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Cornelis Blauwendraat
Cornelis Blauwendraat
NIH/NIA
Verified email at nih.gov
Title
Cited by
Year
A comprehensive analysis of SNCA‐related genetic risk in sporadic parkinson disease
L Pihlstrøm, C Blauwendraat, C Cappelletti, V Berge‐Seidl, M Langmyhr, ...
Annals of neurology 84 (1), 117-129, 2018
572018
A cross‐sectional study of α‐synuclein seed amplification assay in Alzheimer's disease neuroimaging initiative: Prevalence and associations with Alzheimer's disease biomarkers …
D Tosun, Z Hausle, H Iwaki, P Thropp, J Lamoureux, EB Lee, K MacLeod, ...
Alzheimer's & Dementia, 2024
12024
A genetic and transcriptomic assessment of the KTN1 gene in Parkinson’s disease risk
A Moore, PW Crea, M Makarious, S Bandres-Ciga, C Blauwendraat, ...
Neurobiology of Aging 134, 66-73, 2024
2024
A genome wide pleiotropic approach to identify the genetic architecture of multiple system atrophy and its interaction with Parkinson's disease
AAK Sreelatha, A Shadrin, C Blauwendraat, O Frei, T Gasser, G Wenning, ...
MOVEMENT DISORDERS 34, S312-S314, 2019
2019
A genome-wide genetic pleiotropy approach identified shared loci between multiple system atrophy and inflammatory bowel disease
AA Shadrin, S Mucha, D Ellinghaus, MB Makarious, C Blauwendraat, ...
bioRxiv, 751354, 2019
2019
A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypes
K Menden, M Francescatto, T Nyima, C Blauwendraat, A Dhingra, ...
Scientific data 10 (1), 849, 2023
32023
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
1132019
A population scale analysis of rare SNCA variation in the UK Biobank
C Blauwendraat, MB Makarious, HL Leonard, S Bandres-Ciga, H Iwaki, ...
Neurobiology of disease 148, 105182, 2021
112021
A reference human induced pluripotent stem cell line for large-scale collaborative studies
CB Pantazis, A Yang, E Lara, JA McDonough, C Blauwendraat, L Peng, ...
Cell stem cell 29 (12), 1685-1702. e22, 2022
932022
A reference human induced pluripotent stem cell line for large-scale collaborative studies Authors and affiliations
CB Pantazis, A Yang, E Lara, JA McDonough, C Blauwendraat, L Peng, ...
Accelerating medicines partnership: Parkinson's disease. Genetic resource
H Iwaki, HL Leonard, MB Makarious, M Bookman, B Landin, D Vismer, ...
Movement Disorders 36 (8), 1795-1804, 2021
742021
Adaptive Long‐Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4
Z Chen, EK Gustavsson, H Macpherson, C Anderson, C Clarkson, ...
Movement Disorders 39 (3), 486-497, 2024
132024
ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies
C Blauwendraat, MA Nalls, M Federoff, O Pletnikova, J Ding, C Letson, ...
Movement disorders: official journal of the Movement Disorder Society 32 (2 …, 2017
112017
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1
P Alvarez Jerez, PA Wild Crea, D Ramos, EK Gustavsson, M Radefeldt, ...
medRxiv, 2024.02. 20.24302827, 2024
2024
alpha-Synuclein in sympathetic nerve fibers distinguishes PRKN from LRRK2 and other genetic forms of Parkinson's Disease
R Isonaka, D Goldstein, W Zhu, E Yoon, D Ehrlich, A Schindler, A Kokkinis, ...
MOVEMENT DISORDERS 36, S311-S313, 2021
2021
An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of a-synuclein
E Kara, A Crimi, A Wiedmer, M Emmenegger, C Manzoni, S Bandres-Ciga, ...
bioRxiv, 2019.12. 23.886838, 2019
2019
An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of α-synuclein
E Kara, A Crimi, A Wiedmer, M Emmenegger, C Manzoni, S Bandres-Ciga, ...
Cell reports 35 (10), 2021
92021
An introduction to the Global Parkinson's Genetics Program (GP2)
C Blauwendraat, E Riley, A Singleton
MOVEMENT DISORDERS 35, S195-S195, 2020
2020
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease
EE Brown, C Blauwendraat, J Trinh, M Rizig, MA Nalls, E Leveille, ...
Neurobiology of Aging 97, 148. e17-148. e24, 2021
232021
Analysis of rare Parkinson’s disease variants in millions of people
M Nalls, K Heilbron, C Blauwendraat
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Articles 1–20