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Tian Zheng, Ph.D. - Publications

Affiliations: 
2002 Columbia University, New York, NY 
Area:
Statistics
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44 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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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