Genomewide association study for susceptibility genes contributing to familial Parkinson disease - Wikidata - wikimedia - TriplyDB

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

http://www.wikidata.org/entity/Q30437480

about

α-Synuclein genetic variants predict faster motor symptom progression in idiopathic Parkinson disease Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee 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 Parkinson's disease: from monogenic forms to genetic susceptibility factors Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population Glucocerebrosidase is shaking up the synucleinopathies Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease 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 Fish Synucleins: An Update Coffee, Genetic Variants, and Parkinson's Disease: Gene-Environment Interactions The genetics and neuropathology of Parkinson's disease LRRK2 as a Potential Genetic Modifier of Synucleinopathies: Interlacing the Two Major Genetic Factors of Parkinson's Disease Alpha-synuclein biology in Lewy body diseases The role of tau in neurodegenerative diseases and its potential as a therapeutic target Human genetic variation and Parkinson's disease Diacylglycerol Kinases as Emerging Potential Drug Targets for a Variety of Diseases: An Update Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance 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.Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism Circadian dysfunction may be a key component of the non-motor symptoms of Parkinson's disease: insights from a transgenic mouse model Gene-environment interactions: key to unraveling the mystery of Parkinson's disease GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database DNAJC13 mutations in Parkinson disease Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study.Genetic signatures of exceptional longevity in humans Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population Genomic determinants of motor and cognitive outcomes in Parkinson's disease Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.Genomewide association study for onset age in Parkinson disease.Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.Heritability and molecular genetic basis of acoustic startle eye blink and affectively modulated startle response: a genome-wide association study.Cerebrospinal fluid α-synuclein predicts cognitive decline in Parkinson disease progression in the DATATOP cohort.Loss of vesicular dopamine release precedes tauopathy in degenerative dopaminergic neurons in a Drosophila model expressing human tau.Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease.Copy number variation in familial Parkinson disease.Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease

P2860

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P2860

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

http://www.wikidata.org/entity/Q30437480

description

2008 nî lūn-bûn

@nan

2008 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2008年の論文

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2008年論文

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2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

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name

Genomewide association study f ...... to familial Parkinson disease

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Genomewide association study f ...... to familial Parkinson disease

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type

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Genomewide association study f ...... to familial Parkinson disease

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Genomewide association study f ...... to familial Parkinson disease

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Genomewide association study f ...... to familial Parkinson disease

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Genomewide association study f ...... to familial Parkinson disease

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Genomewide association study f ...... to familial Parkinson disease

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Cheryl Halter

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Elizabeth W Pugh

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Jemma B Wilk

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Kimberly F Doheny

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PSG-PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories

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William C Nichols

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P2860

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

PLINK: a tool set for whole-genome association and population-based linkage analyses

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

alpha-Synuclein locus triplication causes Parkinson's disease

Haploview: analysis and visualization of LD and haplotype maps

Whole-genome genotyping

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

Alpha-synuclein locus duplication as a cause of familial Parkinson's disease

P2888

s00439-008-0582-9

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10.1007/S00439-008-0582-9

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6

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124

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James F. Gusella

Richard H Myers

Nathan Pankratz

Anita L DeStefano

Jeanne C Latourelle

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Parkinson's disease

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