Jacque L. Duncan - Publications

Affiliations: 
2000-2005 Ophthalmology University of California, San Francisco, San Francisco, CA 

93 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Oh JK, Vargas Del Valle JG, Lima de Carvalho JR, Sun YJ, Levi SR, Ryu J, Yang J, Nagasaki T, Emanuelli A, Rasool N, Allikmets R, Sparrow JR, Izquierdo NJ, Duncan JL, Mahajan VB, et al. Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series. Orphanet Journal of Rare Diseases. 17: 146. PMID 35365235 DOI: 10.1186/s13023-022-02295-9  0.382
2021 Grudzinska Pechhacker MK, Jacobson SG, Drack AV, Scipio MD, Strubbe I, Pfeifer W, Duncan JL, Dollfus H, Goetz N, Muller J, Vincent AL, Aleman TS, Tumber A, Van Cauwenbergh C, De Baere E, et al. Comparative Natural History of Visual Function From Patients With Biallelic Variants in BBS1 and BBS10. Investigative Ophthalmology & Visual Science. 62: 26. PMID 34940782 DOI: 10.1167/iovs.62.15.26  0.307
2020 Thompson DA, Iannaccone A, Ali RR, Arshavsky VY, Audo I, Bainbridge JWB, Besirli CG, Birch DG, Branham KE, Cideciyan AV, Daiger SP, Dalkara D, Duncan JL, Fahim AT, Flannery JG, et al. Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium. Translational Vision Science & Technology. 9: 2. PMID 32832209 DOI: 10.1167/Tvst.9.7.2  0.311
2020 MacDonald IM, Moen C, Duncan JL, Tsang SH, Cehajic-Kapetanovic J, Aleman TS. Perspectives on Gene Therapy: Choroideremia Represents a Challenging Model for the Treatment of Other Inherited Retinal Degenerations. Translational Vision Science & Technology. 9: 17. PMID 32714643 DOI: 10.1167/Tvst.9.3.17  0.358
2020 Flores Pimentel MA, Duncan JL, de Alba Campomanes AG, Moore A. Dark without pressure retinal changes in a paediatric age group. Eye (London, England). PMID 32690924 DOI: 10.1038/S41433-020-1088-5  0.362
2020 Chen L, Messinger JD, Sloan KR, Wong J, Roorda A, Duncan JL, Curcio CA. Abundance and multimodal visibility of soft drusen in early age-related macular degeneration: a clinicopathologic correlation. Retina (Philadelphia, Pa.). PMID 32568988 DOI: 10.1097/Iae.0000000000002893  0.316
2020 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, Heon E, Hufnagel RB, et al. Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation with Other Measures of Disease Severity. American Journal of Ophthalmology. PMID 32446738 DOI: 10.1016/J.Ajo.2020.05.024  0.385
2020 Foote KG, Wong JJ, Boehm AE, Bensinger E, Porco TC, Roorda A, Duncan JL. Comparing Cone Structure and Function in RHO- and RPGR-Associated Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 61: 42. PMID 32343782 DOI: 10.1167/Iovs.61.4.42  0.478
2020 Zhou H, Dai Y, Gregori G, Rosenfeld PR, Duncan JL, Schwartz DM, Wang RK. Automated morphometric measurement of the retinal pigment epithelium complex and choriocapillaris using swept source OCT. Biomedical Optics Express. 11: 1834-1850. PMID 32341851 DOI: 10.1364/Boe.385113  0.395
2020 MacDonald IM, Moen C, Duncan JL, Tsang SH, Cehajic-Kapetanovic J, Aleman TS. Perspectives on Gene Therapy: Choroideremia Represents a Challenging Model for the Treatment of Other Inherited Retinal Degenerations Translational Vision Science & Technology. 9: 17. DOI: 10.1167/tvst.9.3.17  0.302
2019 Foote KG, Rinella N, Tang J, Bensaid N, Zhou H, Zhang Q, Wang RK, Porco TC, Roorda A, Duncan JL. Cone Structure Persists Beyond Margins of Short-Wavelength Autofluorescence in Choroideremia. Investigative Ophthalmology & Visual Science. 60: 4931-4942. PMID 31770433 DOI: 10.1167/Iovs.19-27979  0.451
