J. Tzeng

发表

Journal of the American Statistical Association: Comment

K. Roeder, C. Sabatti, R. Carroll, 2006 .

Heritability and Genomics of Gene Expression in Peripheral Blood

P. Sullivan, F. Wright, A. Shabalin, 2014, Nature Genetics.

Module-Based Association Analysis for Omics Data with Network Structure

J. Tzeng, D. Voora, R. Kaddurah-Daouk, 2015, PloS one.

Genomewide Association for Major Depressive Disorder: A possible role for the presynaptic protein Piccolo

N. Wray, S. Cichon, M. Rietschel, 2008, Molecular Psychiatry.

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

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

A Powerful Test for SNP Effects on Multivariate Binary Outcomes Using Kernel Machine Regression

P. Sullivan, J. Tzeng, A. Maity, 2017, Statistics in Biosciences.

Analysis of Gene-Gene Interactions Using Gene-Trait Similarity Regression

M. Epstein, J. Tzeng, Xin Wang, 2014, Human Heredity.

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

L. Wasserman, K. Roeder, J. Tzeng, 2003, American journal of human genetics.

Effective SNP ranking improves the performance of eQTL mapping.

J. Tzeng, X. J. Jeng, J. Rhyne, 2020, Genetic epidemiology.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

Testing and estimation in marker‐set association study using semiparametric quantile regression kernel machine

J. Tzeng, F. Hsu, D. Kong, 2016, Biometrics.

Genomewide association for schizophrenia in the CATIE study: results of stage 1

J. Lieberman, P. Sullivan, F. Wright, 2009, Molecular Psychiatry.

A Fast Multiple‐Kernel Method With Applications to Detect Gene‐Environment Interaction

Stephen R. Williams, Shannon T. Holloway, J. Tzeng, 2015, Genetic epidemiology.

Jung-Ying Tzeng, Marie Davidian, Sheng-Mao Chang, 2009, Biometrics.

Regression-based multi-marker analysis for genome-wide association studies using haplotype similarity

Jung-Ying Tzeng, Marie Davidian, M. Davidian, 2007 .

Genomewide association for schizophrenia in the CATIE study: results of stage 1

J. Lieberman, P. Sullivan, F. Wright, 2008, Molecular Psychiatry.

GENE-LEVEL PHARMACOGENETIC ANALYSIS ON SURVIVAL OUTCOMES USING GENE-TRAIT SIMILARITY REGRESSION.

J. Tzeng, Wenbin Lu, F. Hsu, 2014, The annals of applied statistics.

Combining an Evolution-guided Clustering Algorithm and Haplotype-based LRT in Family Association Studies

J. Tzeng, C. K. Hsiao, Mei-Hsien Lee, 2011, BMC Genetics.

A Regression‐based Association Test for Case‐control Studies that Uses Inferred Ancestral Haplotype Similarity

G. Satten, A. Allen, J. Tzeng, 2009, Annals of human genetics.

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

J. Tzeng, Yun Li, Q. Duan, 2018, Genetic epidemiology.

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

Chuhsing Kate Hsiao, Jung-Ying Tzeng, Jau-Tsuen Kao, 2006, American journal of human genetics.

A penalized likelihood approach for investigating gene–drug interactions in pharmacogenetic studies

J. Tzeng, H. Bondell, M. Neely, 2015, Biometrics.

Genetic loci determining total immunoglobulin E levels from birth through adulthood

P. Tsai, E. Burchard, J. Tzeng, 2018, Allergy.

The association between neuraxial anesthesia and the development of childhood asthma – a secondary analysis of the newborn epigenetics study cohort

J. Tzeng, C. Hoyo, T. Allen, 2020, Current medical research and opinion.

A Powerful Test for SNP Effects on Multivariate Binary Outcomes Using Kernel Machine Regression

J. Tzeng, A. Maity, C. Davenport, 2017, Statistics in Biosciences.

Inference on phenotype‐specific effects of genes using multivariate kernel machine regression

Arnab Maity, Jung-Ying Tzeng, Jing Zhao, 2018, Genetic epidemiology.

Duration of exposure to epidural anesthesia at delivery, DNA methylation in umbilical cord blood and their association with offspring asthma in Non-Hispanic Black women

J. Tzeng, C. Hoyo, T. Allen, 2022, Environmental epigenetics.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

An Integrative Co-localization (INCO) Analysis for SNV and CNV Genomic Features With an Application to Taiwan Biobank Data

J. Tzeng, C. K. Hsiao, T. Hsiao, 2021, Frontiers in Genetics.

Rare Variants Association Analysis in Large-Scale Sequencing Studies at the Single Locus Level

Jung-Ying Tzeng, Wenbin Lu, X. Jessie Jeng, 2016, PLoS Comput. Biol..

Across‐Platform Imputation of DNA Methylation Levels Incorporating Nonlocal Information Using Penalized Functional Regression

Jung-Ying Tzeng, Yun Li, Weihua Guan, 2016, Genetic epidemiology.

