Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population - Wikidata - awgldk - TriplyDB

Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population

Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population

http://www.wikidata.org/entity/Q28943392

about

The population genetics of the Jewish people The regulation and deregulation of Wnt signaling by PARK genes in health and disease Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease Physiological and pathological roles of mitochondrial SLC25 carriers Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction.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.An immunohistochemical, enzymatic, and behavioral study of CD157/BST-1 as a neuroregulator.Computational deconvolution of genome wide expression data from Parkinson's and Huntington's disease brain tissues using population-specific expression analysis.Tracking Parkinson's: Study Design and Baseline Patient Data.Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approach Integrated molecular landscape of Parkinson's disease Parkinson's disease-implicated kinases in the brain; insights into disease pathogenesis.Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation A chromosome 5q31.1 locus associates with tuberculin skin test reactivity in HIV-positive individuals from tuberculosis hyper-endemic regions in east Africa.Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.The link between the GBA gene and parkinsonism Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins.Association between GRN rs5848 polymorphism and Parkinson's disease in Taiwanese population Genome-wide association studies in neurology.Genetic association study between STK39 and CCDC62/HIP1R and Parkinson's disease 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.Variants in GBA, SNCA, and MAPT influence Parkinson disease risk, age at onset, and progression.The genetics of Parkinson's disease: progress and therapeutic implications The absence of intrarenal ACE protects against hypertension Next generation sequencing for neurological diseases: new hope or new hype?The Evolution of Genetics: Alzheimer's and Parkinson's Diseases.Calpastatin gene (CAST) is not associated with late onset sporadic Parkinson's disease in the Han Chinese population A non-stop S-antigen gene mutation is associated with late onset hereditary retinal degeneration in dogs.Increased Rate of Sporadic and Recurrent Rare Genic Copy Number Variants in Parkinson's Disease Among Ashkenazi Jews Development of inducible leucine-rich repeat kinase 2 (LRRK2) cell lines for therapeutics development in Parkinson's disease.The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism.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.Association studies of sporadic Parkinson's disease in the genomic era.Parkinson's Disease: From Pathogenesis to Pharmacogenomics Cellular reprogramming: a new approach to modelling Parkinson's disease.Recent advances in Parkinson’s disease genetics.Inflammation in Parkinson's disease: role of glucocorticoids.

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P2860

Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population

http://www.wikidata.org/entity/Q28943392

description

2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

artículu científicu espublizáu en 2011

@ast

scientific journal article

@en

wetenschappelijk artikel (gepubliceerd op 2011/08/03)

@nl

наукова стаття, опублікована в серпні 2011

@uk

مقالة علمية (نشرت في 3-8-2011)

@ar

name

Genome-wide association study ...... an Ashkenazi Jewish population

@ast

Genome-wide association study ...... an Ashkenazi Jewish population

@en

type

label

Genome-wide association study ...... an Ashkenazi Jewish population

@ast

Genome-wide association study ...... an Ashkenazi Jewish population

@en

prefLabel

Genome-wide association study ...... an Ashkenazi Jewish population

@ast

Genome-wide association study ...... an Ashkenazi Jewish population

@en

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1471-2350-12-104

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BMC Medical Genetics

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Genome-wide association study ...... an Ashkenazi Jewish population

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Andrew Browne

http://www.w3.org/2001/XMLSchema#string

Blair Ford

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Cheryl Waters

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Helen Mejia-Sanatana

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Howard Andrews

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Joseph H. Lee

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Karen Marder

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Lorraine N. Clark

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Lucien J. Cote

http://www.w3.org/2001/XMLSchema#string

Miguel Verbitsky

http://www.w3.org/2001/XMLSchema#string

P2860

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

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

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

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

Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

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

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1471-2350-12-104

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10.1186/1471-2350-12-104

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12

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genome-wide association study

Parkinson's disease

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