Year |
Citation |
Score |
2018 |
Hsu Y, Auerbach J, Zheng T, Lo SH. Coping with family structure in genome-wide association studies: a comparative evaluation. Bmc Proceedings. 12: 42. PMID 30263047 DOI: 10.1186/S12919-018-0151-8 |
0.566 |
|
2016 |
Lo A, Agne M, Auerbach J, Fan R, Lo SH, Wang P, Zheng T. Network-guided interaction mining for the blood pressure phenotype of unrelated individuals in genetic analysis workshop 19. Bmc Proceedings. 10: 333-336. PMID 27980658 DOI: 10.1186/S12919-016-0052-7 |
0.599 |
|
2016 |
Auerbach J, Agne M, Fan R, Lo A, Lo SH, Zheng T, Wang P. Identifying regions of disease-related variants in admixed populations with the summation partition approach. Bmc Proceedings. 10: 131-134. PMID 27980624 DOI: 10.1186/S12919-016-0018-9 |
0.575 |
|
2016 |
Lo A, Chernoff H, Zheng T, Lo SH. Framework for making better predictions by directly estimating variables' predictivity. Proceedings of the National Academy of Sciences of the United States of America. 113: 14277-14282. PMID 27911830 DOI: 10.1073/Pnas.1616647113 |
0.538 |
|
2016 |
Tan LSL, Chan AH, Zheng T. Topic-adjusted visibility metric for scientific articles The Annals of Applied Statistics. 10: 1-31. DOI: 10.1214/15-Aoas887 |
0.3 |
|
2015 |
Lo A, Chernoff H, Zheng T, Lo SH. Why significant variables aren't automatically good predictors. Proceedings of the National Academy of Sciences of the United States of America. 112: 13892-7. PMID 26504198 DOI: 10.1073/Pnas.1518285112 |
0.568 |
|
2014 |
Agne M, Huang CH, Hu I, Wang H, Zheng T, Lo SH. Considering interactive effects in the identification of influential regions with extremely rare variants via fixed bin approach. Bmc Proceedings. 8: S7. PMID 25519400 DOI: 10.1186/1753-6561-8-S1-S7 |
0.601 |
|
2014 |
Wang MH, Huang CH, Zheng T, Lo SH, Hu I. Discovering pure gene-environment interactions in blood pressure genome-wide association studies data: a two-step approach incorporating new statistics. Bmc Proceedings. 8: S62. PMID 25519396 DOI: 10.1186/1753-6561-8-S1-S62 |
0.603 |
|
2014 |
Fan R, Huang CH, Hu I, Wang H, Zheng T, Lo SH. A partition-based approach to identify gene-environment interactions in genome wide association studies. Bmc Proceedings. 8: S60. PMID 25519395 DOI: 10.1186/1753-6561-8-S1-S60 |
0.621 |
|
2014 |
Liu Y, Huang CH, Hu I, Lo SH, Zheng T. Correction: A dual clustering framework for association screening with whole genome sequencing data and longitudinal traits. Bmc Proceedings. 8: S112. PMID 25519352 DOI: 10.1186/1753-6561-8-S1-S112 |
0.499 |
|
2014 |
Liu Y, Huang C, Hu I, Lo SH, Zheng T. A dual-clustering framework for association screening with whole genome sequencing data and longitudinal traits. Bmc Proceedings. 8: S47. PMID 25519328 DOI: 10.1186/1753-6561-8-S1-S47 |
0.616 |
|
2014 |
Irshad S, Bansal M, Magnen CL, Dillon R, Castillo-Martin M, Zheng T, Aytes A, Wenske S, Guarnieri P, Sumazin P, Benson M, Shen MM, Califano A, Abate-Shen C. Abstract 2873: A molecular signature predictive of indolent prostate cancer Cancer Research. 74: 2873-2873. DOI: 10.1158/1538-7445.Am2014-2873 |
0.304 |
|
2013 |
Irshad S, Bansal M, Castillo-Martin M, Zheng T, Aytes A, Wenske S, Le Magnen C, Guarnieri P, Sumazin P, Benson MC, Shen MM, Califano A, Abate-Shen C. A molecular signature predictive of indolent prostate cancer. Science Translational Medicine. 5: 202ra122. PMID 24027026 DOI: 10.1126/Scitranslmed.3006408 |
0.31 |
|
2012 |
Wang H, Lo SH, Zheng T, Hu I. Interaction-based feature selection and classification for high-dimensional biological data. Bioinformatics (Oxford, England). 28: 2834-42. PMID 22945786 DOI: 10.1093/Bioinformatics/Bts531 |
0.612 |
|
2011 |
