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Times Cited: 68
Times Cited
Times Co-cited
Similarity
In vivo imaging of human cone photoreceptor inner segments.
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Retinal structure and function in achromatopsia: implications for gene therapy.
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Photoreceptor structure and function in patients with congenital achromatopsia.
Mohamed A Genead, Gerald A Fishman, Jungtae Rha, Adam M Dubis, Daniela Maria O Bonci, Alfredo Dubra, Edwin M Stone, Maureen Neitz, Joseph Carroll. Invest Ophthalmol Vis Sci 2011
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Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone health.
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REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.
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Noninvasive imaging of the human rod photoreceptor mosaic using a confocal adaptive optics scanning ophthalmoscope.
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Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia.
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Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia.
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A prospective longitudinal study of retinal structure and function in achromatopsia.
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A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia.
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Relationship between foveal cone specialization and pit morphology in albinism.
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An Automated Reference Frame Selection (ARFS) Algorithm for Cone Imaging with Adaptive Optics Scanning Light Ophthalmoscopy.
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Characterization of Retinal Structure in ATF6-Associated Achromatopsia.
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Early signs of longitudinal progressive cone photoreceptor degeneration in achromatopsia.
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ASSESSING PHOTORECEPTOR STRUCTURE ASSOCIATED WITH ELLIPSOID ZONE DISRUPTIONS VISUALIZED WITH OPTICAL COHERENCE TOMOGRAPHY.
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Michalis Georgiou, Navjit Singh, Thomas Kane, Anthony G Robson, Angelos Kalitzeos, Nashila Hirji, Andrew R Webster, Alfredo Dubra, Joseph Carroll, Michel Michaelides. Invest Ophthalmol Vis Sci 2020
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The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial.
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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
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In vivo imaging of a cone mosaic in a patient with achromatopsia associated with a GNAT2 variant.
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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.