Proper analysis of secondary phenotype data in case-control association studies. - Wikidata - awgldk - TriplyDB

Proper analysis of secondary phenotype data in case-control association studies.

Proper analysis of secondary phenotype data in case-control association studies.

http://www.wikidata.org/entity/Q33389080

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Replication in Genome-Wide Association Studies Meta-analysis of genome-wide association studies with overlapping subjects A unified method for detecting secondary trait associations with rare variants: application to sequence data.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.An alternative hypothesis testing strategy for secondary phenotype data in case-control genetic association studies.Analysis of Sequence Data Under Multivariate Trait-Dependent Sampling Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data Robust estimation for secondary trait association in case-control genetic studies A general approach to testing for pleiotropy with rare and common variants Secondary phenotype analysis in ascertained family designs: application to the Leiden longevity study.Using cases to strengthen inference on the association between single nucleotide polymorphisms and a secondary phenotype in genome-wide association studies.A flexible likelihood framework for detecting associations with secondary phenotypes in genetic studies using selected samples: application to sequence data The value of reusing prior nested case-control data in new studies with different outcome.SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations.α₁-Antitrypsin protease inhibitor MZ heterozygosity is associated with airflow obstruction in two large cohorts.Investigating the relationship between UMODL1 gene polymorphisms and high myopia: a case-control study in Chinese.Method for evaluating multiple mediators: mediating effects of smoking and COPD on the association between the CHRNA5-A3 variant and lung cancer risk Epidemiology, radiology, and genetics of nicotine dependence in COPD.Estimation of odds ratios of genetic variants for the secondary phenotypes associated with primary diseases.Efficient adaptively weighted analysis of secondary phenotypes in case-control genome-wide association studies.Mendelian randomization studies for a continuous exposure under case-control sampling Dissection of the phenotypic and genotypic associations with nicotinic dependence.Informed genome-wide association analysis with family history as a secondary phenotype identifies novel loci of lung cancer.A Gaussian copula approach for the analysis of secondary phenotypes in case-control genetic association studies A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes A cautionary note on using secondary phenotypes in neuroimaging genetic studies.CHRNA3/5, IREB2, and ADCY2 are associated with severe chronic obstructive pulmonary disease in Poland.Analysis of secondary phenotype involving the interactive effect of the secondary phenotype and genetic variants on the primary disease.Semiparametric Estimation in the Secondary Analysis of Case-Control Studies Commentary: building an evidence base for mendelian randomization studies: assessing the validity and strength of proposed genetic instrumental variables A General and Robust Framework for Secondary Traits Analysis.Genome-wide association analysis for multiple continuous secondary phenotypes.A general semi-parametric approach to the analysis of genetic association studies in population-based designs Quantitative trait analysis in sequencing studies under trait-dependent sampling.PERMANOVA-S: association test for microbial community composition that accommodates confounders and multiple distances Unified Analysis of Secondary Traits in Case-Control Association Studies.Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.Genome-wide association analysis of secondary imaging phenotypes from the Alzheimer's disease neuroimaging initiative study.A general regression framework for a secondary outcome in case-control studies.

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P2860

Proper analysis of secondary phenotype data in case-control association studies.

http://www.wikidata.org/entity/Q33389080

description

2009 nî lūn-bûn

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2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2009 թվականի ապրիլին հրատարակված գիտական հոդված

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2009年の論文

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年學術文章

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Proper analysis of secondary phenotype data in case-control association studies.

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Proper analysis of secondary phenotype data in case-control association studies.

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Proper analysis of secondary phenotype data in case-control association studies.

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Proper analysis of secondary phenotype data in case-control association studies.

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Proper analysis of secondary phenotype data in case-control association studies.

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Proper analysis of secondary phenotype data in case-control association studies.

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Genetic Epidemiology

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Proper analysis of secondary phenotype data in case-control association studies.

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P2860

A common variant of HMGA2 is associated with adult and childhood height in the general population

Common variants near MC4R are associated with fat mass, weight and risk of obesity

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Identification of ten loci associated with height highlights new biological pathways in human growth

Many sequence variants affecting diversity of adult human height

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

Genome-wide association analysis identifies 20 loci that influence adult height

Common variants in the GDF5-UQCC region are associated with variation in human height

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10.1002/GEPI.20377

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3

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