Large-scale replication and heterogeneity in Parkinson disease genetic loci. - Wikidata - wikimedia - TriplyDB

Large-scale replication and heterogeneity in Parkinson disease genetic loci.

Large-scale replication and heterogeneity in Parkinson disease genetic loci.

http://www.wikidata.org/entity/Q36149955

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Phosphatases of α-synuclein, LRRK2, and tau: important players in the phosphorylation-dependent pathology of Parkinsonism Caffeine interaction with glutamate receptor gene GRIN2A: Parkinson's disease in Swedish population Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease 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.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.α-Synuclein oligomers impair neuronal microtubule-kinesin interplay.An immunohistochemical, enzymatic, and behavioral study of CD157/BST-1 as a neuroregulator.A Bayesian mathematical model of motor and cognitive outcomes in Parkinson's disease Parkinson's disease-implicated kinases in the brain; insights into disease pathogenesis.Prevalence of Parkinson disease among the Navajo: a preliminary examination Variants in SNCA Gene Are Associated with Parkinson's Disease Risk and Cognitive Symptoms in a Brazilian Sample.Genetic variations of GAK in two Chinese Parkinson's disease populations: a case-control study.Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study.Genetic association study between STK39 and CCDC62/HIP1R and Parkinson's disease Integrative network analysis unveils convergent molecular pathways in Parkinson's disease and diabetes.Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus STK39, But Not BST1, HLA-DQB1, and SPPL2B Polymorphism, Is Associated With Han-Chinese Parkinson's Disease in Taiwan.Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies.14-3-3 Proteins regulate mutant LRRK2 kinase activity and neurite shortening.Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease.The Evolution of Genetics: Alzheimer's and Parkinson's Diseases.Transcriptome study of differential expression in schizophrenia.GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16.Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort.The impact of mitochondrial DNA and nuclear genes related to mitochondrial functioning on the risk of Parkinson's disease.LRRK2: cause, risk, and mechanism.Association studies of sporadic Parkinson's disease in the genomic era.Mitochondrial proteolytic stress induced by loss of mortalin function is rescued by Parkin and PINK1.The role of inflammation in sporadic and familial Parkinson's disease.Network modeling to identify new mechanisms and therapeutic targets for Parkinson's disease.Ascertainment bias in dementias: a secondary to tertiary centre analysis in Central Italy and conceptual review.Recent advances in Parkinson’s disease genetics.Genes associated with Parkinson's disease: regulation of autophagy and beyond.Genetic Variants in SNCA and the Risk of Sporadic Parkinson's Disease and Clinical Outcomes: A Review Implications of DNA Methylation in Parkinson's Disease.Epigenome-wide DNA methylation analysis in siblings and monozygotic twins discordant for sporadic Parkinson's disease revealed different epigenetic patterns in peripheral blood mononuclear cells.Association between Parkinson's disease and G2019S and R1441C mutations of the LRRK2 gene.LRRK2 levels and phosphorylation in Parkinson's disease brain and cases with restricted Lewy bodies.

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P2860

Large-scale replication and heterogeneity in Parkinson disease genetic loci.

http://www.wikidata.org/entity/Q36149955

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Large-scale replication and heterogeneity in Parkinson disease genetic loci.

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Large-scale replication and heterogeneity in Parkinson disease genetic loci.

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type

label

Large-scale replication and heterogeneity in Parkinson disease genetic loci.

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Large-scale replication and heterogeneity in Parkinson disease genetic loci.

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prefLabel

Large-scale replication and heterogeneity in Parkinson disease genetic loci.

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Large-scale replication and heterogeneity in Parkinson disease genetic loci.

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Large-scale replication and heterogeneity in Parkinson disease genetic loci.

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Christina M Lill

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David Crosiers

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Demetrius Maraganore

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GEO-PD Consortium

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Gaetan Garraux

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Georg Auburger

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Georgia Xiromerisiou

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Georgios M Hadjigeorgiou

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Grzegorz Opala

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Hiroyuki Tomiyama

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P2860

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease

Finding the missing heritability of complex diseases

High-resolution whole-genome association study of Parkinson disease.

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

Genome-wide association study reveals genetic risk underlying Parkinson's disease

Evolutionary toggling of the MAPT 17q21.31 inversion region

Measuring inconsistency in meta-analyses

Quantifying heterogeneity in a meta-analysis

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.

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10.1212/WNL.0B013E318264E353

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7

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Christine Van Broeckhoven

Carles Vilariño-Güell

Ekaterina Rogaeva

Karin Wirdefeldt

Matthew J. Farrer

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2012-07-11T00:00:00Z

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22786590

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Parkinson's disease

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3414661

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