A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB - Wikidata - awgldk - TriplyDB

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

http://www.wikidata.org/entity/Q24644827

about

GWAS of 126,559 individuals identifies genetic variants associated with educational attainment Common genetic variation and performance on standardized cognitive tests A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality Genetic signatures of exceptional longevity in humans Genome-wide association study of comorbid depressive syndrome and alcohol dependence Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study Large-scale genome-wide association study of Asian population reveals genetic factors in FRMD4A and other loci influencing smoking initiation and nicotine dependence.Uniform, optimal signal processing of mapped deep-sequencing data.Genetic copy number variants in sib pairs both affected with schizophrenia.Prefrontal inefficiency is associated with polygenic risk for schizophrenia Childhood intelligence is heritable, highly polygenic and associated with FNBP1L Brain-derived neurotrophic factor val66met polymorphism and hippocampal activation during episodic encoding and retrieval tasks RNA-Seq analysis implicates dysregulation of the immune system in schizophrenia Genetic copy number variation and general cognitive ability No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort.Conserved higher-order chromatin regulates NMDA receptor gene expression and cognition.The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion A common copy number variation (CNV) polymorphism in the CNTNAP4 gene: association with aging in females New genetic loci link adipose and insulin biology to body fat distribution.Genome-Wide Analyses of Working-Memory Ability: A Review.The genetics of cognitive impairment in schizophrenia: a phenomic perspective.Heritability and genetic association analysis of cognition in the Diabetes Heart Study.A systematic eQTL study of cis-trans epistasis in 210 HapMap individuals.The Extended Nutrigenomics - Understanding the Interplay between the Genomes of Food, Gut Microbes, and Human Host Multifactoriality in Psychiatric Disorders: A Computational Study of Schizophrenia Allele-Selective Transcriptome Recruitment to Polysomes Primed for Translation: Protein-Coding and Noncoding RNAs, and RNA Isoforms.Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment.Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain Status of vitamins B-12 and B-6 but not of folate, homocysteine, and the methylenetetrahydrofolate reductase C677T polymorphism are associated with impaired cognition and depression in adults Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait.The COMT Val158 allele is associated with impaired delayed-match-to-sample performance in ADHD.Microsatellite polymorphisms associated with human behavioural and psychological phenotypes including a gene-environment interaction Copy number variations and cognitive phenotypes in unselected populations Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions.Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.GWAS for executive function and processing speed suggests involvement of the CADM2 gene.Loci influencing blood pressure identified using a cardiovascular gene-centric array.Intermediate phenotype analysis of patients, unaffected siblings, and healthy controls identifies VMAT2 as a candidate gene for psychotic disorder and neurocognition Purifying selection shapes the coincident SNP distribution of primate coding sequences.

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A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

http://www.wikidata.org/entity/Q24644827

description

2009 nî lūn-bûn

@nan

2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

@ast

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

@en

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

@nl

type

label

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

@ast

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

@en

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

@nl

prefLabel

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

@ast

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

@en

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

@nl

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Human Molecular Genetics

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A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

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David B Goldstein

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Deborah K Attix

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Dongliang Ge

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Erin L Heinzen

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Gail Clement

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Jessica M Maia

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Jill M McEvoy

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Kevin V Shianna

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Kristen L Linney

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P2860

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

Genetic enhancement of learning and memory in mice

A comprehensive review of genetic association studies

Rare chromosomal deletions and duplications increase risk of schizophrenia

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Disruption of neurexin 1 associated with autism spectrum disorder.

WGAViewer: software for genomic annotation of whole genome association studies

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1053752

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10.1093/HMG/DDP413

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23

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18

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Elizabeth T Cirulli

Michael E. Weale

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2009-12-01T00:00:00Z

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26793589

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19734545

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2773267

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