Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Editor

Personal info

Please enable Javascript support in your browser to use this application.

Instructions on how to enable JavaScript on different browsers can be found here: http://www.google.com/support/bin/answer.py?answer=23852.

Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences & Yunnan Province

Kunming Institute of Zoology

Kunming

Yunnan 650223

China

Name/email consistency: high

Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences & Yunnan Province, Kunming Institute of Zoology, Kunming, Yunnan 650223, China. 2012
Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, USA. 2007
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China. 2005 - 2007

Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients. Zhang, A.M., Jia, X., Guo, X., Zhang, Q., Yao, Y.G. J. Transl. Med (2012) [Pubmed]
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene. Zhang, Q., Zulfiqar, F., Xiao, X., Riazuddin, S.A., Ahmad, Z., Caruso, R., MacDonald, I., Sieving, P., Riazuddin, S., Hejtmancik, J.F. Hum. Genet. (2007) [Pubmed]
FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus. Zhang, Q., Xiao, X., Li, S., Guo, X. Mol. Vis. (2007) [Pubmed]
Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1. Zhang, Q., Li, S., Xiao, X., Jia, X., Guo, X. J. Hum. Genet. (2007) [Pubmed]
The 208delG mutation in FSCN2 does not associate with retinal degeneration in Chinese individuals. Zhang, Q., Li, S., Xiao, X., Jia, X., Guo, X. Invest. Ophthalmol. Vis. Sci. (2007) [Pubmed]
Mutations in NYX of individuals with high myopia, but without night blindness. Zhang, Q., Xiao, X., Li, S., Jia, X., Yang, Z., Huang, S., Caruso, R.C., Guan, T., Sergeev, Y., Guo, X., Hejtmancik, J.F. Mol. Vis. (2007) [Pubmed]
A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612. Zhang, Q., Guo, X., Xiao, X., Jia, X., Li, S., Hejtmancik, J.F. Mol. Vis. (2005) [Pubmed]