| Genome-wide association study reveals genetic risk underlying Parkinson's disease J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ... Nature genetics 41 (12), 1308-1312, 2009 | 2227 | 2009 |
| AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease R Krüger, W Kuhn, T Müller, D Woitalla, M Graeber, S Kösel, H Przuntek, ... Nature genetics 18 (2), 106-108, 1998 | 1711 | 1998 |
| Severe COVID-19 is marked by a dysregulated myeloid cell compartment J Schulte-Schrepping, N Reusch, D Paclik, K Baßler, S Schlickeiser, ... Cell 182 (6), 1419-1440. e23, 2020 | 1322 | 2020 |
| Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis L Schöls, P Bauer, T Schmidt, T Schulte, O Riess The Lancet Neurology 3 (5), 291-304, 2004 | 1296 | 2004 |
| Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study A Rauch, D Wieczorek, E Graf, T Wieland, S Endele, T Schwarzmayr, ... The Lancet 380 (9854), 1674-1682, 2012 | 1251 | 2012 |
| Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease KM Strauss, LM Martins, H Plun-Favreau, FP Marx, S Kautzmann, D Berg, ... Human molecular genetics 14 (15), 2099-2111, 2005 | 751 | 2005 |
| Swarm learning for decentralized and confidential clinical machine learning S Warnat-Herresthal, H Schultze, KL Shastry, S Manamohan, ... Nature 594 (7862), 265-270, 2021 | 650 | 2021 |
| Collaborative analysis of α-synuclein gene promoter variability and Parkinson disease DM Maraganore, M De Andrade, A Elbaz, MJ Farrer, JP Ioannidis, ... Jama 296 (6), 661-670, 2006 | 615 | 2006 |
| Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12 SE Holmes, EE O'Hearn, MG McInnis, DA Gorelick-Feldman, ... Nature genetics 23 (4), 391-392, 1999 | 599 | 1999 |
| 14-3-3 proteins in the nervous system D Berg, C Holzmann, O Riess Nature Reviews Neuroscience 4 (9), 752-762, 2003 | 587 | 2003 |
| Reduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1 G Krebiehl, S Ruckerbauer, LF Burbulla, N Kieper, B Maurer, J Waak, ... PloS one 5 (2), e9367, 2010 | 440 | 2010 |
| The natural history of degenerative ataxia: a retrospective study in 466 patients. T Klockgether, R Lüdtke, B Kramer, M Abele, K Bürk, L Schöls, O Riess, ... Brain: a journal of neurology 121 (4), 589-600, 1998 | 435 | 1998 |
| Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... The American Journal of Human Genetics 98 (3), 500-513, 2016 | 419 | 2016 |
| Transgenic rat model of Huntington's disease S von Hörsten, I Schmitt, HP Nguyen, C Holzmann, T Schmidt, T Walther, ... Human molecular genetics 12 (6), 617-624, 2003 | 419 | 2003 |
| Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ... Brain 140 (12), 3191-3203, 2017 | 404 | 2017 |
| Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes? L Schöls, G Amoiridis, T Büttner, H Przuntek, JT Epplen, O Riess Annals of Neurology: Official Journal of the American Neurological …, 1997 | 402 | 1997 |
| Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ... Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014 | 386 | 2014 |
| Progression-specific genes identified by expression profiling of matched ductal carcinomas in situ and invasive breast tumors, combining laser capture microdissection and … CS Schuetz, M Bonin, SE Clare, K Nieselt, K Sotlar, M Walter, T Fehm, ... Cancer research 66 (10), 5278-5286, 2006 | 383 | 2006 |
| Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds L Schöls, R Krüger, G Amoiridis, H Przuntek, JT Epplen, O Riess Journal of Neurology, Neurosurgery & Psychiatry 64 (1), 67-73, 1998 | 352 | 1998 |
| Increased susceptibility to sporadic Parkinson's disease by a certain combined α‐synuclein/apolipoprotein E genotype R Krüger, AM Menezes Vieira‐Saecker, W Kuhn, D Berg, T Müller, ... Annals of Neurology: Official Journal of the American Neurological …, 1999 | 338 | 1999 |
