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- 杨曹骅；杜亚松；刘文文；张林娜；王红艳；公晓红,核心家系孤独症患儿FOXP1基因的突变及CNV分析.-中国儿童保健杂志-2013-01-01
- Zhao Jian-Yuan；Chen Yi-Jiang；Shen Hong-Bing；Huang Guo-Ying；Jin Li；Wang Hong-Yan；Yang Xue-Yan；Shi Kai-Hu；Sun Shu-Na；Hou Jia；Ye Zhi-Zhou；Wang Jue；Duan Wen-Yuan；Qiao Bin,Zhao Jian-Yuan；Yang Xue-Yan；Shi Kai-Hu；Sun Shu-Na；Hou Jia；Ye Zhi-Zhou；Wang Jue；Duan Wen-Yuan；Qiao Bin；Chen Yi-Jiang；Shen Hong-Bing；Huang Guo-Ying；Jin Li；Wang Hong-Yan,A functional variant in the cystathionine β-synthase gene promoter significantly reduces congenital heart disease susceptibility in a Han Chinese population.-细胞研究（英文版）-2013-01-01-23
- Yang Xue-Yan；Jin Li；Zhang Ting；Wang Hong-Yan；Zhou Xiang-Yu；Wang Qing Qing；Li Hong；Chen Ying；Lei Yun-Ping；Ma Xiao-Hang；Kong Pan；Shi Yan,Yang Xue-Yan；Zhou Xiang-Yu；Wang Qing Qing；Li Hong；Chen Ying；Lei Yun-Ping；Ma Xiao-Hang；Kong Pan；Shi Yan；Jin Li；Zhang Ting；Wang Hong-Yan,Mutations in the COPII Vesicle Component Gene SEC24B are Associated with Human Neural Tube Defects.-HUMAN MUTATION-2013-01-01-34
- Wang Erli；Gu Xun；Jin Li；Wang Hongyan；Sun Shuna；Qiao Bin；Duan Wenyuan；Huang Guoying；An Yu；Xu Shuhua；Zheng Yufang；Su Zhixi,Wang Erli；Sun Shuna；Qiao Bin；Duan Wenyuan；Huang Guoying；An Yu；Xu Shuhua；Zheng Yufang；Su Zhixi；Gu Xun；Jin Li；Wang Hongyan,Identification of Functional Mutations in GATA4 in Patients with Congenital Heart Disease.-PLoS One-2013-01-01-8
- Mei M；Yang L；Zhan G；Wang H；Ma D；Zhou W；Huang G.,以先天性心脏病为主要表现的8p缺失伴重复新生儿全基因组拷贝数变异分析二例.-中华儿科杂志-2014-01-01-52
- Wang X；Zhang J；Cao Y；Diao L；Wang H；Ma X；Ma D；Huang G.,法洛四联症患儿HIRA基因3'UTR区序列分析及相关微RNA.-中华医学杂志-2014-01-01-94
- Wang Jue；Wang Hong-Yan；Zhao Jian-Yuan；Wang Feng；Peng Qian-Qian；Hou Jia；Sun Shu-Na；Gui Yong-Hao；Duan Wen-Yuan；Qiao Bin,Wang Jue；Zhao Jian-Yuan；Wang Feng；Peng Qian-Qian；Hou Jia；Sun Shu-Na；Gui Yong-Hao；Duan Wen-Yuan；Qiao Bin；Wang Hong-Yan,A Genetic Variant in Vitamin B12 Metabolic Genes That Reduces the Risk of Congenital Heart Disease in Han Chinese Populations.-PLoS One-2014-01-01-9
- Zhang Xin；Du Renqian；Li Shilin；Zhang Feng；Jin Li；Wang Hongyan,Evaluation of copy number variation detection for a SNP array platform.-BMC BIOINFORMATICS-2014-01-01-15
- Zhao Jian-Yuan；Huang Guo-Ying；Jin Li；Wang Hong-Yan；Qiao Bin；Duan Wen-Yuan；Gong Xiao-Hong；Peng Qian-Qian；Jiang Song-Shan；Lu Chen-Qi；Chen Yi-Jiang；Shen Hong-Bing,Zhao Jian-Yuan；Qiao Bin；Duan Wen-Yuan；Gong Xiao-Hong；Peng Qian-Qian；Jiang Song-Shan；Lu Chen-Qi；Chen Yi-Jiang；Shen Hong-Bing；Huang Guo-Ying；Jin Li；Wang Hong-Yan,Genetic variants reducing MTR gene expression increase the risk of congenital heart disease in Han Chinese populations.-EUROPEAN HEART JOURNAL-2014-01-01-35
- 王博石；郑煜芳；王红艳；蔡春泉,Notch信号通路基因JAG1、ADAM17和ADAM10与先天性心脏病(CHD)的相关性.-复旦学报(医学版)-2014-01-01-41
