Year |
Citation |
Score |
2024 |
MacLaren RE, Audo I, Fischer MD, Huckfeldt R, Lam B, Pennesi ME, Sisk R, Gow JA, Li J, Zhu K, Tsang SF. An Open-Label Phase II Study Assessing the Safety of Bilateral, Sequential Administration of Retinal Gene Therapy in Participants with Choroideremia: The GEMINI Study. Human Gene Therapy. PMID 38970425 DOI: 10.1089/hum.2024.017 |
0.489 |
|
2024 |
Michaelides M, Besirli CG, Yang Y, de Guimaraes TAC, Sui Chien W, Huckfeldt RM, Comander JI, Sahel JA, Shah SM, Tee JJL, Kumaran N, Georgiadis A, Minnick P, Zeldin R, Naylor S, et al. Phase 1/2 AAV5-hRKp.RPGR (Botaretigene Sparoparvovec) Gene Therapy: Safety and Efficacy in RPGR-associated X-linked Retinitis Pigmentosa. American Journal of Ophthalmology. PMID 38871269 DOI: 10.1016/j.ajo.2024.05.034 |
0.434 |
|
2024 |
Parekh B, Duncan JL, Samarakoon L, Melia M, Abalem MF, Andrews CA, Audo I, Ayala AR, Bradley C, Cheetham JK, Dagnelie G, Durham TA, Huckfeldt RM, Lacy GD, Malbin B, et al. Self-Reported Functional Vision in USH2A-Associated Retinal Degeneration as Measured by the Michigan Retinal Degeneration Questionnaire. Investigative Ophthalmology & Visual Science. 65: 5. PMID 38833260 DOI: 10.1167/iovs.65.6.5 |
0.403 |
|
2024 |
Sangermano R, Gupta P, Price C, Han J, Navarro J, Condroyer C, Place EM, Antonio A, Mukai S, Zanlonghi X, Sahel JA, Duncan JL, Pierce EA, Zeitz C, Audo I, ... Huckfeldt RM, et al. Coding and non-coding variants in the ciliopathy gene cause early-onset non-syndromic retinal degeneration. Research Square. PMID 38405922 DOI: 10.21203/rs.3.rs-3871956/v1 |
0.381 |
|
2023 |
Nano E, Baskin E, Greenberg PB, Huckfeldt RM, Hunter A. Macular dystrophy with associated retinitis pigmentosa-1 like 1 genetic mutation. Clinical & Experimental Optometry. 1-3. PMID 37156228 DOI: 10.1080/08164622.2023.2205013 |
0.34 |
|
2022 |
Raparia E, Ballios BG, Place EM, Husain D, Huckfeldt RM. RP2 X-LINKED RETINITIS PIGMENTOSA CARRIER STATE PRESENTING WITH VASCULAR LEAKAGE AND UNILATERAL MACULAR ATROPHY. Retinal Cases & Brief Reports. 17: 533-537. PMID 37643038 DOI: 10.1097/ICB.0000000000001239 |
0.383 |
|
2022 |
Chorfi S, Place EM, Mallery RM, Huckfeldt RM. Retinal Manifestations in Spinocerebellar Ataxia Type 3. Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society. PMID 36729871 DOI: 10.1097/WNO.0000000000001759 |
0.448 |
|
2022 |
Chorfi S, Place EM, Huckfeldt RM. Disparities in Inherited Retinal Degenerations. Seminars in Ophthalmology. 38: 201-206. PMID 36536519 DOI: 10.1080/08820538.2022.2152715 |
0.349 |
|
2022 |
Girach A, Audo I, Birch DG, Huckfeldt RM, Lam BL, Leroy BP, Michaelides M, Russell SR, Sallum JMF, Stingl K, Tsang SH, Yang P. RNA-based therapies in inherited retinal diseases. Therapeutic Advances in Ophthalmology. 14: 25158414221134602. PMID 36388727 DOI: 10.1177/25158414221134602 |
0.401 |
