Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease - Wikidata - wikimedia - TriplyDB

Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

http://www.wikidata.org/entity/Q24610759

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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease Genome-wide association studies in Alzheimer's disease Role of apolipoprotein E in neurodegenerative diseases The genetics and neuropathology of Alzheimer's disease Association and heterogeneity at the GAPDH locus in Alzheimer's disease Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease Intermediate phenotypes identify divergent pathways to Alzheimer's disease Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities Genome-wide association analysis of age-at-onset in Alzheimer's disease Genome-wide association study of Alzheimer's disease Genomic variants, genes, and pathways of Alzheimer's disease: An overview.Association of CLU and PICALM variants with Alzheimer's disease.Replication study of genome-wide associated SNPs with late-onset Alzheimer's disease Cadherins as targets for genetic diseases.Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels.Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases Systems biology approach to late-onset Alzheimer's disease genome-wide association study identifies novel candidate genes validated using brain expression data and Caenorhabditis elegans experiments.Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease Intercellular protein-protein interactions at synapses.Gene expression levels as endophenotypes in genome-wide association studies of Alzheimer disease Single-nucleotide polymorphisms are associated with cognitive decline at Alzheimer's disease conversion within mild cognitive impairment patients.Clinical genetics of Alzheimer's disease Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data The association of angiotensin-converting enzyme with biomarkers for Alzheimer's disease Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease Recent insights into the molecular genetics of dementia Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE Genetics of Alzheimer disease in the pre- and post-GWAS era Genetic variation at a single locus and age of onset for Alzheimer's disease.Detection of recurrent rearrangement breakpoints from copy number data Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease.Analysis of Genome-Wide Association Study (GWAS) data looking for replicating signals in Alzheimer's disease (AD).Evolution of genetic and genomic features unique to the human lineage.Genome-wide scan of copy number variation in late-onset Alzheimer's disease.Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls.Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS).

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Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

http://www.wikidata.org/entity/Q24610759

description

2009 nî lūn-bûn

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2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի փետրվարին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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name

Genetic variation in PCDH11X i ...... late-onset Alzheimer's disease

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Genetic variation in PCDH11X i ...... late-onset Alzheimer's disease

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Genetic variation in PCDH11X i ...... late-onset Alzheimer's disease

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Genetic variation in PCDH11X i ...... late-onset Alzheimer's disease

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Genetic variation in PCDH11X i ...... late-onset Alzheimer's disease

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Genetic variation in PCDH11X i ...... late-onset Alzheimer's disease

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prefLabel

Genetic variation in PCDH11X i ...... late-onset Alzheimer's disease

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Genetic variation in PCDH11X i ...... late-onset Alzheimer's disease

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Genetic variation in PCDH11X i ...... late-onset Alzheimer's disease

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Nature Genetics

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Genetic variation in PCDH11X i ...... late-onset Alzheimer's disease

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Curtis S Younkin

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Fanggeng Zou

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Gina D Bisceglio

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Julia E Crook

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Li Ma

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Linda H Younkin

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Louise P Walker

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Minerva M Carrasquillo

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Neill R Graff-Radford

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Samantha L Wilcox

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Role of Genes and Environments for Explaining Alzheimer Disease

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

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

Haploview: analysis and visualization of LD and haplotype maps

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

Proteins of the CNR family are multiple receptors for Reelin

Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease

Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium

Inactivation status of PCDH11X: sexual dimorphisms in gene expression levels in brain

Conservation of PCDHX in mammals; expression of human X/Y genes predominantly in brain.

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10.1038/NG.305

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2

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41

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Nilüfer Ertekin-Taner

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Ronald C. Petersen

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2009-02-01T00:00:00Z

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23771198

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1012640708

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19136949

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Alzheimer's disease

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