| 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 | 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 | Retinal Gene Therapy for Usher Syndrome: Current Developments, Challenges, and Perspectives. (Dinculescu A, Link BA, Saperstein DA) Int Ophthalmol Clin 2021 Oct 01;61(4):109-124 7 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 | Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity. (Duncan JL, Liang W, Maguire MG, Audo I, Ayala AR, Birch DG, Carroll J, Cheetham JK, Esposti SD, Durham TA, Erker L, Farsiu S, Ferris FL 3rd, Heon E, Hufnagel RB, Iannaccone A, Jaffe GJ, Kay CN, Michaelides M, Pennesi ME, Sahel JA, Foundation Fighting Blindness Consortium Investigator Group) Am J Ophthalmol 2020 Nov;219:87-100 30 Citations |
| 1 | Identification of a novel pathogenic missense mutation in PRPF31 using whole exome sequencing: a case report. (Bryant L, Lozynska O, Marsh A, Papp TE, van Gorder L, Serrano LW, Gai X, Maguire AM, Aleman TS, Bennett J) Br J Ophthalmol 2019 Jun;103(6):761-767 6 Citations |
| 2 | CELLULAR IMAGING OF THE TAPETAL-LIKE REFLEX IN CARRIERS OF RPGR-ASSOCIATED RETINOPATHY. (Kalitzeos A, Samra R, Kasilian M, Tee JJL, Strampe M, Langlo C, Webster AR, Dubra A, Carroll J, Michaelides M) Retina 2019 Mar;39(3):570-580 23 Citations |
| 2 | Reliability and Repeatability of Cone Density Measurements in Patients With Stargardt Disease and RPGR-Associated Retinopathy. (Tanna P, Kasilian M, Strauss R, Tee J, Kalitzeos A, Tarima S, Visotcky A, Dubra A, Carroll J, Michaelides M) Invest Ophthalmol Vis Sci 2017 Jul 01;58(9):3608-3615 40 Citations |
| 1 | Quantitative Analysis of Retinal Structure Using Spectral-Domain Optical Coherence Tomography in RPGR-Associated Retinopathy. (Tee JJL, Carroll J, Webster AR, Michaelides M) Am J Ophthalmol 2017 Jun;178:18-26 35 Citations |
| 4 | Assessing Photoreceptor Structure in Retinitis Pigmentosa and Usher Syndrome. (Sun LW, Johnson RD, Langlo CS, Cooper RF, Razeen MM, Russillo MC, Dubra A, Connor TB Jr, Han DP, Pennesi ME, Kay CN, Weinberg DV, Stepien KE, Carroll J) Invest Ophthalmol Vis Sci 2016 May 01;57(6):2428-42 92 Citations |
| 2 | ASSESSING PHOTORECEPTOR STRUCTURE ASSOCIATED WITH ELLIPSOID ZONE DISRUPTIONS VISUALIZED WITH OPTICAL COHERENCE TOMOGRAPHY. (Scoles D, Flatter JA, Cooper RF, Langlo CS, Robison S, Neitz M, Weinberg DV, Pennesi ME, Han DP, Dubra A, Carroll J) Retina 2016 Jan;36(1):91-103 74 Citations |
| 1 | CNTF Gene Therapy Confers Lifelong Neuroprotection in a Mouse Model of Human Retinitis Pigmentosa. (Lipinski DM, Barnard AR, Singh MS, Martin C, Lee EJ, Davies WIL, MacLaren RE) Mol Ther 2015 Aug;23(8):1308-1319 67 Citations |
| 1 | Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome. (Bujakowska KM, Zhang Q, Siemiatkowska AM, Liu Q, Place E, Falk MJ, Consugar M, Lancelot ME, Antonio A, Lonjou C, Carpentier W, Mohand-Saïd S, den Hollander AI, Cremers FP, Leroy BP, Gai X, Sahel JA, van den Born LI, Collin RW, Zeitz C, Audo I, Pierce EA) Hum Mol Genet 2015 Jan 01;24(1):230-42 125 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 |
| 3 | Automatic detection of modal spacing (Yellott's ring) in adaptive optics scanning light ophthalmoscope images. (Cooper RF, Langlo CS, Dubra A, Carroll J) Ophthalmic Physiol Opt 2013 Jul;33(4):540-9 41 Citations |
| 1 | X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene. (McClements M, Davies WI, Michaelides M, Carroll J, Rha J, Mollon JD, Neitz M, MacLaren RE, Moore AT, Hunt DM) Vision Res 2013 Mar 22;80:41-50 18 Citations |
| 1 | Transgenic zebrafish expressing mutant human RETGC-1 exhibit aberrant cone and rod morphology. (Collery RF, Cederlund ML, Kennedy BN) Exp Eye Res 2013 Mar;108:120-8 9 Citations |
| 3 | Optical imaging of mitochondrial redox state in rodent model of retinitis pigmentosa. (Maleki S, Gopalakrishnan S, Ghanian Z, Sepehr R, Schmitt H, Eells J, Ranji M) J Biomed Opt 2013 Jan;18(1):16004 24 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 |
| 1 | Assessment of cone survival in response to CNTF, GDNF, and VEGF165b in a novel ex vivo model of end-stage retinitis pigmentosa. (Lipinski DM, Singh MS, MacLaren RE) Invest Ophthalmol Vis Sci 2011 Sep 21;52(10):7340-6 27 Citations |
| 1 | Adaptive optics retinal imaging: applications for studying retinal degeneration. (Carroll J) Arch Ophthalmol 2008 Jun;126(6):857-8 11 Citations |
| 1 | Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency. (Baraas RC, Carroll J, Gunther KL, Chung M, Williams DR, Foster DH, Neitz M) J Opt Soc Am A Opt Image Sci Vis 2007 May;24(5):1438-47 97 Citations |
| 1 | Vitrectomy for large vitreous opacity in retinitis pigmentosa. (Hong PH, Han DP, Burke JM, Wirostko WJ) Am J Ophthalmol 2001 Jan;131(1):133-4 9 Citations |
| 1 | Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15. (Carmi R, Rokhlina T, Kwitek-Black AE, Elbedour K, Nishimura D, Stone EM, Sheffield VC) Hum Mol Genet 1995 Jan;4(1):9-13 169 Citations |
| 1 | Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity. (Kwitek-Black AE, Carmi R, Duyk GM, Buetow KH, Elbedour K, Parvari R, Yandava CN, Stone EM, Sheffield VC) Nat Genet 1993 Dec;5(4):392-6 159 Citations |
