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Genome-wide association study and meta-analysis of intraocular pressure.
Ozel AB, Moroi SE, Reed DM, Nika M, Schmidt CM, Akbari S, Scott K, Rozsa F, Pawar H, Musch DC, Lichter PR, Gaasterland D, Branham K, Gilbert J, Garnai SJ, Chen W, Othman M, Heckenlively J, Swaroop A, Abecasis G, Friedman DS, Zack D, Ashley-Koch A, Ulmer M, Kang JH; NEIGHBOR Consortium; Liu Y, Yaspan BL, Haines J, Allingham RR, Hauser MA, Pasquale L, Wiggs J, Richards JE, Li JZ. Ozel AB, et al. Among authors: reed dm. Hum Genet. 2014 Jan;133(1):41-57. doi: 10.1007/s00439-013-1349-5. Epub 2013 Sep 4. Hum Genet. 2014. PMID: 24002674 Free PMC article.
Variation in optineurin (OPTN) allele frequencies between and within populations.
Ayala-Lugo RM, Pawar H, Reed DM, Lichter PR, Moroi SE, Page M, Eadie J, Azocar V, Maul E, Ntim-Amponsah C, Bromley W, Obeng-Nyarkoh E, Johnson AT, Kijek TG, Downs CA, Johnson JM, Perez-Grossmann RA, Guevara-Fujita ML, Fujita R, Wallace MR, Richards JE. Ayala-Lugo RM, et al. Among authors: reed dm. Mol Vis. 2007 Feb 2;13:151-63. Mol Vis. 2007. PMID: 17293779 Free PMC article.
Geographic and climatic factors associated with exfoliation syndrome.
Stein JD, Pasquale LR, Talwar N, Kim DS, Reed DM, Nan B, Kang JH, Wiggs JL, Richards JE. Stein JD, et al. Among authors: reed dm. Arch Ophthalmol. 2011 Aug;129(8):1053-60. doi: 10.1001/archophthalmol.2011.191. Arch Ophthalmol. 2011. PMID: 21825188 Free PMC article.
Congenital cataracts: de novo gene conversion event in CRYBB2.
Garnai SJ, Huyghe JR, Reed DM, Scott KM, Liebmann JM, Boehnke M, Richards JE, Ritch R, Pawar H. Garnai SJ, et al. Among authors: reed dm. Mol Vis. 2014 Nov 6;20:1579-93. eCollection 2014. Mol Vis. 2014. PMID: 25489230 Free PMC article.
Precision medicine to prevent glaucoma-related blindness.
Moroi SE, Reed DM, Sanders DS, Almazroa A, Kagemann L, Shah N, Shekhawat N, Richards JE. Moroi SE, et al. Among authors: reed dm. Curr Opin Ophthalmol. 2019 May;30(3):187-198. doi: 10.1097/ICU.0000000000000564. Curr Opin Ophthalmol. 2019. PMID: 30883441 Free PMC article. Review.
A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10.
Shimizu S, Krafchak C, Fuse N, Epstein MP, Schteingart MT, Sugar A, Eibschitz-Tsimhoni M, Downs CA, Rozsa F, Trager EH, Reed DM, Boehnke M, Moroi SE, Richards JE. Shimizu S, et al. Among authors: reed dm. Am J Med Genet A. 2004 Nov 1;130A(4):372-7. doi: 10.1002/ajmg.a.30267. Am J Med Genet A. 2004. PMID: 15384081 Free PMC article.
137 results