Year |
Citation |
Score |
2024 |
Hu X, Hu Z, Xu T, Zhang K, Lu HH, Zhao J, Boerwinkle E, Jin L, Xiong M. Equilibrium points and their stability of COVID-19 in US. Scientific Reports. 14: 1628. PMID 38238368 DOI: 10.1038/s41598-024-51729-w |
0.482 |
|
2023 |
Xu T, Zhao J, Xiong M. Graphical Learning and Causal Inference for Drug Repurposing. Medrxiv : the Preprint Server For Health Sciences. PMID 37577650 DOI: 10.1101/2023.07.29.23293346 |
0.466 |
|
2022 |
Chiu CY, Wang S, Zhang B, Luo Y, Simpson C, Zhang W, Wilson AF, Bailey-Wilson JE, Agron E, Chew EY, Zhang J, Xiong M, Fan R. Gene-level association analysis of ordinal traits with functional ordinal logistic regressions. Genetic Epidemiology. PMID 35438198 DOI: 10.1002/gepi.22451 |
0.301 |
|
2022 |
Chang C, Xu L, Zhang R, Jin Y, Jiang P, Wei K, Xu L, Shi Y, Zhao J, Xiong M, Guo S, He D. MicroRNA-Mediated Epigenetic Regulation of Rheumatoid Arthritis Susceptibility and Pathogenesis. Frontiers in Immunology. 13: 838884. PMID 35401568 DOI: 10.3389/fimmu.2022.838884 |
0.509 |
|
2021 |
Jiang Y, Chiu CY, Yan Q, Chen W, Gorin MB, Conley YP, Lakhal-Chaieb ML, Cook RJ, Amos CI, Wilson AF, Bailey-Wilson JE, McMahon FJ, Vazquez AI, Yuan A, Zhong X, ... Xiong M, et al. Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration. Journal of the American Statistical Association. 116: 531-545. PMID 34321704 DOI: 10.1080/01621459.2020.1799809 |
0.311 |
|
2020 |
Ge Q, Huang X, Fang S, Guo S, Liu Y, Lin W, Xiong M. Conditional Generative Adversarial Networks for Individualized Treatment Effect Estimation and Treatment Selection. Frontiers in Genetics. 11: 585804. PMID 33362849 DOI: 10.3389/fgene.2020.585804 |
0.638 |
|
2020 |
Hu Z, Jiao R, Wang P, Zhu Y, Zhao J, De Jager P, Bennett DA, Jin L, Xiong M. Shared Causal Paths underlying Alzheimer's dementia and Type 2 Diabetes. Scientific Reports. 10: 4107. PMID 32139775 DOI: 10.1038/S41598-020-60682-3 |
0.574 |
|
2020 |
Jiang Y, Chiu C, Yan Q, Chen W, Gorin MB, Conley YP, Lakhal-Chaieb ML, Cook RJ, Amos CI, Wilson AF, Bailey-Wilson JE, McMahon FJ, Vazquez AI, Yuan A, Zhong X, ... Xiong M, et al. Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration Journal of the American Statistical Association. 1-15. DOI: 10.1080/01621459.2020.1799809 |
0.355 |
|
2019 |
Chiu CY, Zhang B, Wang S, Shao J, Lakhal-Chaieb ML, Cook RJ, Wilson AF, Bailey-Wilson JE, Xiong M, Fan R. Gene-based association analysis of survival traits via functional regression-based mixed effect cox models for related samples. Genetic Epidemiology. PMID 31502722 DOI: 10.1002/Gepi.22254 |
0.445 |
|
2019 |
Chen J, Wu JS, Mize T, Moreno M, Hamid M, Servin F, Bashy B, Zhao Z, Jia P, Tsuang MT, Kendler KS, Xiong M, Chen X. A Frameshift Variant in the CHST9 Gene Identified by Family-Based Whole Genome Sequencing Is Associated with Schizophrenia in Chinese Population. Scientific Reports. 9: 12717. PMID 31481703 DOI: 10.1038/S41598-019-49052-W |
0.309 |
|
2019 |
Fang S, Xu T, Xiong M, Zhou X, Wang Y, Haydu LE, Ross MI, Gershenwald JE, Prieto VG, Cormier JN, Wargo J, Sui D, Wei Q, Amos CI, Lee JE. Role of immune response, inflammation and tumor immune response-related cytokines/chemokines in melanoma progression. The Journal of Investigative Dermatology. PMID 31176707 DOI: 10.1016/J.Jid.2019.03.1158 |
0.51 |
|
2019 |
Wang Y, Li Y, Hao M, Liu X, Zhang M, Wang J, Xiong M, Shugart YY, Jin L. Robust Reference Powered Association Test of Genome-Wide Association Studies. Frontiers in Genetics. 10: 319. PMID 31024629 DOI: 10.3389/Fgene.2019.00319 |
0.634 |
|
2018 |
Chiu CY, Yuan F, Zhang BS, Yuan A, Li X, Fang HB, Lange K, Weeks DE, Wilson AF, Bailey-Wilson JE, Musolf AM, Stambolian D, Lakhal-Chaieb ML, Cook RJ, McMahon FJ, ... ... Xiong M, et al. Linear mixed models for association analysis of quantitative traits with next-generation sequencing data. Genetic Epidemiology. PMID 30537345 DOI: 10.1002/Gepi.22177 |
0.391 |
|
2018 |
