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

Anthony J. Aldave

Jules Stein Eye Institute and the Department of Ophthalmology

David Geffen School of Medicine at the University of California

Los Angeles

Los Angeles



Name/email consistency: high



  • Jules Stein Eye Institute and the Department of Ophthalmology, David Geffen School of Medicine at the University of California, Los Angeles, Los Angeles, USA. 2002 - 2011
  • Department of Ophthalmology, University of California, San Francisco/Francis I. Proctor Foundation, San Francisco, USA. 2002 - 2005
  • Cornea Service, Department of Ophthalmology, The Jules Stein Eye Institute, The University of California, USA. 2003


  1. Descemet stripping endothelial keratoplasty after Ophtec 311 iris reconstruction lens implantation. Aldave, A.J., Baghdasaryan, E., Miller, K.M. Cornea (2011) [Pubmed]
  2. Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC. Aldave, A.J., Rosenwasser, G.O., Yellore, V.S., Papp, J.C., Sobel, E.M., Pham, M.N., Chen, M.C., Dandekar, S., Sripracha, R., Rayner, S.A., Sassani, J.W., Gorin, M.B. Invest. Ophthalmol. Vis. Sci. (2010) [Pubmed]
  3. Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval. Aldave, A.J., Yellore, V.S., Vo, R.C., Kamal, K.M., Rayner, S.A., Plaisier, C.L., Chen, M.C., Damani, M.R., Pham, M.N., Gorin, M.B., Sobel, E., Papp, J. Cornea (2009) [Pubmed]
  4. The Boston type I keratoprosthesis: improving outcomes and expanding indications. Aldave, A.J., Kamal, K.M., Vo, R.C., Yu, F. Ophthalmology (2009) [Pubmed]
  5. Epithelial debridement and Bowman's layer polishing for visually significant epithelial irregularity and recurrent corneal erosions. Aldave, A.J., Kamal, K.M., Vo, R.C., Yu, F. Cornea (2009) [Pubmed]
  6. A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene. Aldave, A.J., Yellore, V.S., Sonmez, B., Bourla, N., Salem, A.K., Khan, M.A., Rayner, S.A., Glasgow, B.J. Arch. Ophthalmol. (2008) [Pubmed]
  7. Keratoconus is not associated with mutations in COL8A1 and COL8A2. Aldave, A.J., Bourla, N., Yellore, V.S., Rayner, S.A., Khan, M.A., Salem, A.K., Sonmez, B. Cornea (2007) [Pubmed]
  8. Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia. Aldave, A.J., Yellore, V.S., Yu, F., Bourla, N., Sonmez, B., Salem, A.K., Rayner, S.A., Sampat, K.M., Krafchak, C.M., Richards, J.E. Am. J. Med. Genet. A (2007) [Pubmed]
  9. Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11. Aldave, A.J., Yellore, V.S., Bourla, N., Momi, R.S., Khan, M.A., Salem, A.K., Rayner, S.A., Glasgow, B.J., Kurtz, I. Cornea (2007) [Pubmed]
  10. A clinical and histopathologic examination of accelerated TGFBIp deposition after LASIK in combined granular-lattice corneal dystrophy. Aldave, A.J., Sonmez, B., Forstot, S.L., Rayner, S.A., Yellore, V.S., Glasgow, B.J. Am. J. Ophthalmol. (2007) [Pubmed]
  11. Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2. Aldave, A.J., Sonmez, B., Bourla, N., Schultz, G., Papp, J.C., Salem, A.K., Rayner, S.A., Yellore, V.S. Ophthalmic Genet. (2007) [Pubmed]
  12. No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid deposition. Aldave, A.J., Rayner, S.A., King, J.A., Salem, A.K., Prechanond, A., Hashida, S., Affeldt, J.C., Meallet, M.A., Glasgow, B.J., Small, K.W., Yellore, V.S. Cornea (2006) [Pubmed]
  13. Corneal copper deposition associated with chronic lymphocytic leukemia. Aldave, A.J., King, J.A., Kim, B.T., Hopp, L. Am. J. Ophthalmol. (2006) [Pubmed]