2019 Keiner CM, Zhou H, Zhang Q, Wang RK, Rinella NT, Oldenburg CE, Duncan JL, Schwartz DM. Quantifying choriocapillaris hypoperfusion in patients with choroidal neovascularization using swept-source OCT angiography. Clinical Ophthalmology (Auckland, N.Z.). 13: 1613-1620. PMID 31692580 DOI: 10.2147/Opth.S204344  0.332
2019 Rinella NT, Zhou H, Zhang Q, Keiner C, Oldenburg CE, Duncan JL, Wang RK, Schwartz DM. Quantifying Choriocapillaris Flow Voids in Patients With Geographic Atrophy Using Swept-Source OCT Angiography. Ophthalmic Surgery, Lasers & Imaging Retina. 50: e229-e235. PMID 31589763 DOI: 10.3928/23258160-20190905-14  0.304
2019 Lowe RJ, Daniello KM, Duncan JL, Yang H, Yasumura D, Matthes MT, LaVail MM. Influence of eye pigmentation on retinal degeneration in P23H and S334ter mutant rhodopsin transgenic rats. Experimental Eye Research. 107755. PMID 31408630 DOI: 10.1016/J.Exer.2019.107755  0.602
2019 Bensinger E, Rinella N, Saud A, Loumou P, Ratnam K, Griffin S, Qin J, Porco TC, Roorda A, Duncan JL. Loss of Foveal Cone Structure Precedes Loss of Visual Acuity in Patients With Rod-Cone Degeneration. Investigative Ophthalmology & Visual Science. 60: 3187-3196. PMID 31335944 DOI: 10.1167/Iovs.18-26245  0.441
2019 Pennesi ME, Birch DG, Duncan JL, Bennett J, Girach A. CHOROIDEREMIA: Retinal Degeneration With an Unmet Need. Retina (Philadelphia, Pa.). PMID 31021898 DOI: 10.1097/Iae.0000000000002553  0.505
2019 Foote KG, De la Huerta I, Gustafson K, Baldwin A, Zayit-Soudry S, Rinella N, Porco TC, Roorda A, Duncan JL. Cone Spacing Correlates With Retinal Thickness and Microperimetry in Patients With Inherited Retinal Degenerations. Investigative Ophthalmology & Visual Science. 60: 1234-1243. PMID 30924848 DOI: 10.1167/Iovs.18-25688  0.505
2018 Qin J, Rinella N, Zhang Q, Zhou H, Wong J, Deiner M, Roorda A, Porco TC, Wang RK, Schwartz DM, Duncan JL. OCT Angiography and Cone Photoreceptor Imaging in Geographic Atrophy. Investigative Ophthalmology & Visual Science. 59: 5985-5992. PMID 30572343 DOI: 10.1167/Iovs.18-25032  0.397
2018 Flores Pimentel MA, De la Huerta I, Duncan JL, Slavotinek AM, Moore AT, de Alba Campomanes AG. PHENOTYPIC HETEROGENEITY IN A FAMILY WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY WITH PREVENTION OF VISUAL LOSS IN AN AFFECTED MALE CHILD WITH LASER TREATMENT IN INFANCY. Retinal Cases & Brief Reports. PMID 30074570 DOI: 10.1097/Icb.0000000000000796  0.37
2018 Duncan JL, Pierce EA, Laster AM, Daiger SP, Birch DG, Ash JD, Iannaccone A, Flannery JG, Sahel JA, Zack DJ, Zarbin MA. Inherited Retinal Degenerations: Current Landscape and Knowledge Gaps. Translational Vision Science & Technology. 7: 6. PMID 30034950 DOI: 10.1167/Tvst.7.4.6  0.426
2018 Foote KG, Loumou P, Griffin S, Qin J, Ratnam K, Porco TC, Roorda A, Duncan JL. Relationship Between Foveal Cone Structure and Visual Acuity Measured With Adaptive Optics Scanning Laser Ophthalmoscopy in Retinal Degeneration. Investigative Ophthalmology & Visual Science. 59: 3385-3393. PMID 30025078 DOI: 10.1167/Iovs.17-23708  0.465
2017 LaVail MM, Nishikawa S, Steinberg RH, Naash MI, Duncan JL, Trautmann N, Matthes MT, Yasumura D, Lau-Villacorta C, Chen J, Peterson WM, Yang H, Flannery JG. Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration. Experimental Eye Research. PMID 29122605 DOI: 10.1016/J.Exer.2017.10.023  0.658
2017 Lew YJ, Rinella N, Qin J, Chiang J, Moore AT, Porco TC, Roorda A, Duncan JL. High Resolution Imaging in male germ cell associated kinase (MAK)-related Retinal Degeneration. American Journal of Ophthalmology. PMID 29103961 DOI: 10.1016/J.Ajo.2017.10.023  0.412
