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Edwin M. Stone

Affiliations: 
University of Iowa, Iowa City, IA 
Area:
Inherited eye disease
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"Edwin Stone"
Mean distance: 20.75 (cluster 32)
 
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Parents

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Children

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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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BETA: Related publications

Publications

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Mullin NK, Bohrer LR, Anfinson KR, et al. (2024) Exonic splice variant discovery using in vitro models of inherited retinal disease. Hgg Advances. 100357
Scheetz TE, Tollefson MR, Roos BR, et al. (2024) METTL23 Variants and Patients With Normal-Tension Glaucoma. Jama Ophthalmology
Mullin NK, Bohrer LR, Voigt AP, et al. (2024) NR2E3 loss disrupts photoreceptor cell maturation and fate in human organoid models of retinal development. The Journal of Clinical Investigation
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.)
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