公晓红

基本信息

职称：副教授
电话：021-31246609
邮箱：gongxh@fudan.edu.cn
地址：复旦大学生命科学学院 A605室

个人简介

女，1976年出生，博士、副教授。1995-2000年就读北京大学医学部获医学学士学位，2000-2005年就读北京大学精神卫生研究所获医学博士学位。2005-2007年在法国巴斯德研究所从事博士后研究，2007-2012年任复旦大学生命科学学院讲师，2012年至今任复旦大学生命科学学院副教授。

主要研究方向

利用分子遗传、神经生物、脑影像、生物信息等手段，研究人类精神神经系统疾病的遗传基础和分子机制。

代表性成果

1、Xiaohong Gong, Yanyan Liu, Feng-L iang Liu, LiJin, Hongyan Wang, Yong-Tang Zheng. A SDF1 genetic variant confers resistanceto HIV-1 infection in intravenous drug users in China. Infection, Genetics andEvolution. 34 (2015):137-42.

2、Xiaohong Gong* & Hongyan Wang. SHANK1 andautism spectrum disorders. Science China: life sciences. 58(2015): 985–990.

3、Xiaohong Gong*,Wenlian Lu*, Keith M. Kendrick*, Weidan Pu*, Chu Wang, Li Jin, Guangmin Lu,Zhening Liu, Haihong Liu, and Jianfeng Feng. A Brain-Wide Association Study ofDISC1 Genetic Variants Reveals a Relationship With the Structure and FunctionalConnectivity of the Precuneus in Schizophrenia. Human Brain Mapping 35(11)(2014):5414-30.

4、Yanyan Liu*, Yasong Du*, Wenwen Liu, Caohua Yang, Yan Liu,Hongyan Wang, Xiaohong Gong. Lack ofAssociation between NLGN3, NLGN4, SHANK2 and SHANK3 Gene Variants and AutismSpectrumDisorder in a Chinese Population. PLoS ONE 8(2) (2013): e56639.

5、Xiaohong Gong,Yu-wu Jiang, Xin Zhang, Yu An, Jun Zhang, Ye Wu, Li Jin, Bai-Lin Wu, andHongyan Wang. High Proportion of 22q13 Deletions and SHANK3 Mutations inChinese Patients with Intellectual Disability. Plos One. 7(4) (2012), e34739.

6、Yanyan Liu, Feng-Liang Liu, Yanqin He, Liming Li, Shilin Li,Yong-Tang Zheng, Hongyan Wang, XiaohongGong. The genetic variation of CCR5, CXCR4 and SDF-1 in three Chineseethnic populations. Infection, Genetics and Evolution. 12(5) (2012), 1072-1078.

7、Jian-Yuan Zhao*, Xue-Yan Yang*, Xiao-Hong Gong*, Zhuo-Ya Gu, Wen-Yuan Duan, Jue Wang, Li Jin, BinQiao, and Hong-Yan Wang. Functional Variant in Methionine Synthase Reductase Intron-1Significantly Increases the Risk of Congenital Heart Disease in the Han ChinesePopulation. Circulation. 125(3) (2012), 482-490.

8、Xiaohong Gong，Delorme Richard, Fauchereau Fabien, Durand Christelle,Chaste Pauline, Betancur Catalina, Marion Leboyer, and Thomas Bourgeron. Aninvestigation of ribosomal protein L10 gene in autism spectrum disorders. BMCMed Genet. 10:7 (2009), doi:10.1186/1471-2350-10-7.

9、Xiaohong Gong，ElenaBacchelli, Francesca Blasi, Claudio Toma, Catalina Betancur, Pauline Chaste,Elena Maestrini, and Thomas Bourgeron. Analysis of X chromosome inactivation inautism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet. 147B (20