Li Y, Liu X, Ma Y, Wang Y, Zhou W, Hao M, Yuan Z, Liu J, Xiong M, Shugart YY, Wang J, Jin L. knnAUC: an open-source R package for detecting nonlinear dependence between one continuous variable and one binary variable. Bmc Bioinformatics. 19: 448. PMID 30466390 DOI: 10.1186/S12859-018-2427-4 |
0.539 |
|
2018 |
Jiao R, Lin N, Hu Z, Bennett DA, Jin L, Xiong M. Bivariate Causal Discovery and Its Applications to Gene Expression and Imaging Data Analysis. Frontiers in Genetics. 9: 347. PMID 30233639 DOI: 10.3389/Fgene.2018.00347 |
0.49 |
|
2018 |
Hu P, Jiao R, Jin L, Xiong M. Application of Causal Inference to Genomic Analysis: Advances in Methodology. Frontiers in Genetics. 9: 238. PMID 30042787 DOI: 10.3389/Fgene.2018.00238 |
0.505 |
|
2018 |
Wang Y, Li Y, Qiao C, Liu X, Hao M, Shugart YY, Xiong M, Jin L. Nuclear Norm Clustering: a promising alternative method for clustering tasks. Scientific Reports. 8: 10873. PMID 30022093 DOI: 10.1038/S41598-018-29246-4 |
0.378 |
|
2017 |
Lin N, Zhu Y, Fan R, Xiong M. A quadratically regularized functional canonical correlation analysis for identifying the global structure of pleiotropy with NGS data. Plos Computational Biology. 13: e1005788. PMID 29040274 DOI: 10.1371/Journal.Pcbi.1005788 |
0.432 |
|
2017 |
Wang Y, Li Y, Liu X, Pu W, Wang X, Wang J, Xiong M, Yao Shugart Y, Jin L. Bagging Nearest-Neighbor Prediction independence Test: an efficient method for nonlinear dependence of two continuous variables. Scientific Reports. 7: 12736. PMID 28986523 DOI: 10.1038/S41598-017-12783-9 |
0.586 |
|
2017 |
Xu K, Jin L, Xiong M. Functional regression method for whole genome eQTL epistasis analysis with sequencing data. Bmc Genomics. 18: 385. PMID 28521784 DOI: 10.1186/S12864-017-3777-4 |
0.464 |
|
2016 |
Chiu CY, Jung J, Chen W, Weeks DE, Ren H, Boehnke M, Amos CI, Liu A, Mills JL, Ting Lee ML, Xiong M, Fan R. Meta-analysis of quantitative pleiotropic traits for next-generation sequencing with multivariate functional linear models. European Journal of Human Genetics : Ejhg. PMID 28000696 DOI: 10.1038/Ejhg.2016.170 |
0.418 |
|
2016 |
Chiu CY, Jung J, Wang Y, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Mills JL, Boehnke M, Xiong M, Fan R. A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing. Genetic Epidemiology. PMID 27917525 DOI: 10.1002/Gepi.22014 |
0.432 |
|
2016 |
Wang P, Rahman M, Jin L, Xiong M. A new statistical framework for genetic pleiotropic analysis of high dimensional phenotype data. Bmc Genomics. 17: 881. PMID 27821073 DOI: 10.1186/S12864-016-3169-1 |
0.476 |
|
2016 |
Wang Y, Li Y, Pu W, Wen K, Shugart YY, Xiong M, Jin L. Random Bits Forest: a Strong Classifier/Regressor for Big Data. Scientific Reports. 6: 30086. PMID 27444562 DOI: 10.1038/Srep30086 |
0.42 |
|
2016 |
Fan R, Chiu CY, Jung J, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Chen Z, Mills JL, Xiong M. A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits. Genetic Epidemiology. PMID 27374056 DOI: 10.1002/Gepi.21984 |
0.376 |
|
2016 |
Zhang F, Xie D, Liang M, Xiong M. Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits. Plos Genetics. 12: e1005965. PMID 27104857 DOI: 10.1371/Journal.Pgen.1005965 |
0.417 |
|
2016 |
Guo S, Li Y, Wang Y, Chu H, Chen Y, Liu Q, Guo G, Tu W, Wu W, Zou H, Yang L, Xiao R, Ma Y, Zhang F, Xiong M, et al. Copy Number Variation of HLA-DQA1 and APOBEC3A/3B Contribute to the Susceptibility of Systemic Sclerosis in the Chinese Han Population. The Journal of Rheumatology. PMID 27036383 DOI: 10.3899/Jrheum.150945 |
0.694 |
|
2016 |
Xu K, Guo W, Xiong M, Zhu L, Jin L. An estimating equation approach to dimension reduction for longitudinal data. Biometrika. 103: 189-203. PMID 27017956 DOI: 10.1093/Biomet/Asv066 |
0.389 |
|
2016 |
Fan R, Wang Y, Yan Q, Ding Y, Weeks DE, Lu Z, Ren H, Cook RJ, Xiong M, Swaroop A, Chew EY, Chen W. Gene-Based Association Analysis for Censored Traits Via Fixed Effect Functional Regressions. Genetic Epidemiology. PMID 26782979 DOI: 10.1002/Gepi.21947 |
0.42 |
|
2016 |
Wang Y, Li Y, Xiong M, Shugart YY, Jin L. Random bits regression: a strong general predictor for big data Big Data Analytics. 1. DOI: 10.1186/S41044-016-0010-4 |
