Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis.
about
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureGenetic relationship between five psychiatric disorders estimated from genome-wide SNPsA genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.Developing and evaluating polygenic risk prediction models for stratified disease prevention.Crowdsourced estimation of cognitive decline and resilience in Alzheimer's disease.Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke.Statistical power to detect genetic (co)variance of complex traits using SNP data in unrelated samples.Convergent genetic and expression data implicate immunity in Alzheimer's diseaseEvaluation of Penalized and Nonpenalized Methods for Disease Prediction with Large-Scale Genetic Data.Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis.Association and interaction effects of Alzheimer's disease-associated genes and lifestyle on cognitive aging in older adults in a Taiwanese population.Estimation and partition of heritability in human populations using whole-genome analysis methods.Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysis.Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolismEstimating the heritability of colorectal cancer.Large-scale genomics unveils the genetic architecture of psychiatric disordersInvestigation of manic and euthymic episodes identifies state- and trait-specific gene expression and STAB1 as a new candidate gene for bipolar disorderResearch review: Polygenic methods and their application to psychiatric traits.A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsyPopulation genetic differentiation of height and body mass index across Europe.Genotype-environment correlation in the era of DNAGenome-wide association study identifies multiple susceptibility loci for multiple myeloma.Measuring missing heritability: inferring the contribution of common variantsGenetic variation in imprinted genes is associated with risk of late-onset Alzheimer's diseaseSimultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture modelDirect Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC).Genetic burden associated with varying degrees of disease severity in endometriosisPlasma protein biomarkers of Alzheimer's disease endophenotypes in asymptomatic older twins: early cognitive decline and regional brain volumesImplementation of genome-wide complex trait analysis to quantify the heritability in multiple myeloma.Genetic Architecture of Lacunar StrokeHeritability of Individual Psychotic Experiences Captured by Common Genetic Variants in a Community Sample of Adolescents.Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approachesShared genetics underlying epidemiological association between endometriosis and ovarian cancer.Estimation of heritability for nine common cancers using data from genome-wide association studies in Chinese population.Differences in Common Genetic Predisposition to Ischemic Stroke by Age and SexEffects of circadian clock genes and health-related behavior on metabolic syndrome in a Taiwanese population: Evidence from association and interaction analysisQuantifying the heritability of glioma using genome-wide complex trait analysis.Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer's disease.A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants.Shared genetic contribution to Ischaemic Stroke and Alzheimer's Disease.
P2860
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P2860
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Estimation and partitioning of ...... e sclerosis and endometriosis.
@ast
Estimation and partitioning of ...... e sclerosis and endometriosis.
@en
type
label
Estimation and partitioning of ...... e sclerosis and endometriosis.
@ast
Estimation and partitioning of ...... e sclerosis and endometriosis.
@en
prefLabel
Estimation and partitioning of ...... e sclerosis and endometriosis.
@ast
Estimation and partitioning of ...... e sclerosis and endometriosis.
@en
P2093
P2860
P50
P921
P356
P1476
Estimation and partitioning of ...... e sclerosis and endometriosis.
@en
P2093
ANZGene Consortium
Genetic and Environmental Risk for Alzheimer's disease Consortium
International Endogene Consortium
Julie Williams
S Hong Lee
P2860
P304
P356
10.1093/HMG/DDS491
P407
P50
P577
2012-11-28T00:00:00Z