复旦大学生物医学研究院研究员，2000-2003年中科院上海生科院博士后，2003-2008上海交通大学副教授，2008年调入复旦大学生物医学研究院。主要研究方向为出生缺陷和药物基因组学， 已经发表SCI论文30余篇。现任中国神经科学学会精神神经委员会副秘书长，主持完成国家863项目“隔离人群重大疾病等高质量家系的收集、保存和利用”，现主持973字课题一项，作为骨干参与国家973和863课题3项。

联系电话：54237615
Email：xingqinghe@hotmail.com

代表论文——————————————————————————————

·Chen L, Qin S, Xie J, Tang J, Yang L, Shen W, Zhao X, Du J, He G, Feng G, He L, Xing Q*. Genetic polymorphism analysis of CYP2C19 in Chinese Han populations from different geographic areas of mainland China. Pharmacogenomics. 2008 Jun;9(6):691-702.

·2. Xuan J, Zhao X, He G, Yu L, Wang L, Tang W, Li X, Gu N, Feng G, Xing Q*, He L. Effects of the dopamine D3 receptor (DRD3) gene polymorphisms on risperidone response: a pharmacogenetic study. Neuropsychopharmacology. 2008 Jan;33(2):305-11.

·3. Xing Q, Qian X, Li H, Wong S, Wu S, Feng G, Duan S, Xu M, Gao R, Qin W, Gao J, Meng J, He L. The relationship between the therapeutic response to risperidone and the dopamine D2 receptor polymorphism in Chinese schizophrenia patients. Int J Neuropsychopharmacol. 2007 Oct;10(5):631-7.

·4. Xing Q, Chen X, Wang M, Bai W, Peng X, Gao R, Wu S, Qian X, Qin W, Gao J, Feng G, He L. A locus for familial generalized lentiginosis without systemic involvement maps to chromosome 4q21.1-q22.3. Hum Genet. 2005 Jul;117(2-3):154-9.

·5. Xing QH, Wang MT, Chen XD, Feng GY, Ji HY, Yang JD, Gao JJ, Qin W, Qian XQ, Wu SN, He L. A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2. Am J Hum Genet. 2003 Aug;73(2):377-82.