2017 Gustafson K, Duncan JL, Biswas P, Soto-Hermida A, Matsui H, Jakubosky D, Suk J, Telenti A, Frazer KA, Ayyagari R. Correction: Gustafson et al., Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree. Genes 2017, 8, 210. Genes. 8. PMID 29065517 DOI: 10.3390/Genes8100286  0.37
2017 Tu JH, Foote KG, Lujan BJ, Ratnam K, Qin J, Gorin MB, Cunningham ET, Tuten WS, Duncan JL, Roorda A. Dysflective cones: Visual function and cone reflectivity in long-term follow-up of acute bilateral foveolitis. American Journal of Ophthalmology Case Reports. 7: 14-19. PMID 29057371 DOI: 10.1016/J.Ajoc.2017.04.001  0.379
2017 Biswas P, Duncan JL, Ali M, Matsui H, Naeem MA, Raghavendra PB, Frazer KA, Arts HH, Riazuddin S, Akram J, Hejtmancik JF, Riazuddin SA, Ayyagari R. A mutation in IFT43 causes non-syndromic recessive retinal degeneration. Human Molecular Genetics. PMID 28973684 DOI: 10.1093/Hmg/Ddx356  0.466
2017 Litts KM, Cooper RF, Duncan JL, Carroll J. Photoreceptor-Based Biomarkers in AOSLO Retinal Imaging. Investigative Ophthalmology & Visual Science. 58: BIO255-BIO267. PMID 28873135 DOI: 10.1167/Iovs.17-21868  0.478
2017 Gustafson K, Duncan JL, Biswas P, Soto-Hermida A, Matsui H, Jakubosky D, Suk J, Telenti A, Frazer KA, Ayyagari R. Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree. Genes. 8. PMID 28837078 DOI: 10.3390/Genes8090210  0.36
2017 Csaky K, Ferris F, Chew EY, Nair P, Cheetham JK, Duncan JL. Report From the NEI/FDA Endpoints Workshop on Age-Related Macular Degeneration and Inherited Retinal Diseases. Investigative Ophthalmology & Visual Science. 58: 3456-3463. PMID 28702674 DOI: 10.1167/Iovs.17-22339  0.437
2017 Oatts JT, Duncan JL, Hoyt CS, Slavotinek AM, Moore AT. Inner retinal dystrophy in a patient with biallelic sequence variants in BRAT1. Ophthalmic Genetics. 1-3. PMID 28635423 DOI: 10.1080/13816810.2017.1290118  0.376
2017 Biswas P, Duncan JL, Maranhao B, Kozak I, Branham K, Gabriel L, Lin JH, Barteselli G, Navani M, Suk JJ, Parke M, Schlechter C, Weleber R, Heckenlively JR, Dagnelie G, et al. Genetic analysis of ten pedigrees with inherited retinal degeneration (IRD) by exome sequencing and phenotype-genotype association. Physiological Genomics. physiolgenomics.0009. PMID 28130426 DOI: 10.1152/Physiolgenomics.00096.2016  0.419
2016 Dagnelie G, Christopher P, Arditi A, da Cruz L, Duncan JL, Ho AC, de Koo LC, Sahel JA, Stanga PE, Thumann G, Wang Y, Arsiero M, Dorn JD, Greenberg RJ. Performance of real-world functional vision tasks by blind subjects improves after implantation with the Argus® II retinal prosthesis system. Clinical & Experimental Ophthalmology. PMID 27495262 DOI: 10.1111/Ceo.12812  0.301
2016 Birch DG, Bennett LD, Duncan JL, Weleber RG, Pennesi ME. Long-term follow-up of patients with retinitis pigmentosa (RP) receiving intraocular ciliary neurotrophic factor implants. American Journal of Ophthalmology. PMID 27457255 DOI: 10.1016/J.Ajo.2016.07.013  0.396
2016 da Cruz L, Dorn JD, Humayun MS, Dagnelie G, Handa J, Barale PO, Sahel JA, Stanga PE, Hafezi F, Safran AB, Salzmann J, Santos A, Birch D, Spencer R, Cideciyan AV, ... ... Duncan JL, et al. Five-Year Safety and Performance Results from the Argus II Retinal Prosthesis System Clinical Trial. Ophthalmology. PMID 27453256 DOI: 10.1016/J.Ophtha.2016.06.049  0.428
