The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers - Wikidata - wikimedia - TriplyDB

The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers

The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers

http://www.wikidata.org/entity/Q31129910

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Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans Genetic diagnosis and prognosis of Alzheimer's disease: challenges and opportunities Mapping asthma-associated variants in admixed populations 2014 Update of the Alzheimer's Disease Neuroimaging Initiative: A review of papers published since its inception.Alzheimer's disease: relevant molecular and physiopathological events affecting amyloid-β brain balance and the putative role of PPARs.Coding variants in TREM2 increase risk for Alzheimer's disease Identification of rare variants in Alzheimer's disease.Alzheimer's disease risk genes and mechanisms of disease pathogenesis Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease.Text mining facilitates database curation - extraction of mutation-disease associations from Bio-medical literature Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease.Candidate genes for Alzheimer's disease are associated with individual differences in plasma levels of beta amyloid peptides in adults with Down syndrome.Presenilin E318G variant and Alzheimer's disease risk: the Cache County study.Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer's disease.Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease.Genetic discoveries in AD using CSF amyloid and tau.Alzheimer's disease genetics: from the bench to the clinic.Monoaminergic neuropathology in Alzheimer's disease.Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK.Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies.Parkinson disease polygenic risk score is associated with Parkinson disease status and age at onset but not with alpha-synuclein cerebrospinal fluid levels.Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function.Understanding the roles of mutations in the amyloid precursor protein in Alzheimer disease.

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The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers

http://www.wikidata.org/entity/Q31129910

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2013 nî lūn-bûn

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2013 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2013 թվականի օգոստոսին հրատարակված գիտական հոդված

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers

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The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers

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The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers

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JOURNAL.PGEN.1003685

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The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers

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Breanna Cooper

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David Carrell

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Genetic and Environmental Risk for Alzheimer's Disease Consortium GERAD

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Julie A Schneider

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Lori Chibnik

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Sarah Bertelsen

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Yefei Cai

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P2860

SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease

TREM2 Variants in Alzheimer's Disease

Variant of TREM2 Associated with the Risk of Alzheimer's Disease

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

A method and server for predicting damaging missense mutations

Principal components analysis corrects for stratification in genome-wide association studies

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

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e1003685

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scholarly article

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10.1371/JOURNAL.PGEN.1003685

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8

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9

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Bruno A Benitez

Carlos Cruchaga

Alzheimer's Disease Neuroimaging Initiative

Celeste M Karch

David M. Holtzman

David A Bennett

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2013-08-22T00:00:00Z

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262044310

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23990795

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Alzheimer's disease

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3750021

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