1 | Seasonal Variation in ATP-Induced Retinal Damage in the Cone-Dominant 13-Lined Ground Squirrel. (Bowie OR, Follett HM, Yu CT, Guillaume C, Summerfelt PM, Manfredonia N, Grieshop J, Merriman DK, Tarima S, Carroll J) Transl Vis Sci Technol 2024 Nov 04;13(11):5 |
1 | Emc1 is essential for vision and zebrafish photoreceptor outer segment morphogenesis. (McCann T, Sundaramurthi H, Walsh C, Virdi S, Alvarez Y, Sapetto-Rebow B, Collery RF, Carter SP, Moran A, Mulholland R, O'Connor JJ, Taylor MR, Rauch N, Starostik MR, English MA, Swaroop A, Geisler R, Reynolds AL, Kennedy BN) FASEB J 2024 Oct 15;38(19):e70086 |
1 | Chemically induced cone degeneration in the 13-lined ground squirrel. (Follett HM, Warr E, Grieshop J, Yu CT, Gaffney M, Bowie OR, Lee JW, Tarima S, Merriman DK, Carroll J) Vis Neurosci 2024 May 10;41:E002 1 Citation |
3 | Human iPSC-derived photoreceptor transplantation in the cone dominant 13-lined ground squirrel. (Yu CT, Kandoi S, Periasamy R, Reddy LVK, Follett HM, Summerfelt P, Martinez C, Guillaume C, Bowie O, Connor TB, Lipinski DM, Allen KP, Merriman DK, Carroll J, Lamba DA) Stem Cell Reports 2024 Mar 12;19(3):331-342 4 Citations |
1 | Late gene therapy limits the restoration of retinal function in a mouse model of retinitis pigmentosa. (Scalabrino ML, Thapa M, Wang T, Sampath AP, Chen J, Field GD) Nat Commun 2023 Dec 12;14(1):8256 2 Citations |
1 | Cones and cone pathways remain functional in advanced retinal degeneration. (Ellis EM, Paniagua AE, Scalabrino ML, Thapa M, Rathinavelu J, Jiao Y, Williams DS, Field GD, Fain GL, Sampath AP) Curr Biol 2023 Apr 24;33(8):1513-1522.e4 13 Citations |
1 | Change in Cone Structure Over 24 Months in USH2A-Related Retinal Degeneration. (Duncan JL, Liang W, Maguire MG, Porco TC, Wong J, Audo I, Cava JA, Grieve K, Kalitzeos A, Kreis J, Michaelides M, Norberg N, Paques M, Carroll J, Foundation Fighting Blindness Consortium Investigator Group) Am J Ophthalmol 2023 Aug;252:77-93 8 Citations |
1 | Neuroscience: Visual restoration with optogenetics. (Scalabrino ML, Field GD) Curr Biol 2023 Feb 06;33(3):R110-R112 |
1 | Cone Structure and Function in RPGR- and USH2A-Associated Retinal Degeneration. (Micevych PS, Wong J, Zhou H, Wang RK, Porco TC, Carroll J, Roorda A, Duncan JL) Am J Ophthalmol 2023 Jun;250:1-11 2 Citations |
1 | Robust cone-mediated signaling persists late into rod photoreceptor degeneration. (Scalabrino ML, Thapa M, Chew LA, Zhang E, Xu J, Sampath AP, Chen J, Field GD) Elife 2022 Aug 30;11 7 Citations |
1 | Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease Severity. (Lad EM, Duncan JL, Liang W, Maguire MG, Ayala AR, Audo I, Birch DG, Carroll J, Cheetham JK, Durham TA, Fahim AT, Loo J, Deng Z, Mukherjee D, Heon E, Hufnagel RB, Guan B, Iannaccone A, Jaffe GJ, Kay CN, Michaelides M, Pennesi ME, Vincent A, Weng CY, Farsiu S, Foundation Fighting Blindness Consortium Investigator Group) Am J Ophthalmol 2022 Dec;244:98-116 20 Citations |
1 | Photobiomodulation preserves mitochondrial redox state and is retinoprotective in a rodent model of retinitis pigmentosa. (Gopalakrishnan S, Mehrvar S, Maleki S, Schmitt H, Summerfelt P, Dubis AM, Abroe B, Connor TB Jr, Carroll J, Huddleston W, Ranji M, Eells JT) Sci Rep 2020 Nov 23;10(1):20382 29 Citations |
1 | ENHANCED S-CONE SYNDROME: VISUAL FUNCTION, CROSS-SECTIONAL IMAGING, AND CELLULAR STRUCTURE WITH ADAPTIVE OPTICS OPHTHALMOSCOPY. (Ammar MJ, Scavelli KT, Uyhazi KE, Bedoukian EC, Serrano LW, Edelstein ID, Vergilio G, Cooper RF, Morgan JIW, Kumar P, Aleman TS) Retin Cases Brief Rep 2021 Nov 01;15(6):694-701 12 Citations |
