Genome-wide association study confirms extant PD risk loci among the Dutch.
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α-Synuclein genetic variants predict faster motor symptom progression in idiopathic Parkinson diseaseA two-stage meta-analysis identifies several new loci for Parkinson's diseaseImputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studiesInsights into Neuroinflammation in Parkinson's Disease: From Biomarkers to Anti-Inflammatory Based TherapiesThe genetics and neuropathology of Parkinson's diseaseIs inhibition of kinase activity the only therapeutic strategy for LRRK2-associated Parkinson's disease?Diacylglycerol Kinases as Emerging Potential Drug Targets for a Variety of Diseases: An UpdateGenetics in Parkinson disease: Mendelian versus non-Mendelian inheritanceThe Role of MAPT in Neurodegenerative Diseases: Genetics, Mechanisms and TherapyLarge-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseComprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.Selegiline Ameliorates Depression-Like Behavior in Mice Lacking the CD157/BST1 Gene, a Risk Factor for Parkinson's Disease.Communication Impairment in Ultrasonic Vocal Repertoire during the Suckling Period of Cd157 Knockout Mice: Transient Improvement by Oxytocin.Anxiety- and depression-like behavior in mice lacking the CD157/BST1 gene, a risk factor for Parkinson's disease.Common variation in the LRRK2 gene is a risk factor for Parkinson's disease.Risk prediction for complex diseases: application to Parkinson disease.Association mapping of the PARK10 region for Parkinson's disease susceptibility genesAn immunohistochemical, enzymatic, and behavioral study of CD157/BST-1 as a neuroregulator.Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data.Neuroinflammation and non-motor symptoms: the dark passenger of Parkinson's disease?Integrated molecular landscape of Parkinson's diseaseThe genetic contributions of SNCA and LRRK2 genes to Lewy Body pathology in Alzheimer's disease.Evidence for more than one Parkinson's disease-associated variant within the HLA region.Genetic dissection of strain dependent paraquat-induced neurodegeneration in the substantia nigra pars compacta.Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.A novel test of informative missingness using inconsistent linkage disequilibrium signals between case-parent triads and incomplete data.Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation.Novel one-step immunoassays to quantify α-synuclein: applications for biomarker development and high-throughput screening.Results of genome-wide analyses on neurodevelopmental phenotypes at four-year follow-up following cardiac surgery in infancy.HLA-DRB1 alleles are associated with the susceptibility to sporadic Parkinson's disease in Chinese Han populationGenetic variations of GAK in two Chinese Parkinson's disease populations: a case-control study.Genetic association study between STK39 and CCDC62/HIP1R and Parkinson's diseaseThe Broad Impact of TOM40 on Neurodegenerative Diseases in AgingEvidence for Immune Response, Axonal Dysfunction and Reduced Endocytosis in the Substantia Nigra in Early Stage Parkinson's Disease.The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane.Large-scale replication and heterogeneity in Parkinson disease genetic loci.A cytosine-thymine (CT)-rich haplotype in intron 4 of SNCA confers risk for Lewy body pathology in Alzheimer's disease and affects SNCA expression.High-Throughput Characterization of Blood Serum Proteomics of IBD Patients with Respect to Aging and Genetic Factors.Polygenic risk of Parkinson disease is correlated with disease age at onset.A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.
P2860
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P2860
Genome-wide association study confirms extant PD risk loci among the Dutch.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Genome-wide association study confirms extant PD risk loci among the Dutch.
@ast
Genome-wide association study confirms extant PD risk loci among the Dutch.
@en
type
label
Genome-wide association study confirms extant PD risk loci among the Dutch.
@ast
Genome-wide association study confirms extant PD risk loci among the Dutch.
@en
prefLabel
Genome-wide association study confirms extant PD risk loci among the Dutch.
@ast
Genome-wide association study confirms extant PD risk loci among the Dutch.
@en
P2093
P2860
P50
P356
P1476
Genome-wide association study confirms extant PD risk loci among the Dutch.
@en
P2093
Bart van de Warrenburg
Dena G Hernandez
Jacobus J van Hilten
Javier Simón-Sánchez
Karin D van Dijk
Patrizia Rizzu
Rob M A de Bie
Sampath Arepalli
P2860
P2888
P304
P356
10.1038/EJHG.2010.254
P50
P577
2011-01-19T00:00:00Z