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Penalized multivariate linear mixed model for longitudinal genome-wide association studies.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S73
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- Article
Bivariate genetic association analysis of systolic and diastolic blood pressure by copula models.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S72
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- Article
Prediction of genetic contributions to complex traits using whole genome sequencing data.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S68
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- Article
Evaluation of estimated genetic values and their application to genome-wide investigation of systolic blood pressure.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S66
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- Article
Identifying rare variant associations in population-based and family-based designs.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S58
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- Publication type:
- Article
Prediction of hypertension based on the genetic analysis of longitudinal phenotypes: a comparison of different modeling approaches for the binary trait of hypertension.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S78
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- Article
Using a Bayesian latent variable approach to detect pleiotropy in the Genetic Analysis Workshop 18 data.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S77
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- Article
Genetic association analysis using weighted false discovery rate approach on Genetic Analysis Workshop 18 data.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S76
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- Publication type:
- Article
Bivariate linear mixed model analysis to test joint associations of genetic variants on systolic and diastolic blood pressure.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S75
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- Article
A novel transmission-based test of association for multivariate phenotypes: an application to systolic and diastolic blood pressure levels.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S71
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- Article
A penalized linear mixed model for genomic prediction using pedigree structures.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S67
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- Article
Genetic association analysis for common variants in the Genetic Analysis Workshop 18 data: a Dirichlet regression approach.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S70
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- Publication type:
- Article
Application of noncollapsing methods to the gene-based association test: a comparison study using Genetic Analysis Workshop 18 data.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S53
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- Article
Identifying rare variants associated with hypertension using the C-alpha test.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S56
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- Publication type:
- Article
Family-based Bayesian collapsing method for rare-variant association study.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S37
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- Publication type:
- Article
Evaluation of logistic Bayesian LASSO for identifying association with rare haplotypes.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S54
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- Article
Practical investigation of the performance of robust logistic regression to predict the genetic risk of hypertension.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S65
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- Publication type:
- Article
Genotype imputation accuracy with different reference panels in admixed populations.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S64
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- Publication type:
- Article
Single-marker and multi-marker mixed models for polygenic score analysis in family-based data.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S63
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- Publication type:
- Article
Discovering pure gene-environment interactions in blood pressure genome-wide association studies data: a two-step approach incorporating new statistics.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S62
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- Article
A powerful statistical method identifies novel loci associated with diastolic blood pressure triggered by nonlinear gene-environment interaction.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S61
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- Article
A partition-based approach to identify gene-environment interactions in genome wide association studies.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S60
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- Article
Testing optimally weighted combination of variants for hypertension.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S59
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- Article
Haplotype approach for association analysis on hypertension.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S57
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- Article
Detection of imprinting effects for hypertension based on general pedigrees utilizing all affected and unaffected individuals.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S52
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- Publication type:
- Article
A goodness-of-fit association test for whole genome sequencing data.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S51
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- Article
Population structure at different minor allele frequency levels.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S55
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- Article
A variance component-based gene burden test.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S49
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- Article
Comparison of several sequence-based association methods in pedigrees.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S48
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- Article
A dual-clustering framework for association screening with whole genome sequencing data and longitudinal traits.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S47
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- Article
Collapsing singletons may boost signal for associating rare variants in sequencing study.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S50
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- Article
Kernel score statistic for dependent data.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S41
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- Article
A comparison of whole genome sequencing with exome sequencing for family-based association studies.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S38
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- Publication type:
- Article
A Bayesian hierarchical gene model on latent genotypes for genome-wide association studies.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S45
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- Article
Gene-based analysis of rare and common variants to determine association with blood pressure.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S46
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- Article
Evaluation of the power and type I error of recently proposed family-based tests of association for rare variants.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S36
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- Publication type:
- Article
Analysis of Genetic Analysis Workshop 18 data with gene-based penalized regression.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S43
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- Publication type:
- Article
Whole genome sequencing data from pedigrees suggests linkage disequilibrium among rare variants created by population admixture.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S44
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- Article
Adjusting for population stratification and relatedness with sequencing data.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S42
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- Publication type:
- Article
Rare genetic variant analysis on blood pressure in related samples.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S35
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- Publication type:
- Article
Extended T<sup>2</sup> tests for longitudinal family data in whole genome sequencing studies.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S40
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- Article
Adjustment of familial relatedness in association test for rare variants.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S39
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- Publication type:
- Article
Combining information from linkage and association mapping for next-generation sequencing longitudinal family data.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S34
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- Publication type:
- Article
A generalized least-squares framework for rare-variant analysis in family data.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S28
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- Publication type:
- Article
Family-based tests applied to extended pedigrees identify rare variants related to hypertension.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S31
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- Publication type:
- Article
A comparative analysis of family-based and population-based association tests using whole genome sequence data.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S33
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- Publication type:
- Article
De novo mutations discovered in 8 Mexican American families through whole genome sequencing.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S24
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- Publication type:
- Article
Two-stage family-based designs for sequencing studies.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S32
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- Publication type:
- Article
Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S27
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- Publication type:
- Article
On family-based genome-wide association studies with large pedigrees: observations and recommendations.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S26
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- Article