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

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N. Zhong

Department of Human Genetics

New York State Institute for Basic Research

Staten Island 10314

USA

[email]@aol.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Human Genetics, New York State Institute for Basic Research, Staten Island 10314, USA. 1998 - 2001
  • New York State Institute for Basic Research in Developmental Disabilities, 1050 Forest Hill Road, Staten Island, New York 10314, USA. 2000 - 2001

References

  1. Molecular genetic testing for neuronal ceroid lipofuscinoses. Zhong, N. Adv. Genet. (2001) [Pubmed]
  2. Outlook for future treatment. Zhong, N., Wisniewski, K.E. Adv. Genet. (2001) [Pubmed]
  3. Neuronal ceroid lipofuscinoses and possible pathogenic mechanism. Zhong, N. Mol. Genet. Metab. (2000) [Pubmed]
  4. CLN-encoded proteins do not interact with each other. Zhong, N.A., Moroziewicz, D.N., Ju, W., Wisniewski, K.E., Jurkiewicz, A., Brown, W.T. Neurogenetics (2000) [Pubmed]
  5. Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinoses. Zhong, N.A., Wisniewski, K.E., Ju, W., Moroziewicz, D.N., Jurkiewicz, A., McLendon, L., Jenkins, E.C., Brown, W.T. Genet. Test. (2000) [Pubmed]
  6. Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians. Zhong, N., Ju, W., Xu, W., Ye, L., Shen, Y., Wu, G., Chen, S.H., Jin, R., Hu, X.F., Yang, A., Liu, X., Poon, P., Pang, C., Zheng, Y., Song, L., Zhao, P., Fu, B., Gu, H., Brown, W.T. Am. J. Med. Genet. (1999) [Pubmed]
  7. Reduced mRNA for G3BP in fragile X cells: evidence of FMR1 gene regulation. Zhong, N., Ju, W., Nelson, D., Dobkin, C., Brown, W.T. Am. J. Med. Genet. (1999) [Pubmed]
  8. 5-HTTLPR variants not associated with autistic spectrum disorders. Zhong, N., Ye, L., Ju, W., Brown, W.T., Tsiouris, J., Cohen, I. Neurogenetics (1999) [Pubmed]
  9. Molecular screening of Batten disease: identification of a missense mutation (E295K) in the CLN3 gene. Zhong, N., Wisniewski, K.E., Kaczmarski, A.L., Ju, W., Xu, W.M., Xu, W.W., Mclendon, L., Liu, B., Kaczmarski, W., Sklower Brooks, S.S., Brown, W.T. Hum. Genet. (1998) [Pubmed]
  10. Two common mutations in the CLN2 gene underlie late infantile neuronal ceroid lipofuscinosis. Zhong, N., Wisniewski, K.E., Hartikainen, J., Ju, W., Moroziewicz, D.N., McLendon, L., Sklower Brooks, S.S., Brown, W.T. Clin. Genet. (1998) [Pubmed]
 
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