| Year |
Citation |
Score |
| 2021 |
Yu QY, Lu TP, Hsiao TH, Lin CH, Wu CY, Tzeng JY, Hsiao CK. An Integrative Co-localization (INCO) Analysis for SNV and CNV Genomic Features With an Application to Taiwan Biobank Data. Frontiers in Genetics. 12: 709555. PMID 34567069 DOI: 10.3389/fgene.2021.709555 |
0.311 |
|
| 2020 |
Brucker A, Lu W, Marceau West R, Yu QY, Hsiao CK, Hsiao TH, Lin CH, Magnusson PKE, Sullivan PF, Szatkiewicz JP, Lu TP, Tzeng JY. Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis. Plos Computational Biology. 16: e1007797. PMID 32365089 DOI: 10.1371/Journal.Pcbi.1007797 |
0.34 |
|
| 2020 |
Martinez K, Maity A, Yolken RH, Sullivan PF, Tzeng JY. Robust kernel association testing (RobKAT). Genetic Epidemiology. PMID 31943371 DOI: 10.1002/Gepi.22280 |
0.305 |
|
| 2018 |
Wang C, Tzeng JY, Wu PZ, Preisig M, Hsiao CK. Re-examining Dis/Similarity-Based Tests for Rare-Variant Association with Case-Control Samples. Genetics. PMID 29545466 DOI: 10.1534/Genetics.118.300769 |
0.387 |
|
| 2018 |
Maity A, Zhao J, Sullivan PF, Tzeng JY. Inference on phenotype-specific effects of genes using multivariate kernel machine regression. Genetic Epidemiology. PMID 29314255 DOI: 10.1002/Gepi.22096 |
0.416 |
|
| 2016 |
Jeng XJ, Daye ZJ, Lu W, Tzeng JY. Rare Variants Association Analysis in Large-Scale Sequencing Studies at the Single Locus Level. Plos Computational Biology. 12: e1004993. PMID 27355347 DOI: 10.1371/journal.pcbi.1004993 |
0.308 |
|
| 2015 |
Tzeng JY, Magnusson PK, Sullivan PF, Szatkiewicz JP. A New Method for Detecting Associations with Rare Copy-Number Variants. Plos Genetics. 11: e1005403. PMID 26431523 DOI: 10.1371/Journal.Pgen.1005403 |
0.425 |
|
| 2015 |
Hung H, Lin YT, Chen P, Wang CC, Huang SY, Tzeng JY. Detection of gene-gene interactions using multistage sparse and low-rank regression. Biometrics. PMID 26288029 DOI: 10.1111/Biom.12374 |
0.314 |
|
| 2015 |
Marceau R, Lu W, Holloway S, Sale MM, Worrall BB, Williams SR, Hsu FC, Tzeng JY. A Fast Multiple-Kernel Method With Applications to Detect Gene-Environment Interaction. Genetic Epidemiology. PMID 26139508 DOI: 10.1002/Gepi.21909 |
0.421 |
|
| 2015 |
Neely ML, Bondell HD, Tzeng JY. A penalized likelihood approach for investigating gene-drug interactions in pharmacogenetic studies. Biometrics. 71: 529-37. PMID 25604216 DOI: 10.1111/Biom.12259 |
0.373 |
|
| 2015 |
Zhao G, Marceau R, Zhang D, Tzeng JY. Assessing gene-environment interactions for common and rare variants with binary traits using gene-trait similarity regression. Genetics. 199: 695-710. PMID 25585620 DOI: 10.1534/Genetics.114.171686 |
0.426 |
|
| 2015 |
Wang Z, Maity A, Luo Y, Neely ML, Tzeng JY. Complete effect-profile assessment in association studies with multiple genetic and multiple environmental factors. Genetic Epidemiology. 39: 122-33. PMID 25538034 DOI: 10.1002/Gepi.21877 |
0.377 |
|
| 2014 |
Tzeng JY, Lu W, Hsu FC. GENE-LEVEL PHARMACOGENETIC ANALYSIS ON SURVIVAL OUTCOMES USING GENE-TRAIT SIMILARITY REGRESSION. The Annals of Applied Statistics. 8: 1232-1255. PMID 25018788 DOI: 10.1214/14-Aoas735 |
0.345 |
|
| 2014 |
Wang X, Epstein MP, Tzeng JY. Analysis of gene-gene interactions using gene-trait similarity regression. Human Heredity. 78: 17-26. PMID 24969398 DOI: 10.1159/000360161 |
0.314 |
|
| 2014 |
Hu J, Tzeng JY. Integrative gene set analysis of multi-platform data with sample heterogeneity. Bioinformatics (Oxford, England). 30: 1501-7. PMID 24489370 DOI: 10.1093/Bioinformatics/Btu060 |
0.346 |
|
| 2013 |
Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, ... ... Tzeng JY, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/Ng.2711 |
0.404 |
|
| 2012 |
Maity A, Sullivan PF, Tzeng JY. Multivariate phenotype association analysis by marker-set kernel machine regression. Genetic Epidemiology. 36: 686-95. PMID 22899176 DOI: 10.1002/Gepi.21663 |
0.392 |
|
| 2011 |
