gongxh@fudan.edu.cn

摘要

研究方向: 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。

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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).