1 | Photoreceptor Survival Is Regulated by GSTO1-1 in the Degenerating Retina. (Fernando N, Wooff Y, Aggio-Bruce R, Chu-Tan JA, Jiao H, Dietrich C, Rutar M, Rooke M, Menon D, Eells JT, Valter K, Board PG, Provis J, Natoli R) Invest Ophthalmol Vis Sci 2018 Sep 04;59(11):4362-4374 9 Citations |
1 | Brain-Derived Neurotrophic Factor as a Treatment Option for Retinal Degeneration. (Daly C, Ward R, Reynolds AL, Galvin O, Collery RF, Kennedy BN) Adv Exp Med Biol 2018;1074:465-471 18 Citations |
2 | Photoreceptor-Based Biomarkers in AOSLO Retinal Imaging. (Litts KM, Cooper RF, Duncan JL, Carroll J) Invest Ophthalmol Vis Sci 2017 May 01;58(6):BIO255-BIO267 50 Citations |
2 | Loss of Zebrafish Mfrp Causes Nanophthalmia, Hyperopia, and Accumulation of Subretinal Macrophages. (Collery RF, Volberding PJ, Bostrom JR, Link BA, Besharse JC) Invest Ophthalmol Vis Sci 2016 Dec 01;57(15):6805-6814 31 Citations |
1 | Multimodal Imaging of Photoreceptor Structure in Choroideremia. (Sun LW, Johnson RD, Williams V, Summerfelt P, Dubra A, Weinberg DV, Stepien KE, Fishman GA, Carroll J) PLoS One 2016;11(12):e0167526 56 Citations |
1 | Single residue AAV capsid mutation improves transduction of photoreceptors in the Abca4-/- mouse and bipolar cells in the rd1 mouse and human retina ex vivo. (De Silva SR, Charbel Issa P, Singh MS, Lipinski DM, Barnea-Cramer AO, Walker NJ, Barnard AR, Hankins MW, MacLaren RE) Gene Ther 2016 Nov;23(11):767-774 26 Citations |
1 | Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations. (Bujakowska KM, Fernandez-Godino R, Place E, Consugar M, Navarro-Gomez D, White J, Bedoukian EC, Zhu X, Xie HM, Gai X, Leroy BP, Pierce EA) Genet Med 2017 Jun;19(6):643-651 48 Citations |
1 | Characterization of Fatty Acid Binding Protein 7 (FABP7) in the Murine Retina. (Su X, Tan QS, Parikh BH, Tan A, Mehta MN, Sia Wey Y, Tun SB, Li LJ, Han XY, Wong TY, Hunziker W, Luu CD, Owada Y, Barathi VA, Zhang SS, Chaurasia SS) Invest Ophthalmol Vis Sci 2016 Jun 01;57(7):3397-408 17 Citations |
1 | Long time remodeling during retinal degeneration evaluated by optical coherence tomography, immunocytochemistry and fundus autofluorescence. (Pinilla I, Fernández-Sánchez L, Segura FJ, Sánchez-Cano AI, Tamarit JM, Fuentes-Broto L, Eells JT, Lax P, Cuenca N) Exp Eye Res 2016 Sep;150:122-34 24 Citations |
2 | In vivo imaging of human cone photoreceptor inner segments. (Scoles D, Sulai YN, Langlo CS, Fishman GA, Curcio CA, Carroll J, Dubra A) Invest Ophthalmol Vis Sci 2014 Jun 06;55(7):4244-51 321 Citations |
1 | Urocortin 2 treatment is protective in excitotoxic retinal degeneration. (Szabadfi K, Kiss P, Reglodi D, Fekete EM, Tamas A, Danyadi B, Atlasz T, Gabriel R) Acta Physiol Hung 2014 Mar;101(1):67-76 4 Citations |
1 | Relationship between foveal cone structure and clinical measures of visual function in patients with inherited retinal degenerations. (Ratnam K, Carroll J, Porco TC, Duncan JL, Roorda A) Invest Ophthalmol Vis Sci 2013 Aug 28;54(8):5836-47 94 Citations |
1 | Assessment of tropism and effectiveness of new primate-derived hybrid recombinant AAV serotypes in the mouse and primate retina. (Charbel Issa P, De Silva SR, Lipinski DM, Singh MS, Mouravlev A, You Q, Barnard AR, Hankins MW, During MJ, Maclaren RE) PLoS One 2013;8(4):e60361 43 Citations |