Pongpanich M, Neely ML, Tzeng JY. On the Aggregation of Multimarker Information for Marker-Set and Sequencing Data Analysis: Genotype Collapsing vs. Similarity Collapsing. Frontiers in Genetics. 2: 110. PMID 22303404 DOI: 10.3389/Fgene.2011.00110 |
0.381 |
|
| 2011 |
Tzeng JY, Zhang D, Pongpanich M, Smith C, McCarthy MI, Sale MM, Worrall BB, Hsu FC, Thomas DC, Sullivan PF. Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression. American Journal of Human Genetics. 89: 277-88. PMID 21835306 DOI: 10.1016/J.Ajhg.2011.07.007 |
0.352 |
|
| 2011 |
Lee MH, Tzeng JY, Huang SY, Hsiao CK. Combining an evolution-guided clustering algorithm and haplotype-based LRT in family association studies. Bmc Genetics. 12: 48. PMID 21592403 DOI: 10.1186/1471-2156-12-48 |
0.372 |
|
| 2010 |
Koehler ML, Bondell HD, Tzeng JY. Evaluating haplotype effects in case-control studies via penalized-likelihood approaches: prospective or retrospective analysis? Genetic Epidemiology. 34: 892-911. PMID 21104891 DOI: 10.1002/Gepi.20545 |
0.424 |
|
| 2010 |
Pongpanich M, Sullivan PF, Tzeng JY. A quality control algorithm for filtering SNPs in genome-wide association studies. Bioinformatics (Oxford, England). 26: 1731-7. PMID 20501555 DOI: 10.1093/Bioinformatics/Btq272 |
0.354 |
|
| 2010 |
Tzeng JY, Bondell HD. A comprehensive approach to haplotype-specific analysis by penalized likelihood. European Journal of Human Genetics : Ejhg. 18: 95-103. PMID 19584902 DOI: 10.1038/Ejhg.2009.118 |
0.439 |
|
| 2009 |
Liu Y, Li YJ, Satten GA, Allen AS, Tzeng JY. A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity. Annals of Human Genetics. 73: 520-6. PMID 19622101 DOI: 10.1111/J.1469-1809.2009.00536.X |
0.451 |
|
| 2009 |
Tzeng JY, Zhang D, Chang SM, Thomas DC, Davidian M. Gene-trait similarity regression for multimarker-based association analysis. Biometrics. 65: 822-32. PMID 19210740 DOI: 10.1111/J.1541-0420.2008.01176.X |
0.36 |
|
| 2007 |
Tzeng JY, Zhang D. Haplotype-based association analysis via variance-components score test. American Journal of Human Genetics. 81: 927-38. PMID 17924336 DOI: 10.1086/521558 |
0.467 |
|
| 2006 |
Wen SH, Tzeng JY, Kao JT, Hsiao CK. A two-stage design for multiple testing in large-scale association studies. Journal of Human Genetics. 51: 523-32. PMID 16691321 DOI: 10.1007/S10038-006-0393-6 |
0.344 |
|
| 2006 |
Tzeng JY, Wang CH, Kao JT, Hsiao CK. Regression-based association analysis with clustered haplotypes through use of genotypes. American Journal of Human Genetics. 78: 231-42. PMID 16365833 DOI: 10.1086/500025 |
0.435 |
|
| 2006 |
Sabatti C, Satten GA, Allen AS, Epstein MP, Chatterjee N, Spinka C, Chen J, Carroll RJ, Tzeng JY, Roeder K, Li H, Lin DY, Zeng D. Journal of the American Statistical Association: Comment Journal of the American Statistical Association. 101: 104-118. DOI: 10.1198/016214505000000817 |
0.404 |
|
| 2005 |
Tzeng JY. Evolutionary-based grouping of haplotypes in association analysis. Genetic Epidemiology. 28: 220-31. PMID 15726584 DOI: 10.1002/Gepi.20063 |
0.398 |
|
| 2003 |
Tzeng JY, Devlin B, Wasserman L, Roeder K. On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit. American Journal of Human Genetics. 72: 891-902. PMID 12610778 DOI: 10.1086/373881 |
0.53 |
|
| 2003 |
Tzeng J, Byerley W, Devlin B, Roeder K, Wasserman L. Outlier Detection and False Discovery Rates for Whole-Genome DNA Matching Journal of the American Statistical Association. 98: 236-246. DOI: 10.1198/016214503388619256 |
0.519 |
|
| 2000 |
Hsiao CK, Tzeng J, Wang C. Comparing the performance of two indices for spatial model selection: application to two mortality data. Statistics in Medicine. 19: 1915-1930. PMID 10867680 DOI: 10.1002/1097-0258(20000730)19:14<1915::Aid-Sim503>3.0.Co;2-M |
0.319 |
|
| 1998 |
Tzeng J, Hsiao CK, Chen C. Spatial Model Selection Using Bayes Factor and Ratio of Variabilities for Asthma Mortality Data Canadian Journal of Public Health-Revue Canadienne De Sante Publique. 17: 158-169. DOI: 10.6288/Cjph1998-17-02-09 |
0.316 |
|
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