0.417 |
|
2015 |
Jiang J, Lin N, Guo S, Chen J, Xiong M. Multiple functional linear model for association analysis of RNA-seq with imaging. Quantitative Biology (Beijing, China). 3: 90-102. PMID 26753102 DOI: 10.1007/s40484-015-0048-8 |
0.58 |
|
2015 |
Fan R, Wang Y, Chiu CY, Chen W, Ren H, Li Y, Boehnke M, Amos CI, Moore JH, Xiong M. Meta-analysis of Complex Diseases at Gene Level by Generalized Functional Linear Models. Genetics. PMID 26715663 DOI: 10.1534/Genetics.115.180869 |
0.444 |
|
2015 |
Park T, Van Steen K, Lou XY, Xiong M. Statistical Analysis of High-Dimensional Genetic Data in Complex Traits. Biomed Research International. 2015: 564273. PMID 26346557 DOI: 10.1155/2015/564273 |
0.458 |
|
2015 |
Wang Y, Li Y, Cao H, Xiong M, Shugart YY, Jin L. Efficient test for nonlinear dependence of two continuous variables. Bmc Bioinformatics. 16: 260. PMID 26283601 DOI: 10.1186/S12859-015-0697-7 |
0.439 |
|
2015 |
Lin N, Jiang J, Guo S, Xiong M. Functional Principal Component Analysis and Randomized Sparse Clustering Algorithm for Medical Image Analysis. Plos One. 10: e0132945. PMID 26196383 DOI: 10.1371/Journal.Pone.0132945 |
0.568 |
|
2015 |
Zhao J, Zhu Y, Xiong M. Genome-wide gene-gene interaction analysis for next-generation sequencing. European Journal of Human Genetics : Ejhg. PMID 26173972 DOI: 10.1038/Ejhg.2015.147 |
0.567 |
|
2015 |
Fan R, Wang Y, Boehnke M, Chen W, Li Y, Ren H, Lobach I, Xiong M. Gene Level Meta-Analysis of Quantitative Traits by Functional Linear Models. Genetics. PMID 26058849 DOI: 10.1534/Genetics.115.178343 |
0.432 |
|
2015 |
Wang Y, Liu A, Mills JL, Boehnke M, Wilson AF, Bailey-Wilson JE, Xiong M, Wu CO, Fan R. Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models. Genetic Epidemiology. 39: 259-75. PMID 25809955 DOI: 10.1002/Gepi.21895 |
0.379 |
|
2015 |
Guo S, Yan F, Xu J, Bao Y, Zhu J, Wang X, Wu J, Li Y, Pu W, Liu Y, Jiang Z, Ma Y, Chen X, Xiong M, Jin L, et al. Identification and validation of the methylation biomarkers of non-small cell lung cancer (NSCLC). Clinical Epigenetics. 7: 3. PMID 25657825 DOI: 10.1186/S13148-014-0035-3 |
0.679 |
|
2015 |
Zhao J, Zhu Y, Boerwinkle E, Xiong M. Pathway analysis with next-generation sequencing data. European Journal of Human Genetics : Ejhg. 23: 507-15. PMID 24986826 DOI: 10.1038/Ejhg.2014.121 |
0.563 |
|
2014 |
Fan R, Wang Y, Mills JL, Carter TC, Lobach I, Wilson AF, Bailey-Wilson JE, Weeks DE, Xiong M. Generalized functional linear models for gene-based case-control association studies. Genetic Epidemiology. 38: 622-37. PMID 25203683 DOI: 10.1002/Gepi.21840 |
0.412 |
|
2014 |
Zhang F, Boerwinkle E, Xiong M. Epistasis analysis for quantitative traits by functional regression model. Genome Research. 24: 989-98. PMID 24803592 DOI: 10.1101/Gr.161760.113 |
0.383 |
|
2014 |
Ma J, Xiong M, You M, Lozano G, Amos CI. Genome-wide association tests of inversions with application to psoriasis. Human Genetics. 133: 967-74. PMID 24623382 DOI: 10.1007/S00439-014-1437-1 |
0.426 |
|
2014 |
Guo S, Wang YL, Li Y, Jin L, Xiong M, Ji QH, Wang J. Significant SNPs have limited prediction ability for thyroid cancer. Cancer Medicine. 3: 731-5. PMID 24591304 DOI: 10.1002/Cam4.211 |
0.695 |
|
2013 |
Fan R, Wang Y, Mills JL, Wilson AF, Bailey-Wilson JE, Xiong M. Functional linear models for association analysis of quantitative traits. Genetic Epidemiology. 37: 726-42. PMID 24130119 DOI: 10.1002/Gepi.21757 |
0.413 |
|
2013 |
Liang F, Xiong M. Bayesian detection of causal rare variants under posterior consistency. Plos One. 8: e69633. PMID 23922764 DOI: 10.1371/Journal.Pone.0069633 |
0.382 |
|
2013 |
Hong S, Chen X, Jin L, Xiong M. Canonical correlation analysis for RNA-seq co-expression networks. Nucleic Acids Research. 41: e95. PMID 23460206 DOI: 10.1093/Nar/Gkt145 |
0.445 |
|
2013 |
Luo L, Zhu Y, Xiong M. Smoothed functional principal component analysis for testing association of the entire allelic spectrum of genetic variation. European Journal of Human Genetics : Ejhg. 21: 217-24. PMID 22781089 DOI: 10.1038/Ejhg.2012.141 |
