Big data: astronomical or genomical? ZD Stephens, SY Lee, F Faghri, RH Campbell, C Zhai, MJ Efron, R Iyer, ... PLoS biology 13 (7), e1002195, 2015 | 1498 | 2015 |
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 | 1211 | 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 | 976 | 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), 1268-1283. e6, 2018 | 507 | 2018 |
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 | 150 | 2019 |
Estimating the causal influence of body mass index on risk of Parkinson disease: a Mendelian randomisation study AJ Noyce, DA Kia, G Hemani, A Nicolas, TR Price, E De Pablo-Fernandez, ... PLoS medicine 14 (6), e1002314, 2017 | 143 | 2017 |
Analysis and prediction of unplanned intensive care unit readmission using recurrent neural networks with long short-term memory YW Lin, Y Zhou, F Faghri, MJ Shaw, RH Campbell PloS one 14 (7), e0218942, 2019 | 133 | 2019 |
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 | 132 | 2016 |
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 | 118 | 2021 |
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 | 112 | 2017 |
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), 2019 | 109 | 2019 |
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 | 93 | 2019 |
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 | 85 | 2019 |
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 | 83 | 2019 |
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 | 77 | 2021 |
The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease S Bandres‐Ciga, S Saez‐Atienzar, L Bonet‐Ponce, K Billingsley, D Vitale, ... Movement Disorders 34 (4), 460-468, 2019 | 73 | 2019 |
The Parkinson's disease genome‐wide association study locus browser FP Grenn, JJ Kim, MB Makarious, H Iwaki, A Illarionova, K Brolin, ... Movement Disorders 35 (11), 2056-2067, 2020 | 69 | 2020 |
Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease S Bandres-Ciga, S Saez-Atienzar, JJ Kim, MB Makarious, F Faghri, ... Acta neuropathologica 140, 341-358, 2020 | 68 | 2020 |
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 | 68 | 2019 |
Frequency of loss of function variants in LRRK2 in Parkinson disease C Blauwendraat, X Reed, DA Kia, Z Gan-Or, S Lesage, L Pihlstrøm, ... JAMA neurology 75 (11), 1416-1422, 2018 | 65 | 2018 |