Lista de obras - Jung-Ying Tzeng - Dominio Público Uruguay

A comprehensive approach to haplotype-specific analysis by penalized likelihood.

artículo científico publicado en 2010

A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity

artículo científico publicado en 2009

A two-stage design for multiple testing in large-scale association studies

artículo científico publicado en 2006

Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis

artículo científico publicado en 2020

Combining an evolution-guided clustering algorithm and haplotype-based LRT in family association studies.

artículo científico publicado en 2011

Comment

2006 article by Tzeng & Roeder

Comparing the performance of two indices for spatial model selection: application to two mortality data.

artículo científico publicado en 2000

Evaluating haplotype effects in case-control studies via penalized-likelihood approaches: prospective or retrospective analysis?

artículo científico publicado en 2010

Evolutionary-based grouping of haplotypes in association analysis

artículo científico publicado en 2005

FastLORS: Joint modelling for expression quantitative trait loci mapping in R

artículo científico publicado en 2020

Gene-trait similarity regression for multimarker-based association analysis.

artículo científico publicado en 2009

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Haplotype-based association analysis via variance-components score test.

artículo científico publicado en 2007

Identifying individual risk rare variants using protein structure guided local tests (POINT)

artículo científico publicado en 2019

On the Aggregation of Multimarker Information for Marker-Set and Sequencing Data Analysis: Genotype Collapsing vs. Similarity Collapsing.

artículo científico publicado en 2011

On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.

artículo científico publicado en 2003

On the substructure controls in rare variant analysis: Principal components or variance components?

artículo científico publicado en 2017

Outlier Detection and False Discovery Rates for Whole-Genome DNA Matching

article

Regression-based association analysis with clustered haplotypes through use of genotypes.

artículo científico publicado en 2005

Robust kernel association testing (RobKAT)

scientific article published on 14 January 2020

Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression

artículo científico publicado en 2011

Lista de obras de Jung-Ying Tzeng

A comprehensive approach to haplotype-specific analysis by penalized likelihood.

A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity

A two-stage design for multiple testing in large-scale association studies

Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis

Combining an evolution-guided clustering algorithm and haplotype-based LRT in family association studies.

Comment

Comparing the performance of two indices for spatial model selection: application to two mortality data.

Evaluating haplotype effects in case-control studies via penalized-likelihood approaches: prospective or retrospective analysis?

Evolutionary-based grouping of haplotypes in association analysis

FastLORS: Joint modelling for expression quantitative trait loci mapping in R

Gene-trait similarity regression for multimarker-based association analysis.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Haplotype-based association analysis via variance-components score test.

Identifying individual risk rare variants using protein structure guided local tests (POINT)

On the Aggregation of Multimarker Information for Marker-Set and Sequencing Data Analysis: Genotype Collapsing vs. Similarity Collapsing.

On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.

On the substructure controls in rare variant analysis: Principal components or variance components?

Outlier Detection and False Discovery Rates for Whole-Genome DNA Matching

Regression-based association analysis with clustered haplotypes through use of genotypes.

Robust kernel association testing (RobKAT)

Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression