Related references
Note: Only part of the references are listed.Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study
Rita Guerreiro et al.
LANCET NEUROLOGY (2018)
Genetic risk factors for cognitive decline in Parkinson's disease: a review of the literature
E. S. Fagan et al.
EUROPEAN JOURNAL OF NEUROLOGY (2017)
Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci
John F. Fullard et al.
HUMAN MOLECULAR GENETICS (2017)
Targeting -Synuclein as a therapy for Parkinson's disease: The battle begins
C. Warren Olanow et al.
MOVEMENT DISORDERS (2017)
Genetic effects on gene expression across human tissues
Francois Aguet et al.
NATURE (2017)
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Diana Chang et al.
NATURE GENETICS (2017)
Fast, scalable prediction of deleterious noncoding variants from functional and population genomic data
Yi-Fei Huang et al.
NATURE GENETICS (2017)
β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson's disease
Shuchi Mittal et al.
SCIENCE (2017)
Interpreting Gene Expression Effects of Disease-Associated Variants: A Lesson from SNCA rs356168
Omolara-Chinue Glenn et al.
FRONTIERS IN GENETICS (2017)
Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)
Mike A. Nalls et al.
MOVEMENT DISORDERS (2016)
The NINDS Parkinson's Disease Biomarkers Program
Liana S. Rosenthal et al.
MOVEMENT DISORDERS (2016)
A cumulative genetic risk score predicts progression in Parkinson's disease
Lasse Pihlstrom et al.
MOVEMENT DISORDERS (2016)
Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression
Frank Soldner et al.
NATURE (2016)
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy et al.
NATURE GENETICS (2016)
Next-generation genotype imputation service and methods
Sayantan Das et al.
NATURE GENETICS (2016)
Genome-wide assessment of Parkinson's disease in a Southern Spanish population
Sara Bandres-Ciga et al.
NEUROBIOLOGY OF AGING (2016)
Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe
Cornelis Blauwendraat et al.
GENOME MEDICINE (2016)
Polygenic Risk of Parkinson Disease Is Correlated with Disease Age at Onset
Valentina Escott-Price et al.
ANNALS OF NEUROLOGY (2015)
The Prion Hypothesis of Parkinson's Disease
Yaping Chu et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2015)
Structure of the toxic core of α-synuclein from invisible crystals
Jose A. Rodriguez et al.
NATURE (2015)
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
Mike A. Nalls et al.
NEUROBIOLOGY OF AGING (2015)
Second-generation PLINK: rising to the challenge of larger and richer datasets
Christopher C. Chang et al.
GIGASCIENCE (2015)
A promoter-level mammalian expression atlas
Alistair R. R. Forrest et al.
NATURE (2014)
A general framework for estimating the relative pathogenicity of human genetic variants
Martin Kircher et al.
NATURE GENETICS (2014)
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Mike A. Nalls et al.
NATURE GENETICS (2014)
Genetic variability in the regulation of gene expression in ten regions of the human brain
Adaikalavan Ramasamy et al.
NATURE NEUROSCIENCE (2014)
Large-Scale Identification of Coregulated Enhancer Networks in the Adult Human Brain
Marit W. Vermunt et al.
CELL REPORTS (2014)
Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease
Lasse Pihlstrom et al.
NEUROBIOLOGY OF AGING (2013)
Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2
Nathan Pankratz et al.
ANNALS OF NEUROLOGY (2012)
Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses
Oliver Stegle et al.
NATURE PROTOCOLS (2012)
Genome Wide Assessment of Young Onset Parkinson's Disease from Finland
Dena G. Hernandez et al.
PLOS ONE (2012)
Alternative α-synuclein transcript usage as a convergent mechanism in Parkinson's disease pathology
Herve Rhinn et al.
NATURE COMMUNICATIONS (2012)
Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
Chris C. A. Spencer et al.
HUMAN MOLECULAR GENETICS (2011)
α-Synuclein and tau concentrations in cerebrospinal fluid of patients presenting with parkinsonism: a cohort study (vol 10, pg 230, 2011)
B. Mollenhauer et al.
LANCET NEUROLOGY (2011)
The effect of SNCA 3' region on the levels of SNCA-112 splicing variant
Jeanette J. McCarthy et al.
NEUROGENETICS (2011)
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease
Chuong B. Do et al.
PLOS GENETICS (2011)
A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease
Vincent Plagnol et al.
PLOS GENETICS (2011)
α-Synuclein and tau concentrations in cerebrospinal fluid of patients presenting with parkinsonism: a cohort study
Brit Mollenhauer et al.
LANCET NEUROLOGY (2011)
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
Taye H. Hamza et al.
NATURE GENETICS (2010)
Genomewide association study for susceptibility genes contributing to familial Parkinson disease
Nathan Pankratz et al.
HUMAN GENETICS (2009)
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
Wataru Satake et al.
NATURE GENETICS (2009)
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Javier Simon-Sanchez et al.
NATURE GENETICS (2009)
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
E. Sidransky et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
A fast and flexible statistical model for large-scale population genotype data: Applications to inferring missing genotypes and haplotypic phase
P Scheet et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix
J Li et al.
HEREDITY (2005)
A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other
DR Nyholt
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
α-synuclein locus triplication causes Parkinson's disease
AB Singleton et al.
SCIENCE (2003)
A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: Application to HLA in type 1 diabetes
HJ Cordell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Share Paper