2016 Biswas P, Chavali VR, Agnello G, Stone E, Chakarova C, Duncan JL, Kannabiran C, Homsher M, Bhattacharya SS, Naeem MA, Kimchi A, Sharon D, Iwata T, Riazuddin S, Reddy GB, et al. A missense mutation in the ASRGL1 gene is involved in causing autosomal recessive retinal degeneration. Human Molecular Genetics. PMID 27106100 DOI: 10.1093/Hmg/Ddw113  0.452
2016 Alavi MV, Mao M, Pawlikowski BT, Kvezereli M, Duncan JL, Libby RT, John SW, Gould DB. Col4a1 mutations cause progressive retinal neovascular defects and retinopathy. Scientific Reports. 6: 18602. PMID 26813606 DOI: 10.1038/Srep18602  0.494
2016 Geruschat DR, Richards TP, Arditi A, da Cruz L, Dagnelie G, Dorn JD, Duncan JL, Ho AC, Olmos de Koo LC, Sahel JA, Stanga PE, Thumann G, Wang V, Greenberg RJ. An analysis of observer-rated functional vision in patients implanted with the Argus II Retinal Prosthesis System at three years. Clinical & Experimental Optometry. PMID 26804484 DOI: 10.1111/Cxo.12359  0.354
2015 Zayit-Soudry S, Sippl-Swezey N, Porco TC, Lynch SK, Syed R, Ratnam K, Menghini M, Roorda AJ, Duncan JL. Repeatability of Cone Spacing Measures in Eyes With Inherited Retinal Degenerations. Investigative Ophthalmology & Visual Science. 56: 6179-89. PMID 26416092 DOI: 10.1167/Iovs.15-17010  0.437
2015 Horton JC, Parker AB, Botelho JV, Duncan JL. Spontaneous Regeneration of Human Photoreceptor Outer Segments. Scientific Reports. 5: 12364. PMID 26213154 DOI: 10.1038/Srep12364  0.467
2015 Kuo DS, Ou Y, Jeng BH, Bhisitkul R, Stewart JM, Duncan JL, Han Y. Correlation of Serial Scleral and Corneal Pneumatonometry. Ophthalmology. 122: 1771-6. PMID 26165473 DOI: 10.1016/J.Ophtha.2015.05.033  0.351
2015 Ho AC, Humayun MS, Dorn JD, da Cruz L, Dagnelie G, Handa J, Barale PO, Sahel JA, Stanga PE, Hafezi F, Safran AB, Salzmann J, Santos A, Birch D, Spencer R, ... ... Duncan JL, et al. Long-Term Results from an Epiretinal Prosthesis to Restore Sight to the Blind. Ophthalmology. 122: 1547-54. PMID 26162233 DOI: 10.1016/J.Ophtha.2015.04.032  0.39
2015 Lujan BJ, Roorda A, Croskrey JA, Dubis AM, Cooper RF, Bayabo JK, Duncan JL, Antony BJ, Carroll J. DIRECTIONAL OPTICAL COHERENCE TOMOGRAPHY PROVIDES ACCURATE OUTER NUCLEAR LAYER AND HENLE FIBER LAYER MEASUREMENTS. Retina (Philadelphia, Pa.). PMID 25829348 DOI: 10.1097/Iae.0000000000000527  0.329
2015 Wang Q, Tuten WS, Lujan BJ, Holland J, Bernstein PS, Schwartz SD, Duncan JL, Roorda A. Adaptive optics microperimetry and OCT images show preserved function and recovery of cone visibility in macular telangiectasia type 2 retinal lesions. Investigative Ophthalmology & Visual Science. 56: 778-86. PMID 25587056 DOI: 10.1167/Iovs.14-15576  0.462
2015 Menghini M, Lujan BJ, Zayit-Soudry S, Syed R, Porco TC, Bayabo K, Carroll J, Roorda A, Duncan JL. Correlation of outer nuclear layer thickness with cone density values in patients with retinitis pigmentosa and healthy subjects. Investigative Ophthalmology & Visual Science. 56: 372-81. PMID 25515570 DOI: 10.1167/Iovs.14-15521  0.429
2014 Mak AC, Pullinger CR, Tang LF, Wong JS, Deo RC, Schwarz JM, Gugliucci A, Movsesyan I, Ishida BY, Chu C, Poon A, Kim P, Stock EO, Schaefer EJ, Asztalos BF, ... ... Duncan JL, et al. Effects of the absence of apolipoprotein e on lipoproteins, neurocognitive function, and retinal function. Jama Neurology. 71: 1228-36. PMID 25111166 DOI: 10.1001/Jamaneurol.2014.2011  0.349
2014 Duncan JL, Biswas P, Kozak I, Navani M, Syed R, Soudry S, Menghini M, Caruso RC, Jeffrey BG, Heckenlively JR, Reddy GB, Lee P, Roorda A, Ayyagari R. Ocular Phenotype of a Family with FAM161A-associated Retinal Degeneration. Ophthalmic Genetics. 1-9. PMID 25007332 DOI: 10.3109/13816810.2014.929716  0.476
