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- 叶建宏；杨雪艳；王红艳,CNNM2基因和人类神经管畸形发生的相关性研究.-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
- Yufang Zheng；Bing Su；Keping Hu；Zilong Qiu；Hongyan Wang；Yumeng Wang；Yahui Liu；Yasong Du；Zhangmin Yang；Yanqing He；Xiaohong Gong；Xing Liu；Jian Huang,Yufang Zheng；Yumeng Wang；Yahui Liu；Yasong Du；Zhangmin Yang；Yanqing He；Xiaohong Gong；Xing Liu；Jian Huang；Bing Su；Keping Hu；Zilong Qiu；Hongyan Wang,MeCP2 in autism-displays allelic expression imbalance and affects both nerve system and heart development through Notch pathway.-遗传多样性：前沿与挑战——中国的遗传学研究（2013-2015）——2015中国遗传学会大会论文摘要汇编-2015-01-01
- Chen Zhongzhong；Lei Yunping；Zheng Yufang；Aguiar-Pulido Vanessa；Ross M.Elizabeth；Peng Rui；Jin Li；Zhang Ting；Finnell Richard H.；Wang Hongyan,Threshold for neural tube defect risk by accumulated singleton loss-of-function variants (vol 28, 1039, 2018).-细胞研究（英文版）-2019-01-01-29
- Huang Zhongyuan；Lu Renguo；Huang Ting；Wang Hongyan；Li Tongsheng,An Investigation into the Migration of Segments in Crosslinked Fluorinated Polyimide Adhesive.-Journal of Macromolecular Science Part B-Physics-2013-01-01-52
- Xu Shuhua；Pan Xuedong；He Yungang；Yang Yajun；Wang Yi；Fu Wenqing；An Yu；Wang Jiucun；Tan Jingze；Qian Ji；Chen Xiaoli；Yin Xianyong；Zhang Xin；Sun Yangfei；Zhang Xuejun；Wu Bailin；Jin Li；Li Shilin；Jin Wenfei；Lou Haiyi；Yang Ling；Gong Xiaohong；Wang Hongyan；Shen Yiping,Xu Shuhua；Yin Xianyong；Li Shilin；Jin Wenfei；Lou Haiyi；Yang Ling；Gong Xiaohong；Wang Hongyan；Shen Yiping；Pan Xuedong；He Yungang；Yang Yajun；Wang Yi；Fu Wenqing；An Yu；Wang Jiucun；Tan Jingze；Qian Ji；Chen Xiaoli；Zhang Xin；Sun Yangfei；Zhang Xuejun；Wu Bailin；Jin Li,Genomic Dissection of Population Substructure of Han Chinese and Its Implication in Association Studies.-AMERICAN JOURNAL OF HUMAN GENETICS-2009-01-01-85
- Liu Pei；Lu Renguo；Wang Hongyan；Huang Ting；Li Tongsheng,The Mechanical and Tribological Properties of Aramid (Twaron) Fabric/Polytetrafluoroethylene Composites.-Journal of Macromolecular Science Part B-Physics-2012-01-01-51
- Wang Erli；Jin Wenfei；Duan Wenyuan；Qiao Bin；Sun Shuna；Huang Guoying；Shi Kaihu；Jin Li；Wang Hongyan,Association of Two Variants in SMAD7 with the Risk of Congenital Heart Disease in the Han Chinese Population.-PLoS One-2013-01-01-8
- Qiao Xiaojin；Qiao Bin；Zheng Yufang；Wang Hongyan；Liu Yahui；Li Peiqiang；Chen Zhongzhong；Li Huili；Yang Xueyan；Finnell Richard H.；Yang Zhangmin；Zhang Ting,Qiao Xiaojin；Liu Yahui；Li Peiqiang；Chen Zhongzhong；Li Huili；Yang Xueyan；Finnell Richard H.；Yang Zhangmin；Zhang Ting；Qiao Bin；Zheng Yufang；Wang Hongyan,Genetic analysis of rare coding mutations of CELSR1-3 in congenital heart and neural tube defects in Chinese people.-CLINICAL SCIENCE-2016-01-01-130
- Zhou Xiangyu；Zeng Weijia；Li Huili；Chen Haitao；Wei Gang；Yang Xueyan；Zhang Ting；Wang Hongyan,Rare mutations in apoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects.-Cell Death and Disease-2018-01-01-9
- Zhang Linna；Qin Yue；Gong Xiaohong；Peng Rui；Cai Chunquan；Zheng Yufang；Du Yasong；Wang Hongyan,A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population.-Translational Psychiatry-2019-01-01-9
