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Claudia Schulte
Claudia Schulte
University of Tuebingen, Hertie Institute for Clinical Brain Research, DZNE
Verified email at uni-tuebingen.de
Title
Cited by
Cited by
Year
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
22432009
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
21922009
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
19932014
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
15582019
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
4132016
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
3812014
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ...
Brain 140 (12), 3191-3203, 2017
3762017
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*
D Berg, KJ Schweitzer, P Leitner, A Zimprich, P Lichtner, P Belcredi, ...
Brain 128 (12), 3000-3011, 2005
3222005
SNCA variants are associated with increased risk for multiple system atrophy
SW Scholz, H Houlden, C Schulte, M Sharma, A Li, D Berg, A Melchers, ...
Annals of Neurology: Official Journal of the American Neurological …, 2009
3192009
GBA-associated PD presents with nonmotor characteristics
K Brockmann, K Srulijes, AK Hauser, C Schulte, I Csoti, T Gasser, D Berg
Neurology 77 (3), 276-280, 2011
3002011
Parkinson's disease age at onset genome‐wide association study: defining heritability, genetic loci, and α‐synuclein mechanisms
C Blauwendraat, K Heilbron, CL Vallerga, S Bandres‐Ciga, R Von Coelln, ...
Movement Disorders 34 (6), 866-875, 2019
2892019
GBA‐associated Parkinson's disease: Reduced survival and more rapid progression in a prospective longitudinal study
K Brockmann, K Srulijes, S Pflederer, AK Hauser, C Schulte, W Maetzler, ...
Movement Disorders 30 (3), 407-411, 2015
2662015
Using genome-wide complex trait analysis to quantify ‘missing heritability’in Parkinson's disease
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simón-Sánchez, ...
Human molecular genetics 21 (22), 4996-5009, 2012
2372012
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
R Chia, MS Sabir, S Bandres-Ciga, S Saez-Atienzar, RH Reynolds, ...
Nature genetics 53 (3), 294-303, 2021
2162021
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
MA Van Es, HJ Schelhaas, PWJ Van Vught, N Ticozzi, PM Andersen, ...
Annals of neurology 70 (6), 964-973, 2011
2132011
S100B is increased in Parkinson’s disease and ablation protects against MPTP-induced toxicity through the RAGE and TNF-α pathway
K Sathe, W Maetzler, JD Lang, RB Mounsey, C Fleckenstein, HL Martin, ...
Brain 135 (11), 3336-3347, 2012
2112012
Cortical PIB binding in Lewy body disease is associated with Alzheimer-like characteristics
W Maetzler, I Liepelt, M Reimold, G Reischl, C Solbach, C Becker, ...
Neurobiology of disease 34 (1), 107-112, 2009
2042009
Genetic basis of Parkinson’s disease: inheritance, penetrance, and expression
C Schulte, T Gasser
The application of clinical genetics, 67-80, 2011
1962011
Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia
C Blauwendraat, X Reed, L Krohn, K Heilbron, S Bandres-Ciga, M Tan, ...
Brain 143 (1), 234-248, 2020
1812020
Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasis
LF Burbulla, C Schelling, H Kato, D Rapaport, D Woitalla, C Schiesling, ...
Human molecular genetics 19 (22), 4437-4452, 2010
1622010
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