Adam M Dubis, Robert F Cooper, Jonathan Aboshiha, Christopher S Langlo, Venki Sundaram, Benjamin Liu, Frederick Collison, Gerald A Fishman, Anthony T Moore, Andrew R Webster, Alfredo Dubra, Joseph Carroll, Michel Michaelides. Invest Ophthalmol Vis Sci 2014
Times Cited: 54
Times Cited: 54
Times Cited
Times Co-cited
Similarity
In vivo imaging of human cone photoreceptor inner segments.
Drew Scoles, Yusufu N Sulai, Christopher S Langlo, Gerald A Fishman, Christine A Curcio, Joseph Carroll, Alfredo Dubra. Invest Ophthalmol Vis Sci 2014
Drew Scoles, Yusufu N Sulai, Christopher S Langlo, Gerald A Fishman, Christine A Curcio, Joseph Carroll, Alfredo Dubra. Invest Ophthalmol Vis Sci 2014
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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
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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Retinal structure and function in achromatopsia: implications for gene therapy.
Venki Sundaram, Caroline Wilde, Jonathan Aboshiha, Jill Cowing, Colin Han, Christopher S Langlo, Ravinder Chana, Alice E Davidson, Panagiotis I Sergouniotis, James W Bainbridge,[...]. Ophthalmology 2014
Venki Sundaram, Caroline Wilde, Jonathan Aboshiha, Jill Cowing, Colin Han, Christopher S Langlo, Ravinder Chana, Alice E Davidson, Panagiotis I Sergouniotis, James W Bainbridge,[...]. Ophthalmology 2014
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Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia.
Christopher S Langlo, Emily J Patterson, Brian P Higgins, Phyllis Summerfelt, Moataz M Razeen, Laura R Erker, Maria Parker, Frederick T Collison, Gerald A Fishman, Christine N Kay,[...]. Invest Ophthalmol Vis Sci 2016
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44
A prospective longitudinal study of retinal structure and function in achromatopsia.
Jonathan Aboshiha, Adam M Dubis, Jill Cowing, Rachel T A Fahy, Venki Sundaram, James W Bainbridge, Robin R Ali, Alfredo Dubra, Marko Nardini, Andrew R Webster,[...]. Invest Ophthalmol Vis Sci 2014
Jonathan Aboshiha, Adam M Dubis, Jill Cowing, Rachel T A Fahy, Venki Sundaram, James W Bainbridge, Robin R Ali, Alfredo Dubra, Marko Nardini, Andrew R Webster,[...]. Invest Ophthalmol Vis Sci 2014
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Human photoreceptor topography.
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Noninvasive imaging of the human rod photoreceptor mosaic using a confocal adaptive optics scanning ophthalmoscope.
Alfredo Dubra, Yusufu Sulai, Jennifer L Norris, Robert F Cooper, Adam M Dubis, David R Williams, Joseph Carroll. Biomed Opt Express 2011
Alfredo Dubra, Yusufu Sulai, Jennifer L Norris, Robert F Cooper, Adam M Dubis, David R Williams, Joseph Carroll. Biomed Opt Express 2011
38
Reflective afocal broadband adaptive optics scanning ophthalmoscope.
Alfredo Dubra, Yusufu Sulai. Biomed Opt Express 2011
Alfredo Dubra, Yusufu Sulai. Biomed Opt Express 2011
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A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia.
Susanne Kohl, Frauke Coppieters, Françoise Meire, Simone Schaich, Susanne Roosing, Christina Brennenstuhl, Sylvia Bolz, Maria M van Genderen, Frans C C Riemslag, Robert Lukowski,[...]. Am J Hum Genet 2012
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Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia.
Susanne Kohl, Britta Baumann, Thomas Rosenberg, Ulrich Kellner, Birgit Lorenz, Maria Vadalà, Samuel G Jacobson, Bernd Wissinger. Am J Hum Genet 2002
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In vivo imaging of the photoreceptor mosaic of a rod monochromat.
Joseph Carroll, Stacey S Choi, David R Williams. Vision Res 2008
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Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography.
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Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia.
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Reliability and Repeatability of Cone Density Measurements in Patients with Congenital Achromatopsia.
Mortada A Abozaid, Christopher S Langlo, Adam M Dubis, Michel Michaelides, Sergey Tarima, Joseph Carroll. Adv Exp Med Biol 2016
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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
Susanne Kohl, Balazs Varsanyi, Gesine Abadin Antunes, Britta Baumann, Carel B Hoyng, Herbert Jägle, Thomas Rosenberg, Ulrich Kellner, Birgit Lorenz, Roberto Salati,[...]. Eur J Hum Genet 2005
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Mervyn G Thomas, Anil Kumar, Susanne Kohl, Frank A Proudlock, Irene Gottlob. Ophthalmology 2011
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REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.
Christopher S Langlo, Laura R Erker, Maria Parker, Emily J Patterson, Brian P Higgins, Phyllis Summerfelt, Moataz M Razeen, Frederick T Collison, Gerald A Fishman, Christine N Kay,[...]. Retina 2017
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Longitudinal study of cone photoreceptors during retinal degeneration and in response to ciliary neurotrophic factor treatment.
