Follow
Olaf Riess
Olaf Riess
Professor der Humangenetik, Universität Tübingen
Verified email at med.uni-tuebingen.de - Homepage
Title
Cited by
Cited by
Year
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
46531998
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
19862009
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
13142012
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
11682004
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
8682020
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
6912005
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
5782006
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
5641999
14-3-3 proteins in the nervous system
D Berg, C Holzmann, O Riess
Nature Reviews Neuroscience 4 (9), 752-762, 2003
5432003
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
4052010
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
3992003
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
3771998
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
3771997
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
3522006
Next-generation sequencing in X-linked intellectual disability
A Tzschach, U Grasshoff, S Beck-Woedl, C Dufke, C Bauer, M Kehrer, ...
European Journal of Human Genetics 23 (11), 1513-1518, 2015
3492015
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
3492014
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
3351999
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
3301998
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
3301998
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
3062016
The system can't perform the operation now. Try again later.
Articles 1–20