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Times Cited: 95
Times Cited
Times Co-cited
Similarity
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 Russell, Jean Bennett, Jennifer A Wellman, Daniel C Chung, Zi-Fan Yu, Amy Tillman, Janet Wittes, Julie Pappas, Okan Elci, Sarah McCague,[...]. Lancet 2017
Stephen Russell, Jean Bennett, Jennifer A Wellman, Daniel C Chung, Zi-Fan Yu, Amy Tillman, Janet Wittes, Julie Pappas, Okan Elci, Sarah McCague,[...]. Lancet 2017
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Non-syndromic retinitis pigmentosa.
Sanne K Verbakel, Ramon A C van Huet, Camiel J F Boon, Anneke I den Hollander, Rob W J Collin, Caroline C W Klaver, Carel B Hoyng, Ronald Roepman, B Jeroen Klevering. Prog Retin Eye Res 2018
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Effect of gene therapy on visual function in Leber's congenital amaurosis.
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Special Issue Introduction: Inherited Retinal Disease: Novel Candidate Genes, Genotype-Phenotype Correlations, and Inheritance Models.
Frans P M Cremers, Camiel J F Boon, Kinga Bujakowska, Christina Zeitz. Genes (Basel) 2018
Frans P M Cremers, Camiel J F Boon, Kinga Bujakowska, Christina Zeitz. Genes (Basel) 2018
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The molecular basis of human retinal and vitreoretinal diseases.
Wolfgang Berger, Barbara Kloeckener-Gruissem, John Neidhardt. Prog Retin Eye Res 2010
Wolfgang Berger, Barbara Kloeckener-Gruissem, John Neidhardt. Prog Retin Eye Res 2010
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Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
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Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing.
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Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease.
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Safety and efficacy of gene transfer for Leber's congenital amaurosis.
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Long-term effect of gene therapy on Leber's congenital amaurosis.
James W B Bainbridge, Manjit S Mehat, Venki Sundaram, Scott J Robbie, Susie E Barker, Caterina Ripamonti, Anastasios Georgiadis, Freya M Mowat, Stuart G Beattie, Peter J Gardner,[...]. N Engl J Med 2015
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Emerging therapies for inherited retinal degeneration.
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The mechanism of cone cell death in Retinitis Pigmentosa.
Peter A Campochiaro, Tahreem A Mir. Prog Retin Eye Res 2018
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Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases.
Mor Hanany, Carlo Rivolta, Dror Sharon. Proc Natl Acad Sci U S A 2020
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Biochemical adaptations of the retina and retinal pigment epithelium support a metabolic ecosystem in the vertebrate eye.
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7
Rod-derived cone viability factor promotes cone survival by stimulating aerobic glycolysis.
Najate Aït-Ali, Ram Fridlich, Géraldine Millet-Puel, Emmanuelle Clérin, François Delalande, Céline Jaillard, Frédéric Blond, Ludivine Perrocheau, Sacha Reichman, Leah C Byrne,[...]. Cell 2015
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Development of a gene-editing approach to restore vision loss in Leber congenital amaurosis type 10.
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7
Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium.
Debra A Thompson, Robin R Ali, Eyal Banin, Kari E Branham, John G Flannery, David M Gamm, William W Hauswirth, John R Heckenlively, Alessandro Iannaccone, K Thiran Jayasundera,[...]. Invest Ophthalmol Vis Sci 2015
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10
Toward an elucidation of the molecular genetics of inherited retinal degenerations.
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Efficacy, Safety, and Durability of Voretigene Neparvovec-rzyl in RPE65 Mutation-Associated Inherited Retinal Dystrophy: Results of Phase 1 and 3 Trials.
Albert M Maguire, Stephen Russell, Jennifer A Wellman, Daniel C Chung, Zi-Fan Yu, Amy Tillman, Janet Wittes, Julie Pappas, Okan Elci, Kathleen A Marshall,[...]. Ophthalmology 2019
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Clinical characteristics and current therapies for inherited retinal degenerations.
