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Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1 EM Valente, PM Abou-Sleiman, V Caputo, MMK Muqit, K Harvey, ... Science 304 (5674), 1158-1160, 2004 | 4294 | 2004 |
The ubiquitin pathway in Parkinson's disease E Leroy, R Boyer, G Auburger, B Leube, G Ulm, E Mezey, G Harta, ... Nature 395 (6701), 451-452, 1998 | 2142 | 1998 |
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28 C Alexander, M Votruba, UEA Pesch, DL Thiselton, S Mayer, A Moore, ... Nature genetics 26 (2), 211-215, 2000 | 1618 | 2000 |
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS AC Elden, HJ Kim, MP Hart, AS Chen-Plotkin, BS Johnson, X Fang, ... Nature 466 (7310), 1069-1075, 2010 | 1474 | 2010 |
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2 SM Pulst, A Nechiporuk, T Nechiporuk, S Gispert, XN Chen, ... Nature genetics 14 (3), 269-276, 1996 | 1343 | 1996 |
Levels of nerve growth factor and its mRNA in the central nervous system of the rat correlate with cholinergic innervation. S Korsching, G Auburger, R Heumann, J Scott, H Thoenen The EMBO journal 4 (6), 1389-1393, 1985 | 1075 | 1985 |
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 | 625 | 2007 |
Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice LA Becker, B Huang, G Bieri, R Ma, DA Knowles, P Jafar-Nejad, ... Nature 544 (7650), 367-371, 2017 | 571 | 2017 |
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Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7 U Rüb, L Schöls, H Paulson, G Auburger, P Kermer, JC Jen, K Seidel, ... Progress in neurobiology 104, 38-66, 2013 | 388 | 2013 |
Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1 S Gispert, R Twells, G Orozco, A Brice, J Weber, L Heredero, K Scheufler, ... Nature genetics 4 (3), 295-299, 1993 | 388 | 1993 |
Genome-wide association study of intracranial aneurysm identifies three new risk loci K Yasuno, K Bilguvar, P Bijlenga, SK Low, B Krischek, G Auburger, ... Nature genetics 42 (5), 420-425, 2010 | 364 | 2010 |
MPTP susceptibility in the mouse: behavioral, neurochemical, and histological analysis of gender and strain differences M Sedelis, K Hofele, GW Auburger, S Morgan, JP Huston, ... Behavior genetics 30, 171-182, 2000 | 321 | 2000 |
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 | 305 | 2015 |
An isoform of ataxin‐3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients T Schmidt, GB Landwehrmeyer, I Schmitt, Y Trottier, G Auburger, ... Brain pathology 8 (4), 669-679, 1998 | 270 | 1998 |
Decreased expression of Drp1 and Fis1 mediates mitochondrial elongation in senescent cells and enhances resistance to oxidative stress through PINK1 S Mai, M Klinkenberg, G Auburger, J Bereiter-Hahn, M Jendrach Journal of cell science 123 (6), 917-926, 2010 | 265 | 2010 |
Spinocerebellar ataxia 2 (SCA2) I Lastres-Becker, U Rüb, G Auburger The cerebellum 7, 115-124, 2008 | 256 | 2008 |
Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6 HH Hoepken, S Gispert, B Morales, O Wingerter, D Del Turco, A Mülsch, ... Neurobiology of disease 25 (2), 401-411, 2007 | 252 | 2007 |
Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger Acta neuropathologica 97, 306-310, 1999 | 252 | 1999 |