Liu Y, Huang CH, Hu I, Lo SH, Zheng T. Association screening for genes with multiple potentially rare variants: an inverse-probability weighted clustering approach. Bmc Proceedings. 5: S106. PMID 22373536 DOI: 10.1186/1753-6561-5-S9-S106 |
0.624 |
|
2011 |
Wang H, Huang CH, Lo SH, Zheng T, Hu I. New insights into old methods for identifying causal rare variants. Bmc Proceedings. 5: S50. PMID 22373518 DOI: 10.1186/1753-6561-5-S9-S50 |
0.608 |
|
2011 |
Agne M, Huang CH, Hu I, Wang H, Zheng T, Lo SH. Identifying influential regions in extremely rare variants using a fixed-bin approach. Bmc Proceedings. 5: S3. PMID 22373412 DOI: 10.1186/1753-6561-5-S9-S3 |
0.581 |
|
2011 |
Fan R, Huang CH, Lo SH, Zheng T, Ionita-Laza I. Identifying rare disease variants in the Genetic Analysis Workshop 17 simulated data: a comparison of several statistical approaches. Bmc Proceedings. 5: S17. PMID 22373071 DOI: 10.1186/1753-6561-5-S9-S17 |
0.612 |
|
2010 |
Wang S, Zheng T, Chanock S, Jedrychowski W, Perera FP. Methods for detecting interactions between genetic polymorphisms and prenatal environment exposure with a mother-child design. Genetic Epidemiology. 34: 125-32. PMID 19582785 DOI: 10.1002/Gepi.20441 |
0.339 |
|
2009 |
Huang CH, Cong L, Xie J, Qiao B, Lo SH, Zheng T. Rheumatoid arthritis-associated gene-gene interaction network for rheumatoid arthritis candidate genes. Bmc Proceedings. 3: S75. PMID 20018070 DOI: 10.1186/1753-6561-3-S7-S75 |
0.596 |
|
2009 |
Qiao B, Huang CH, Cong L, Xie J, Lo SH, Zheng T. Genome-wide gene-based analysis of rheumatoid arthritis-associated interaction with PTPN22 and HLA-DRB1. Bmc Proceedings. 3: S132. PMID 20017999 DOI: 10.1186/1753-6561-3-S7-S132 |
0.567 |
|
2009 |
An P, Mukherjee O, Chanda P, Yao L, Engelman CD, Huang CH, Zheng T, Kovac IP, Dubé MP, Liang X, Li J, de Andrade M, Culverhouse R, Malzahn D, Manning AK, et al. The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16. Genetic Epidemiology. 33: S58-67. PMID 19924703 DOI: 10.1002/Gepi.20474 |
0.371 |
|
2009 |
Watkinson J, Liang KC, Wang X, Zheng T, Anastassiou D. Inference of regulatory gene interactions from expression data using three-way mutual information. Annals of the New York Academy of Sciences. 1158: 302-13. PMID 19348651 DOI: 10.1111/J.1749-6632.2008.03757.X |
0.394 |
|
2009 |
Chernoff H, Lo S, Zheng T. Discovering influential variables: A method of partitions The Annals of Applied Statistics. 3: 1335-1369. DOI: 10.1214/09-Aoas265 |
0.557 |
|
2008 |
Zheng T, Lo SH. Comment: Quantifying the Fraction of Missing Information for Hypothesis Testing in Statistical and Genetic Studies. Statistical Science : a Review Journal of the Institute of Mathematical Statistics. 23: 318-320. PMID 19946612 DOI: 10.1214/08-Sts244A |
0.553 |
|
2008 |
Yan X, Zheng T. Selecting informative genes for discriminant analysis using multigene expression profiles. Bmc Genomics. 9: S14. PMID 18831779 DOI: 10.1186/1471-2164-9-S2-S14 |
0.323 |
|
2008 |
Lo SH, Chernoff H, Cong L, Ding Y, Zheng T. Discovering interactions among BRCA1 and other candidate genes associated with sporadic breast cancer. Proceedings of the National Academy of Sciences of the United States of America. 105: 12387-92. PMID 18711133 DOI: 10.1073/Pnas.0805242105 |
0.585 |
|
2008 |
Iossifov I, Zheng T, Baron M, Gilliam TC, Rzhetsky A. Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network. Genome Research. 18: 1150-62. PMID 18417725 DOI: 10.1101/Gr.075622.107 |
0.364 |
|
2008 |
Watkinson J, Wang X, Zheng T, Anastassiou D. Identification of gene interactions associated with disease from gene expression data using synergy networks. Bmc Systems Biology. 2: 10. PMID 18234101 DOI: 10.1186/1752-0509-2-10 |
0.383 |
|
2008 |
