公晓红

基本信息

职称:博士、副教授
电话:021-51630609
邮箱:
gongxh@fudan.edu.cn 
地址:复旦大学生命科学学院

 

个人简介

女,博士,副教授。2000年获北京大学临床医学学士学位。2005年获北京大学医学博士学位。2005-2007年在法国巴斯德研究所从事博士后研究。2007年起任复旦大学生命科学学院讲师,副教授。

 

主要研究方向 (Research Interests)

人类复杂疾病的遗传学研究,主要集中在精神疾病和出生缺陷。利用分子遗传、神经生物、脑影像、生物信息等手段,研究复杂疾病的遗传基础,揭示分子机制。

 

获奖情况 (Awards)

 

代表性成果

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).

 

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