0.503 |
|
2012 |
Wei ZZ, Luo LB, Zhang HL, Xiong M, Wang X, Zhou D. Identification and characterization of 43 novel polymorphic EST-SSR markers for arum lily, Zantedeschia aethiopica (Araceae). American Journal of Botany. 99: e493-7. PMID 23196401 DOI: 10.3732/ajb.1200228 |
0.405 |
|
2012 |
Shugart YY, Zhu Y, Guo W, Xiong M. Weighted pedigree-based statistics for testing the association of rare variants. Bmc Genomics. 13: 667. PMID 23176082 DOI: 10.1186/1471-2164-13-667 |
0.381 |
|
2012 |
Fan R, Zhang Y, Albert PS, Liu A, Wang Y, Xiong M. Longitudinal association analysis of quantitative traits. Genetic Epidemiology. 36: 856-69. PMID 22965819 DOI: 10.1002/Gepi.21673 |
0.391 |
|
2012 |
Ma J, Xiao F, Xiong M, Andrew AS, Brenner H, Duell EJ, Haugen A, Hoggart C, Hung RJ, Lazarus P, Liu C, Matsuo K, Mayordomo JI, Schwartz AG, Staratschek-Jox A, et al. Natural and orthogonal interaction framework for modeling gene-environment interactions with application to lung cancer. Human Heredity. 73: 185-94. PMID 22889990 DOI: 10.1159/000339906 |
0.342 |
|
2012 |
Luo L, Zhu Y, Xiong M. Quantitative trait locus analysis for next-generation sequencing with the functional linear models. Journal of Medical Genetics. 49: 513-24. PMID 22889854 DOI: 10.1136/Jmedgenet-2012-100798 |
0.526 |
|
2012 |
Zhu Y, Xiong M. Family-based association studies for next-generation sequencing. American Journal of Human Genetics. 90: 1028-45. PMID 22682329 DOI: 10.1016/J.Ajhg.2012.04.022 |
0.386 |
|
2012 |
Luo L, Zhu Y, Xiong M. A novel genome-information content-based statistic for genome-wide association analysis designed for next-generation sequencing data. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 19: 731-44. PMID 22651812 DOI: 10.1089/Cmb.2012.0035 |
0.517 |
|
2012 |
Wei S, Wang LE, McHugh MK, Han Y, Xiong M, Amos CI, Spitz MR, Wei QW. Genome-wide gene-environment interaction analysis for asbestos exposure in lung cancer susceptibility. Carcinogenesis. 33: 1531-7. PMID 22637743 DOI: 10.1093/Carcin/Bgs188 |
0.375 |
|
2012 |
Qu HQ, Li Q, Xu S, McCormick JB, Fisher-Hoch SP, Xiong M, Qian J, Jin L. Ancestry informative marker set for han chinese population. G3 (Bethesda, Md.). 2: 339-41. PMID 22413087 DOI: 10.1534/G3.112.001941 |
0.423 |
|
2012 |
Siu H, Jin L, Xiong M. Manifold learning for human population structure studies. Plos One. 7: e29901. PMID 22272259 DOI: 10.1371/Journal.Pone.0029901 |
0.469 |
|
2012 |
Wang C, Yan S, Hou Z, Fu W, Xiong M, Han S, Jin L, Li H. Present Y chromosomes reveal the ancestry of Emperor CAO Cao of 1800 years ago. Journal of Human Genetics. 57: 216-8. PMID 22189622 DOI: 10.1038/Jhg.2011.147 |
0.404 |
|
2012 |
Fan R, Zhong M, Wang S, Zhang Y, Andrew A, Karagas M, Chen H, Amos CI, Xiong M, Moore JH. Entropy-based information gain approaches to detect and to characterize gene-gene and gene-environment interactions/correlations of complex diseases. Genetic Epidemiology. 35: 706-21. PMID 22009792 DOI: 10.1002/Gepi.20621 |
0.408 |
|
2011 |
Tong CR, Wang H, Lin YH, Yang JF, Zhao J, Zhang X, Yin YM, Fei XH, Wu P, Wang T, Liu HX, Cai P, Wei ZJ, Xiao J, Liu DY, ... Xiong M, et al. [The clinical and laboratory features of 9 cases with gammadeltaT cell lymphoma or leukemia]. Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi. 32: 445-9. PMID 22213862 |
0.398 |
|
2011 |
He Y, Li C, Amos CI, Xiong M, Ling H, Jin L. Accelerating haplotype-based genome-wide association study using perfect phylogeny and phase-known reference data. Plos One. 6: e22097. PMID 21789217 DOI: 10.1371/Journal.Pone.0022097 |
0.486 |
|
2011 |
Hong S, Dong H, Jin L, Xiong M. Gene co-expression network and functional module analysis of ovarian cancer. International Journal of Computational Biology and Drug Design. 4: 147-64. PMID 21712565 DOI: 10.1504/Ijcbdd.2011.041008 |
0.431 |
|
2011 |
Siu H, Zhu Y, Jin L, Xiong M. Implication of next-generation sequencing on association studies. Bmc Genomics. 12: 322. PMID 21682891 DOI: 10.1186/1471-2164-12-322 |
0.471 |
|
2011 |
