| Shields' textbook of glaucoma RR Allingham, S Moroi, MB Shields, K Damji Lippincott Williams & Wilkins, 2020 | 784 | 2020 |
| Primary open-angle glaucoma preferred practice pattern® guidelines BE Prum, LF Rosenberg, SJ Gedde, SL Mansberger, JD Stein, SE Moroi, ... Ophthalmology 123 (1), P41-P111, 2016 | 649 | 2016 |
| Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus Y Lu, V Vitart, KP Burdon, CC Khor, Y Bykhovskaya, A Mirshahi, ... Nature genetics 45 (2), 155-163, 2013 | 354 | 2013 |
| Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma JL Wiggs, BL Yaspan, MA Hauser, JH Kang, RR Allingham, LM Olson, ... PLoS genetics 8 (4), e1002654, 2012 | 338 | 2012 |
| Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma JNC Bailey, SJ Loomis, JH Kang, RR Allingham, P Gharahkhani, CC Khor, ... Nature genetics 48 (2), 189-194, 2016 | 257 | 2016 |
| Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma PG Hysi, CY Cheng, H Springelkamp, S Macgregor, JNC Bailey, ... Nature genetics 46 (10), 1126-1130, 2014 | 252 | 2014 |
| Age-dependent prevalence of mutations at the GLC1A locus in primary open-angle glaucoma S Shimizu, PR Lichter, AT Johnson, Z Zhou, M Higashi, M Gottfredsdottir, ... American journal of ophthalmology 130 (2), 165-177, 2000 | 240 | 2000 |
| Toll-like receptor 4 variant D299G is associated with susceptibility to age-related macular degeneration S Zareparsi, M Buraczynska, KEH Branham, S Shah, D Eng, M Li, ... Human molecular genetics 14 (11), 1449-1455, 2005 | 225 | 2005 |
| Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells CM Krafchak, H Pawar, SE Moroi, A Sugar, PR Lichter, DA Mackey, ... The American Journal of Human Genetics 77 (5), 694-708, 2005 | 223 | 2005 |
| Primary angle closure preferred practice pattern® guidelines BE Prum, LW Herndon, SE Moroi, SL Mansberger, JD Stein, MC Lim, ... Ophthalmology 123 (1), P1-P40, 2016 | 219 | 2016 |
| Primary open-angle glaucoma suspect preferred practice pattern® guidelines BE Prum, MC Lim, SL Mansberger, JD Stein, SE Moroi, SJ Gedde, ... Ophthalmology 123 (1), P112-P151, 2016 | 183 | 2016 |
| Cystoid macular edema associated with latanoprost therapy in a case series of patients with glaucoma and ocular hypertension SE Moroi, MS Gottfredsdottir, MT Schteingart, SG Elner, CM Lee, ... Ophthalmology 106 (5), 1024-1029, 1999 | 171 | 1999 |
| Cataract surgery in patients with nanophthalmos: results and complications W Wu, DG Dawson, A Sugar, SG Elner, KA Meyer, JB McKey, SE Moroi Journal of Cataract & Refractive Surgery 30 (3), 584-590, 2004 | 143 | 2004 |
| Late-onset macular degeneration and long anterior lens zonules result from a CTRP5 gene mutation R Ayyagari, MNA Mandal, AJ Karoukis, L Chen, NC McLaren, M Lichter, ... Investigative ophthalmology & visual science 46 (9), 3363-3371, 2005 | 142 | 2005 |
| Gene expression profile of human trabecular meshwork cells in response to long-term dexamethasone exposure FW Rozsa, DM Reed, KM Scott, H Pawar, SE Moroi, TG Kijek, ... Mol Vis 12 (14-15), 125-41, 2006 | 138 | 2006 |
| A common variant near TGFBR3 is associated with primary open angle glaucoma Z Li, RR Allingham, M Nakano, L Jia, Y Chen, Y Ikeda, B Mani, LJ Chen, ... Human molecular genetics 24 (13), 3880-3892, 2015 | 125 | 2015 |
| Glaucoma associated with Boston type I keratoprosthesis R Kamyar, JS Weizer, FH De Paula, JD Stein, SE Moroi, D John, ... Cornea 31 (2), 134-139, 2012 | 119 | 2012 |
| Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss SJ Loomis, JH Kang, RN Weinreb, BL Yaspan, JNC Bailey, ... Ophthalmology 121 (2), 508-516, 2014 | 117 | 2014 |
| Genome-wide association study and meta-analysis of intraocular pressure AB Ozel, SE Moroi, DM Reed, M Nika, CM Schmidt, S Akbari, K Scott, ... Human genetics 133, 41-57, 2014 | 115 | 2014 |
| Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene … DJ Brown, TB Kim, EM Petty, CA Downs, DM Martin, PJ Strouse, SE Moroi, ... The American Journal of Human Genetics 71 (3), 618-624, 2002 | 110 | 2002 |
