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Michel Michaelides

UCL Institute of Ophthalmology

11-43 Bath Street

London EC1V 9EL

UK;

[email]@ucl.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • UCL Institute of Ophthalmology, 11-43 Bath Street, London EC1V 9EL, UK;. 2012
  • UCL Institute of Ophthalmology, London, United Kingdom. 2010
  • Department of Medical Retina, Moorfields Eye Hospital, London, United Kingdom. 2010
  • Moorfields Eye Hospital, London, England. 2008
  • Department of Paediatric Ophthalmology and Strabismus, Moorfields Eye Hospital, City Road, London, UK. 2007
  • Moorfields Eye Hospital, and Institute of Ophthalmology, University College London, London, United Kingdom. 2006

References

  1. Developmental macular disorders: phenotypes and underlying molecular genetic basis. Michaelides, M., Jeffery, G., Moore, A.T. Br. J. Ophthalmol (2012) [Pubmed]
  2. The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy. Michaelides, M., Gaillard, M.C., Escher, P., Tiab, L., Bedell, M., Borruat, F.X., Barthelmes, D., Carmona, R., Zhang, K., White, E., McClements, M., Robson, A.G., Holder, G.E., Bradshaw, K., Hunt, D.M., Webster, A.R., Moore, A.T., Schorderet, D.F., Munier, F.L. Invest. Ophthalmol. Vis. Sci. (2010) [Pubmed]
  3. A prospective randomized trial of intravitreal bevacizumab or laser therapy in the management of diabetic macular edema (BOLT study) 12-month data: report 2. Michaelides, M., Kaines, A., Hamilton, R.D., Fraser-Bell, S., Rajendram, R., Quhill, F., Boos, C.J., Xing, W., Egan, C., Peto, T., Bunce, C., Leslie, R.D., Hykin, P.G. Ophthalmology (2010) [Pubmed]
  4. Macular dystrophy associated with the A3243G mitochondrial DNA mutation. Distinct retinal and associated features, disease variability, and characterization of asymptomatic family members. Michaelides, M., Jenkins, S.A., Bamiou, D.E., Sweeney, M.G., Davis, M.B., Luxon, L., Bird, A.C., Rath, P.P. Arch. Ophthalmol. (2008) [Pubmed]
  5. Glaucoma following congenital cataract surgery--the role of early surgery and posterior capsulotomy. Michaelides, M., Bunce, C., Adams, G.G. BMC. Ophthalmol (2007) [Pubmed]
  6. Evidence of genetic heterogeneity in MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome. Michaelides, M., Urquhart, J., Holder, G.E., Restori, M., Kayali, N., Manson, F.D., Black, G.C. Am. J. Ophthalmol. (2006) [Pubmed]
 
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