Yue-bin Li

KCNQ1 gain-of-function mutation in familial atrial fibrillation.

Ying Wang, Zhu Chen, S. Bendahhou, 2003, Science.

KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation

Wei Huang, Shi-Jie Xu, Yi Liu, 2003, Science.

Evidence for a major psoriasis susceptibility locus at 6p21(PSORS1) and a novel candidate region at 4q31 by genome-wide scan in Chinese hans.

Li Jin, Xuejun Zhang, Wei Huang, 2002, The Journal of investigative dermatology.

Mutation analysis of the ED1 gene in two Chinese Han families with X-linked hypohidrotic ectodermal dysplasia

Xiao-yan Xiong, Xuejun Zhang, Wei Huang, 2003, Archives of Dermatological Research.

A mutation in the connexin 30 gene in Chinese Han patients with hidrotic ectodermal dysplasia.

Xiao-yan Xiong, Y. Wang, Xuejun Zhang, 2003, Journal of dermatological science.

[A genome-wide screening for pathological myopia suggests a novel locus on chromosome 15q12 - 13].

D. Hu, Wei Huang, Zong-hou Shen, 2005, [Zhonghua yan ke za zhi] Chinese journal of ophthalmology.