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- GONG XiaoHong；WANG HongYan,SHANK1 and autism spectrum disorders.-中国科学. 生命科学-2015-01-01-58
- Li Peiqiang；Li Haijie；Zheng Yufang；Qiao Bin；Duan Wenyuan；Huang Lijuan；Liu Weiqi；Wang Hongyan,Variants in the Regulatory Region of WNT5A Reduced Risk of Cardiac Conotruncal Malformations in the Chinese Population.-Scientific Reports-2015-01-01-5
- Zheng Yufang；Wu Xiaohui；Wang Hongyan；Jing Yingchun；Chen Zhongzhong；Shi Zhiwen；Liu Weiqi；Liu Jiaojiao；Wang Chunyan；Chen Shuxia；Xu Hong,Zheng Yufang；Jing Yingchun；Chen Zhongzhong；Shi Zhiwen；Liu Weiqi；Liu Jiaojiao；Wang Chunyan；Chen Shuxia；Xu Hong；Wu Xiaohui；Wang Hongyan,A screening in Piggy Bac transgenic mice for new candidate genes in neural tube and congenital heart defects.-中华医学会第十五次全国医学遗传学学术会议暨中国医师协会医学遗传医师分会第一届全国学术会议暨2016年浙江省医学遗传学年会论文汇编-2016-01-01
- Peng Rui；Li Binbin；Zheng Yufang；Wang Hongyan,The association study of mutations in GLI family and Congenital Heart Diseases.-中华医学会第十五次全国医学遗传学学术会议暨中国医师协会医学遗传医师分会第一届全国学术会议暨2016年浙江省医学遗传学年会论文汇编-2016-01-01
- Wang Hongyan；Lv Renguo；Huang Zhongyuan；Liu Pei；Cong Peihong；Li Tongsheng,Synthesis and Characterization of a Fluorinated Phenolic Resin/phenolic Resin Blend.-Journal of Macromolecular Science Part B-Physics-2016-01-01-55
- 黄丽娟；李培强；郑煜芳；杨雪艳；王红艳,先天性心脏病(CHD)中MESP1稀有突变的功能分析.-中华医学会第十五次全国医学遗传学学术会议暨中国医师协会医学遗传医师分会第一届全国学术会议暨2016年浙江省医学遗传学年会论文汇编-2016-01-01
- An Yu；Zhang Feng；Shen Yiping；Wu Bailin；Wang Hongyan；Duan Wenyuan；Huang Guoying；Chen Xiaoli；Li Li；Nie Chenxia；Hou Jia；Gui Yonghao；Wu Yiming,An Yu；Duan Wenyuan；Huang Guoying；Chen Xiaoli；Li Li；Nie Chenxia；Hou Jia；Gui Yonghao；Wu Yiming；Zhang Feng；Shen Yiping；Wu Bailin；Wang Hongyan,Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population.-BMC Medical Genomics-2016-01-01-9
- Yu Li-Wei；Wang Feng；Yang Xue-Yan；Sun Shu-Na；Zheng Yu-Fang；Li Bin-Bin；Gui Yong-Hao；Wang Hong-Yan,Mild decrease in TBX20 promoter activity is a potentially protective factor against congenital heart defects in the Han Chinese population.-Scientific Reports-2016-01-01-6
- Hongyan Wang；Yumeng Wang；Yufang Zheng；Yasong Du,MiR-197 rescues the neurogenesis defects caused by autistic MECP2 mutation.-中华医学会第十五次全国医学遗传学学术会议暨中国医师协会医学遗传医师分会第一届全国学术会议暨2016年浙江省医学遗传学年会论文汇编-2016-01-01
- Mutations in TUBB8 and Human Oocyte Meiotic Arrest.-NEW ENGLAND JOURNAL OF MEDICINE-2016-01-01-374
