| PINK1 loss-of-function mutations affect mitochondrial complex I activity via NdufA10 ubiquinone uncoupling VA Morais, D Haddad, K Craessaerts, PJ De Bock, J Swerts, S Vilain, ... Science 344 (6180), 203-207, 2014 | 232 | 2014 |
| 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 | 195 | 2011 |
| Phosphatase and Tensin Homolog (PTEN)-induced Putative Kinase 1 (PINK1)-dependent Ubiquitination of Endogenous Parkin Attenuates Mitophagy STUDY IN HUMAN PRIMARY FIBROBLASTS … A Rakovic, K Shurkewitsch, P Seibler, A Grünewald, A Zanon, J Hagenah, ... Journal of Biological Chemistry 288 (4), 2223-2237, 2013 | 186 | 2013 |
| Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness SB Wortmann, FM Vaz, T Gardeitchik, LELM Vissers, GH Renkema, ... Nature genetics 44 (7), 797-802, 2012 | 160 | 2012 |
| Mutant Parkin impairs mitochondrial function and morphology in human fibroblasts A Grünewald, L Voges, A Rakovic, M Kasten, H Vandebona, ... PloS one 5 (9), e12962, 2010 | 139 | 2010 |
| Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit? K Hedrich, J Hagenah, A Djarmati, A Hiller, T Lohnau, K Lasek, ... Archives of neurology 63 (6), 833-838, 2006 | 132 | 2006 |
| Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients A Rakovic, A Grünewald, P Seibler, A Ramirez, N Kock, S Orolicki, ... Human molecular genetics 19 (16), 3124-3137, 2010 | 128 | 2010 |
| Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology A Grünewald, ME Gegg, JW Taanman, RH King, N Kock, C Klein, ... Experimental neurology 219 (1), 266-273, 2009 | 120 | 2009 |
| Myoclonus‐dystonia: significance of large SGCE deletions A Grünewald, A Djarmati, K Lohmann‐Hedrich, K Farrell, JA Zeller, ... Human mutation 29 (2), 331-332, 2008 | 117 | 2008 |
| Mitochondrial DNA Depletion in Respiratory Chain–Deficient P arkinson Disease Neurons A Grünewald, KA Rygiel, PD Hepplewhite, CM Morris, M Picard, ... Annals of neurology 79 (3), 366-378, 2016 | 104 | 2016 |
| ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome A Grünewald, B Arns, P Seibler, A Rakovic, A Münchau, A Ramirez, ... Neurobiology of aging 33 (8), 1843. e1-1843. e7, 2012 | 102 | 2012 |
| Bee venom and its component apamin as neuroprotective agents in a Parkinson disease mouse model D Alvarez-Fischer, C Noelker, F Vulinović, A Grünewald, C Chevarin, ... PLoS One 8 (4), e61700, 2013 | 91 | 2013 |
| Bioenergetic consequences of PINK1 mutations in Parkinson disease AY Abramov, M Gegg, A Grunewald, NW Wood, C Klein, AHV Schapira PLoS One 6 (10), e25622, 2011 | 88 | 2011 |
| A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis MC Rocha, JP Grady, A Grünewald, A Vincent, PF Dobson, RW Taylor, ... Scientific reports 5, 15037, 2015 | 85 | 2015 |
| Genetics of Parkinson's disease KR Kumar, A Djarmati-Westenberger, A Grünewald Seminars in neurology 31 (05), 433-440, 2011 | 75 | 2011 |
| New insights into the complex role of mitochondria in Parkinson’s disease A Grünewald, KR Kumar, CM Sue Progress in neurobiology 177, 73-93, 2019 | 72 | 2019 |
| Next-Generation Phenotyping Using the Parkin Example: Time to Catch Up With Genetics A Grünewald, M Kasten, A Ziegler, C Klein JAMA neurology 70 (9), 1186-1191, 2013 | 61 | 2013 |
| SCNT-derived ESCs with mismatched mitochondria trigger an immune response in allogeneic hosts T Deuse, D Wang, M Stubbendorff, R Itagaki, A Grabosch, LC Greaves, ... Cell Stem Cell 16 (1), 33-38, 2015 | 51 | 2015 |
| Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegia KR Kumar, NF Blair, H Vandebona, C Liang, K Ng, DM Sharpe, ... Journal of neurology 260 (10), 2516-2522, 2013 | 50 | 2013 |
| Genome‐wide association study in musician's dystonia: A risk variant at the arylsulfatase G locus? K Lohmann, A Schmidt, A Schillert, S Winkler, A Albanese, F Baas, ... Movement Disorders 29 (7), 921-927, 2014 | 49 | 2014 |
