorial two-step account of agency M Synofzik, G Vosgerau, A Newen Consciousness and cognition 17 (1), 219-239, 2008 | 1124 | 2008 |
| Misattributions of agency in schizophrenia are based on imprecise predictions about the sensory consequences of one's actions M Synofzik, P Thier, DT Leube, P Schlotterbeck, A Lindner Brain 133 (1), 262-271, 2010 | 428 | 2010 |
| Targeted next generation sequencing as a diagnostic tool in epileptic disorders JR Lemke, E Riesch, T Scheurenbrand, M Schubach, C Wilhelm, I Steiner, ... Epilepsia 53 (8), 1387-1398, 2012 | 413 | 2012 |
| Intensive coordinative training improves motor performance in degenerative cerebellar disease W Ilg, M Synofzik, D Brotz, S Burkard, MA Giese, L Schols Neurology 73 (22), 1823-1830, 2009 | 410 | 2009 |
| The experience of agency: an interplay between prediction and postdiction M Synofzik, G Vosgerau, M Voss Frontiers in psychology 4, 127, 2013 | 393 | 2013 |
| I move, therefore I am: A new theoretical framework to investigate agency and ownership M Synofzik, G Vosgerau, A Newen Consciousness and cognition 17 (2), 411-424, 2008 | 392 | 2008 |
| A Pan‐European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats J van der Zee, I Gijselinck, L Dillen, T Van Langenhove, J Theuns, ... Human mutation 34 (2), 363-373, 2013 | 342 | 2013 |
| De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy S Syrbe, UBS Hedrich, E Riesch, T Djémié, S Müller, RS Møller, B Maher, ... Nature genetics 47 (4), 393-399, 2015 | 303 | 2015 |
| Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study KM Moore, J Nicholas, M Grossman, CT McMillan, DJ Irwin, L Massimo, ... The Lancet Neurology 19 (2), 145-156, 2020 | 298 | 2020 |
| Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients M Anheim, B Monga, M Fleury, P Charles, C Barbot, M Salih, JP Delaunoy, ... Brain 132 (10), 2688-2698, 2009 | 267 | 2009 |
| The cerebellum updates predictions about the visual consequences of one's behavior M Synofzik, A Lindner, P Thier Current Biology 18 (11), 814-818, 2008 | 252 | 2008 |
| Video game–based coordinative training improves ataxia in children with degenerative ataxia W Ilg, C Schatton, J Schicks, MA Giese, L Schöls, M Synofzik Neurology 79 (20), 2056-2060, 2012 | 239 | 2012 |
| PNPLA6 mutations cause Boucher-Neuhäuser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum M Synofzik, MA Gonzalez, CM Lourenco, M Coutelier, TB Haack, ... Brain 137 (1), 69-77, 2014 | 238 | 2014 |
| Long‐term effects of coordinative training in degenerative cerebellar disease W Ilg, D Brötz, S Burkard, MA Giese, L Schöls, M Synofzik Movement disorders 25 (13), 2239-2246, 2010 | 228 | 2010 |
| S100B is increased in Parkinson’s disease and ablation protects against MPTP-induced toxicity through the RAGE and TNF-α pathway K Sathe, W Maetzler, JD Lang, RB Mounsey, C Fleckenstein, HL Martin, ... Brain 135 (11), 3336-3347, 2012 | 227 | 2012 |
| Consensus paper: management of degenerative cerebellar disorders W Ilg, AJ Bastian, S Boesch, RG Burciu, P Celnik, J Claaßen, K Feil, ... The Cerebellum 13, 248-268, 2014 | 226 | 2014 |
| Stimulating personality: ethical criteria for deep brain stimulation in psychiatric patients and for enhancement purposes M Synofzik, TE Schlaepfer Biotechnology Journal: Healthcare Nutrition Technology 3 (12), 1511-1520, 2008 | 213 | 2008 |
| Overcoming the divide between ataxias and spastic paraplegias: shared phenotypes, genes, and pathways M Synofzik, R Schüle Movement Disorders 32 (3), 332-345, 2017 | 199 | 2017 |
| Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum M Synofzik, AS Soehn, J Gburek-Augustat, J Schicks, KN Karle, R Schüle, ... Orphanet journal of rare diseases 8 (1), 41, 2013 | 198 | 2013 |
| Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78) A Estrada-Cuzcano, S Martin, T Chamova, M Synofzik, D Timmann, ... Brain 140 (2), 287-305, 2017 | 179 | 2017 |
