Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ... autophagy 17 (1), 1-382, 2021 | 12040* | 2021 |
Ala30Pro 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 | 4777 | 1998 |
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 | 2068 | 2009 |
Neurostimulation for Parkinson's disease with early motor complications WMM Schuepbach, J Rau, K Knudsen, J Volkmann, P Krack, ... New England Journal of Medicine 368 (7), 610-622, 2013 | 1354 | 2013 |
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 | 715 | 2005 |
Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson’s disease LF Burbulla, P Song, JR Mazzulli, E Zampese, YC Wong, S Jeon, ... Science 357 (6357), 1255-1261, 2017 | 610 | 2017 |
Loss-of-function of human PINK1 results in mitochondrial pathology and can be rescued by parkin N Exner, B Treske, D Paquet, K Holmström, C Schiesling, S Gispert, ... Journal of Neuroscience 27 (45), 12413-12418, 2007 | 606 | 2007 |
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 | 588 | 2006 |
Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expression P Reinhardt, B Schmid, LF Burbulla, DC Schöndorf, L Wagner, M Glatza, ... Cell stem cell 12 (3), 354-367, 2013 | 519 | 2013 |
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 | 417 | 2010 |
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 | 343 | 1999 |
UCHL1 is a Parkinson's disease susceptibility gene DM Maraganore, TG Lesnick, A Elbaz, MC Chartier‐Harlin, T Gasser, ... Annals of neurology 55 (4), 512-521, 2004 | 324 | 2004 |
The hallmarks of P arkinson's disease PMA Antony, NJ Diederich, R Krüger, R Balling The FEBS journal 280 (23), 5981-5993, 2013 | 296 | 2013 |
The brainstem pathologies of Parkinson's disease and dementia with Lewy bodies K Seidel, J Mahlke, S Siswanto, R Krüger, H Heinsen, G Auburger, ... Brain pathology 25 (2), 121-135, 2015 | 239 | 2015 |
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 | 209 | 1998 |
Nigral stimulation for resistant axial motor impairment in Parkinson’s disease? A randomized controlled trial D Weiss, M Walach, C Meisner, M Fritz, M Scholten, S Breit, C Plewnia, ... Brain 136 (7), 2098-2108, 2013 | 203 | 2013 |
Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease FP Marx, C Holzmann, KM Strauss, L Li, O Eberhardt, E Gerhardt, ... Human molecular genetics 12 (11), 1223-1231, 2003 | 189 | 2003 |
Familial Parkinson's disease–genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the disease C Schiesling, N Kieper, K Seidel, R Krüger Neuropathology and applied neurobiology 34 (3), 255-271, 2008 | 188 | 2008 |
Mitochondrial protein quality control by the proteasome involves ubiquitination and the protease Omi S Radke, H Chander, P Schäfer, G Meiss, R Krüger, JB Schulz, ... Journal of Biological Chemistry 283 (19), 12681-12685, 2008 | 188 | 2008 |
Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers R Krüger, W Kuhn, KL Leenders, R Sprengelmeyer, T Müller, D Woitalla, ... Neurology 56 (10), 1355-1362, 2001 | 187 | 2001 |