Woo JH, Zheng T, Kim JH. DACE: Differential Allelic Co-Expression test for estimating regulatory associations of SNP and biological pathway International Journal of Functional Informatics and Personalised Medicine. 1: 407-418. DOI: 10.1504/Ijfipm.2008.022156 |
0.389 |
|
2007 |
Zheng T, Lo SH. A Modified Kendall Rank-Order Association Test For Evaluating The Repeatability Of Two Studies With A Large Number Of Objects. Lecture Notes-Monograph Series / Institute of Mathematical Statistics. 3: 515-528. PMID 21687777 |
0.534 |
|
2007 |
Wang S, Zheng T, Wang Y. Transcription activity hot spot, is it real or an artifact? Bmc Proceedings. 1: S94. PMID 18466598 DOI: 10.1186/1753-6561-1-S1-S94 |
0.376 |
|
2007 |
Li Z, Zheng T, Califano A, Floratos A. Pattern-based mining strategy to detect multi-locus association and gene x environment interaction. Bmc Proceedings. 1: S16. PMID 18466505 DOI: 10.1186/1753-6561-1-S1-S16 |
0.425 |
|
2007 |
Ding Y, Cong L, Ionita-Laza I, Lo SH, Zheng T. Constructing gene association networks for rheumatoid arthritis using the backward genotype-trait association (BGTA) algorithm. Bmc Proceedings. 1: S13. PMID 18466472 DOI: 10.1186/1753-6561-1-S1-S13 |
0.616 |
|
2007 |
Zheng T, Wang S, Cong L, Ding Y, Ionita-Laza I, Lo SH. Joint study of genetic regulators for expression traits related to breast cancer. Bmc Proceedings. 1: S10. PMID 18466439 DOI: 10.1186/1753-6561-1-S1-S10 |
0.579 |
|
2007 |
Wilcox MA, Li Z, Tapper W, Browning S, Curtin K, Ding J, Ding Y, Gagnon F, He Q, Kuo TY, Li M, Matthew G, Mei L, Rao S, Shaw J, ... ... Zheng T, et al. Genetic association with rheumatoid arthritis-Genetic Analysis Workshop 15: summary of contributions from Group 2. Genetic Epidemiology. 31: S12-21. PMID 18046771 DOI: 10.1002/gepi.20276 |
0.302 |
|
2007 |
Chen GK, Zheng T, Witte JS, Goode EL, Gao L, Hu P, Suh YJ, Suktitipat B, Szymczak S, Woo JH, Zhang W. Genome-wide association analyses of expression phenotypes. Genetic Epidemiology. 31: S7-S11. PMID 18046762 DOI: 10.1002/Gepi.20275 |
0.413 |
|
2007 |
Rzhetsky A, Wajngurt D, Park N, Zheng T. Probing genetic overlap among complex human phenotypes. Proceedings of the National Academy of Sciences of the United States of America. 104: 11694-9. PMID 17609372 DOI: 10.1073/Pnas.0704820104 |
0.337 |
|
2006 |
Rzhetsky A, Zheng T, Weinreb C. Self-correcting maps of molecular pathways. Plos One. 1: e61. PMID 17183692 DOI: 10.1371/Journal.Pone.0000061 |
0.319 |
|
2006 |
Zheng T, Wang H, Lo SH. Backward genotype-trait association (BGTA)-based dissection of complex traits in case-control designs. Human Heredity. 62: 196-212. PMID 17114886 DOI: 10.1159/000096995 |
0.592 |
|
2006 |
Lin C, Wang H, Chen Y, Freimer N, Zheng T, Lo S, Moura-Neto RS, Bydlowski SP, Pena SDJ, Rocha J, Passarino G, Montesanto A, Dato S, Giordano S, Domma F, et al. Contents Vol. 62, 2006 Human Heredity. 62: 225-226. DOI: 10.1159/000098096 |
0.469 |
|
2006 |
Lin C, Wang H, Chen Y, Freimer N, Zheng T, Lo S, Moura-Neto RS, Bydlowski SP, Pena SDJ, Rocha J, Passarino G, Montesanto A, Dato S, Giordano S, Domma F, et al. Subject Index Vol. 62, 2006 Human Heredity. 62: 224-224. DOI: 10.1159/000098095 |
0.485 |
|
2004 |
Lo SH, Zheng T. A demonstration and findings of a statistical approach through reanalysis of inflammatory bowel disease data. Proceedings of the National Academy of Sciences of the United States of America. 101: 10386-91. PMID 15231995 DOI: 10.1073/Pnas.0403662101 |
0.585 |
|
2002 |
Lo SH, Zheng T. Backward Haplotype Transmission Association (BHTA) algorithm - a fast multiple-marker screening method. Human Heredity. 53: 197-215. PMID 12435884 DOI: 10.1159/000066194 |
0.608 |
|
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