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Cornelis Blauwendraat
Cornelis Blauwendraat
NIH/NIA
Verified email at nih.gov
Title
Cited by
Cited by
Year
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
16152019
The genetic architecture of Parkinson's disease
C Blauwendraat, MA Nalls, AB Singleton
The Lancet Neurology 19 (2), 170-178, 2020
7992020
MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease
PA Juge, JS Lee, E Ebstein, H Furukawa, E Dobrinskikh, S Gazal, ...
New England Journal of Medicine 379 (23), 2209-2219, 2018
3802018
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
2842019
Genome-wide pleiotropy between Parkinson disease and autoimmune diseases
A Witoelar, IE Jansen, Y Wang, RS Desikan, JR Gibbs, C Blauwendraat, ...
JAMA neurology 74 (7), 780-792, 2017
2582017
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
2072021
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
1732020
Identification of risk loci for Parkinson disease in Asians and comparison of risk between Asians and Europeans: a genome-wide association study
JN Foo, EGY Chew, SJ Chung, R Peng, C Blauwendraat, MA Nalls, ...
JAMA neurology 77 (6), 746-754, 2020
1672020
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
C Blauwendraat, F Faghri, L Pihlstrom, JT Geiger, A Elbaz, S Lesage, ...
Neurobiology of aging 57, 247. e9-247. e13, 2017
1372017
Genetic risk of Parkinson disease and progression: an analysis of 13 longitudinal cohorts
H Iwaki, C Blauwendraat, HL Leonard, G Liu, J Maple-Grødem, JC Corvol, ...
Neurology: Genetics 5 (4), e348, 2019
1352019
The role of monogenic genes in idiopathic Parkinson’s disease
X Reed, S Bandrés-Ciga, C Blauwendraat, MR Cookson
Neurobiology of disease 124, 230-239, 2019
1292019
Genome‐wide association studies of cognitive and motor progression in Parkinson's disease
MMX Tan, MA Lawton, E Jabbari, RH Reynolds, H Iwaki, C Blauwendraat, ...
Movement Disorders 36 (2), 424-433, 2021
1242021
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing
IE Jansen, H Ye, S Heetveld, MC Lechler, H Michels, RI Seinstra, ...
Genome biology 18, 1-26, 2017
1172017
Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets
DA Kia, D Zhang, S Guelfi, C Manzoni, L Hubbard, RH Reynolds, J Botía, ...
JAMA neurology 78 (4), 464-472, 2021
1122021
Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts
H Iwaki, C Blauwendraat, HL Leonard, JJ Kim, G Liu, J Maple‐Grødem, ...
Movement Disorders 34 (12), 1839-1850, 2019
1122019
Virus exposure and neurodegenerative disease risk across national biobanks
KS Levine, HL Leonard, C Blauwendraat, H Iwaki, N Johnson, ...
Neuron 111 (7), 1086-1093. e2, 2023
1062023
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the …
SJ Van Der Lee, OJ Conway, I Jansen, MM Carrasquillo, L Kleineidam, ...
Acta neuropathologica 138, 237-250, 2019
1012019
Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset
KJ Billingsley, IA Barbosa, S Bandrés-Ciga, JP Quinn, VJ Bubb, ...
npj Parkinson's Disease 5 (1), 8, 2019
972019
System Genomics of Parkinson’s Disease Consortium; International Parkinson’s Disease Genomics Consortium. Identification of novel risk loci, causal insights, and heritable risk …
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
Lancet Neurol 18 (12), 1091-1102, 2019
932019
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability
RH Reynolds, J Botía, MA Nalls, J Hardy, SA Gagliano Taliun, M Ryten
npj Parkinson's Disease 5 (1), 6, 2019
902019
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