| Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertension X Zhu, T Feng, BO Tayo, J Liang, JH Young, N Franceschini, JA Smith, ... The American Journal of Human Genetics 96 (1), 21-36, 2015 | 342 | 2015 |
| Detecting rare variants for complex traits using family and unrelated data X Zhu, T Feng, Y Li, Q Lu, RC Elston Genetic epidemiology 34 (2), 171-187, 2010 | 147 | 2010 |
| Two-marker association tests yield new disease associations for coronary artery disease and hypertension TP Slavin, T Feng, A Schnell, X Zhu, RC Elston Human genetics 130, 725-733, 2011 | 110 | 2011 |
| Genome-wide association of anthropometric traits in African-and African-derived populations SJ Kang, CWK Chiang, CD Palmer, BO Tayo, G Lettre, JL Butler, ... Human molecular genetics 19 (13), 2725-2738, 2010 | 106 | 2010 |
| Genome-wide searching of rare genetic variants in WTCCC data T Feng, X Zhu Human genetics 128 (3), 269-280, 2010 | 61 | 2010 |
| Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS) T Feng, RC Elston, X Zhu Genetic epidemiology 35 (5), 398-409, 2011 | 60 | 2011 |
| Gene, pathway and network frameworks to identify epistatic interactions of single nucleotide polymorphisms derived from GWAS data Y Liu, S Maxwell, T Feng, X Zhu, RC Elston, M Koyutürk, MR Chance BMC systems biology 6, 1-12, 2012 | 54 | 2012 |
| A variable‐sized sliding‐window approach for genetic association studies via principal component analysis R Tang, T Feng, Q Sha, S Zhang Annals of human genetics 73 (6), 631-637, 2009 | 32 | 2009 |
| Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level H Wang, BE Cade, H Chen, KJ Gleason, R Saxena, T Feng, EK Larkin, ... Human molecular genetics 25 (23), 5244-5253, 2016 | 31 | 2016 |
| Assessing the impact of global versus local ancestry in association studies SJ Kang, EK Larkin, Y Song, J Barnholtz-Sloan, D Baechle, T Feng, X Zhu BMC proceedings 3, 1-6, 2009 | 29 | 2009 |
| An efficient method to identify differentially expressed genes in microarray experiments H Qin, T Feng, SA Harding, CJ Tsai, S Zhang Bioinformatics 24 (14), 1583-1589, 2008 | 27 | 2008 |
| Two-stage association tests for genome-wide association studies based on family data with arbitrary family structure T Feng, S Zhang, Q Sha European Journal of Human Genetics 15 (11), 1169-1175, 2007 | 21 | 2007 |
| The association of the vanin-1 N131S variant with blood pressure is mediated by endoplasmic reticulum-associated degradation and loss of function YJ Wang, BO Tayo, A Bandyopadhyay, H Wang, T Feng, N Franceschini, ... PLoS genetics 10 (9), e1004641, 2014 | 18 | 2014 |
| Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American families PB Shetty, H Tang, T Feng, B Tayo, AC Morrison, SLR Kardia, CL Hanis, ... Circulation: Cardiovascular Genetics 8 (1), 106-113, 2015 | 16 | 2015 |
| 基于听觉特性的音频水印能量估计及自适应嵌入算法研究 冯涛， 韩纪庆 声学学报 31 (1), 48-54, 2006 | 12 | 2006 |
| A method to correct for population structure using a segregation model Q Feng, J Abraham, T Feng, Y Song, RC Elston, X Zhu BMC proceedings 3, 1-5, 2009 | 9 | 2009 |
| A data-driven weighting scheme for family-based genome-wide association studies H Qin, T Feng, S Zhang, Q Sha European journal of human genetics 18 (5), 596-603, 2010 | 7 | 2010 |
| 稳健数字水印结构的性质研究 冯涛， 王承发， 韩纪庆 计算机学报 27 (007), 971-976, 2004 | 7 | 2004 |
| Whole genome sequencing data from pedigrees suggests linkage disequilibrium among rare variants created by population admixture T Feng, X Zhu BMC proceedings 8, 1-4, 2014 | 5 | 2014 |
| Detecting association with rare variants for common diseases using haplotype-based methods T Feng, Y Li, X Zhu Statistics and its Interface 4 (3), 273-283, 2011 | 5 | 2011 |
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