Faraz Faghri
Title
Cited by
Cited by
Year
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
10802015
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, 2017
5882017
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
3232019
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
2542018
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
882017
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
862016
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
592019
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
592017
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
542019
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
502019
Failure scenario as a service (FSaaS) for Hadoop clusters
F Faghri, S Bazarbayev, M Overholt, R Farivar, RH Campbell, ...
Proceedings of the Workshop on Secure and Dependable Middleware for Cloud …, 2012
462012
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
442019
Parkinson’s disease genetics: identifying novel risk loci, providing causal insights and improving estimates of heritable risk
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
BioRxiv, 388165, 2018
442018
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
392018
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
352019
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
342019
System Genomics of Parkinson's Disease Consortium International Parkinson's Disease Genomics Consortium
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
Lancet Neurol 18, 1091-1102, 2019
252019
Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease
DA Kia, AJ Noyce, J White, D Speed, A Nicolas, IPDGC collaborators, ...
Annals of neurology 84 (2), 191-199, 2018
232018
Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease
C Blauwendraat, DA Kia, L Pihlstrøm, Z Gan-Or, S Lesage, JR Gibbs, ...
Neurobiology of aging 64, 159. e5-159. e8, 2018
232018
Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population
A Giri, KY Mok, I Jansen, M Sharma, C Tesson, G Mangone, S Lesage, ...
Neurobiology of aging 50, 167. e11-167. e13, 2017
232017
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Articles 1–20