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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 | 1635 | 2019 |
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci D Chang, MA Nalls, IB Hallgrímsdóttir, J Hunkapiller, M Van Der Brug, ... Nature genetics 49 (10), 1511-1516, 2017 | 1100 | 2017 |
Genome-wide analyses identify KIF5A as a novel ALS gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1267-1288, 2018 | 598 | 2018 |
Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis R Tian, A Abarientos, J Hong, SH Hashemi, R Yan, N Dräger, K Leng, ... Nature neuroscience 24 (7), 1020-1034, 2021 | 210 | 2021 |
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis S Bandres‐Ciga, AJ Noyce, G Hemani, A Nicolas, A Calvo, G Mora, ... Annals of neurology 85 (4), 470-481, 2019 | 166 | 2019 |
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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 | 147 | 2023 |
World of empowered IoT users SH Hashemi, F Faghri, P Rausch, RH Campbell 2016 IEEE first international conference on internet-of-things design and …, 2016 | 142 | 2016 |
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 | 140 | 2019 |
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 | 140 | 2017 |
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 | 121 | 2021 |
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 | 117 | 2019 |
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 | 103 | 2019 |
A CRISPRi/a platform in human iPSC-derived microglia uncovers regulators of disease states NM Dräger, SM Sattler, CTL Huang, OM Teter, K Leng, SH Hashemi, ... Nature neuroscience 25 (9), 1149-1162, 2022 | 98 | 2022 |
Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... BioRxiv, 388165, 2019 | 96 | 2019 |
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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 | 88 | 2022 |