The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Brian P. Brooks

National Eye Institute

National Institutes of Health

Bethesda

MD 20892

USA

[email]@mail.nih.gov

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA. 2007
  • National Eye Institute, USA. 2006
  • Department of Ophthalmology, Kellogg Eye Center, University of Michigan, Ann Arbor, USA. 2002 - 2004
  • National Human Genome Research Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, USA. 2004

References

  1. Analysis of ocular hypopigmentation in Rab38cht/cht mice. Brooks, B.P., Larson, D.M., Chan, C.C., Kjellstrom, S., Smith, R.S., Crawford, M.A., Lamoreux, L., Huizing, M., Hess, R., Jiao, X., Hejtmancik, J.F., Maminishkis, A., John, S.W., Bush, R., Pavan, W.J. Invest. Ophthalmol. Vis. Sci. (2007) [Pubmed]
  2. Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature. Brooks, B.P., Meck, J.M., Haddad, B.R., Bendavid, C., Blain, D., Toretsky, J.A. BMC Med. Genet. (2006) [Pubmed]
  3. Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case report. Brooks, B.P., Kleta, R., Caruso, R.C., Stuart, C., Ludlow, J., Stratakis, C.A. BMC. Ophthalmol (2004) [Pubmed]
  4. A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome. Brooks, B.P., Moroi, S.E., Downs, C.A., Wiltse, S., Othman, M.I., Semina, E.V., Richards, J.E. Ophthalmic Genet. (2004) [Pubmed]
  5. Infantile spasms as a cause of acquired perinatal visual loss. Brooks, B.P., Simpson, J.L., Leber, S.M., Robertson, P.L., Archer, S.M. J. AAPOS (2002) [Pubmed]
 
WikiGenes - Universities