| . "TEAM: Efficient two-locus epistasis tests in human genome-wide association study.." Bioinformatics. 2010;26(12):i217-27. Pub Med |
| . "Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny.." Bioinformatics. 2018;34(12):2126-2128. Pub Med |
| . "Statistical significance of hierarchical clustering.." Biometrics. 2017;73(3):811-821. Pub Med |
| . "Sparse meta-analysis with high-dimensional data.." Biostatistics. 2016;17(2):205-20. Pub Med |
| . "Prediction of a time-to-event trait using genome wide SNP data.." BMC Bioinformatics. 2013;14():58. Pub Med |
| . "Consistency and overfitting of multi-omics methods on experimental data.." Brief Bioinform. 2020;21(4):1277-1284. Pub Med |
| . "SCOPE: A normalization and copy-number estimation method for single-cell DNA sequencing.." Cell Syst. 2020;10(5):445-452.e6. Pub Med |
| . "A general framework for association tests with multivariate traits in large-scale genomics studies.." Genet Epidemiol. 2013;37(8):759-67. Pub Med |
| . "A general framework for integrative analysis of incomplete multiomics data.." Genet Epidemiol. 2020;44(7):646-664. Pub Med |
| . "CODEX2: Full-spectrum copy number variation detection by high-throughput DNA sequencing.." Genome Biol. 2018;19(1):202. Pub Med |
| . "I-Boost: An integrative boosting approach for predicting survival time with multiple genomics platforms.." Genome Biol. 2019;20(1):52. Pub Med |
| . "Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis.." Hum Genomics. 2010;5(1):5-16. Pub Med |
| . "Allele-specific copy-number discovery from whole-genome and whole-exome sequencing.." Nucleic Acids Res. 2015;43(14):e90. Pub Med |
| . "Rare variants association analysis in large-scale sequencing studies at the single locus level.." PLoS Comput Biol. 2016;12(6):e1004993. Pub Med |
| . "Tximeta: Reference sequence checksums for provenance identification in RNA-seq.." PLoS Comput Biol. 2020;16(2):e1007664. 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 |
| . "Generation of a transcriptional radiation exposure signature in human blood using long-read nanopore sequencing.." Radiat Res. 2020;193(2):143-154. 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 |
| . "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 |
| . "Pathway-guided identification of gene-gene interactions.." Ann Hum Genet. 2014;78(6):478-91. Pub Med |
| . "A general framework for studying genetic effects and gene-environment interactions with missing data.." Biostatistics. 2010;11(4):583-98. Pub Med |
| . "Common variants in psychiatric risk genes predict brain structure at birth.." Cereb Cortex. 2014;24(5):1230-46. Pub Med |
| . "A genome-wide association study identifies novel loci for paclitaxel-induced sensory peripheral neuropathy in CALGB 40101.." Clin Cancer Res. 2012;18(18):5099-109. Pub Med |
| . "Pathway-based identification of SNPs predictive of survival.." Eur J Hum Genet. 2011;19(6):704-9. Pub Med |
| . "Evaluating haplotype effects in case-control studies via penalized-likelihood approaches: Prospective or retrospective analysis?." Genet Epidemiol. 2010;34(8):892-911. Pub Med |
| . "Analysis of untyped SNPs: Maximum likelihood and imputation methods.." Genet Epidemiol. 2010;34(8):803-15. Pub Med |
| . "A general framework for integrative analysis of incomplete multiomics data.." Genet Epidemiol. 2020;44(7):646-664. Pub Med |
| . "A simple and accurate method to determine genomewide significance for association tests in sequencing studies.." Genet Epidemiol. 2019;43(4):365-372. 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 |
| . "Analysis of gene-gene interactions using gene-trait similarity regression.." Hum Hered. 2014;78(1):17-26. Pub Med |
| . "Nomenclature for alleles of the thiopurine methyltransferase gene.." Pharmacogenet Genomics. 2013;23(4):242-8. Pub Med |
| . "Integrative analysis of sequencing and array genotype data for discovering disease associations with rare mutations.." Proc Natl Acad Sci U S A. 2015;112(4):1019-24. Pub Med |
| . "Intergenerational response to the endocrine disruptor vinclozolin is influenced by maternal genotype and crossing scheme.." Reprod Toxicol. 2018;78():9-19. Pub Med |
| . "Integrative analysis of sequencing and array genotype data for discovering disease associations with rare mutations.." Proc Natl Acad Sci U S A. 2015;112(4):1019-24. Pub Med |
| . "Spatial regression with covariate measurement error: A semiparametric approach.." Biometrics. 2016;72(3):678-86. Pub Med |
| . "Cancer pharmacogenomics: early promise, but concerted effort needed.." Science. 2013;339(6127):1563-6. Pub Med |
| . "FADTTS: Functional analysis of diffusion tensor tract statistics.." Neuroimage. 2011;56(3):1412-25. Pub Med |
| . "Time course and prognostic value of serum GFAP, pNFH, and S100β concentrations in dogs with complete spinal cord injury because of intervertebral disc extrusion.." J Vet Intern Med. 2019;33(2):726-734. 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 |
| . "The association between copy number aberration, DNA methylation and gene expression in tumor samples.." Nucleic Acids Res. 2018;46(6):3009-3018. Pub Med |
| . "Statistical design of noninferiority multiple region clinical trials to assess global and consistent treatment effects.." J Biopharm Stat. 2017;27(6):933-944. Pub Med |
| . "Common variants in psychiatric risk genes predict brain structure at birth.." Cereb Cortex. 2014;24(5):1230-46. Pub Med |
| . "Assessing model fit in joint models of longitudinal and survival data with applications to cancer clinical trials.." Stat Med. 2014;33(27):4715-33. Pub Med |
| . "Characterizing expected benefits of biomarkers in treatment selection.." Biostatistics. 2015;16(2):383-99. Pub Med |
| . "Impact of sex and gonadal steroids on neonatal brain structure.." Cereb Cortex. 2014;24(10):2721-31. Pub Med |
| . "Joint modeling of survival and longitudinal non-survival data: current methods and issues. Report of the DIA Bayesian joint modeling working group.." Stat Med. 2015;34(14):2181-95. Pub Med |
| . "Randomized, double-blind study comparing proposed biosimilar LA-EP2006 with reference pegfilgrastim in breast cancer.." Future Oncol. 2016;12(11):1359-67. Pub Med |
| . "A comparison of proposed biosimilar LA-EP2006 and reference Pegfilgrastim for the prevention of neutropenia in patients with early-stage breast cancer receiving Myelosuppressive adjuvant or Neoadjuvant chemotherapy: Pegfilgrastim Randomized Oncology (Supp." Oncologist. 2016;21(7):789-94. Pub Med |
| . "Checking semiparametric transformation models with censored data.." Biostatistics. 2012;13(1):18-31. Pub Med |
| . "Fixed and random effects selection in mixed effects models.." Biometrics. 2011;67(2):495-503. Pub Med |
