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PubMed

• Geographic and climatic factors associated with exfoliation syndrome.
  Stein, J.D., Pasquale, L.R., Talwar, N., Kim, D.S., Reed, D.M., Nan, B., Kang, J.H., Wiggs, J.L., Richards, J.E.> ;Arch Ophthalmol. 2011 Aug
• Differences in Rates of Glaucoma among Asian Americans and Other Racial Groups, and among Various Asian Ethnic Groups.
  Stein, J.D., Kim, D.S., Niziol, L.M., Talwar, N., Nan, B., Musch, D.C., Richards, J.E.> ;Ophthalmology. 2011 Jun
• Effects of timolol on MYOC, OPTN, and WDR36 RNA levels.
  Rozsa, F.W., Scott, K., Pawar, H., Moroi, S., Richards, J.E.> ;Arch Ophthalmol. 2008 Jan
• Recurrent Myocilin Asn480Lys glaucoma causative mutation arises de novo in a family of Andean descent.
  Guevara-Fujita, M.L., Perez-Grossmann, R.A., Estrada-Cuzcano, A., Pawar, H., Vargas, E., Richards, J.E., Fujita, R.> ;J Glaucoma. 2008-01-01
• 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 Nov 1
• Molecular testing for hereditary retinal disease as part of clinical care.
  Downs, K., Zacks, D.N., Caruso, R., Karoukis, A.J., Branham, K., Yashar, B.M., Haimann, M.H., Trzupek, K., Meltzer, M., Blain, D., Richards, J.E., Weleber, R.G., Hecke...> ;Arch Ophthalmol. 2007 Feb
• Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individuals.
  Hewitt, A. W., Bennett, S. L., Richards, J. E., Dimasi, D. P., Booth, A. P., Inglehearn, C., Anwar, R., Yamamoto, T., Fingert, J. H., Héon, E., Craig, J. E., Mackey, D...> ;Arch Ophthalmol. 2007 Jan
• Evaluation of the beta2-adrenergic receptor gene as a candidate glaucoma gene in 2 ancestral populations.
  McLaren, N., Reed, D.M., Musch, D.C., Downs, C.A., Higashi, M.E., Santiago, C., Radenbaugh, P.A., Allingham, R.R., Richards, J.E., Moroi, S.E.> ;Arch Ophthalmol. 2007 Jan
• Differential expression profile prioritization of positional candidate glaucoma genes: the GLC1C locus.
  Rozsa, F.W., Scott, K.M., Pawar, H., Samples, J.R., Wirtz, M.K., Richards, J.E.> ;Arch Ophthalmol. 2007 Jan
• Variation in optineurin (OPTN) allele frequencies between and within populations.
  Ayala-Lugo, R.M., Pawar, H., Reed, D.M., Lichter, P.R., Moroi, S.E., Page, M., Eadie, J., Azocar, V., Maul, E., Ntim-Amponsah, C., Bromley, W., Obeng-Nyarkoh, E., John...> ;Mol Vis. 2007
• Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds.
  Hewitt, A. W., Samples, J. R., Allingham, R. R., Järvelä, I., Kitsos, G., Krishnadas, S. R., Richards, J. E., Lichter, P. R., Petersen, M. B., Sundaresan, P., Wiggs, J...> ;Mol Vis. 2007
• Concordance of aqueous humor flow in the morning and at night in normal humans.
  Radenbaugh, P.A., Goyal, A., McLaren, N.C., Reed, D.M., Musch, D.C., Richards, J.E., Moroi, S.E.> ;Invest Ophthalmol Vis Sci. 2006 Nov
• Gene expression profile of human trabecular meshwork cells in response to long-term dexamethasone exposure.
  Rozsa, F.W., Reed, D.M., Scott, K.M., Pawar, H., Moroi, S.E., Kijek, T.G., Krafchak, C.M., Othman, M.I., Vollrath, D., Elner, V.M., Richards, J.E.> ;Mol Vis. 2006
• Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells.
  Krafchak, C.M., Pawar, H., Moroi, S.E., Sugar, A., Lichter, P.R., Mackey, D.A., Mian, S., Nairus, T., Elner, V., Schteingart, M.T., Downs, C.A., Kijek, T.G., Johnson, ...> ;Am J Hum Genet. 2005 Nov
• Effect of intravitreal triamcinolone acetonide on susceptibility to experimental bacterial endophthalmitis and subsequent response to treatment.
  Bucher, R. S.,Hall, E.,Reed, D. M.,Richards, J. E.,Johnson, M. W.,Zacks, D. N.> ;Arch Ophthalmol. 2005 May
• A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10.
  Shimizu, S., Krafchak, C., Fuse, N., Epstein, M.P., Schteingart, M.T., Sugar, A., Eibschitz-Tsimhoni, M., Downs, C.A., Rozsa, F., Trager, E.H., Reed, D.M., Boehnke, M....> ;Am J Med Genet A. 2004 Nov 1
• Stem cell therapy for ocular disorders.
  Levin, L. A., Ritch, R., Richards, J. E., Borrás, T.> ;Arch Ophthalmol. 2004 Apr
• Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease.
  Abecasis, G.R., Yashar, B.M., Zhao, Y., Ghiasvand, N.M., Zareparsi, S., Branham, K.H., Reddick, A.C., Trager, E.H., Yoshida, S., Bahling, J., Filippova, E., Elner, S.,...> ;Am J Hum Genet. 2004 Mar
• Clinicopathologic correlation and genetic analysis in a case of posterior polymorphous corneal dystrophy.
  Moroi, S.E., Gokhale, P.A., Schteingart, M.T., Sugar, A., Downs, C.A., Shimizu, S., Krafchak, C., Fuse, N., Elner, S.G., Elner, V.M., Flint, A., Epstein, M.P., Boehnke...> ;Am J Ophthalmol. 2003 Apr
• Septuagenarian's phenotype leads to ascertainment of familial MYOC gene mutation.
  Lim, P., Lichter, P.R., Higashi, M., Downs, C.A., Richards, J.E.> ;J Glaucoma. 2003 Apr
• X-linked recessive atrophic macular degeneration from RPGR mutation.
  Ayyagari, R., Demirci, F.Y., Liu, J., Bingham, E.L., Stringham, H., Kakuk, L.E., Boehnke, M., Gorin, M.B., Richards, J.E., Sieving, P.A.> ;Genomics. 2002 Aug
• Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectively.
  Thompson, D.A., McHenry, C.L., Li, Y., Richards, J.E., Othman, M.I., Schwinger, E., Vollrath, D., Jacobson, S.G., Gal, A.> ;Am J Hum Genet. 2002 Jan
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