Author details

Full Name

Jung-Ying Tzeng

Affiliation

ORCID

Career Start Year

2000

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36694712	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.		2023
37745545	Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects.	medRxiv	2023
38011285	Transfer learning with false negative control improves polygenic risk prediction.		2023
37577355	The prediction of Alzheimer's disease through multi-trait genetic modeling.		2023
35668471	Phylogeny-guided microbiome OTU-specific association test (POST).	Microbiome	2022
34567069	An Integrative Co-localization (INCO) Analysis for SNV and CNV Genomic Features With an Application to Taiwan Biobank Data.	Frontiers in Genetics	2021
33674827	Gene-set integrative analysis of multi-omics data using tensor-based association test.		2021
34804120	Copy Number Variation Identification on 3,800 Alzheimer's Disease Whole Genome Sequencing Data from the Alzheimer's Disease Sequencing Project.	Frontiers in Genetics	2021
34795690	SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data.	Frontiers in Genetics	2021
32212939	The association between neuraxial anesthesia and the development of childhood asthma - a secondary analysis of the newborn epigenetics study cohort.	Current Medical Research and Opinion	2020
32365089	Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis.	PLoS Comput Biol	2020
31943371	Robust kernel association testing (RobKAT).	Genet Epidemiol	2020
32216117	Effective SNP ranking improves the performance of eQTL mapping.	Genetic Epidemiology	2020
30779729	Identifying individual risk rare variants using protein structure guided local tests (POINT).	PLoS Comput Biol	2019
31929665	Efficient Signal Inclusion With Genomic Applications.	Journal of the American Statistical Association	2019
31709028	Reference equations for spirometry in healthyÂ Asian children aged 5 to 18 years inÂ Taiwan.	World Allergy Organization Journal	2019
30378687	Genetic loci determining total immunoglobulin E levels from birth through adulthood.	Allergy	2019
31528362	Cadmium exposure and <i>MEG3</i> methylation differences between Whites and African Americans in the NEST Cohort.	Environ Epigenet	2019
29314255	Inference on phenotype-specific effects of genes using multivariate kernel machine regression.	Genet Epidemiol	2018
30420901	A Powerful Test for SNP Effects on Multivariate Binary Outcomes using Kernel Machine Regression.	Stat Biosci	2018
29096038	Rejoinder to "A note on testing and estimation in marker-set association study using semiparametric quantile regression kernel machine".	Biometrics	2018
29511319	Cadmium exposure increases the risk of juvenile obesity: a human and zebrafish comparative study.	Int J Obes (Lond)	2018
29280188	On the substructure controls in rare variant analysis: Principal components or variance components?	Genet Epidemiol	2018
29545466	Reexamining Dis/Similarity-Based Tests for Rare-Variant Association with Case-Control Samples.	Genetics	2018
29075047	Fast Bayesian Variable Screenings for Binary Response Regressions with Small Sample Size.	Journal of Statistical Computation and Simulation	2017
28438148	Maternal blood cadmium, lead and arsenic levels, nutrient combinations, and offspring birthweight.	BMC Public Health	2017
26575303	Testing and estimation in marker-set association study using semiparametric quantile regression kernel machine.	Biometrics	2016
27061717	Across-Platform Imputation of DNA Methylation Levels Incorporating Nonlocal Information Using Penalized Functional Regression.	Genet Epidemiol	2016
27355347	Rare Variants Association Analysis in Large-Scale Sequencing Studies at the Single Locus Level.	PLoS Computational Biology	2016
26288029	Detection of gene-gene interactions using multistage sparse and low-rank regression.	Biometrics	2016
26568645	Proper Use of Allele-Specific Expression Improves Statistical Power for -eQTL Mapping with RNA-Seq Data.	Journal of the American Statistical Association	2015
25585620	Assessing gene-environment interactions for common and rare variants with binary traits using gene-trait similarity regression.	Genetics	2015
25538034	Complete effect-profile assessment in association studies with multiple genetic and multiple environmental factors.	Genetic Epidemiology	2015
25822417	Module-based association analysis for omics data with network structure.	PLoS One	2015
25604216	A penalized likelihood approach for investigating gene-drug interactions in pharmacogenetic studies.	Biometrics	2015
26139508	A Fast Multiple-Kernel Method With Applications to Detect Gene-Environment Interaction.	Genet Epidemiol	2015
26431523	A New Method for Detecting Associations with Rare Copy-Number Variants.	PLoS Genet	2015
24969398	Analysis of gene-gene interactions using gene-trait similarity regression.	Human Heredity	2014
24489370	Integrative gene set analysis of multi-platform data with sample heterogeneity.		2014
24728292	Heritability and genomics of gene expression in peripheral blood.	Nat Genet	2014
25227508	Pathway-guided identification of gene-gene interactions.	Annals of Human Genetics	2014
25018788	GENE-LEVEL PHARMACOGENETIC ANALYSIS ON SURVIVAL OUTCOMES USING GENE-TRAIT SIMILARITY REGRESSION.	Annals of Applied Statistics	2014
24683298	Statistical considerations in biosimilar assessment using biosimilarity index.	Journal of Bioequivalence and Bioavailability (discontinued)	2013
22472876	A mega-analysis of genome-wide association studies for major depressive disorder.	Mol Psychiatry	2013
23933821	Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.	Nat Genet	2013
24734164	Establishment of reference standards in biosimilar studies.	GaBI Journal	2013
22899176	Multivariate phenotype association analysis by marker-set kernel machine regression.	Genet Epidemiol	2012
22303404	On the Aggregation of Multimarker Information for Marker-Set and Sequencing Data Analysis: Genotype Collapsing vs. Similarity Collapsing.	Front Genet	2012
21592403	Combining an evolution-guided clustering algorithm and haplotype-based LRT in family association studies.	BMC Genetics	2011
21835306	Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression.	Am J Hum Genet	2011