Articles By Keyword

. "A general framework for association tests with multivariate traits in large-scale genomics studies.." Genet Epidemiol. 2013;37(8):759-67. Pub Med
. "Multivariate recurrent events in the presence of multivariate informative censoring with applications to bleeding and transfusion events in myelodysplastic syndrome.." J Biopharm Stat. 2014;24(2):429-42. Pub Med
. "A regularized variable selection procedure in additive hazards model with stratified case-cohort design.." Lifetime Data Anal. 2018;24(3):443-463. Pub Med
. "Accelerated failure time model for data from outcome-dependent sampling.." Lifetime Data Anal. 2021;27(1):15-37. Pub Med
. "Multiplicative rates model for recurrent events in case-cohort studies.." Lifetime Data Anal. 2020;26(1):134-157. Pub Med
. "Marginal hazard regression for correlated failure time data with auxiliary covariates.." Lifetime Data Anal. 2012;18(1):116-38. Pub Med
. "Genetic analyses of diverse populations improves discovery for complex traits.." Nature. 2019;570(7762):514-518. Pub Med
. "Joint modeling of longitudinal and survival data with missing and left-censored time-varying covariates.." Stat Med. 2014;33(26):4560-76. Pub Med
. "Sample size/power calculation for stratified case-cohort design.." Stat Med. 2014;33(23):3973-85. Pub Med
. "Improving the efficiency of estimation in the additive hazards model for stratified case-cohort design with multiple diseases.." Stat Med. 2016;35(2):282-93. Pub Med
. "Parameter estimation in Cox models with missing failure indicators and the OPPERA study.." Stat Med. 2015;34(30):3984-96. Pub Med
. "A hybrid Bayesian hierarchical model combining cohort and case-control studies for meta-analysis of diagnostic tests: Accounting for partial verification bias.." Stat Methods Med Res. 2016;25(6):3015-3037. Pub Med
. "Checking semiparametric transformation models with censored data.." Biostatistics. 2012;13(1):18-31. Pub Med
. "Comparative effectiveness of oxaliplatin vs non-oxaliplatin-containing adjuvant chemotherapy for stage III colon cancer.." J Natl Cancer Inst. 2012;104(3):211-27. Pub Med
. "The association between copy number aberration, DNA methylation and gene expression in tumor samples.." Nucleic Acids Res. 2018;46(6):3009-3018. Pub Med
. "Bayesian gamma frailty models for survival data with semi-competing risks and treatment switching.." Lifetime Data Anal. 2014;20(1):76-105. Pub Med
. "Genetic variation determines VEGF-A plasma levels in cancer patients.." Sci Rep. 2018;8(1):16332. Pub Med
. "Pattern mixture models for clinical validation of biomarkers in the presence of missing data.." Stat Med. 2017;36(19):2994-3004. Pub Med
. "Bayesian analysis on meta-analysis of case-control studies accounting for within-study correlation.." Stat Methods Med Res. 2015;24(6):836-55. Pub Med
. "PIK3CA mutations enable targeting of a breast tumor dependency through mTOR-mediated MCL-1 translation.." Sci Transl Med. 2016;8(369):369ra175. Pub Med
. "Clinical characteristics, response to exercise training, and outcomes in patients with heart failure and chronic obstructive pulmonary disease: findings from Heart Failure and A Controlled Trial Investigating Outcomes of Exercise TraiNing (HF-ACTION).." Am Heart J. 2013;165(2):193-9. Pub Med
. "Data for cancer comparative effectiveness research: past, present, and future potential.." Cancer. 2012;118(21):5186-97. Pub Med
. "A framework for understanding cancer comparative effectiveness research data needs.." J Clin Epidemiol. 2012;65(11):1150-8. Pub Med
. "Comparative effectiveness of oxaliplatin vs non-oxaliplatin-containing adjuvant chemotherapy for stage III colon cancer.." J Natl Cancer Inst. 2012;104(3):211-27. Pub Med
. "DiNAMIC: A method to identify recurrent DNA copy number aberrations in tumors.." Bioinformatics. 2011;27(5):678-85. Pub Med
. "PreMeta: A tool to facilitate meta-analysis of rare-variant associations.." BMC Genomics. 2017;18(1):160. Pub Med
. "Consistency and overfitting of multi-omics methods on experimental data.." Brief Bioinform. 2020;21(4):1277-1284. Pub Med
. "Purity independent subtyping of tumors (PurIST), a clinically robust, single-sample classifier for tumor subtyping in pancreatic cancer.." Clin Cancer Res. 2020;26(1):82-92. Pub Med
. "Statistical considerations for analysis of microarray experiments.." Clin Transl Sci. 2011;4(6):466-77. Pub Med
. "Swimming downstream: Statistical analysis of differential transcript usage following Salmon quantification.." F1000Res. 2018;7():952. Pub Med
. "Rapid and robust resampling-based multiple-testing correction with application in a genome-wide expression quantitative trait loci study.." Genetics. 2012;190(4):1511-20. Pub Med
. "SynthEx: a synthetic-normal-based DNA sequencing tool for copy number alteration detection and tumor heterogeneity profiling.." Genome Biol. 2017;18(1):66. Pub Med
. "Ten simple rules for effective statistical practice.." PLoS Comput Biol. 2016;12(6):e1004961. Pub Med
. "Tximeta: Reference sequence checksums for provenance identification in RNA-seq.." PLoS Comput Biol. 2020;16(2):e1007664. Pub Med
. "Identifying individual risk rare variants using protein structure guided local tests (POINT).." PLoS Comput Biol. 2019;15(2):e1006722. Pub Med
. "Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis.." PLoS Comput Biol. 2020;16(5):e1007797. Pub Med
. "Module-based association analysis for omics data with network structure.." PLoS One. 2015;10(3):e0122309. Pub Med
. "Joint skeleton estimation of multiple directed acyclic graphs for heterogeneous population.." Biometrics. 2019;75(1):36-47. Pub Med
. "Data for cancer comparative effectiveness research: past, present, and future potential.." Cancer. 2012;118(21):5186-97. Pub Med
. "Meta-analysis of gene-level associations for rare variants based on single-variant statistics.." Am J Hum Genet. 2013;93(2):236-48. Pub Med
. "Incorporating functional information in tests of excess De Novo mutational load.." Am J Hum Genet. 2015;97(2):272-83. Pub Med
. "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;89(2):277-88. Pub Med
. "Genetic association analysis under complex survey sampling: the Hispanic Community Health Study/Study of Latinos.." Am J Hum Genet. 2014;95(6):675-88. Pub Med
. "A general framework for detecting disease associations with rare variants in sequencing studies.." Am J Hum Genet. 2011;89(3):354-67. Pub Med
. "Meta-analysis for discovering rare-variant associations: Statistical methods and software programs.." Am J Hum Genet. 2015;97(1):35-53. Pub Med
. "Pathway-guided identification of gene-gene interactions.." Ann Hum Genet. 2014;78(6):478-91. Pub Med
. "Component-wise gradient boosting and false discovery control in survival analysis with high-dimensional covariates.." Bioinformatics. 2016;32(1):50-7. Pub Med
. "A variable selection method for genome-wide association studies.." Bioinformatics. 2011;27(1):1-8. Pub Med
. "Multiple kernel learning with random effects for predicting longitudinal outcomes and data integration.." Biometrics. 2015;71(4):918-28. Pub Med
. "Bayesian design of noninferiority trials for medical devices using historical data.." Biometrics. 2011;67(3):1163-70. Pub Med