Luo L, Boerwinkle E, Xiong M. Association studies for next-generation sequencing. Genome Research. 21: 1099-108. PMID 21521787 DOI: 10.1101/Gr.115998.110 |
0.512 |
|
2011 |
Fang S, Fang X, Xiong M. Psoriasis prediction from genome-wide SNP profiles. Bmc Dermatology. 11: 1. PMID 21214922 DOI: 10.1186/1471-5945-11-1 |
0.579 |
|
2011 |
Wei S, Wang L, McHugh MK, Han Y, Amos CI, Spitz MR, Xiong M, Wei Q. Abstract LB-441: The genome wide gene-environment interaction analysis for asbestos exposure on lung cancer susceptibility Epidemiology. 71. DOI: 10.1158/1538-7445.Am2011-Lb-441 |
0.312 |
|
2010 |
Xiong M, Zhao Z, Arnold J, Yu F. Next-generation sequencing. Journal of Biomedicine & Biotechnology. 2010: 370710. PMID 21512588 DOI: 10.1155/2010/370710 |
0.334 |
|
2010 |
Dong H, Siu H, Luo L, Fang X, Jin L, Xiong M. Investigation gene and microRNA expression in glioblastoma. Bmc Genomics. 11: S16. PMID 21143783 DOI: 10.1186/1471-2164-11-S3-S16 |
0.52 |
|
2010 |
Dong H, Luo L, Hong S, Siu H, Xiao Y, Jin L, Chen R, Xiong M. Integrated analysis of mutations, miRNA and mRNA expression in glioblastoma. Bmc Systems Biology. 4: 163. PMID 21114830 DOI: 10.1186/1752-0509-4-163 |
0.516 |
|
2010 |
Wu X, Dong H, Luo L, Zhu Y, Peng G, Reveille JD, Xiong M. A novel statistic for genome-wide interaction analysis. Plos Genetics. 6: e1001131. PMID 20885795 DOI: 10.1371/Journal.Pgen.1001131 |
0.494 |
|
2010 |
Luo L, Peng G, Zhu Y, Dong H, Amos CI, Xiong M. Genome-wide gene and pathway analysis. European Journal of Human Genetics : Ejhg. 18: 1045-53. PMID 20442747 DOI: 10.1038/Ejhg.2010.62 |
0.537 |
|
2010 |
Peng G, Luo L, Siu H, Zhu Y, Hu P, Hong S, Zhao J, Zhou X, Reveille JD, Jin L, Amos CI, Xiong M. Gene and pathway-based second-wave analysis of genome-wide association studies. European Journal of Human Genetics : Ejhg. 18: 111-7. PMID 19584899 DOI: 10.1038/Ejhg.2009.115 |
0.686 |
|
2009 |
Zhou X, Lee JE, Arnett FC, Xiong M, Park MY, Yoo YK, Shin ES, Reveille JD, Mayes MD, Kim JH, Song R, Choi JY, Park JA, Lee YJ, Lee EY, et al. HLA-DPB1 and DPB2 are genetic loci for systemic sclerosis: a genome-wide association study in Koreans with replication in North Americans. Arthritis and Rheumatism. 60: 3807-14. PMID 19950302 DOI: 10.1002/Art.24982 |
0.346 |
|
2009 |
Chu X, Dong C, Lei R, Sun L, Wang Z, Dong Y, Shen M, Wang Y, Wang B, Zhang K, Yang L, Li Y, Yuan W, Wang Y, Song H, ... ... Xiong M, et al. Polymorphisms in the interleukin 3 gene show strong association with susceptibility to Graves' disease in Chinese population. Genes and Immunity. 10: 260-6. PMID 19262575 DOI: 10.1038/Gene.2009.3 |
0.494 |
|
2009 |
Lin R, Wang X, Wang Y, Zhang F, Wang Y, Fu W, Yu T, Li S, Xiong M, Huang W, Jin L. Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations. Human Mutation. 30: 609-15. PMID 19243019 DOI: 10.1002/Humu.20895 |
0.466 |
|
2009 |
Wu X, Jin L, Xiong M. Mutual information for testing gene-environment interaction. Plos One. 4: e4578. PMID 19238204 DOI: 10.1371/Journal.Pone.0004578 |
0.479 |
|
2009 |
Lin R, Wang Y, Wang Y, Fu W, Zhang D, Zheng H, Yu T, Wang Y, Shen M, Lei R, Wu H, Sun A, Zhang R, Wang X, Xiong M, et al. Common variants of four bilirubin metabolism genes and their association with serum bilirubin and coronary artery disease in Chinese Han population. Pharmacogenetics and Genomics. 19: 310-8. PMID 19238116 DOI: 10.1097/Fpc.0B013E328328F818 |
0.411 |
|
2009 |
Fang X, Luo L, Reveille JD, Xiong M. Discussion: Why do we test multiple traits in genetic association studies Journal of the Korean Statistical Society. 38: 17-23. DOI: 10.1016/J.Jkss.2008.10.008 |
0.511 |
|
2008 |
Sun X, Jin L, Xiong M. Extended kalman filter for estimation of parameters in nonlinear state-space models of biochemical networks. Plos One. 3: e3758. PMID 19018286 DOI: 10.1371/Journal.Pone.0003758 |
0.384 |
|
2008 |
Wu X, Jin L, Xiong M. Composite measure of linkage disequilibrium for testing interaction between unlinked loci. European Journal of Human Genetics : Ejhg. 16: 644-51. PMID 18212814 DOI: 10.1038/Sj.Ejhg.5202004 |
