Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q24606055

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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 Phosphatases of α-synuclein, LRRK2, and tau: important players in the phosphorylation-dependent pathology of Parkinsonism Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases 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 Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson disease Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease Meta-analysis of early nonmotor features and risk factors for Parkinson disease Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease A large study reveals no association between APOE and Parkinson's disease Aldehyde dehydrogenase inhibition as a pathogenic mechanism in Parkinson disease A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease Toward precision medicine in neurological diseases Using iPS Cells toward the Understanding of Parkinson's Disease Coffee, Genetic Variants, and Parkinson's Disease: Gene-Environment Interactions Parkinson's disease, insulin resistance and novel agents of neuroprotection The genetics and neuropathology of Parkinson's disease State of play in amyotrophic lateral sclerosis genetics Intrabodies as neuroprotective therapeutics Late-Onset Alzheimer's Disease Genes and the Potentially Implicated Pathways Genetics of Parkinson's disease - a clinical perspective Is inhibition of kinase activity the only therapeutic strategy for LRRK2-associated Parkinson's disease?Genetic risk prediction in complex disease Neuroimmunological processes in Parkinson's disease and their relation to α-synuclein: microglia as the referee between neuronal processes and peripheral immunity PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease Roco kinase structures give insights into the mechanism of Parkinson disease-related leucine-rich-repeat kinase 2 mutations Pathogenic Parkinson's disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation Parkinson's disease genes VPS35 and EIF4G1 interact genetically and converge on α-synuclein Inhibition of LRRK2 kinase activity stimulates macroautophagy 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 CNS infections, sepsis and risk of Parkinson's disease Developmental exposure to organophosphates triggers transcriptional changes in genes associated with Parkinson's disease in vitro and in vivo Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees Gene-wise association of variants in four lysosomal storage disorder genes in neuropathologically confirmed Lewy body disease Synaptotagmin-11 inhibits clathrin-mediated and bulk endocytosis

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

http://www.wikidata.org/entity/Q24606055

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2011 nî lūn-bûn

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2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2011 թվականի փետրվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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Imputation of sequence variant ...... enome-wide association studies

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Imputation of sequence variant ...... enome-wide association studies

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Imputation of sequence variant ...... enome-wide association studies

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Imputation of sequence variant ...... enome-wide association studies

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Imputation of sequence variant ...... enome-wide association studies

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Imputation of sequence variant ...... enome-wide association studies

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Imputation of sequence variant ...... enome-wide association studies

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Dena G Hernandez

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J Simón-Sánchez

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Manu Sharma

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Michael A Nalls

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Mohamad Saad

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Sigurlaug Sveinbjörnsdóttir

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Una-Marie Sheerin

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P2860

Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

The NCBI dbGaP database of genotypes and phenotypes

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

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

The crystal structure of human alpha-amino-beta-carboxymuconate-epsilon-semialdehyde decarboxylase in complex with 1,3-dihydroxyacetonephosphate suggests a regulatory link between NAD synthesis and glycolysis

Measuring inconsistency in meta-analyses

The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI

Practical aspects of imputation-driven meta-analysis of genome-wide association studies

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

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Vincent Plagnol

Claudia Schulte

Nicholas W. Wood

Andrew Singleton

John Anthony Hardy

Kári Stefánsson

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2011-02-19T00:00:00Z

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genome-wide association study

Parkinson's disease

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