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, 2009
16672009
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
13092013
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
12082014
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
11742008
Genetics of Parkinson’s disease
C Klein, A Westenberger
Cold Spring Harbor perspectives in medicine 2 (1), a008888, 2012
8522012
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
6912006
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
4792012
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
4092012
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
3822000
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
3742004
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
3692011
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
3442005
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
2912007
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
2762018
Parkin deletions in a family with adult‐onset, tremor‐dominant parkinsonism: Expanding the phenotype
C Klein, PP Pramstaller, B Kis, CC Page, M Kann, J Leung, H Woodward, ...
Annals of neurology 48 (1), 65-71, 2000
2712000
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
2692001
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
2662005
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
2662004
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
2522017
Lysosomal impairment in Parkinson's disease
B Dehay, M Martinez‐Vicente, GA Caldwell, KA Caldwell, Z Yue, ...
Movement Disorders 28 (6), 725-732, 2013
2522013
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