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Xiaohong Gong
Published:2013-11-13 Hits:2031

Xiaohong Gong
Associate Professor
School of Life Sciences, Fudan University
Office Phone: 86-21-65643279


2005-2007 Post-doctoral fellow, Pasteur institute, France
2000 –2005 Ph.D degree in Psychiatry Genetics, Peking University
1996 - 2000 B.S. degree in Medicine, Peking University


 Her research interests are genetic study of human complex diseases, especially focused on psychiatric diseases and birth defects. Projects include:1)Genetic imaging study of major depressive disorder and schizophrenia ; 2) Identification of susceptibility genes in autism spectrum disorders and intellectual disability; 3) Functional study of Neurexin-Neuroligin pathway genes.

Representative Publications:
1. Liu YY, Du YS, Liu WW, Yang CH, Liu Y, Wang HY, Gong XH. (2013)Lack of Association between NLGN3, NLGN4, SHANK2 and SHANK3 Gene Variants and Autism SpectrumDisorder in a Chinese Population. PLoS ONE
2. Liu YY, Liu FL, He YQ, Li LM, Li SL, Zheng YT, Wang HY, Gong XH . (2012) The genetic variation of CCR5, CXCR4 and SDF-1 in three Chinese ethnic populations. Infection, Genetics and Evolution.
3. Gong XH,Jiang YW, Zhang X, An Y. Zhang J, Wu Y, Wang JM, Sun YF, Qiu ZL, Jin L, Wu BL, Wang HY (2012). High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability. PLoS ONE.
4. Zhao JY*, Yang XY*, Gong XH*,Gu ZY, Duan WY, Wang J, Ye ZZ, Shen HB, Shi KH, Hou J, Huang GY, Jin L, Qiao B, and Wang HY . (2012). A functional variant in MTRR intron-1 significantly increases risk of congenital heart disease in Han Chinese population. Circulation.
5. Gong XH,Delorme R, Fauchereau F, Durand CM, Chaste P, Betancur C et al.(2009) An investigation of ribosomal protein L10 gene in autism spectrum disorders. BMC Med Genet.
6. Gong XH, Bacchelli E, Blasi F, Toma C, Betancur C, Chaste P et al. (2008)Analysis of X chromosome inactivation in autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet.


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