1 | Reversal of end-stage retinal degeneration and restoration of visual function by photoreceptor transplantation. (Singh MS, Charbel Issa P, Butler R, Martin C, Lipinski DM, Sekaran S, Barnard AR, MacLaren RE) Proc Natl Acad Sci U S A 2013 Jan 15;110(3):1101-6 213 Citations |
3 | The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic. (Carroll J, Dubra A, Gardner JC, Mizrahi-Meissonnier L, Cooper RF, Dubis AM, Nordgren R, Genead M, Connor TB Jr, Stepien KE, Sharon D, Hunt DM, Banin E, Hardcastle AJ, Moore AT, Williams DR, Fishman G, Neitz J, Neitz M, Michaelides M) Invest Ophthalmol Vis Sci 2012 Dec 05;53(13):8006-15 83 Citations |
1 | NMNAT1 mutations cause Leber congenital amaurosis. (Falk MJ, Zhang Q, Nakamaru-Ogiso E, Kannabiran C, Fonseca-Kelly Z, Chakarova C, Audo I, Mackay DS, Zeitz C, Borman AD, Staniszewska M, Shukla R, Palavalli L, Mohand-Said S, Waseem NH, Jalali S, Perin JC, Place E, Ostrovsky J, Xiao R, Bhattacharya SS, Consugar M, Webster AR, Sahel JA, Moore AT, Berson EL, Liu Q, Gai X, Pierce EA) Nat Genet 2012 Sep;44(9):1040-5 165 Citations |
1 | Optimization of in vivo confocal autofluorescence imaging of the ocular fundus in mice and its application to models of human retinal degeneration. (Charbel Issa P, Singh MS, Lipinski DM, Chong NV, Delori FC, Barnard AR, MacLaren RE) Invest Ophthalmol Vis Sci 2012 Feb;53(2):1066-75 57 Citations |
1 | Characterization of a dominant cone degeneration in a green fluorescent protein-reporter mouse with disruption of Loci associated with human dominant retinal dystrophy. (Lipinski DM, Yusuf M, Barnard AR, Damant C, Charbel Issa P, Singh MS, Lee E, Davies WL, Volpi EV, MacLaren RE) Invest Ophthalmol Vis Sci 2011 Aug 22;52(9):6617-23 12 Citations |
1 | Photobiomodulation protects the retina from light-induced photoreceptor degeneration. (Albarracin R, Eells J, Valter K) Invest Ophthalmol Vis Sci 2011 Jun 01;52(6):3582-92 118 Citations |
1 | Adaptive optics retinal imaging: emerging clinical applications. (Godara P, Dubis AM, Roorda A, Duncan JL, Carroll J) Optom Vis Sci 2010 Dec;87(12):930-41 139 Citations |
1 | Unusual adaptive optics findings in a patient with bilateral maculopathy. (Godara P, Rha J, Tait DM, McAllister J, Dubis A, Carroll J, Weinberg DV) Arch Ophthalmol 2010 Feb;128(2):253-4 9 Citations |
1 | Urocortin 2 protects against retinal degeneration following bilateral common carotid artery occlusion in the rat. (Szabadfi K, Atlasz T, Reglodi D, Kiss P, Dányádi B, Fekete EM, Zorrilla EP, Tamás A, Szabó K, Gábriel R) Neurosci Lett 2009 May 08;455(1):42-5 18 Citations |
1 | Adaptive optics retinal imaging: applications for studying retinal degeneration. (Carroll J) Arch Ophthalmol 2008 Jun;126(6):857-8 11 Citations |
1 | Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod-cone degeneration interval and identifies ancestral disease-transmitting chromosome. (Goldstein O, Zangerl B, Pearce-Kelling S, Sidjanin DJ, Kijas JW, Felix J, Acland GM, Aguirre GD) Genomics 2006 Nov;88(5):541-50 63 Citations |
1 | High-resolution retinal imaging of cone-rod dystrophy. (Wolfing JI, Chung M, Carroll J, Roorda A, Williams DR) Ophthalmology 2006 Jun;113(6):1019.e1 158 Citations |
1 | Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome. (Fath MA, Mullins RF, Searby C, Nishimura DY, Wei J, Rahmouni K, Davis RE, Tayeh MK, Andrews M, Yang B, Sigmund CD, Stone EM, Sheffield VC) Hum Mol Genet 2005 May 01;14(9):1109-18 166 Citations |