0.448 |
|
2008 |
Dong H, Xiao Y, Wang W, Jin L, Xiong M. Symmetry of Metabolic Network Journal of Computer Science & Systems Biology. 1: 1-20. DOI: 10.4172/Jcsb.1000001 |
0.367 |
|
2008 |
Peng G, Luo L, Siu H, Zhu Y, Hu P, Hong S, Zhao J, Zhou X, Reveille J, Jin L, Amos C, Xiong M. Gene and Pathway-Based Analysis: Second Wave of Genome-wide Association Studies Nature Precedings. DOI: 10.1038/Npre.2008.2068.1 |
0.596 |
|
2008 |
Wu X, Jin L, Xiong M. Erratum: Composite measure of linkage disequilibrium for testing interaction between unlinked loci (European Journal of Human Genetics) (2008) vol. 16 (644-651) 10.1038/sj.ejhg.5202004) European Journal of Human Genetics. 16. DOI: 10.1038/Ejhg.2008.53 |
0.433 |
|
2007 |
Xu S, Huang W, Wang H, He Y, Wang Y, Wang Y, Qian J, Xiong M, Jin L. Dissecting linkage disequilibrium in African-American genomes: roles of markers and individuals. Molecular Biology and Evolution. 24: 2049-58. PMID 17630283 DOI: 10.1093/Molbev/Msm135 |
0.451 |
|
2007 |
Lee EB, Zhao J, Kim JY, Xiong M, Song YW. Evidence of potential interaction of chemokine genes in susceptibility to systemic sclerosis. Arthritis and Rheumatism. 56: 2443-8. PMID 17599774 DOI: 10.1002/Art.22742 |
0.582 |
|
2007 |
Zhao J, Boerwinkle E, Xiong M. An entropy-based genome-wide transmission/disequilibrium test. Human Genetics. 121: 357-67. PMID 17297624 DOI: 10.1007/S00439-007-0322-6 |
0.613 |
|
2006 |
Zhao J, Jin L, Xiong M. Test for interaction between two unlinked loci. American Journal of Human Genetics. 79: 831-45. PMID 17033960 DOI: 10.1086/508571 |
0.626 |
|
2006 |
Zhao J, Jin L, Xiong M. Nonlinear tests for genomewide association studies. Genetics. 174: 1529-38. PMID 16816420 DOI: 10.1534/Genetics.106.060491 |
0.6 |
|
2006 |
Zhao J, Boerwinkle E, Xiong M. Impact of Haplotype-Frequency Estimation Error on Test Statistics in Association Studies The American Journal of Human Genetics. 78: 728-729. DOI: 10.1086/501074 |
0.472 |
|
2005 |
Zhou X, Tan FK, Xiong M, Arnett FC, Feghali-Bostwick CA. Monozygotic twins clinically discordant for scleroderma show concordance for fibroblast gene expression profiles. Arthritis and Rheumatism. 52: 3305-14. PMID 16200604 DOI: 10.1002/Art.21355 |
0.317 |
|
2005 |
Xiong M, Feghali-Bostwick CA, Arnett FC, Zhou X. A systems biology approach to genetic studies of complex diseases. Febs Letters. 579: 5325-32. PMID 16182293 DOI: 10.1016/J.Febslet.2005.08.058 |
0.404 |
|
2005 |
Zhao J, Boerwinkle E, Xiong M. An entropy-based statistic for genomewide association studies. American Journal of Human Genetics. 77: 27-40. PMID 15931594 DOI: 10.1086/431243 |
0.595 |
|
2005 |
Zhao JY, Xiong MM, Huang W, Wang H, Zuo J, Wu GD, Chen Z, Qiang BQ, Zhang ML, Chen JL, Ding W, Yuan WT, Xu HY, Jin L, Li YX, et al. An autosomal genomic scan for loci linked to type 2 diabetes in northern Han Chinese. Journal of Molecular Medicine (Berlin, Germany). 83: 209-15. PMID 15776287 DOI: 10.1007/S00109-004-0587-3 |
0.562 |
|
2005 |
Fan R, Knapp M, Wjst M, Zhao C, Xiong M. High resolution T association tests of complex diseases based on family data. Annals of Human Genetics. 69: 187-208. PMID 15720300 DOI: 10.1046/J.1529-8817.2004.00151.X |
0.368 |
|
2004 |
Xiong M, Zhao J, Xiong H. Network-based regulatory pathways analysis. Bioinformatics (Oxford, England). 20: 2056-66. PMID 15072999 DOI: 10.1093/Bioinformatics/Bth201 |
0.489 |
|
2004 |
Xiong M, Li J, Fang X. Identification of genetic networks. Genetics. 166: 1037-52. PMID 15020486 DOI: 10.1534/Genetics.166.2.1037 |
0.341 |
|
2004 |
Luo A, Kong J, Hu G, Liew CC, Xiong M, Wang X, Ji J, Wang T, Zhi H, Wu M, Liu Z. Discovery of Ca2+-relevant and differentiation-associated genes downregulated in esophageal squamous cell carcinoma using cDNA microarray. Oncogene. 23: 1291-9. PMID 14647409 DOI: 10.1038/Sj.Onc.1207218 |
0.326 |
|
2003 |
Zhou X, Tan FK, Wang N, Xiong M, Maghidman S, Reveille JD, Milewicz DM, Chakraborty R, Arnett FC. Genome-wide association study for regions of systemic sclerosis susceptibility in a Choctaw Indian population with high disease prevalence. Arthritis and Rheumatism. 48: 2585-92. PMID 13130478 DOI: 10.1002/Art.11220 |