2014 Liu BS, Tarima S, Visotcky A, Pechauer A, Cooper RF, Landsem L, Wilk MA, Godara P, Makhijani V, Sulai YN, Syed N, Yasumura G, Garg AK, Pennesi ME, Lujan BJ, ... ... Duncan JL, et al. The reliability of parafoveal cone density measurements. The British Journal of Ophthalmology. 98: 1126-31. PMID 24855115 DOI: 10.1136/Bjophthalmol-2013-304823  0.308
2013 Bowne SJ, Sullivan LS, Avery CE, Sasser EM, Roorda A, Duncan JL, Wheaton DH, Birch DG, Branham KE, Heckenlively JR, Sieving PA, Daiger SP. Mutations in the small nuclear riboprotein 200 kDa gene (SNRNP200) cause 1.6% of autosomal dominant retinitis pigmentosa. Molecular Vision. 19: 2407-17. PMID 24319334  0.307
2013 Ratnam K, Carroll J, Porco TC, Duncan JL, Roorda A. Relationship between foveal cone structure and clinical measures of visual function in patients with inherited retinal degenerations. Investigative Ophthalmology & Visual Science. 54: 5836-47. PMID 23908179 DOI: 10.1167/Iovs.13-12557  0.416
2013 Birch DG, Weleber RG, Duncan JL, Jaffe GJ, Tao W. Randomized trial of ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for retinitis pigmentosa. American Journal of Ophthalmology. 156: 283-292.e1. PMID 23668681 DOI: 10.1016/J.Ajo.2013.03.021  0.417
2013 Syed R, Sundquist SM, Ratnam K, Zayit-Soudry S, Zhang Y, Crawford JB, MacDonald IM, Godara P, Rha J, Carroll J, Roorda A, Stepien KE, Duncan JL. High-resolution images of retinal structure in patients with choroideremia. Investigative Ophthalmology & Visual Science. 54: 950-61. PMID 23299470 DOI: 10.1167/Iovs.12-10707  0.386
2013 Ratnam K, Västinsalo H, Roorda A, Sankila EM, Duncan JL. Cone structure in patients with usher syndrome type III and mutations in the Clarin 1 gene. Jama Ophthalmology. 131: 67-74. PMID 22964989 DOI: 10.1001/2013.Jamaophthalmol.2  0.324
2012 Branham K, Othman M, Brumm M, Karoukis AJ, Atmaca-Sonmez P, Yashar BM, Schwartz SB, Stover NB, Trzupek K, Wheaton D, Jennings B, Ciccarelli ML, Jayasundera KT, Lewis RA, Birch D, ... ... Duncan JL, et al. Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease. Investigative Ophthalmology & Visual Science. 53: 8232-7. PMID 23150612 DOI: 10.1167/Iovs.12-11025  0.42
2012 Duncan JL, Roorda A, Navani M, Vishweswaraiah S, Syed R, Soudry S, Ratnam K, Gudiseva HV, Lee P, Gaasterland T, Ayyagari R. Identification of a novel mutation in the CDHR1 gene in a family with recessive retinal degeneration. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 1301-8. PMID 23044944 DOI: 10.1001/Archophthalmol.2012.1906  0.329
2012 McGill TJ, Prusky GT, Douglas RM, Yasumura D, Matthes MT, Lowe RJ, Duncan JL, Yang H, Ahern K, Daniello KM, Silver B, LaVail MM. Discordant anatomical, electrophysiological, and visual behavioral profiles of retinal degeneration in rat models of retinal degenerative disease. Investigative Ophthalmology & Visual Science. 53: 6232-44. PMID 22899760 DOI: 10.1167/Iovs.12-9569  0.636
2012 Humayun MS, Dorn JD, da Cruz L, Dagnelie G, Sahel JA, Stanga PE, Cideciyan AV, Duncan JL, Eliott D, Filley E, Ho AC, Santos A, Safran AB, Arditi A, Del Priore LV, et al. Interim results from the international trial of Second Sight's visual prosthesis. Ophthalmology. 119: 779-88. PMID 22244176 DOI: 10.1016/J.Ophtha.2011.09.028  0.346
2011 Duncan JL, Ratnam K, Birch DG, Sundquist SM, Lucero AS, Zhang Y, Meltzer M, Smaoui N, Roorda A. Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene. Investigative Ophthalmology & Visual Science. 52: 9614-23. PMID 22110067 DOI: 10.1167/Iovs.11-8600  0.329
