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
. "Analysis of untyped SNPs: Maximum likelihood and imputation methods.." Genet Epidemiol. 2010;34(8):803-15. Pub Med
. "On the substructure controls in rare variant analysis: Principal components or variance components?." Genet Epidemiol. 2018;42(3):276-287. Pub Med
. "Reexamining dis/similarity-based tests for rare-variant association with case-control samples.." Genetics. 2018;209(1):105-113. 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
. "Identifying individual risk rare variants using protein structure guided local tests (POINT).." PLoS Comput Biol. 2019;15(2):e1006722. Pub Med
. "Genetic analyses of diverse populations improves discovery for complex traits.." Nature. 2019;570(7762):514-518. Pub Med
. "A spatial dirichlet process mixture model for clustering population genetics data.." Biometrics. 2011;67(2):381-90. Pub Med
. "Predicting Alzheimer's disease using combined imaging-whole genome SNP data.." J Alzheimers Dis. 2015;46(3):695-702. Pub Med
. "TEAM: Efficient two-locus epistasis tests in human genome-wide association study.." Bioinformatics. 2010;26(12):i217-27. Pub Med
. "Global copy number profiling of cancer genomes.." Bioinformatics. 2016;32(6):926-8. Pub Med
. "Genome analysis and pleiotropy assessment using causal networks with loss of function mutation and metabolomics.." BMC Genomics. 2019;20(1):395. 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 simple and accurate method to determine genomewide significance for association tests in sequencing studies.." Genet Epidemiol. 2019;43(4):365-372. Pub Med
. "Analysis of untyped SNPs: Maximum likelihood and imputation methods.." Genet Epidemiol. 2010;34(8):803-15. 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
. "A junction coverage compatibility score to quantify the reliability of transcript abundance estimates and annotation catalogs.." Life Sci Alliance. 2019;2(1):. Pub Med
. "Genome-wide association study identifies five new schizophrenia loci.." Nat Genet. 2011;43(10):969-76. 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
. "Cancer pharmacogenomics: early promise, but concerted effort needed.." Science. 2013;339(6127):1563-6. 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 of gene-level associations for rare variants based on single-variant statistics.." Am J Hum Genet. 2013;93(2):236-48. Pub Med
. "A variable selection method for genome-wide association studies.." Bioinformatics. 2011;27(1):1-8. Pub Med
. "TEAM: Efficient two-locus epistasis tests in human genome-wide association study.." Bioinformatics. 2010;26(12):i217-27. Pub Med
. "Sparse meta-analysis with high-dimensional data.." Biostatistics. 2016;17(2):205-20. Pub Med
. "fastJT: An R package for robust and efficient feature selection for machine learning and genome-wide association studies.." BMC Bioinformatics. 2019;20(1):333. Pub Med
. "Prediction of a time-to-event trait using genome wide SNP data.." BMC Bioinformatics. 2013;14():58. Pub Med
. "Exploiting expression patterns across multiple tissues to map expression quantitative trait loci.." BMC Bioinformatics. 2016;17():257. Pub Med
. "Efficient estimation of grouped survival models.." BMC Bioinformatics. 2019;20(1):269. Pub Med
. "Combining an evolution-guided clustering algorithm and haplotype-based LRT in family association studies.." BMC Genet. 2011;12():48. Pub Med
. "Whole-genome and epigenomic landscapes of etiologically distinct subtypes of cholangiocarcinoma.." Cancer Discov. 2017;7(10):1116-1135. 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
. "Genomewide meta-analysis validates a role for S1PR1 in microtubule targeting agent-induced sensory peripheral neuropathy.." Clin Pharmacol Ther. 2020;108(3):625-634. Pub Med
. "Meta-analysis of genome-wide association studies: No efficiency gain in using individual participant data.." Genet Epidemiol. 2010;34(1):60-6. Pub Med
. "Sample size considerations of prediction-validation methods in high-dimensional data for survival outcomes.." Genet Epidemiol. 2013;37(3):276-82. Pub Med
. "Multivariate phenotype association analysis by marker-set kernel machine regression.." Genet Epidemiol. 2012;36(7):686-95. Pub Med
. "Power and sample size calculations for SNP association studies with censored time-to-event outcomes.." Genet Epidemiol. 2012;36(6):538-48. 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
. "Analysis of untyped SNPs: Maximum likelihood and imputation methods.." Genet Epidemiol. 2010;34(8):803-15. Pub Med
. "Effective SNP ranking improves the performance of eQTL mapping.." Genet Epidemiol. 2020;44(6):611-619. Pub Med
. "Complete effect-profile assessment in association studies with multiple genetic and multiple environmental factors.." Genet Epidemiol. 2015;39(2):122-33. Pub Med
. "A framework for transcriptome-wide association studies in breast cancer in diverse study populations.." Genome Biol. 2020;21(1):42. Pub Med
. "Genome-wide association study identifies five new schizophrenia loci.." Nat Genet. 2011;43(10):969-76. Pub Med
. "Genetic analyses of diverse populations improves discovery for complex traits.." Nature. 2019;570(7762):514-518. 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
. "A new method for detecting associations with rare copy-number variants.." PLoS Genet. 2015;11(10):e1005403. Pub Med
. "SNPpy--database management for SNP data from genome wide association studies.." PLoS One. 2011;6(10):e24982. Pub Med
. "A junction coverage compatibility score to quantify the reliability of transcript abundance estimates and annotation catalogs.." Life Sci Alliance. 2019;2(1):. Pub Med
. "TEAM: Efficient two-locus epistasis tests in human genome-wide association study.." Bioinformatics. 2010;26(12):i217-27. Pub Med