Gene-set integrative analysis of multi-omics data using tensor-based association test

Jung-Ying Tzeng, Wenbin Lu, Hung Hung, 2021, Bioinform..

A New Method for Detecting Associations with Rare Copy-Number Variants

Patrick F. Sullivan, Jung-Ying Tzeng, Jin P. Szatkiewicz, 2015, PLoS genetics.

Transfer Learning with False Negative Control Improves Polygenic Risk Prediction

J. Tzeng, X. J. Jeng, Yifei Hu, 2023, bioRxiv.

Copy Number Variation Identification on 3,800 Alzheimer’s Disease Whole Genome Sequencing Data from the Alzheimer’s Disease Sequencing Project

G. Schellenberg, J. Tzeng, Wenbin Lu, 2021, Frontiers in Genetics.

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

Patrick F. Sullivan, Jung-Ying Tzeng, Tzu-Pin Lu, 2020, PLoS Comput. Biol..

Association Tests Using Copy Number Profile Curves (CONCUR) Enhances Power in Rare Copy Number Variant Analysis

Chuhsing Kate Hsiao, Patrick F. Sullivan, Patrik K. E. Magnusson, 2019, bioRxiv.

Reexamining Dis/Similarity-Based Tests for Rare-Variant Association with Case-Control Samples

J. Tzeng, M. Preisig, Charlotte Wang, 2018, Genetics.

Assessing Gene-Environment Interactions for Common and Rare Variants with Binary Traits Using Gene-Trait Similarity Regression

Jung-Ying Tzeng, Rachel Marceau, J. Tzeng, 2015, Genetics.

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

Jung-Ying Tzeng, Mark I McCarthy, Fang-Chi Hsu, 2011, American journal of human genetics.

Cadmium exposure and MEG3 methylation differences between Whites and African Americans in the NEST Cohort

Jonathan R. Hall, Eric S. Money, J. Tzeng, 2019, Environmental epigenetics.

Cadmium Exposure Increases the Risk of Juvenile Obesity: A Human and Zebrafish Comparative Study

Adrian J. Green, J. Tzeng, S. Murphy, 2017, bioRxiv.

Maternal blood cadmium, lead and arsenic levels, nutrient combinations, and offspring birthweight

J. Tzeng, S. Murphy, C. Samuel-Hodge, 2017, BMC Public Health.

Complete Effect‐Profile Assessment in Association Studies With Multiple Genetic and Multiple Environmental Factors

Arnab Maity, Zhi Wang, Jung-Ying Tzeng, 2015, Genetic epidemiology.

Erratum: Genomewide association for schizophrenia in the CATIE study: Results of stage 1 (Molecular Psychiatry (2008) 13 (570-584) DOI: 10.1038/mp.2008.25)

Fred A. Wright, Jung-Ying Tzeng, Fei Zou, 2009 .

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

Larry Wasserman, Kathryn Roeder, Jung-Ying Tzeng, 2003 .

Reference equations for spirometry in healthy Asian children aged 5 to 18 years in Taiwan☆

J. Tzeng, S. Liao, H. Tsai, 2019, The World Allergy Organization journal.

Phylogeny-guided microbiome OTU-specific association test (POST)

Shannon T. Holloway, J. Tzeng, Wenbin Lu, 2021, Microbiome.

POSTm: Phylogeney-Guided OTU-Specific Association Test for Microbiome Data

Shannon T. Holloway, J. Tzeng, Caizhi Huang, 2022 .

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

J. Tzeng, C. K. Hsiao, Chih-Hao Wang, 2000, Statistics in medicine.

Design and Statistical Analysis for the Myopia Intervention Trial in Taiwan

Chien-Jen Chen, J. Tzeng, C. K. Hsiao, 2000 .

Proper Use of Allele-Specific Expression Improves Statistical Power for cis-eQTL Mapping with RNA-Seq Data

Jung-Ying Tzeng, Wei Sun, Charles M Perou, 2015, Journal of the American Statistical Association.

Integrative gene set analysis of multi-platform data with sample heterogeneity

Jun Hu, Jung-Ying Tzeng, J. Tzeng, 2014, Bioinform..

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

Jung-Ying Tzeng, J. Tzeng, Daowen Zhang, 2007, American journal of human genetics.

Efficient Signal Inclusion With Genomic Applications

Jung-Ying Tzeng, Teng Zhang, X. Jessie Jeng, 2018, Journal of the American Statistical Association.

Genomewide Association for Major Depressive Disorder: A possible role for the presynaptic protein Piccolo

N. Wray, S. Cichon, M. Rietschel, 2008, Molecular Psychiatry.

Haplotype-Based Pharmacogenetic Analysis for Longitudinal Quantitative Traits in the Presence of Dropout

Jung-Ying Tzeng, Wenbin Lu, Mark W Farmen, 2010, Journal of biopharmaceutical statistics.