High-resolution whole-genome association study of Parkinson disease. - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q24535861

about

Parkinson's disease: from monogenic forms to genetic susceptibility factors A genomic pathway approach to a complex disease: axon guidance and Parkinson disease SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population Human G-proteins, ObgH1 and Mtg1, associate with the large mitochondrial ribosome subunit and are involved in translation and assembly of respiratory complexes Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease Genome-wide association studies in neurological disorders Genome-wide association study reveals genetic risk underlying Parkinson's disease Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease Immunotherapy in Parkinson's Disease: Micromanaging Alpha-Synuclein Aggregation The genetics and neuropathology of Parkinson's disease Genome-wide association studies of late-onset cardiovascular disease Human genetic variation and Parkinson's disease Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.Gene-environment interactions: key to unraveling the mystery of Parkinson's disease The power of meta-analysis in genome-wide association studies The HapMap and genome-wide association studies in diagnosis and therapy Parkinson disease loci in the mid-western Amish A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.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.Loss of vesicular dopamine release precedes tauopathy in degenerative dopaminergic neurons in a Drosophila model expressing human tau.Lack of replication of association between GIGYF2 variants and Parkinson disease.Genomewide association study for susceptibility genes contributing to 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 SNCA variant associated with Parkinson disease and plasma alpha-synuclein level.Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.Spatial distribution of Parkinson's disease mortality in Spain, 1989-1998, as a guide for focused aetiological research or health-care intervention Efficient study designs for test of genetic association using sibship data and unrelated cases and controls.CGI: a new approach for prioritizing genes by combining gene expression and protein-protein interaction data.Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease.Structural basis for the dissociation of α-synuclein fibrils triggered by pressure perturbation of the hydrophobic core.Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set.Family-based versus unrelated case-control designs for genetic associations.Application of genome-wide single nucleotide polymorphism typing: simple association and beyond

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P2860

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

http://www.wikidata.org/entity/Q24535861

description

2005 nî lūn-bûn

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2005 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

High-resolution whole-genome association study of Parkinson disease

@nl

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

@ast

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

@en

type

label

High-resolution whole-genome association study of Parkinson disease

@nl

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

@ast

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

@en

prefLabel

High-resolution whole-genome association study of Parkinson disease

@nl

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

@ast

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

@en

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American Journal of Human Genetics

P1476

High-resolution whole-genome association study of Parkinson disease

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P2093

David R Cox

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Demetrius M Maraganore

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Dennis G Ballinger

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Kari J Strain

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P V Krishna Pant

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Timothy G Lesnick

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Walter A Rocca

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P2860

X-inactivation profile reveals extensive variability in X-linked gene expression in females

Intergenic transcription is required to repress the Saccharomyces cerevisiae SER3 gene

The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders

Plexin-B3 is a functional receptor for semaphorin 5A.

Molecular cloning and mapping of human semaphorin F from the Cri-du-chat candidate interval

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

Complement factor H polymorphism in age-related macular degeneration

Statistical significance for genomewide studies

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685-693

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2392081

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10.1086/496902

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5

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77

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Matthew J. Farrer

Mariza de Andrade

Kelly A. Frazer

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2005-09-09T00:00:00Z

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7514998

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16252231

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Parkinson's disease

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1271381

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