2011 Deveault C, Billingsley G, Duncan JL, Bin J, Theal R, Vincent A, Fieggen KJ, Gerth C, Noordeh N, Traboulsi EI, Fishman GA, Chitayat D, Knueppel T, Millán JM, Munier FL, et al. BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definition. Human Mutation. 32: 610-9. PMID 21344540 DOI: 10.1002/Humu.21480  0.345
2011 Chen Y, Ratnam K, Sundquist SM, Lujan B, Ayyagari R, Gudiseva VH, Roorda A, Duncan JL. Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease. Investigative Ophthalmology & Visual Science. 52: 3281-92. PMID 21296825 DOI: 10.1167/Iovs.10-6538  0.471
2011 Thorne JE, Van Natta ML, Jabs DA, Duncan JL, Srivastava SK. Visual field loss in patients with cytomegalovirus retinitis. Ophthalmology. 118: 895-901. PMID 21146225 DOI: 10.1016/J.Ophtha.2010.09.017  0.422
2011 Talcott KE, Ratnam K, Sundquist SM, Lucero AS, Lujan BJ, Tao W, Porco TC, Roorda A, Duncan JL. Longitudinal study of cone photoreceptors during retinal degeneration and in response to ciliary neurotrophic factor treatment. Investigative Ophthalmology & Visual Science. 52: 2219-26. PMID 21087953 DOI: 10.1167/Iovs.10-6479  0.484
2011 Duncan JL, Talcott KE, Ratnam K, Sundquist SM, Lucero AS, Day S, Zhang Y, Roorda A. Cone structure in retinal degeneration associated with mutations in the peripherin/RDS gene. Investigative Ophthalmology & Visual Science. 52: 1557-66. PMID 21071739 DOI: 10.1167/Iovs.10-6549  0.425
2011 Gelfand JM, Duncan JL, Racine CA, Gillum LA, Chin CT, Zhang Y, Zhang Q, Wong LJ, Roorda A, Green AJ. Heterogeneous patterns of tissue injury in NARP syndrome. Journal of Neurology. 258: 440-8. PMID 20953793 DOI: 10.1007/S00415-010-5775-1  0.384
2010 Godara P, Dubis AM, Roorda A, Duncan JL, Carroll J. Adaptive optics retinal imaging: emerging clinical applications. Optometry and Vision Science : Official Publication of the American Academy of Optometry. 87: 930-41. PMID 21057346 DOI: 10.1097/Opx.0B013E3181Ff9A8B  0.432
2010 Lin P, Shankar SP, Duncan J, Slavotinek A, Stone EM, Rutar T. Retinal vascular abnormalities and dragged maculae in a carrier with a new NDP mutation (c.268delC) that caused severe Norrie disease in the proband. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 14: 93-6. PMID 20227630 DOI: 10.1016/J.Jaapos.2009.11.012  0.392
2010 Duncan JL, LaVail MM. Intense cyclic light-induced retinal degeneration in rats. Archives of Ophthalmology (Chicago, Ill. : 1960). 128: 244-5. PMID 20142550 DOI: 10.1001/Archophthalmol.2009.399  0.532
2009 Sohn EH, Francis PJ, Duncan JL, Weleber RG, Saperstein DA, Farrell DF, Stone EM. Phenotypic variability due to a novel Glu292Lys variation in exon 8 of the BEST1 gene causing best macular dystrophy. Archives of Ophthalmology (Chicago, Ill. : 1960). 127: 913-20. PMID 19597114 DOI: 10.1001/Archophthalmol.2009.148  0.444
2009 Duncan KG, Hosseini K, Bailey KR, Yang H, Lowe RJ, Matthes MT, Kane JP, LaVail MM, Schwartz DM, Duncan JL. Expression of reverse cholesterol transport proteins ATP-binding cassette A1 (ABCA1) and scavenger receptor BI (SR-BI) in the retina and retinal pigment epithelium. The British Journal of Ophthalmology. 93: 1116-20. PMID 19304587 DOI: 10.1136/Bjo.2008.144006  0.594
2009 Yoon MK, Roorda A, Zhang Y, Nakanishi C, Wong LJ, Zhang Q, Gillum L, Green A, Duncan JL. Adaptive optics scanning laser ophthalmoscopy images in a family with the mitochondrial DNA T8993C mutation. Investigative Ophthalmology & Visual Science. 50: 1838-47. PMID 18997096 DOI: 10.1167/Iovs.08-2029  0.326
