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Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factorsTransdisciplinary approaches enhance the production of translational knowledgeAssociation between Expression Quantitative Trait Loci and Metabolic Traits in Two Korean PopulationsHuman GRK4γ142V Variant Promotes Angiotensin II Type I Receptor-Mediated Hypertension via Renal Histone Deacetylase Type 1 Inhibition.Common variants of the G protein-coupled receptor type 4 are associated with human essential hypertension and predict the blood pressure response to angiotensin receptor blockade.Gain-of-function mutation in Gnao1: a murine model of epileptiform encephalopathy (EIEE17)?Phenome-Wide Association Studies: Leveraging Comprehensive Phenotypic and Genotypic Data for Discovery.Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data setThe impact of population demography and selection on the genetic architecture of complex traits.Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5Pooled sample-based GWAS: a cost-effective alternative for identifying colorectal and prostate cancer risk variants in the Polish population.Are APOE ɛ genotype and TOMM40 poly-T repeat length associations with cognitive ageing mediated by brain white matter tract integrity?GWAS-based pathway analysis differentiates between fluid and crystallized intelligence.The impact of improved microarray coverage and larger sample sizes on future genome-wide association studiesAddressing population-specific multiple testing burdens in genetic association studies.TFF2-CXCR4 Axis Is Associated with BRAF V600E Colon Cancer.Polymorphisms and minihaplotypes in the VvNAC26 gene associate with berry size variation in grapevineGut microbiota in hypertension.A novel approach to genome-wide association analysis identifies genetic associations with primary biliary cholangitis and primary sclerosing cholangitis in Polish patients.Cardiovascular and noncardiovascular disease associations with hip fractures.Genetic predictors of cue- and stress-induced cigarette craving: an exploratory study.Genome-wide prediction of childhood asthma and related phenotypes in a longitudinal birth cohort.Integrative mutation, haplotype and G × G interaction evidence connects ABGL4, LRP8 and PCSK9 genes to cardiometabolic risk.Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.Alzheimer's disease susceptibility genes APOE and TOMM40, and brain white matter integrity in the Lothian Birth Cohort 1936.Identifying population differences in genes that affect body mass index.Controlling false discoveries in genome scans for selection.Association of Body Mass Index With Cardiometabolic Disease in the UK Biobank: A Mendelian Randomization Study.The genetic contribution to disease risk and variability in response to diet: where is the hidden heritability?The more you test, the more you find: The smallest P-values become increasingly enriched with real findings as more tests are conducted.ADRB2, brain white matter integrity and cognitive ageing in the Lothian Birth Cohort 1936.Interhemispheric gene expression differences in the cerebral cortex of humans and macaque monkeys.Gene coexpression networks reveal key drivers of phenotypic divergence in lake whitefish.What is the natural measurement unit of temperament: single traits or profiles?Pooling-Based Genome-Wide Association Study Identifies Risk Loci in the Pathogenesis of Ovarian Endometrioma in Chinese Han Women.Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networks.
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 24 February 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Correcting away the hidden heritability.
@en
Correcting away the hidden heritability.
@nl
type
label
Correcting away the hidden heritability.
@en
Correcting away the hidden heritability.
@nl
prefLabel
Correcting away the hidden heritability.
@en
Correcting away the hidden heritability.
@nl
P2860
P1476
Correcting away the hidden heritability.
@en
P2093
Scott M Williams
P2860
P304
P356
10.1111/J.1469-1809.2011.00640.X
P407
P577
2011-02-24T00:00:00Z