Elizabeth A. M. Windsor

Johns Hopkins University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

27h-index4.0kcitations47works0.02yr avg
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Research Topics

Retinal Development and Disorders(33), Retinal Diseases and Treatments(25), Photoreceptor and optogenetics research(13), Retinal and Optic Conditions(9), Advanced Fluorescence Microscopy Techniques(5)

Publications45 total

Risk factors for poor visual outcome in patients with idiopathic intracranial hypertension
Neurology·2015· 87 citedOpen Access
Quality of life in idiopathic intracranial hypertension at diagnosis
Neurology·2015· 102 citedOpen Access
Assessment of Signs of Anterior Blepharitis Using Standardized Color Photographs
Cornea·2013· 9 citedOpen Access
Retinal and Visual Function Phenotype Associated With CEP290 Mutations
Investigative Ophthalmology & Visual Science·2010
Evaluation of Central Visual Function Using a Foveo-Papillary Profile in Macular/Retinal Degenerations Caused by ABCA4 (ABCR) Mutations
Investigative Ophthalmology & Visual Science·2010
Normal Central Retinal Function and Structure Preserved in Retinitis Pigmentosa
Investigative Ophthalmology & Visual Science·2010· 93 cited
<i>CERKL</i>Mutations Cause an Autosomal Recessive Cone-Rod Dystrophy with Inner Retinopathy
Investigative Ophthalmology & Visual Science·2009· 88 cited
Leber Congenital Amaurosis gene therapy clinical trial
Journal of Vision·2009· 3 citedOpen Access
Vision 1 Year after Gene Therapy for Leber's Congenital Amaurosis
New England Journal of Medicine·2009· 199 citedOpen Access
Human <i>RPE65</i> Gene Therapy for Leber Congenital Amaurosis: Persistence of Early Visual Improvements and Safety at 1 Year
Human Gene Therapy·2009· 311 citedOpen Access
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization.
PubMed·2009· 32 citedOpen Access
Predicting Abca4 Disease Progression: A Strategy for Gene Therapy
Investigative Ophthalmology & Visual Science·2009
CERKL Mutations Cause Retina-Wide Cone and Rod Disease With Prominent Maculopathy
2009
Defining the Residual Vision in Leber Congenital Amaurosis Caused by<i>RPE65</i>Mutations
Investigative Ophthalmology & Visual Science·2009· 121 citedOpen Access
Disease Boundaries in the Retina of Patients with Usher Syndrome Caused by<i>MYO7A</i>Gene Mutations
Investigative Ophthalmology & Visual Science·2009· 91 cited
ABCA4 disease progression and a proposed strategy for gene therapy
Human Molecular Genetics·2008· 185 citedOpen Access
Photoreceptor Layer Topography in Children with Leber Congenital Amaurosis Caused by<i>RPE65</i>Mutations
Investigative Ophthalmology & Visual Science·2008· 99 citedOpen Access
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics
Proceedings of the National Academy of Sciences·2008· 661 citedOpen Access
Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic wavelets
Eye·2008· 17 citedOpen Access
Retinal Disease in Usher Syndrome III Caused by Mutations in the Clarin-1 Gene
Investigative Ophthalmology & Visual Science·2008· 82 cited
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Frequent Co-authors

Samuel G. Jacobson(41), Artur V. Cideciyan(40), Sharon Schwartz(40), Tomás S. Alemán(35), Alexander Sumaroka(33), Alejandro J. Román(27), Edwin M. Stone(26), Elise Héon(7), Małgorzata Świder(7), Janet D. Steinberg(7), Waldo Herrera(7), Sanford L. Boye(6), T. S. Aleman(6), Shalesh Kaushal(5), William W. Hauswirth(5), Krzysztof Palczewski(5), Jean Bennett(5), Geoffrey K. Aguirre(5), E.E. Smilko(5), Terence R. Flotte(4)