  14. Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene. Aldave, A.J., Rayner, S.A., Kim, B.T., Prechanond, A., Yellore, V.S. Mol. Vis. (2006) [Pubmed]
  15. No VSX1 gene mutations associated with keratoconus. Aldave, A.J., Yellore, V.S., Salem, A.K., Yoo, G.L., Rayner, S.A., Yang, H., Tang, G.Y., Piconell, Y., Rabinowitz, Y.S. Invest. Ophthalmol. Vis. Sci. (2006) [Pubmed]
  16. No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophy. Aldave, A.J., Rayner, S.A., Salem, A.K., Yoo, G.L., Kim, B.T., Saeedian, M., Sonmez, B., Yellore, V.S. Invest. Ophthalmol. Vis. Sci. (2006) [Pubmed]
  17. Lattice dystrophy-like localized amyloidosis of the cornea secondary to trichiasis. Aldave, A.J., Principe, A.H., Lin, D.Y., Yellore, V.S., Small, K.W. Cornea (2005) [Pubmed]
  18. Candidate gene screening for posterior polymorphous dystrophy. Aldave, A.J., Yellore, V.S., Principe, A.H., Abedi, G., Merrill, K., Chalukya, M., Small, K.W., Udar, N. Cornea (2005) [Pubmed]
  19. A unique corneal dystrophy of Bowman's layer and stroma associated with the Gly623Asp mutation in the transforming growth factor beta-induced (TGFBI) gene. Aldave, A.J., Rayner, S.A., King, J.A., Affeldt, J.A., Yellore, V.S. Ophthalmology (2005) [Pubmed]
  20. Primary graft failure associated with epithelial downgrowth: a case report. Aldave, A.J., Hollander, D.A., Branco, B., Crawford, B., Abbott, R.L. BMC. Ophthalmol (2005) [Pubmed]
  21. Analysis of fifteen positional candidate genes for Schnyder crystalline corneal dystrophy. Aldave, A.J., Rayner, S.A., Principe, A.H., Affeldt, J.A., Katsev, D., Yellore, V.S. Mol. Vis. (2005) [Pubmed]
  22. Novel mutations in the carbohydrate sulfotransferase gene (CHST6) in American patients with macular corneal dystrophy. Aldave, A.J., Yellore, V.S., Thonar, E.J., Udar, N., Warren, J.F., Yoon, M.K., Cohen, E.J., Rapuano, C.J., Laibson, P.R., Margolis, T.P., Small, K. Am. J. Ophthalmol. (2004) [Pubmed]
  23. Anterior basement membrane corneal dystrophy and pseudo-unilateral lattice corneal dystrophy in a patient with recurrent corneal erosions. Aldave, A.J., Lin, D.Y., Principe, A.H., Yellore, V.S., Weissman, B.A. Am. J. Ophthalmol. (2004) [Pubmed]
  24. The usefulness of buccal swabs for mutation screening in patients with suspected corneal dystrophies. Aldave, A.J., Yellore, V.S., Self, C.A., Holsclaw, D., Small, K. Ophthalmology (2004) [Pubmed]
  25. Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene. Aldave, A.J., Gutmark, J.G., Yellore, V.S., Affeldt, J.A., Meallet, M.A., Udar, N., Rao, N.A., Small, K.W., Klintworth, G.K. Am. J. Ophthalmol. (2004) [Pubmed]
  26. Spontaneous corneal hydrops and perforation in keratoconus and pellucid marginal degeneration. Aldave, A.J., Mabon, M., Hollander, D.A., McLeod, S.D., Spencer, W.H., Abbott, R.L. Cornea (2003) [Pubmed]
  27. Peripheral keratitis associated with erythema elevatum diutinum. Aldave, A.J., Shih, J.L., Jovkar, S., McLeod, S.D. Am. J. Ophthalmol. (2003) [Pubmed]
  28. Atypical vortex pattern of corneal deposits in granular corneal dystrophy. Aldave, A.J., Yellore, V.S., Hwang, D.G. Cornea (2003) [Pubmed]
  29. Central discoid corneal dystrophy. Aldave, A.J., Edward, D.P., Park, A.J., Raber, I.M., Eagle, R.C. Cornea (2002) [Pubmed]
  30. A novel technique for harvesting keratolimbal allografts from corneoscleral buttons. Aldave, A.J., Wong, I.G. Am. J. Ophthalmol. (2002) [Pubmed]
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