Georg Auburger
Georg Auburger
Research Professor, Exp. Neurology, Klinikum Goethe Universität, Frankfurt am Main, Germany
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Guidelines for the use and interpretation of assays for monitoring autophagy
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy, 1-382, 2021
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
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
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
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
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
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
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
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
Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration
S Gispert, F Ricciardi, A Kurz, M Azizov, HH Hoepken, D Becker, W Voos, ...
PloS one 4 (6), e5777, 2009
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
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
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
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 (3), 171-182, 2000
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
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
Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution
B Leube, D Rudnicki, T Ratzlaff, KR Kessler, R Benecke, G Auburger
Human molecular genetics 5 (10), 1673-1677, 1996
Spinocerebellar ataxia 2 (SCA2)
I Lastres-Becker, U Rüb, G Auburger
The cerebellum 7 (2), 115-124, 2008
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
Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger
Acta neuropathologica 97 (3), 306-310, 1999
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