A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies
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Robust estimation for homoscedastic regression in the secondary analysis of case-control data.A Note on Penalized Regression Spline Estimation in the Secondary Analysis of Case-Control Data.Multinomial logistic regression approach to haplotype association analysis in population-based case-control studies.A haplotype-based test of association using data from cohort and nested case-control epidemiologic studies.Fine mapping functional sites or regions from case-control data using haplotypes of multiple linked SNPs.Inference on haplotype effects in case-control studies using unphased genotype data.Decision forest analysis of 61 single nucleotide polymorphisms in a case-control study of esophageal cancer; a novel method.Polymorphisms of the XRCC1, XRCC3 and XPD genes and risk of colorectal adenoma and carcinoma, in a Norwegian cohort: a case control study.Empirical vs Bayesian approach for estimating haplotypes from genotypes of unrelated individualsIncorporating single-locus tests into haplotype cladistic analysis in case-control studies.Estimating effects of rare haplotypes on failure time using a penalized Cox proportional hazards regression model.Importance of TP53 codon 72 and intron 3 duplication 16bp polymorphisms in prediction of susceptibility on breast cancerSimple and efficient analysis of disease association with missing genotype dataHaplotype reconstruction error as a classical misclassification problem: introducing sensitivity and specificity as error measures.On combining triads and unrelated subjects data in candidate gene studies: an application to data on testicular cancer.A systematic search for SNPs/haplotypes associated with disease phenotypes using a haplotype-based stepwise procedure.STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement.Toll-like receptor polymorphisms and susceptibility to urinary tract infections in adult women.Estimating haplotype effects for survival data.Genetic variation of the human urinary tract innate immune response and asymptomatic bacteriuria in women.A general framework for studying genetic effects and gene-environment interactions with missing data.Modeling Informatively Missing Genotypes in Haplotype Analysis.Toll-like receptor 4 polymorphisms are associated with resistance to Legionnaires' disease.Analysis of Case-Control Association Studies: SNPs, Imputation and Haplotypes.The future of association studies: gene-based analysis and replication.Associations between NBS1 polymorphisms, haplotypes and smoking-related cancers.Polymorphisms in nucleotide excision repair genes and endometrial cancer risk.Polymorphisms in toll-like receptor 4 and toll-like receptor 9 influence viral load in a seroincident cohort of HIV-1-infected individualsRegression-based association analysis with clustered haplotypes through use of genotypes.Genetic association of the antiviral restriction factor TRIM5alpha with human immunodeficiency virus type 1 infectionMixed modeling and multiple imputation for unobservable genotype clustersPowerful haplotype-based Hardy-Weinberg equilibrium tests for tightly linked loci.Dual effect of the macrophage migration inhibitory factor gene on the development and severity of human systemic lupus erythematosus.Genetic variation in bactericidal/permeability-increasing protein influences the risk of developing rapid airflow decline after hematopoietic cell transplantation.A comprehensive literature review of haplotyping software and methods for use with unrelated individuals.A common dominant TLR5 stop codon polymorphism abolishes flagellin signaling and is associated with susceptibility to legionnaires' diseaseLipopolysaccharide binding protein promoter variants influence the risk for Gram-negative bacteremia and mortality after allogeneic hematopoietic cell transplantation.Recursive organizer (ROR): an analytic framework for sequence-based association analysis.Analysis of case-control studies of genetic and environmental factors with missing genetic information and haplotype-phase ambiguityShrinkage Estimators for Robust and Efficient Inference in Haplotype-Based Case-Control Studies.
P2860
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P2860
A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies
description
2003 nî lūn-bûn
@nan
2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի ապրիլին 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
A method for the assessment of ...... iables in case-control studies
@ast
A method for the assessment of ...... iables in case-control studies
@en
type
label
A method for the assessment of ...... iables in case-control studies
@ast
A method for the assessment of ...... iables in case-control studies
@en
prefLabel
A method for the assessment of ...... iables in case-control studies
@ast
A method for the assessment of ...... iables in case-control studies
@en
P2093
P2860
P356
P1476
A method for the assessment of ...... iables in case-control studies
@en
P2093
Lue Ping Zhao
Najma Khalid
Shuying Sue Li
P2860
P304
P356
10.1086/375140
P407
P577
2003-04-16T00:00:00Z