Thomas Gasser
Thomas Gasser
Professor of Neurology
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Cited by
Cited by
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
A Zimprich, S Biskup, P Leitner, P Lichtner, M Farrer, S Lincoln, ...
Neuron 44 (4), 601-607, 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
MDS clinical diagnostic criteria for Parkinson's disease
RB Postuma, D Berg, M Stern, W Poewe, CW Olanow, W Oertel, J Obeso, ...
Movement disorders 30 (12), 1591-1601, 2015
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, 2009
Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
CB Lücking, A Dürr, V Bonifati, J Vaughan, G De Michele, T Gasser, ...
New England Journal of Medicine 342 (21), 1560-1567, 2000
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ...
New England Journal of Medicine 361 (17), 1651-1661, 2009
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
DG Healy, M Falchi, SS O'Sullivan, V Bonifati, A Durr, S Bressman, ...
The Lancet Neurology 7 (7), 583-590, 2008
The phenotypic spectrum of CADASIL: clinical findings in 102 cases
M Dichgans, M Mayer, I Uttner, R Brüning, J Müller‐Höcker, G Rungger, ...
Annals of neurology 44 (5), 731-739, 1998
MDS research criteria for prodromal Parkinson's disease
D Berg, RB Postuma, CH Adler, BR Bloem, P Chan, B Dubois, T Gasser, ...
Movement Disorders 30 (12), 1600-1611, 2015
Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria
DW Dickson, H Braak, JE Duda, C Duyckaerts, T Gasser, GM Halliday, ...
The Lancet Neurology 8 (12), 1150-1157, 2009
A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe
N Abbas, CB Lücking, S Ricard, A Dürr, V Bonifati, G De Michele, ...
Human molecular genetics 8 (4), 567-574, 1999
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
Intraoperative MRI guidance and extent of resection in glioma surgery: a randomised, controlled trial
C Senft, A Bink, K Franz, H Vatter, T Gasser, V Seifert
The lancet oncology 12 (11), 997-1003, 2011
A susceptibility locus for Parkinson's disease maps to chromosome 2p13
T Gasser, B Müller-Myhsok, ZK Wszolek, R Oehlmann, DB Calne, ...
Nature genetics 18 (3), 262-265, 1998
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
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome
A Zimprich, M Grabowski, F Asmus, M Naumann, D Berg, M Bertram, ...
Nature genetics 29 (1), 66-69, 2001
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
CM Lill, JT Roehr, MB McQueen, FK Kavvoura, S Bagade, BMM Schjeide, ...
PLoS Genet 8 (3), e1002548, 2012
Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients
J Winkelmann, TC Wetter, V Collado-Seidel, T Gasser, M Dichgans, ...
Sleep 23 (5), 1-6, 2000
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