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

Artur V. Cideciyan

Scheie Eye Institute

Department of Ophthalmology

University of Pennsylvania Perelman School of Medicine




Name/email consistency: high



  • Scheie Eye Institute, Department of Ophthalmology, University of Pennsylvania Perelman School of Medicine, Philadelphia, USA. 2013
  • Scheie Eye Institute, University of Pennsylvania, 51 North 39th St, Philadelphia, USA. 1998 - 2010


  1. Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement. Cideciyan, A.V., Jacobson, S.G., Beltran, W.A., Sumaroka, A., Swider, M., Iwabe, S., Roman, A.J., Olivares, M.B., Schwartz, S.B., Komáromy, A.M., Hauswirth, W.W., Aguirre, G.D. Proc. Natl. Acad. Sci. U.S.A. (2013) [Pubmed]
  2. Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy. Cideciyan, A.V. Prog. Retin. Eye. Res (2010) [Pubmed]
  3. ABCA4 disease progression and a proposed strategy for gene therapy. Cideciyan, A.V., Swider, M., Aleman, T.S., Tsybovsky, Y., Schwartz, S.B., Windsor, E.A., Roman, A.J., Sumaroka, A., Steinberg, J.D., Jacobson, S.G., Stone, E.M., Palczewski, K. Hum. Mol. Genet. (2009) [Pubmed]
  4. Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year. Cideciyan, A.V., Hauswirth, W.W., Aleman, T.S., Kaushal, S., Schwartz, S.B., Boye, S.L., Windsor, E.A., Conlon, T.J., Sumaroka, A., Pang, J.J., Roman, A.J., Byrne, B.J., Jacobson, S.G. Hum. Gene Ther. (2009) [Pubmed]
  5. Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics. Cideciyan, A.V., Aleman, T.S., Boye, S.L., Schwartz, S.B., Kaushal, S., Roman, A.J., Pang, J.J., Sumaroka, A., Windsor, E.A., Wilson, J.M., Flotte, T.R., Fishman, G.A., Heon, E., Stone, E.M., Byrne, B.J., Jacobson, S.G., Hauswirth, W.W. Proc. Natl. Acad. Sci. U.S.A. (2008) [Pubmed]
  6. Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis. Cideciyan, A.V., Aleman, T.S., Jacobson, S.G., Khanna, H., Sumaroka, A., Aguirre, G.K., Schwartz, S.B., Windsor, E.A., He, S., Chang, B., Stone, E.M., Swaroop, A. Hum. Mutat. (2007) [Pubmed]
  7. Reduced-illuminance autofluorescence imaging in ABCA4-associated retinal degenerations. Cideciyan, A.V., Swider, M., Aleman, T.S., Roman, M.I., Sumaroka, A., Schwartz, S.B., Stone, E.M., Jacobson, S.G. J. Opt. Soc. Am. A. Opt. Image. Sci. Vis (2007) [Pubmed]
  8. In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosa. Cideciyan, A.V., Jacobson, S.G., Aleman, T.S., Gu, D., Pearce-Kelling, S.E., Sumaroka, A., Acland, G.M., Aguirre, G.D. Proc. Natl. Acad. Sci. U.S.A. (2005) [Pubmed]
  9. ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retina. Cideciyan, A.V., Swider, M., Aleman, T.S., Sumaroka, A., Schwartz, S.B., Roman, M.I., Milam, A.H., Bennett, J., Stone, E.M., Jacobson, S.G. Invest. Ophthalmol. Vis. Sci. (2005) [Pubmed]
  10. Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence. Cideciyan, A.V., Aleman, T.S., Swider, M., Schwartz, S.B., Steinberg, J.D., Brucker, A.J., Maguire, A.M., Bennett, J., Stone, E.M., Jacobson, S.G. Hum. Mol. Genet. (2004) [Pubmed]
  11. Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3. Cideciyan, A.V., Jacobson, S.G., Gupta, N., Osawa, S., Locke, K.G., Weiss, E.R., Wright, A.F., Birch, D.G., Milam, A.H. Invest. Ophthalmol. Vis. Sci. (2003) [Pubmed]
  12. Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man. Cideciyan, A.V., Haeseleer, F., Fariss, R.N., Aleman, T.S., Jang, G.F., Verlinde, C.L., Marmor, M.F., Jacobson, S.G., Palczewski, K. Vis. Neurosci. (2000) [Pubmed]
  13. Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man. Cideciyan, A.V., Zhao, X., Nielsen, L., Khani, S.C., Jacobson, S.G., Palczewski, K. Proc. Natl. Acad. Sci. U.S.A. (1998) [Pubmed]
  14. Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man. Cideciyan, A.V., Hood, D.C., Huang, Y., Banin, E., Li, Z.Y., Stone, E.M., Milam, A.H., Jacobson, S.G. Proc. Natl. Acad. Sci. U.S.A. (1998) [Pubmed]
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