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Randi J. Hagerman

Department of Pediatrics

University of California

Davis

School of Medicine

USA

[email]@*.ucdavis.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Pediatrics, University of California, Davis, School of Medicine, USA. 2008 - 2011
  • M.I.N.D. Institute and Department of Pediatrics, University of California at Davis Medical Center, Sacramento, California 95817, USA. 2001 - 2008
  • M.I.N.D. Institute, and Department of Pediatrics, School of Medicine, University of California, USA. 2008

References

  1. FMR1 premutation and full mutation molecular mechanisms related to autism. Hagerman, R., Au, J., Hagerman, P. J. Neurodev. Disord (2011) [Pubmed]
  2. Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome. Greco, C.M., Navarro, C.S., Hunsaker, M.R., Maezawa, I., Shuler, J.F., Tassone, F., Delany, M., Au, J.W., Berman, R.F., Jin, L.W., Schumann, C., Hagerman, P.J., Hagerman, R.J. Mol. Autism (2011) [Pubmed]
  3. Fragile X and autism: Intertwined at the molecular level leading to targeted treatments. Hagerman, R., Hoem, G., Hagerman, P. Mol. Autism (2010) [Pubmed]
  4. Advances in the treatment of fragile X syndrome. Hagerman, R.J., Berry-Kravis, E., Kaufmann, W.E., Ono, M.Y., Tartaglia, N., Lachiewicz, A., Kronk, R., Delahunty, C., Hessl, D., Visootsak, J., Picker, J., Gane, L., Tranfaglia, M. Pediatrics (2009) [Pubmed]
  5. Treatment of fragile X-associated tremor ataxia syndrome (FXTAS) and related neurological problems. Hagerman, R.J., Hall, D.A., Coffey, S., Leehey, M., Bourgeois, J., Gould, J., Zhang, L., Seritan, A., Berry-Kravis, E., Olichney, J., Miller, J.W., Fong, A.L., Carpenter, R., Bodine, C., Gane, L.W., Rainin, E., Hagerman, H., Hagerman, P.J. Clin. Interv. Aging (2008) [Pubmed]
  6. Testing for fragile X gene mutations throughout the life span. Hagerman, R.J., Hagerman, P.J. JAMA (2008) [Pubmed]
  7. Autism profiles of males with fragile X syndrome. Harris, S.W., Hessl, D., Goodlin-Jones, B., Ferranti, J., Bacalman, S., Barbato, I., Tassone, F., Hagerman, P.J., Herman, H., Hagerman, R.J. Am. J. Ment. Retard (2008) [Pubmed]
  8. Neuropathy as a presenting feature in fragile X-associated tremor/ataxia syndrome. Hagerman, R.J., Coffey, S.M., Maselli, R., Soontarapornchai, K., Brunberg, J.A., Leehey, M.A., Zhang, L., Gane, L.W., Fenton-Farrell, G., Tassone, F., Hagerman, P.J. Am. J. Med. Genet. A (2007) [Pubmed]
  9. Lessons from fragile X regarding neurobiology, autism, and neurodegeneration. Hagerman, R.J. J. Dev. Behav. Pediatr (2006) [Pubmed]
  10. Recent advances in fragile X: a model for autism and neurodegeneration. Hagerman, R.J., Ono, M.Y., Hagerman, P.J. Curr. Opin. Psychiatry (2005) [Pubmed]
  11. Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation. Hagerman, R.J., Leavitt, B.R., Farzin, F., Jacquemont, S., Greco, C.M., Brunberg, J.A., Tassone, F., Hessl, D., Harris, S.W., Zhang, L., Jardini, T., Gane, L.W., Ferranti, J., Ruiz, L., Leehey, M.A., Grigsby, J., Hagerman, P.J. Am. J. Hum. Genet. (2004) [Pubmed]
  12. The fragile X premutation: into the phenotypic fold. Hagerman, R.J., Hagerman, P.J. Curr. Opin. Genet. Dev. (2002) [Pubmed]
  13. Influence of stimulants on electrodermal studies in Fragile X syndrome. Hagerman, R.J., Miller, L.J., McGrath-Clarke, J., Riley, K., Goldson, E., Harris, S.W., Simon, J., Church, K., Bonnell, J., Ognibene, T.C., McIntosh, D.N. Microsc. Res. Tech. (2002) [Pubmed]
  14. Fragile X syndrome: a model of gene-brain-behavior relationships. Hagerman, R.J., Hagerman, P.J. Mol. Genet. Metab. (2001) [Pubmed]
 
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