2008 Lavail MM, Nishikawa S, Duncan JL, Yang H, Matthes MT, Yasumura D, Vollrath D, Overbeek PA, Ash JD, Robinson ML. Sustained delivery of NT-3 from lens fiber cells in transgenic mice reveals specificity of neuroprotection in retinal degenerations. The Journal of Comparative Neurology. 511: 724-35. PMID 18925574 DOI: 10.1002/Cne.21858  0.615
2008 Grishanin RN, Yang H, Liu X, Donohue-Rolfe K, Nune GC, Zang K, Xu B, Duncan JL, Lavail MM, Copenhagen DR, Reichardt LF. Retinal TrkB receptors regulate neural development in the inner, but not outer, retina. Molecular and Cellular Neurosciences. 38: 431-43. PMID 18511296 DOI: 10.1016/J.Mcn.2008.04.004  0.637
2007 McGill TJ, Prusky GT, Douglas RM, Yasumura D, Matthes MT, Nune G, Donohue-Rolfe K, Yang H, Niculescu D, Hauswirth WW, Girman SV, Lund RD, Duncan JL, LaVail MM. Intraocular CNTF reduces vision in normal rats in a dose-dependent manner. Investigative Ophthalmology & Visual Science. 48: 5756-66. PMID 18055829 DOI: 10.1167/Iovs.07-0054  0.629
2007 Paskowitz DM, Greenberg KP, Yasumura D, Grimm D, Yang H, Duncan JL, Kay MA, Lavail MM, Flannery JG, Vollrath D. Rapid and stable knockdown of an endogenous gene in retinal pigment epithelium. Human Gene Therapy. 18: 871-80. PMID 17892416 DOI: 10.1089/Hum.2007.065  0.617
2007 Johnson J, Fremeau RT, Duncan JL, Rentería RC, Yang H, Hua Z, Liu X, LaVail MM, Edwards RH, Copenhagen DR. Vesicular glutamate transporter 1 is required for photoreceptor synaptic signaling but not for intrinsic visual functions. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 7245-55. PMID 17611277 DOI: 10.1523/Jneurosci.0815-07.2007  0.609
2007 Duncan JL, Zhang Y, Gandhi J, Nakanishi C, Othman M, Branham KE, Swaroop A, Roorda A. High-resolution imaging with adaptive optics in patients with inherited retinal degeneration. Investigative Ophthalmology & Visual Science. 48: 3283-91. PMID 17591900 DOI: 10.1167/Iovs.06-1422  0.445
2007 Roorda A, Zhang Y, Duncan JL. High-resolution in vivo imaging of the RPE mosaic in eyes with retinal disease. Investigative Ophthalmology & Visual Science. 48: 2297-303. PMID 17460294 DOI: 10.1167/Iovs.06-1450  0.472
2007 Rhee KD, Ruiz A, Duncan JL, Hauswirth WW, Lavail MM, Bok D, Yang XJ. Molecular and cellular alterations induced by sustained expression of ciliary neurotrophic factor in a mouse model of retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 48: 1389-400. PMID 17325188 DOI: 10.1167/Iovs.06-0677  0.634
2007 Paskowitz DM, Donohue-Rolfe KM, Yang H, Yasumura D, Matthes MT, Hosseini K, Graybeal CM, Nune G, Zarbin MA, Lavail MM, Duncan JL. Neurotrophic factors minimize the retinal toxicity of verteporfin photodynamic therapy. Investigative Ophthalmology & Visual Science. 48: 430-7. PMID 17197564 DOI: 10.1167/Iovs.06-0690  0.637
2006 Duncan JL, Paskowitz DM, Nune GC, Yasumura D, Yang H, Matthes MT, Zarbin MA, LaVail MM. Retinal damage caused by photodynamic therapy can be reduced using BDNF. Advances in Experimental Medicine and Biology. 572: 297-302. PMID 17249587 DOI: 10.1007/0-387-32442-9_41  0.57
2006 Duncan JL, Yang H, Doan T, Silverstein RS, Murphy GJ, Nune G, Liu X, Copenhagen D, Tempel BL, Rieke F, Krizaj D. Scotopic visual signaling in the mouse retina is modulated by high-affinity plasma membrane calcium extrusion. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 7201-11. PMID 16822977 DOI: 10.1523/Jneurosci.5230-05.2006  0.423
2006 Paskowitz DM, LaVail MM, Duncan JL. Light and inherited retinal degeneration. The British Journal of Ophthalmology. 90: 1060-6. PMID 16707518 DOI: 10.1136/Bjo.2006.097436  0.653
