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A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration.
Hageman GS, Anderson DH, Johnson LV, Hancox LS, Taiber AJ, Hardisty LI, Hageman JL, Stockman HA, Borchardt JD, Gehrs KM, Smith RJ, Silvestri G, Russell SR, Klaver CC, Barbazetto I, Chang S, Yannuzzi LA, Barile GR, Merriam JC, Smith RT, Olsh AK, Bergeron J, Zernant J, Merriam JE, Gold B, Dean M, Allikmets R. Hageman GS, et al. Among authors: chang s. Proc Natl Acad Sci U S A. 2005 May 17;102(20):7227-32. doi: 10.1073/pnas.0501536102. Epub 2005 May 3. Proc Natl Acad Sci U S A. 2005. PMID: 15870199 Free PMC article.
Peripapillary atrophy in Stargardt disease.
Hwang JC, Zernant J, Allikmets R, Barile GR, Chang S, Smith RT. Hwang JC, et al. Among authors: chang s. Retina. 2009 Feb;29(2):181-6. doi: 10.1097/IAE.0b013e31818a2c01. Retina. 2009. PMID: 18854780 Free PMC article.
Cadherin 5 is regulated by corticosteroids and associated with central serous chorioretinopathy.
Schubert C, Pryds A, Zeng S, Xie Y, Freund KB, Spaide RF, Merriam JC, Barbazetto I, Slakter JS, Chang S, Munch IC, Drack AV, Hernandez J, Yzer S, Merriam JE, Linneberg A, Larsen M, Yannuzzi LA, Mullins RF, Allikmets R. Schubert C, et al. Among authors: chang s. Hum Mutat. 2014 Jul;35(7):859-67. doi: 10.1002/humu.22551. Hum Mutat. 2014. PMID: 24665005 Free PMC article.
Disruption in Bruch membrane in patients with Stargardt disease.
Park SP, Chang S, Allikmets R, Smith RT, Burke TR, Gregory-Roberts E, Tsang SH. Park SP, et al. Among authors: chang s. Ophthalmic Genet. 2012 Mar;33(1):49-52. doi: 10.3109/13816810.2011.628358. Epub 2011 Nov 7. Ophthalmic Genet. 2012. PMID: 22060670 Free PMC article.
Optical coherence tomography in asteroid hyalosis.
Hwang JC, Barile GR, Schiff WM, Ober MD, Smith RT, Del Priore LV, Turano MR, Chang S. Hwang JC, et al. Among authors: chang s. Retina. 2006 Jul-Aug;26(6):661-5. doi: 10.1097/01.iae.0000224502.33905.66. Retina. 2006. PMID: 16829809 Free PMC article.
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