0.332 |
|
2003 |
Fan R, Xiong M. Linkage and association studies of QTL for nuclear families by mixed models. Biostatistics (Oxford, England). 4: 75-95. PMID 12925331 DOI: 10.1093/Biostatistics/4.1.75 |
0.323 |
|
2003 |
Mu J, Ferdig MT, Feng X, Joy DA, Duan J, Furuya T, Subramanian G, Aravind L, Cooper RA, Wootton JC, Xiong M, Su XZ. Multiple transporters associated with malaria parasite responses to chloroquine and quinine. Molecular Microbiology. 49: 977-89. PMID 12890022 DOI: 10.1046/J.1365-2958.2003.03627.X |
0.301 |
|
2003 |
Chen Z, Zhang K, Zhang X, Yuan XH, Yuan Z, Jin L, Xiong M. Comparison of gene expression between metastatic derivatives and their poorly metastatic parental cells implicates crucial tumor-environment interaction in metastasis of head and neck squamous cell carcinoma. Clinical & Experimental Metastasis. 20: 335-42. PMID 12856721 DOI: 10.1023/A:1024039802134 |
0.398 |
|
2003 |
Xiong M, Zhao J, Boerwinkle E. Haplotype block linkage disequilibrium mapping. Frontiers in Bioscience : a Journal and Virtual Library. 8: a85-93. PMID 12700120 DOI: 10.2741/919 |
0.526 |
|
2003 |
Zhang K, Akey JM, Wang N, Xiong M, Chakraborty R, Jin L. Randomly distributed crossovers may generate block-like patterns of linkage disequilibrium: an act of genetic drift. Human Genetics. 113: 51-9. PMID 12677424 DOI: 10.1007/S00439-003-0941-5 |
0.462 |
|
2003 |
Fan R, Xiong M. Combined high resolution linkage and association mapping of quantitative trait loci. European Journal of Human Genetics : Ejhg. 11: 125-37. PMID 12634860 DOI: 10.1038/Sj.Ejhg.5200941 |
0.338 |
|
2003 |
Akey JM, Zhang K, Xiong M, Jin L. The effect of single nucleotide polymorphism identification strategies on estimates of linkage disequilibrium. Molecular Biology and Evolution. 20: 232-42. PMID 12598690 DOI: 10.1093/Molbev/Msg032 |
0.496 |
|
2002 |
Fan R, Xiong M. High resolution mapping of quantitative trait loci by linkage disequilibrium analysis. European Journal of Human Genetics : Ejhg. 10: 607-15. PMID 12357331 DOI: 10.1038/Sj.Ejhg.5200843 |
0.307 |
|
2002 |
Xiong M, Fan R, Jin L. Linkage disequilibrium mapping of quantitative trait loci under truncation selection Human Heredity. 53: 158-172. PMID 12145552 DOI: 10.1159/000064978 |
0.348 |
|
2002 |
Fan R, Floros J, Xiong M. Models and tests of linkage and association studies of quantitative trait locus for multi-allele marker Loci Human Heredity. 53: 130-145. PMID 12145549 DOI: 10.1159/000064975 |
0.317 |
|
2002 |
Chu S, Zhu D, Wang G, Xiong M, Jin L. [Linkage analysis of 13 vasoactivity-regulating short tandem genes loci in essential hypertension in Chinese]. Zhonghua Nei Ke Za Zhi. 41: 295-7. PMID 12133419 |
0.354 |
|
2002 |
Chu S, Zhu D, Wang G, Xiong M, Jin L. [Linkage analysis of cytokine and cytokine-related receptor gene loci and essential hypertension in Chinese]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 19: 221-4. PMID 12048683 |
0.351 |
|
2002 |
Xiong M, Zhao J, Boerwinkle E. Generalized T2 test for genome association studies. American Journal of Human Genetics. 70: 1257-68. PMID 11923914 DOI: 10.1086/340392 |
0.591 |
|
2001 |
Zhao J, Li W, Xiong M. Population based linkage disequilibrium mapping of QTL: an application to simulated data in an isolated population. Genetic Epidemiology. 21: S655-9. PMID 11793756 DOI: 10.1002/Gepi.2001.21.S1.S655 |
0.545 |
|
2001 |
Zhou X, Tan FK, Xiong M, Milewicz DM, Feghali CA, Fritzler MJ, Reveille JD, Arnett FC. Systemic sclerosis (scleroderma): specific autoantigen genes are selectively overexpressed in scleroderma fibroblasts. Journal of Immunology (Baltimore, Md. : 1950). 167: 7126-33. PMID 11739535 DOI: 10.4049/Jimmunol.167.12.7126 |
0.304 |
|
2001 |
Xiong M, Fang X, Zhao J. Biomarker identification by feature wrappers. Genome Research. 11: 1878-87. PMID 11691853 DOI: 10.1101/Gr.190001 |
0.534 |
|
2001 |
