Edwin M. Stone
Affiliations: | University of Iowa, Iowa City, IA |
Area:
Inherited eye diseaseGoogle:
"Edwin Stone"Mean distance: 20.75 (cluster 32)
Children
Sign in to add trainee| Amanda C Owings | research assistant | 2006-2008 | University of Iowa |
| John H. Fingert | grad student | 2000 | University of Iowa |
| Suma P. Shankar | grad student | 2005 | University of Iowa |
| Emily I. Schindler | grad student | 2011 | University of Iowa |
| Alex H. Wagner | grad student | 2014 | University of Iowa |
| Stewart Thompson | post-doc | University of Iowa |
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Publications
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| Burnight ER, Wiley LA, Mullin NK, et al. (2023) CRISPRi-Mediated Treatment of Dominant Rhodopsin-Associated Retinitis Pigmentosa. The Crispr Journal. 6: 502-513 |
| Burnight ER, Fenner BJ, Han IC, et al. (2023) Demonstration of the pathogenicity of a common non-exomic mutation in ABCA4 using iPSC-derived retinal organoids and retrospective clinical data. Human Molecular Genetics |
| Boese EA, Drack AV, Roos BR, et al. (2023) GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract Surgery. Jama Ophthalmology |
| Voigt AP, Mullin NK, Navratil EM, et al. (2023) GENE EXPRESSION WITHIN A HUMAN CHOROIDAL NEOVASCULAR MEMBRANE USING SPATIAL TRANSCRIPTOMICS. Biorxiv : the Preprint Server For Biology |
| Boese EA, Alward WLM, Kwon YH, et al. (2023) Thrombospondin Mutations and Primary Congenital Glaucoma Patients in a United States Population. Journal of Glaucoma |
| Tejan-Kamara AZ, Boese EA, Pouw A, et al. (2023) Mutations in EFEMP1 in patients with juvenile open-angle glaucoma (JOAG). Ophthalmology. Glaucoma |
| Ricca AM, Han IC, Hoffman J, et al. (2023) Macular Atrophy and Phenotypic Variability in Autosomal Dominant Stargardt-like Macular Dystrophy due to PROM1 mutation. Retina (Philadelphia, Pa.) |
| Mullin NK, Voigt AP, Boese EA, et al. (2023) Transcriptomic and chromatin accessibility analysis of the human macular and peripheral retinal pigment epithelium at the single cell level. The American Journal of Pathology |
| Han IC, Wiley LA, Ochoa D, et al. (2022) Characterization of a novel Pde6b-deficient rat model of retinal degeneration and treatment with adeno-associated virus (AAV) gene therapy. Gene Therapy |
| Quigley HA, Stone EM, Fingert JH. (2022) Familial Glaucoma-A Pedigree Revisited With Genetic Testing After 70 Years. Jama Ophthalmology |