Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. - Wikidata - wikimedia - TriplyDB

Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.

Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.

http://www.wikidata.org/entity/Q44428663

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A two-stage meta-analysis identifies several new loci for Parkinson's disease Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies Coffee, Genetic Variants, and Parkinson's Disease: Gene-Environment Interactions Is inhibition of kinase activity the only therapeutic strategy for LRRK2-associated Parkinson's disease?Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population Comprehensive 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.Anxiety- and depression-like behavior in mice lacking the CD157/BST1 gene, 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 genes An immunohistochemical, enzymatic, and behavioral study of CD157/BST-1 as a neuroregulator.Rationale for therapeutic silencing of alpha-synuclein in Parkinson's disease Integrated molecular landscape of Parkinson's disease A Bayesian mathematical model of motor and cognitive outcomes in Parkinson's disease Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.Genome wide assessment of young onset Parkinson's disease from Finland Results of genome-wide analyses on neurodevelopmental phenotypes at four-year follow-up following cardiac surgery in infancy.Evaluation of Parkinson disease risk variants as expression-QTLs.Association between GRN rs5848 polymorphism and Parkinson's disease in Taiwanese population Genome-wide association studies in neurology.Testing the utility of an integrated analysis of copy number and transcriptomics datasets for inferring gene regulatory relationships Genetic variations of GAK in two Chinese Parkinson's disease populations: a case-control study.Genome-wide association study confirms extant PD risk loci among the Dutch.Genetic association study between STK39 and CCDC62/HIP1R and Parkinson's disease SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population Gene expression in the Parkinson's disease brain.Large-scale replication and heterogeneity in Parkinson disease genetic loci.High-Throughput Characterization of Blood Serum Proteomics of IBD Patients with Respect to Aging and Genetic Factors.A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.The genetics of Parkinson's disease: progress and therapeutic implications The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism.Identifying the genetic components underlying the pathophysiology of movement disorders.The Evolution of Genetics: Alzheimer's and Parkinson's Diseases.

P2860

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P2860

Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.

http://www.wikidata.org/entity/Q44428663

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2010 nî lūn-bûn

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Genome-wide association study ...... se in the European population.

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Genome-wide association study ...... se in the European population.

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Genome-wide association study ...... se in the European population.

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Genome-wide association study ...... se in the European population.

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Parkinson's disease