Akey JM, Wang H, Xiong M, Wu H, Liu W, Shriver MD, Jin L. Interaction between the melanocortin-1 receptor and P genes contributes to inter-individual variation in skin pigmentation phenotypes in a Tibetan population. Human Genetics. 108: 516-20. PMID 11499678 DOI: 10.1007/S004390100524 |
0.367 |
|
2001 |
Jiang Z, Akey JM, Shi J, Xiong M, Wang Y, Shen Y, Xu X, Chen H, Wu H, Xiao J, Lu D, Huang W, Jin L. A polymorphism in the promoter region of catalase is associated with blood pressure levels. Human Genetics. 109: 95-8. PMID 11479740 DOI: 10.1007/S004390100553 |
0.463 |
|
2001 |
Xiong M, Li W, Zhao J, Jin L, Boerwinkle E. Feature (gene) selection in gene expression-based tumor classification. Molecular Genetics and Metabolism. 73: 239-47. PMID 11461191 DOI: 10.1006/Mgme.2001.3193 |
0.512 |
|
2001 |
Zhang H, Yu CY, Singer B, Xiong M. Recursive partitioning for tumor classification with gene expression microarray data. Proceedings of the National Academy of Sciences of the United States of America. 98: 6730-5. PMID 11381113 DOI: 10.1073/Pnas.111153698 |
0.315 |
|
2001 |
Akey J, Jin L, Xiong M. Haplotypes vs single marker linkage disequilibrium tests: what do we gain? European Journal of Human Genetics : Ejhg. 9: 291-300. PMID 11313774 DOI: 10.1038/Sj.Ejhg.5200619 |
0.42 |
|
2001 |
Zhu DL, Wang HY, Xiong MM, He X, Chu SL, Jin L, Wang GL, Yuan WT, Zhao GS, Boerwinkle E, Huang W. Linkage of hypertension to chromosome 2q14-q23 in Chinese families. Journal of Hypertension. 19: 55-61. PMID 11204305 DOI: 10.1097/00004872-200101000-00008 |
0.377 |
|
2001 |
Lu J, Liu Z, Xiong M, Wang Q, Wang X, Yang G, Zhao L, Qiu Z, Zhou C, Wu M. Gene expression profile changes in initiation and progression of squamous cell carcinoma of esophagus. International Journal of Cancer. 91: 288-294. PMID 11169949 DOI: 10.1002/1097-0215(200002)9999:9999<::Aid-Ijc1063>3.0.Co;2-S |
0.326 |
|
2001 |
Xiong M, Jin L, Li W, Boerwinkle E. Computational methods for gene expression-based tumor classification. Biotechniques. 29: 1264-8, 1270. PMID 11126130 DOI: 10.2144/00296Bc02 |
0.327 |
|
2000 |
Xiong M, Jin L. Combined linkage and linkage disequilibrium mapping for genome screen Genetic Epidemiology. 19: 211-234. PMID 11015125 DOI: 10.1002/1098-2272(200010)19:3<211::Aid-Gepi3>3.0.Co;2-L |
0.379 |
|
2000 |
Xiong M, Guo S. Multiple regression approach to mapping of quantitative trait loci (QTL) based on sib-pair data: A theoretical analysis Annals of Statistics. 28: 1245-1278. DOI: 10.1214/Aos/1015957393 |
0.36 |
|
2000 |
Zhao J, Wang H, Xiong M, Huang W, Zuo J, Chen Z, Qiang B, Sun Q, Li Y, Liu Q, Du W, Chen J, Ding W, Yuan W, Zhao Y, et al. The localization of type 2 diabetes susceptibility gene loci in northern Chinese Han families Chinese Science Bulletin. 45: 1792-1795. DOI: 10.1007/Bf02886269 |
0.367 |
|
1999 |
Xiong M, Jin L. Comparison of the power and accuracy of biallelic and microsatellite markers in population-based gene-mapping methods American Journal of Human Genetics. 64: 629-640. PMID 9973302 DOI: 10.1086/302231 |
0.389 |
|
1998 |
Xiong M, Guo SW. The power of linkage detection by the transmission/disequilibrium tests Human Heredity. 48: 295-312. PMID 9813451 DOI: 10.1159/000022821 |
0.322 |
|
1998 |
Krushkal J, Xiong M, Ferrell R, Sing CF, Turner ST, Boerwinkle E. Linkage and association of adrenergic and dopamine receptor genes in the distal portion of the long arm of chromosome 5 with systolic blood pressure variation. Human Molecular Genetics. 7: 1379-83. PMID 9700190 DOI: 10.1093/Hmg/7.9.1379 |
0.31 |
|
1997 |
Guo SW, Xiong M. Estimating the age of mutant disease alleles based on linkage disequilibrium Human Heredity. 47: 315-337. PMID 9391824 DOI: 10.1159/000154431 |
0.337 |
|
1997 |
Xiong M, Guo SW. Fine-scale genetic mapping based on linkage disequilibrium: Theory and applications American Journal of Human Genetics. 60: 1513-1531. PMID 9199574 DOI: 10.1086/515475 |
0.354 |
|
1997 |
Guo SW, Xiong M. Genes preserved in relatives. Human Heredity. 47: 138-54. PMID 9156325 DOI: 10.1159/000154402 |
0.328 |
|
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