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
16382009
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
12422013
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
11592014
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
11402008
Genetics of Parkinson’s disease
C Klein, A Westenberger
Cold Spring Harbor perspectives in medicine 2 (1), a008888, 2012
8112012
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
6842006
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
4652012
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
4002012
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
3782000
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
3732004
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
3662011
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
3382005
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
2882007
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
2702000
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
2682001
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
2642004
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease
K Hedrich, A Djarmati, N Schäfer, R Hering, C Wellenbrock, PH Weiss, ...
Neurology 62 (3), 389-394, 2004
2472004
Lysosomal impairment in Parkinson's disease
B Dehay, M Martinez‐Vicente, GA Caldwell, KA Caldwell, Z Yue, ...
Movement Disorders 28 (6), 725-732, 2013
2452013
Parkinson disease, 10 years after its genetic revolution: multiple clues to a complex disorder
C Klein, MG Schlossmacher
Neurology 69 (22), 2093-2104, 2007
2412007
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