Quantifying the underestimation of relative risks from genome-wide association studies
about
Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritabilityImputation-based meta-analysis of severe malaria in three African populations.Genome-wide association of body fat distribution in African ancestry populations suggests new loci.Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac diseaseImputation of KIR Types from SNP Variation Data.Estimating causal effects of genetic risk variants for breast cancer using marker data from bilateral and familial cases.Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation.Cohen's h for detection of disease association with rare genetic variants.Quantifying missing heritability at known GWAS loci.Identifying breast cancer risk loci by global differential allele-specific expression (DASE) analysis in mammary epithelial transcriptome.Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.Using genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experiments.Genome wide association studies in presence of misclassified binary responsesFine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regionsThe genetics of asthma and allergic disease: a 21st century perspectiveResolving the variable genome and epigenome in human disease.Dissecting Allele Architecture of Early Onset IBD Using High-Density GenotypingCase-Only Survival Analysis Reveals Unique Effects of Genotype, Sex, and Coronary Disease Severity on Survivorship.From markers to molecular mechanisms: type 1 diabetes in the post-GWAS era.Common, germline genetic variations in the novel tumor suppressor BAP1 and risk of developing different types of cancer.Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations.A two-platform design for next generation genome-wide association studies.A note on the efficiencies of sampling strategies in two-stage Bayesian regional fine mapping of a quantitative trait.Elucidating the Underlying Functional Mechanisms of Breast Cancer Susceptibility Through Post-GWAS Analyses
P2860
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P2860
Quantifying the underestimation of relative risks 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
Quantifying the underestimation of relative risks from genome-wide association studies
@ast
Quantifying the underestimation of relative risks from genome-wide association studies
@en
type
label
Quantifying the underestimation of relative risks from genome-wide association studies
@ast
Quantifying the underestimation of relative risks from genome-wide association studies
@en
prefLabel
Quantifying the underestimation of relative risks from genome-wide association studies
@ast
Quantifying the underestimation of relative risks from genome-wide association studies
@en
P2093
P2860
P1433
P1476
Quantifying the underestimation of relative risks from genome-wide association studies
@en
P2093
Chris Spencer
Damjan Vukcevic
Eliana Hechter
P2860
P304
P356
10.1371/JOURNAL.PGEN.1001337
P577
2011-03-17T00:00:00Z