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

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Qiufen Wang

Center for Molecular Genetics

Lerner Research Institute

The Cleveland Clinic Foundation

9500 Euclid Ave.

USA

[email]@ccf.org

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Center for Molecular Genetics, Lerner Research Institute, The Cleveland Clinic Foundation, 9500 Euclid Ave., USA. 2001 - 2005
  • Center for Human Genome Research, Huazhong University of Science and Technology, Wuhan, Hubei, China. 2005
  • Department of Molecular Cardiology, Lerner Research Institute, and Center for Cardiovascular Genetics, The Cleveland Clinic Foundation, USA. 2004

References

  1. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family. Wang, Q., Liu, M., Xu, C., Tang, Z., Liao, Y., Du, R., Li, W., Wu, X., Wang, X., Liu, P., Zhang, X., Zhu, J., Ren, X., Ke, T., Wang, Q., Yang, J. J. Mol. Med. (2005) [Pubmed]
  2. Advances in the genetic basis of coronary artery disease. Wang, Q. Curr. Atheroscler. Rep (2005) [Pubmed]
  3. Molecular genetics of coronary artery disease. Wang, Q. Curr. Opin. Cardiol. (2005) [Pubmed]
  4. Update on the molecular genetics of vascular anomalies. Wang, Q.K. Lymphat. Res. Biol (2005) [Pubmed]
  5. The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel. Wang, Q., Chen, S., Chen, Q., Wan, X., Shen, J., Hoeltge, G.A., Timur, A.A., Keating, M.T., Kirsch, G.E. J. Med. Genet. (2004) [Pubmed]
  6. Cytogenetic analysis of obsessive-compulsive disorder (OCD): identification of a FRAXE fragile site. Wang, Q., Gu, Y., Ferguson, J.M., Chen, Q., Boatwright, S., Gardiner, J., Below, C., Espinosa, J., Nelson, D.L., Shaffer, L.G. Am. J. Med. Genet. A (2003) [Pubmed]
  7. Update on the molecular genetics of retinitis pigmentosa. Wang, Q., Chen, Q., Zhao, K., Wang, L., Wang, L., Traboulsi, E.I. Ophthalmic Genet. (2001) [Pubmed]
  8. Identification and molecular characterization of de novo translocation t(8;14)(q22.3;q13) associated with a vascular and tissue overgrowth syndrome. Wang, Q., Timur, A.A., Szafranski, P., Sadgephour, A., Jurecic, V., Cowell, J., Baldini, A., Driscoll, D.J. Cytogenet. Cell Genet. (2001) [Pubmed]
 
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