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

Gerald A. Fishman

Department of Ophthalmology and Visual Sciences (MC 648)

Room 3.85

Eye and Ear Infirmary

1855W Taylor Street

USA;

[email]@uic.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Ophthalmology and Visual Sciences (MC 648), Room 3.85, Eye and Ear Infirmary, 1855W Taylor Street, USA;. 2011
  • Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, IL 60612, USA. 1998 - 2008

References

  1. Spectral-domain OCT peripapillary retinal nerve fibre layer thickness measurements in patients with stargardt disease. Genead, M.A., Fishman, G.A., Anastasakis, A. Br. J. Ophthalmol (2011) [Pubmed]
  2. John dalton: though in error, he still influenced our understanding of congenital color deficiency. Fishman, G.A. Ophthalmic Genet. (2008) [Pubmed]
  3. Continued use of dorzolamide for the treatment of cystoid macular oedema in patients with retinitis pigmentosa. Fishman, G.A., Apushkin, M.A. Br. J. Ophthalmol (2007) [Pubmed]
  4. Natural course of visual field loss in patients with Type 2 Usher syndrome. Fishman, G.A., Bozbeyoglu, S., Massof, R.W., Kimberling, W. Retina (Philadelphia, Pa.) (2007) [Pubmed]
  5. Outcome measures and their application in clinical trials for retinal degenerative diseases: outline, review, and perspective. Fishman, G.A., Jacobson, S.G., Alexander, K.R., Cideciyan, A.V., Birch, D.G., Weleber, R.G., Hood, D.C. Retina (Philadelphia, Pa.) (2005) [Pubmed]
  6. Short-term inter-visit variability of erg amplitudes in normal subjects and patients with retinitis pigmentosa. Fishman, G.A., Chappelow, A.V., Anderson, R.J., Rotenstreich, Y., Derlacki, D.J. Retina (Philadelphia, Pa.) (2005) [Pubmed]
  7. Novel mutations in the cellular retinaldehyde-binding protein gene (RLBP1) associated with retinitis punctata albescens: evidence of interfamilial genetic heterogeneity and fundus changes in heterozygotes. Fishman, G.A., Roberts, M.F., Derlacki, D.J., Grimsby, J.L., Yamamoto, H., Sharon, D., Nishiguchi, K.M., Dryja, T.P. Arch. Ophthalmol. (2004) [Pubmed]
  8. ABCA4 gene sequence variations in patients with autosomal recessive cone-rod dystrophy. Fishman, G.A., Stone, E.M., Eliason, D.A., Taylor, C.M., Lindeman, M., Derlacki, D.J. Arch. Ophthalmol. (2003) [Pubmed]
  9. Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR gene. Fishman, G.A., Stone, E.M., Grover, S., Derlacki, D.J., Haines, H.L., Hockey, R.R. Arch. Ophthalmol. (1999) [Pubmed]
  10. A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa. Fishman, G.A., Grover, S., Buraczynska, M., Wu, W., Swaroop, A. Arch. Ophthalmol. (1998) [Pubmed]
 
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