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

Diana M. Juriloff

Department of Medical Genetics

University of British Columbia

6174 University Boulevard

Vancouver

Canada

[email]@interchange.ubc.ca

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Medical Genetics, University of British Columbia, 6174 University Boulevard, Vancouver, Canada. 2000 - 2008

References

  1. Mouse genetic models of cleft lip with or without cleft palate. Juriloff, D.M., Harris, M.J. Birth Defects Res. Part A Clin. Mol. Teratol. (2008) [Pubmed]
  2. Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test. Juriloff, D.M., Harris, M.J., McMahon, A.P., Carroll, T.J., Lidral, A.C. Birth Defects Res. Part A Clin. Mol. Teratol. (2006) [Pubmed]
  3. The open-eyelid mutation, lidgap-Gates, is an eight-exon deletion in the mouse Map3k1 gene. Juriloff, D.M., Harris, M.J., Mah, D.G. Genomics (2005) [Pubmed]
  4. Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice. Juriloff, D.M., Harris, M.J., Dewell, S.L., Brown, C.J., Mager, D.L., Gagnier, L., Mah, D.G. Birth Defects Res. Part A Clin. Mol. Teratol. (2005) [Pubmed]
  5. A digenic cause of cleft lip in A-strain mice and definition of candidate genes for the two loci. Juriloff, D.M., Harris, M.J., Dewell, S.L. Birth Defects Res. Part A Clin. Mol. Teratol. (2004) [Pubmed]
  6. Unravelling the complex genetics of cleft lip in the mouse model. Juriloff, D.M., Harris, M.J., Brown, C.J. Mamm. Genome (2001) [Pubmed]
  7. Multifactorial genetics of exencephaly in SELH/Bc mice. Juriloff, D.M., Gunn, T.M., Harris, M.J., Mah, D.G., Wu, M.K., Dewell, S.L. Teratology (2001) [Pubmed]
  8. Mouse models for neural tube closure defects. Juriloff, D.M., Harris, M.J. Hum. Mol. Genet. (2000) [Pubmed]
  9. Gaping lids, gp, a mutation on centromeric chromosome 11 that causes defective eyelid development in mice. Juriloff, D.M., Harris, M.J., Banks, K.G., Mah, D.G. Mamm. Genome (2000) [Pubmed]
 
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