José-Alain Sahel, Katia Marazova, Isabelle Audo. Cold Spring Harb Perspect Med 2014
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Gene Therapy in Retinal Dystrophies.
Lucia Ziccardi, Viviana Cordeddu, Lucia Gaddini, Andrea Matteucci, Mariacristina Parravano, Fiorella Malchiodi-Albedi, Monica Varano. Int J Mol Sci 2019
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Visual Acuity Change Over 24 Months and Its Association With Foveal Phenotype and Genotype in Individuals With Stargardt Disease: ProgStar Study Report No. 10.
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18
Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect.
Artur V Cideciyan, Samuel G Jacobson, Arlene V Drack, Allen C Ho, Jason Charng, Alexandra V Garafalo, Alejandro J Roman, Alexander Sumaroka, Ian C Han, Maria D Hochstedler,[...]. Nat Med 2019
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6
Improvement and decline in vision with gene therapy in childhood blindness.
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Samuel G Jacobson, Artur V Cideciyan, Alejandro J Roman, Alexander Sumaroka, Sharon B Schwartz, Elise Heon, William W Hauswirth. N Engl J Med 2015
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Biology and therapy of inherited retinal degenerative disease: insights from mouse models.
Shobi Veleri, Csilla H Lazar, Bo Chang, Paul A Sieving, Eyal Banin, Anand Swaroop. Dis Model Mech 2015
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Choroideremia Gene Therapy Phase 2 Clinical Trial: 24-Month Results.
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7
Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial.
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Seeing the Light after 25 Years of Retinal Gene Therapy.
Ivana Trapani, Alberto Auricchio. Trends Mol Med 2018
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Molecular Therapies for Inherited Retinal Diseases-Current Standing, Opportunities and Challenges.
Irene Vázquez-Domínguez, Alejandro Garanto, Rob W J Collin. Genes (Basel) 2019
Irene Vázquez-Domínguez, Alejandro Garanto, Rob W J Collin. Genes (Basel) 2019
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Initial results from a first-in-human gene therapy trial on X-linked retinitis pigmentosa caused by mutations in RPGR.
Jasmina Cehajic-Kapetanovic, Kanmin Xue, Cristina Martinez-Fernandez de la Camara, Anika Nanda, Alexandra Davies, Laura J Wood, Anna Paola Salvetti, M Dominik Fischer, James W Aylward, Alun R Barnard,[...]. Nat Med 2020
Jasmina Cehajic-Kapetanovic, Kanmin Xue, Cristina Martinez-Fernandez de la Camara, Anika Nanda, Alexandra Davies, Laura J Wood, Anna Paola Salvetti, M Dominik Fischer, James W Aylward, Alun R Barnard,[...]. Nat Med 2020
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Spectral-domain optical coherence tomography measures of outer segment layer progression in patients with X-linked retinitis pigmentosa.
David G Birch, Kirsten G Locke, Yuquan Wen, Kelly I Locke, Dennis R Hoffman, Donald C Hood. JAMA Ophthalmol 2013
David G Birch, Kirsten G Locke, Yuquan Wen, Kelly I Locke, Dennis R Hoffman, Donald C Hood. JAMA Ophthalmol 2013
5
Effect of Oral Valproic Acid vs Placebo for Vision Loss in Patients With Autosomal Dominant Retinitis Pigmentosa: A Randomized Phase 2 Multicenter Placebo-Controlled Clinical Trial.
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A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
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5
Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies.
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A general framework for estimating the relative pathogenicity of human genetic variants.
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Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vector.
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6
Gene therapy restores vision in a canine model of childhood blindness.
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Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success.
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A comparison of the causes of blindness certifications in England and Wales in working age adults (16-64 years), 1999-2000 with 2009-2010.
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Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement.
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Reprogramming metabolism by targeting sirtuin 6 attenuates retinal degeneration.
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8
Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.
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Beneficial effects on vision in patients undergoing retinal gene therapy for choroideremia.
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5
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.