Estimating missing heritability for disease from genome-wide association studies.
about
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureWeb-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's diseaseAccurate and robust genomic prediction of celiac disease using statistical learningAnalysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer typesThe molecular genetic architecture of self-employmentThe ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataUncovering the Genetic Architectures of Quantitative TraitsChild development and molecular genetics: 14 years laterHeritability in the genome-wide association eraWhere GWAS and epidemiology meet: opportunities for the simultaneous study of genetic and environmental risk factors in schizophreniaGenetic risk prediction in complex diseaseEpigenomic elements analyses for promoters identify ESRRG as a new susceptibility gene for obesity-related traitsProspective association of a genetic risk score and lifestyle intervention with cardiovascular morbidity and mortality among individuals with type 2 diabetes: the Look AHEAD randomised controlled trial.The Red Queen in mitochondria: cyto-nuclear co-evolution, hybrid breakdown and human diseaseGenome-wide association study identifies five new schizophrenia lociGenome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphomaLarge-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesDNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12Genetic relationship between five psychiatric disorders estimated from genome-wide SNPsHost genetics and viral load in primary HIV-1 infection: clear evidence for gene by sex interactionsAnalysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared lociThe association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjectsIdentification of pathways for bipolar disorder: a meta-analysisGenome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureGenome-wide association study identifies multiple risk loci for chronic lymphocytic leukemiaA genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine AdsorbedGenome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans.Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.Systematic assessment of environmental risk factors for bipolar disorder: an umbrella review of systematic reviews and meta-analyses.Dissecting the genetics of complex traits using summary association statisticsDeveloping and evaluating polygenic risk prediction models for stratified disease prevention.Assessing the genetic architecture of epithelial ovarian cancer histological subtypes.Genetic overlap between diagnostic subtypes of ischemic strokeA Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health RecordsComparison of the heritability of schizophrenia and endophenotypes in the COGS-1 family study.Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke.Heritability estimates identify a substantial genetic contribution to risk and outcome of intracerebral hemorrhageEvidence of gene-gene interaction and age-at-diagnosis effects in type 1 diabetes.
P2860
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P2860
Estimating missing heritability for disease from genome-wide association studies.
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Estimating missing heritability for disease from genome-wide association studies.
@ast
Estimating missing heritability for disease from genome-wide association studies.
@en
Estimating missing heritability for disease from genome-wide association studies.
@nl
type
label
Estimating missing heritability for disease from genome-wide association studies.
@ast
Estimating missing heritability for disease from genome-wide association studies.
@en
Estimating missing heritability for disease from genome-wide association studies.
@nl
prefLabel
Estimating missing heritability for disease from genome-wide association studies.
@ast
Estimating missing heritability for disease from genome-wide association studies.
@en
Estimating missing heritability for disease from genome-wide association studies.
@nl
P2860
P50
P1476
Estimating missing heritability for disease from genome-wide association studies.
@en
P2860
P304
P356
10.1016/J.AJHG.2011.02.002
P407
P577
2011-03-03T00:00:00Z