Christine Klein
Title
Cited by
Cited by
Year
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
17942009
Phenomenology and classification of dystonia: a consensus update
A Albanese, K Bhatia, SB Bressman, MR DeLong, S Fahn, VSC Fung, ...
Movement disorders 28 (7), 863-873, 2013
15192013
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
13912014
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
12832008
Genetics of Parkinson’s disease
C Klein, A Westenberger
Cold Spring Harbor perspectives in medicine 2 (1), a008888, 2012
10112012
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
LJ Ozelius, G Senthil, R Saunders-Pullman, E Ohmann, A Deligtisch, ...
New England Journal of Medicine 354 (4), 424-425, 2006
7272006
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 genetics 8 (3), e1002548, 2012
5092012
Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson’s disease
O Cooper, H Seo, S Andrabi, C Guardia-Laguarta, J Graziotto, ...
Science translational medicine 4 (141), 141ra90-141ra90, 2012
4442012
Parkin and PINK1 mitigate STING-induced inflammation
DA Sliter, J Martinez, L Hao, X Chen, N Sun, TD Fischer, JL Burman, Y Li, ...
Nature 561 (7722), 258-262, 2018
4202018
The DYT1 phenotype and guidelines for diagnostic testing
SB Bressman, C Sabatti, D Raymond, D De Leon, C Klein, PL Kramer, ...
Neurology 54 (9), 1746-1753, 2000
3942000
Mitochondrial Parkin recruitment is impaired in neurons derived from mutant PINK1 induced pluripotent stem cells
P Seibler, J Graziotto, H Jeong, F Simunovic, C Klein, D Krainc
Journal of Neuroscience 31 (16), 5970-5976, 2011
3932011
A major lung cancer susceptibility locus maps to chromosome 6q23–25
JE Bailey-Wilson, CI Amos, SM Pinney, GM Petersen, M De Andrade, ...
The American Journal of Human Genetics 75 (3), 460-474, 2004
3872004
Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking Palsy
JA Obeso, M Stamelou, CG Goetz, W Poewe, AE Lang, D Weintraub, ...
Movement Disorders 32 (9), 1264-1310, 2017
3842017
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes
V Bonifati, CF Rohe, GJ Breedveld, E Fabrizio, M De Mari, C Tassorelli, ...
Neurology 65 (1), 87-95, 2005
3582005
Deciphering the role of heterozygous mutations in genes associated with parkinsonism
C Klein, K Lohmann-Hedrich, E Rogaeva, MG Schlossmacher, AE Lang
The Lancet Neurology 6 (7), 652-662, 2007
3052007
Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers
PP Pramstaller, MG Schlossmacher, TS Jacques, F Scaravilli, C Eskelson, ...
Annals of neurology 58 (3), 411-422, 2005
2942005
Lysosomal impairment in Parkinson's disease
B Dehay, M Martinez‐Vicente, GA Caldwell, KA Caldwell, Z Yue, ...
Movement Disorders 28 (6), 725-732, 2013
2832013
Distribution, type, and origin of Parkin mutations: Review and case studies
K Hedrich, C Eskelson, B Wilmot, K Marder, J Harris, J Garrels, ...
Movement disorders: official journal of the Movement Disorder Society 19 (10 …, 2004
2832004
Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene
R Hilker, C Klein, M Ghaemi, B Kis, T Strotmann, LJ Ozelius, O Lenz, ...
Annals of neurology 49 (3), 367-376, 2001
2782001
Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration
B Dehay, A Ramirez, M Martinez-Vicente, C Perier, MH Canron, ...
Proceedings of the National Academy of Sciences 109 (24), 9611-9616, 2012
2762012
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