Edwin M. Stone - Concepedia

Author

Edwin M. Stone

University of Iowa ORCID

Also Known As

Albert O. Edwards, Budd Tucker, E M Stone, E STONE, E Stone, E. M. Stone, E. M. Stoned, E. STONE, E. Stone, E.M. Stone

857

Publications

49.5K

Citations

118

H-Index

265

Concepts

All Affiliations

University of Iowa Howard Hughes Medical Institute University of Pennsylvania Penn Presbyterian Medical Center University of Iowa Hospitals and Clinics

About

Edwin M. Stone is an author at University of Iowa specializing in medicine, genetics, and ophthalmology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	73	164	21.9K
2	Engineering	11	11	1.1K
3	Health Sciences	4	4	510
4	Arts	1	1	268
5	Education	1	1	23

Edwin M. Stone

396

Publications

43.1K

Citations

113

H-Index

Page 1

	Year	Citations
Safety and Efficacy of Gene Transfer for Leber's Congenital Amaurosis Albert M. Maguire, Francesca Simonelli, Eric A. Pierce, New England Journal of Medicine Ocular DiseaseGeneticsImmunologyPathologyDisease Gene Identification	2008	2.1K
Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65 -mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial Stephen R. Russell, Jean Bennett, Jennifer Wellman, The Lancet Ocular DiseaseRetinaOphthalmologyExperimental OphthalmologyVoretigene Neparvovec	2017	1.8K
Identification of a Gene That Causes Primary Open Angle Glaucoma Edwin M. Stone, John H. Fingert, Wallace L.M. Alward, Science	1997	1.4K
Mutations in the <i>SMAD4/DPC4</i> Gene in Juvenile Polyposis James R. Howe, Stina Roth, John C. Ringold, Science	1998	895
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial Albert M. Maguire, Katherine A. High, Alberto Auricchio, The Lancet Gene TherapiesGenetic DisorderGeneticsClinical TrialsTranslational Research	2009	849
The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions Val C. Sheffield, John S. Beck, Anne E. Kwitek, Genomics Sequence MotifStructural BioinformaticsSingle Base SubstitutionsGeneticsNatural Sciences	1993	675
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics Artur V. Cideciyan, Tomás S. Alemán, Sanford L. Boye, Proceedings of the National Academy of Sciences Slow Rod KineticsGene TherapiesOcular DiseaseHuman Gene TherapyRpe65 Gene	2008	660
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate Neena B. Haider, Samuel G. Jacobson, Artur V. Cideciyan, Nature Genetics Ocular DiseaseDevelopmental BiologySignal TransductionOphthalmologyRetina	2000	497
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy Edwin M. Stone, Andrew Lotery, Francis L. Munier, Nature Genetics Ocular DiseaseRetinal DystrophyOphthalmologyGenetic DisorderMedicine	1999	491
Cloning and sequencing of a deoxyribonucleic acid copy of glyceraldehyde 3-phosphate dehydrogenase messenger ribonucleic acid isolated from chicken muscle Achilles Dugaiczyk, Jay A. Haron, Edwin M. Stone, Biochemistry	1983	481

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