Katherine E Talcott, Kavitha Ratnam, Sanna M Sundquist, Anna S Lucero, Brandon J Lujan, Weng Tao, Travis C Porco, Austin Roorda, Jacque L Duncan. Invest Ophthalmol Vis Sci 2011
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Relationship between foveal cone specialization and pit morphology in albinism.
Melissa A Wilk, John T McAllister, Robert F Cooper, Adam M Dubis, Teresa N Patitucci, Phyllis Summerfelt, Jennifer L Anderson, Kimberly E Stepien, Deborah M Costakos, Thomas B Connor,[...]. Invest Ophthalmol Vis Sci 2014
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27
Adaptive Optics Retinal Imaging in CNGA3-Associated Achromatopsia: Retinal Characterization, Interocular Symmetry, and Intrafamilial Variability.
Michalis Georgiou, Katie M Litts, Angelos Kalitzeos, Christopher S Langlo, Thomas Kane, Navjit Singh, Melissa Kassilian, Nashila Hirji, Neruban Kumaran, Alfredo Dubra,[...]. Invest Ophthalmol Vis Sci 2019
Michalis Georgiou, Katie M Litts, Angelos Kalitzeos, Christopher S Langlo, Thomas Kane, Navjit Singh, Melissa Kassilian, Nashila Hirji, Neruban Kumaran, Alfredo Dubra,[...]. Invest Ophthalmol Vis Sci 2019
50
Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy.
Livia S Carvalho, Jianhua Xu, Rachael A Pearson, Alexander J Smith, James W Bainbridge, Lynsie M Morris, Steven J Fliesler, Xi-Qin Ding, Robin R Ali. Hum Mol Genet 2011
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25
Observation of cone and rod photoreceptors in normal subjects and patients using a new generation adaptive optics scanning laser ophthalmoscope.
David Merino, Jacque L Duncan, Pavan Tiruveedhula, Austin Roorda. Biomed Opt Express 2011
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25
Genetic etiology and clinical consequences of complete and incomplete achromatopsia.
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Early signs of longitudinal progressive cone photoreceptor degeneration in achromatopsia.
Mervyn George Thomas, Rebecca Jane McLean, Susanne Kohl, Viral Sheth, Irene Gottlob. Br J Ophthalmol 2012
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The cone dysfunction syndromes.
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Repeatability of in vivo parafoveal cone density and spacing measurements.
Robert Garrioch, Christopher Langlo, Adam M Dubis, Robert F Cooper, Alfredo Dubra, Joseph Carroll. Optom Vis Sci 2012
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Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.
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CNGA3 mutations in hereditary cone photoreceptor disorders.
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High-resolution imaging with adaptive optics in patients with inherited retinal degeneration.
Jacque L Duncan, Yuhua Zhang, Jarel Gandhi, Chiaki Nakanishi, Mohammad Othman, Kari E H Branham, Anand Swaroop, Austin Roorda. Invest Ophthalmol Vis Sci 2007
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Achromatopsia: clinical features, molecular genetics, animal models and therapeutic options.
Nashila Hirji, Jonathan Aboshiha, Michalis Georgiou, James Bainbridge, Michel Michaelides. Ophthalmic Genet 2018
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Gene therapy rescues cone function in congenital achromatopsia.
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22
A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene.
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22
The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic.
Joseph Carroll, Alfredo Dubra, Jessica C Gardner, Liliana Mizrahi-Meissonnier, Robert F Cooper, Adam M Dubis, Rick Nordgren, Mohamed Genead, Thomas B Connor, Kimberly E Stepien,[...]. Invest Ophthalmol Vis Sci 2012
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Spatial and temporal variation of rod photoreceptor reflectance in the human retina.
Robert F Cooper, Adam M Dubis, Ashavini Pavaskar, Jungtae Rha, Alfredo Dubra, Joseph Carroll. Biomed Opt Express 2011
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Adaptive optics microperimetry and OCT images show preserved function and recovery of cone visibility in macular telangiectasia type 2 retinal lesions.
Qinyun Wang, William S Tuten, Brandon J Lujan, Jennifer Holland, Paul S Bernstein, Steven D Schwartz, Jacque L Duncan, Austin Roorda. Invest Ophthalmol Vis Sci 2015
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Normal Perceptual Sensitivity Arising From Weakly Reflective Cone Photoreceptors.
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Evaluating Descriptive Metrics of the Human Cone Mosaic.
Robert F Cooper, Melissa A Wilk, Sergey Tarima, Joseph Carroll. Invest Ophthalmol Vis Sci 2016
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Restoration of cone vision in the CNGA3-/- mouse model of congenital complete lack of cone photoreceptor function.
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Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.
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Assessing Photoreceptor Structure in Retinitis Pigmentosa and Usher Syndrome.
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20
Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy.
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High-resolution images of retinal structure in patients with choroideremia.
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18
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.