2005 Vagefi MR, Kim ET, Alvarado RG, Duncan JL, Howes EL, Crawford JB. Bilateral endogenous Scedosporium prolificans endophthalmitis after lung transplantation. American Journal of Ophthalmology. 139: 370-3. PMID 15734012 DOI: 10.1016/J.Ajo.2004.08.005  0.363
2005 Kuo YM, Duncan JL, Westaway SK, Yang H, Nune G, Xu EY, Hayflick SJ, Gitschier J. Deficiency of pantothenate kinase 2 (Pank2) in mice leads to retinal degeneration and azoospermia. Human Molecular Genetics. 14: 49-57. PMID 15525657 DOI: 10.1093/Hmg/Ddi005  0.406
2004 Paskowitz DM, Nune G, Yasumura D, Yang H, Bhisitkul RB, Sharma S, Matthes MT, Zarbin MA, Lavail MM, Duncan JL. BDNF reduces the retinal toxicity of verteporfin photodynamic therapy. Investigative Ophthalmology & Visual Science. 45: 4190-6. PMID 15505074 DOI: 10.1167/Iovs.04-0676  0.652
2004 Wilson HL, Schwartz DM, Bhatt HR, McCulloch CE, Duncan JL. Statin and aspirin therapy are associated with decreased rates of choroidal neovascularization among patients with age-related macular degeneration. American Journal of Ophthalmology. 137: 615-24. PMID 15059698 DOI: 10.1016/J.Ajo.2003.10.025  0.341
2004 Cheung MC, Nune GC, Wang M, McTaggart KE, MacDonald IM, Duncan JL. Detection of localized retinal dysfunction in a choroideremia carrier. American Journal of Ophthalmology. 137: 189-91. PMID 14700671 DOI: 10.1016/S0002-9394(03)00783-9  0.427
2003 Duncan JL, Yang H, Vollrath D, Yasumura D, Matthes MT, Trautmann N, Chappelow AV, Feng W, Earp HS, Matsushima GK, LaVail MM. Inherited retinal dystrophy in Mer knockout mice. Advances in Experimental Medicine and Biology. 533: 165-72. PMID 15180261 DOI: 10.1007/978-1-4615-0067-4_21  0.566
2003 Duncan JL, LaVail MM, Yasumura D, Matthes MT, Yang H, Trautmann N, Chappelow AV, Feng W, Earp HS, Matsushima GK, Vollrath D. An RCS-like retinal dystrophy phenotype in mer knockout mice. Investigative Ophthalmology & Visual Science. 44: 826-38. PMID 12556419 DOI: 10.1167/Iovs.02-0438  0.648
2002 Bok D, Yasumura D, Matthes MT, Ruiz A, Duncan JL, Chappelow AV, Zolutukhin S, Hauswirth W, LaVail MM. Effects of adeno-associated virus-vectored ciliary neurotrophic factor on retinal structure and function in mice with a P216L rds/peripherin mutation. Experimental Eye Research. 74: 719-35. PMID 12126945 DOI: 10.1006/Exer.2002.1176  0.651
2002 Duncan JL, Aleman TS, Gardner LM, De Castro E, Marks DA, Emmons JM, Bieber ML, Steinberg JD, Bennett J, Stone EM, MacDonald IM, Cideciyan AV, Maguire MG, Jacobson SG. Macular pigment and lutein supplementation in choroideremia. Experimental Eye Research. 74: 371-81. PMID 12014918 DOI: 10.1006/Exer.2001.1126  0.487
2001 Gordon KB, Rugo HS, Duncan JL, Irvine AR, Howes EL, O'Brien JM, Carter SR. Ocular manifestations of leukemia: leukemic infiltration versus infectious process. Ophthalmology. 108: 2293-300. PMID 11733273 DOI: 10.1016/S0161-6420(01)00817-X  0.41
2001 Vollrath D, Feng W, Duncan JL, Yasumura D, D'Cruz PM, Chappelow A, Matthes MT, Kay MA, LaVail MM. Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk. Proceedings of the National Academy of Sciences of the United States of America. 98: 12584-9. PMID 11592982 DOI: 10.1073/Pnas.221364198  0.67
1998 Duncan JL, Golabi M, Fredrick DR, Hoyt CS, Hwang DG, Kramer SG, Howes EL, Cunningham ET. Complex limbal choristomas in linear nevus sebaceous syndrome. Ophthalmology. 105: 1459-65. PMID 9709758 DOI: 10.1016/S0161-6420(98)98029-0  0.314
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