基本信息：
电话：021-51630609
邮箱：gongxh@fudan.edu.cn
地址：复旦大学生命科学学院A605
工作经历：
研究方向：
代表论文：
1. Yanyan Liu, Yasong Du, Wenwen Liu, Caohua Yang, Yan Liu, Hongyan Wang, Xiaohong Gong*. Lack of Association between NLGN3, NLGN4, SHANK2 and SHANK3 Gene Variants and Autism Spectrum Disorder in a Chinese Population. Plos One. 8(2): e56639 (2013).
2. Xiaohong Gong, Yu-wu Jiang, Xin Zhang, Yu An, Jun Zhang, Ye Wu, Li Jin, Bai-Lin Wu, Hongyan Wang. High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability. Plos One. 7(4) e34739 (2012).
3. Yanyan Liu, Feng-Liang Liu, Yanqin He, Liming Li, Shilin Li, Yong-Tang Zheng, Hongyan Wang*, Xiaohong Gong*. The genetic variation of CCR5, CXCR4 and SDF-1 in three Chinese ethnic populations. Infection, Genetics and Evolution. 12(5), 1072-1078 (2012).
4. Jian-Yuan Zhao, Xue-Yan Yang, Xiao-Hong Gong, Zhuo-Ya Gu, Wen-Yuan Duan, Jue Wang, Li Jin, Bin Qiao, Hong-Yan Wang. Functional Variant in Methionine Synthase Reductase Intron-1 Significantly Increases the Risk of Congenital Heart Disease in the Han Chinese Population. Circulation. 125(3), 482-490 (2012).
5. Xiaohong Gong，Elena Bacchelli, Francesca Blasi, Claudio Toma, Catalina Betancur, Pauline Chaste, Elena Maestrini, Thomas Bourgeron*. Analysis of X chromosome inactivation in autism spectrum disorder. American Journal of Medical Genetics B. 147B, 830–835 (2008).