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的个人主页 http://faculty.ustc.edu.cn/zhanghong123/zh_CN/index.htm

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[11] Hu J, Li T, Xiu Z, Zhang H# (2015). MAFsnp: A Multi-sample Accurate and Flexible SNP Caller Using Next-generation Sequencing Data. PLoS ONE 10(8): e0135332.
[12] Zhang H#, Xu J, Jiang N, Hu X, Luo Z (2015). PLNseq: a multivariate Poisson lognormal distribution for high-throughput matched RNA-sequencing read count data. Statistics in Medicine 34: 1577-1589.
[13] Zhang H, Qin J, Landi M, Caporaso N, Yu K (2013). A copula-model based semiparametric interaction test under the case-control design. Statistica Sinica. 23: 1505-1521.
[14] Zhang H, Zeng D, Olschwang S, Yu K (2013). Semiparametric inference on the penetrances of rare genetic mutations based on a case-family design. Journal of Statistical Planning and Inference. 143: 368-377.
[15] Zhang H, Wacholder S, Qin J, Hildesheim A, Yu K (2011). Improved genetic association tests for an ordinal outcome representing the disease progression process. Genetic Epidemiology 35:499-505.
[16] Zhang H, Ahn J, Yu K (2011). Comparing statistical methods for removing seasonal variation from vitamin D measurements in case-control studies. Statistics and Its Interface. 4:85-93.
[17] Li T, Li Z, Ying Z, Zhang H#. (2010). Influence of population stratification on population based marker-disease association analysis. Annals of Human Genetics. 74:351-360.
[18] Zhang H, Olschwang S, Yu K. (2010). Statistical inference on the penetrances of rare genetic mutations based on a case-family design. Biostatistics 11:519-532.
[19] Wu C*, Zhang H*, Liu X, DeWan A, Dubrow R, Ying Z, Yang Y, Hoh J (2009). Detecting essential and removable interactions in genome-wide association studies. Statistics and Its Interface 2:161-170.
[20] Zhang H, Chen H, Li Z. (2009). Large sample interval mapping method for genetic trait loci infinite regression mixture models. Journal of Statistical Planning and Inference 139:764-779.

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