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

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John M. Graham

Medical Genetics Institute at Cedars-Sinai Medical Center

Los Angeles

CA 90048

USA

[email]@cshs.org

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Medical Genetics Institute at Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA. 2001 - 2010
  • Medical Genetics Institute, Steven Spielberg Pediatric Research Center, Cedars-Sinai Medical Center, Department of Pediatrics, USA. 2005
  • Ahmanson Department of Pediatrics, Steven Spielberg Pediatric Research Center, SHARE's Child Disability Center, UCLA School of Medicine, USA. 2004

References

  1. Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome). Graham, J.M., Clark, R.D., Moeschler, J.B., Rogers, R.C. Am. J. Med. Genet. C. Semin. Med. Genet (2010) [Pubmed]
  2. Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome. Graham, J.M., Kramer, N., Bejjani, B.A., Thiel, C.T., Carta, C., Neri, G., Tartaglia, M., Zenker, M. Am. J. Med. Genet. A (2009) [Pubmed]
  3. Behavioral features of CHARGE syndrome (Hall-Hittner syndrome) comparison with Down syndrome, Prader-Willi syndrome, and Williams syndrome. Graham, J.M., Rosner, B., Dykens, E., Visootsak, J. Am. J. Med. Genet. A (2005) [Pubmed]
  4. Marshall J. Edwards: discoverer of maternal hyperthermia as a human teratogen. Graham, J.M. Birth Defects Res. Part A Clin. Mol. Teratol. (2005) [Pubmed]
  5. Gene-environment interactions in rare diseases that include common birth defects. Graham, J.M., Shaw, G.M. Birth Defects Res. Part A Clin. Mol. Teratol. (2005) [Pubmed]
  6. MICRO syndrome: an entity distinct from COFS syndrome. Graham, J.M., Hennekam, R., Dobyns, W.B., Roeder, E., Busch, D. Am. J. Med. Genet. A (2004) [Pubmed]
  7. A new X-linked syndrome with agenesis of the corpus callosum, mental retardation, coloboma, micrognathia, and a mutation in the Alpha 4 gene at Xq13. Graham, J.M., Wheeler, P., Tackels-Horne, D., Lin, A.E., Hall, B.D., May, M., Short, K.M., Schwartz, C.E., Cox, T.C. Am. J. Med. Genet. A (2003) [Pubmed]
  8. Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy. Graham, J.M., Anyane-Yeboa, K., Raams, A., Appeldoorn, E., Kleijer, W.J., Garritsen, V.H., Busch, D., Edersheim, T.G., Jaspers, N.G. Am. J. Hum. Genet. (2001) [Pubmed]
 
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