Informative missingness in genetic association studies: case-parent designs.
about
Population structure and eigenanalysisReview and evaluation of methods correcting for population stratification with a focus on underlying statistical principlesHandling missing data in transmission disequilibrium test in nuclear families with one affected offspring.Bootstrap calibration of TRANSMIT for informative missingness of parental genotype dataHigh resolution T association tests of complex diseases based on family data.An evaluation of power and type I error of single-nucleotide polymorphism transmission/disequilibrium-based statistical methods under different family structures, missing parental data, and population stratification.Genetic association analysis using data from triads and unrelated subjectsImpact of non-ignorable missingness on genetic tests of linkage and/or association using case-parent trios.Approaches to handling incomplete data in family-based association testing.The impact of complex informative missingness on the validity of the transmission/disequilibrium test (TDT)Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls.On combining triads and unrelated subjects data in candidate gene studies: an application to data on testicular cancer.Missingness in the T1DGC MHC fine-mapping SNP data: association with HLA genotype and potential influence on genetic association studies.Modeling Informatively Missing Genotypes in Haplotype Analysis.Detection of parent-of-origin effects based on complete and incomplete nuclear families with multiple affected children.Family-based association tests using genotype data with uncertainty.Reducing bias of allele frequency estimates by modeling SNP genotype data with informative missingnessA novel test of informative missingness using inconsistent linkage disequilibrium signals between case-parent triads and incomplete data.Detection of parent-of-origin effects in complete and incomplete nuclear families with multiple affected children using multiple tightly linked markers.Robust transmission/disequilibrium test for incomplete family genotypes.Dosage transmission disequilibrium test (dTDT) for linkage and association detection.Association analysis of complex diseases using triads, parent-child dyads and singleton monads.Replication in genetic studies of complex traits.Sibship T2 association tests of complex diseases for tightly linked markers.Family-based association tests for different family structures using pooled DNAPower analysis of C-TDT for small sample size genome-wide association studies by the joint use of case-parent trios and pairs.Combined linkage disequilibrium and linkage mapping: Bayesian multilocus approach.RHD maternal-fetal genotype incompatibility and schizophrenia: extending the MFG test to include multiple siblings and birth order.Rare variant association analysis in case-parents studies by allowing for missing parental genotypes.A robust TDT-type association test under informative parental missingness.Differential dropout among SNP genotypes and impacts on association tests.Testing informative missingness in genetic studies using case–parent triads
P2860
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P2860
Informative missingness in genetic association studies: case-parent designs.
description
2003 nî lūn-bûn
@nan
2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Informative missingness in genetic association studies: case-parent designs.
@ast
Informative missingness in genetic association studies: case-parent designs.
@en
type
label
Informative missingness in genetic association studies: case-parent designs.
@ast
Informative missingness in genetic association studies: case-parent designs.
@en
prefLabel
Informative missingness in genetic association studies: case-parent designs.
@ast
Informative missingness in genetic association studies: case-parent designs.
@en
P2093
P2860
P356
P1476
Informative missingness in genetic association studies: case-parent designs.
@en
P2093
Andrew S Allen
Glen A Satten
Paul J Rathouz
P2860
P304
P356
10.1086/368276
P407
P577
2003-02-14T00:00:00Z