|
2022 |
Aleman TS, Huckfeldt RM, Serrano LW, Pearson DJ, Vergilio GK, McCague S, Marshall KA, Ashtari M, Doan TM, Weigel-DiFranco CA, Biron BS, Wen XH, Chung DC, Liu E, Ferenchak K, et al. AAV2-hCHM Subretinal Delivery to the Macula in Choroideremia: Two Year Interim Results of an Ongoing Phase I/II Gene Therapy Trial. Ophthalmology. PMID 35714735 DOI: 10.1016/j.ophtha.2022.06.006 |
0.499 |
|
2022 |
Nikonov S, Aravand P, Lyubarsky A, Nikonov R, Luo AJ, Wei Z, Maguire AM, Phelps NT, Shpylchak I, Willett K, Aleman TS, Huckfeldt RM, Ramachandran PS, Bennett J. Restoration of Vision and Retinal Responses After Adeno-Associated Virus-Mediated Optogenetic Therapy in Blind Dogs. Translational Vision Science & Technology. 11: 24. PMID 35604672 DOI: 10.1167/tvst.11.5.24 |
0.783 |
|
2022 |
Catomeris AJ, Ballios BG, Sangermano R, Wagner NE, Comander JI, Pierce EA, Place EM, Bujakowska KM, Huckfeldt RM. Novel variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophy. Ophthalmic Genetics. 1-8. PMID 35057699 DOI: 10.1080/13816810.2021.2023196 |
0.455 |
|
2021 |
Ballios BG, Place EM, Martinez-Velazquez L, Pierce EA, Comander JI, Huckfeldt RM. Beyond Sector Retinitis Pigmentosa: Expanding the Phenotype and Natural History of the Rhodopsin Gene Codon 106 Mutation (Gly-to-Arg) in Autosomal Dominant Retinitis Pigmentosa. Genes. 12. PMID 34946802 DOI: 10.3390/genes12121853 |
0.357 |
|
2021 |
Richard AJ, Huckfeldt RM, Reichel E, Liang MC. Variants of Uncertain Significance: Twins With Identical Pathogenic Gene Mutations in Retinitis Punctata Albescens. Ophthalmic Surgery, Lasers & Imaging Retina. 52: 450-453. PMID 34410188 DOI: 10.3928/23258160-20210727-08 |
0.349 |
|
2021 |
Ferenchak K, Deitch I, Huckfeldt R. Antisense Oligonucleotide Therapy for Ophthalmic Conditions. Seminars in Ophthalmology. 1-6. PMID 34010086 DOI: 10.1080/08820538.2021.1914116 |
0.414 |
|
2021 |
Georgiou M, Fujinami K, Vincent A, Nasser F, Khateb S, Vargas ME, Thiadens AAHJ, de Carvalho ER, Nguyen XT, De Guimarães TAC, Robson AG, Mahroo OA, Pontikos N, Arno G, Fujinami-Yokokawa Y, ... ... Huckfeldt RM, et al. KCNV2-associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints - KCNV2 Study Group Report 2. American Journal of Ophthalmology. PMID 33737031 DOI: 10.1016/j.ajo.2021.03.004 |
0.443 |
|
2021 |
Ballios BG, Pierce EA, Huckfeldt RM. Gene editing technology: Towards precision medicine in inherited retinal diseases. Seminars in Ophthalmology. 1-9. PMID 33621144 DOI: 10.1080/08820538.2021.1887903 |
0.388 |
|
2020 |
Park EA, Huckfeldt RM, Comander JI, Sobrin L. Peripheral Leakage on Ultra-Widefield Fluorescein Angiography in Patients With Inherited Retinal Degeneration. Journal of Vitreoretinal Diseases. 5: 147-156. PMID 37009079 DOI: 10.1177/2474126420951988 |
0.357 |
|
2020 |
Park EA, Huckfeldt RM, Comander JI, Sobrin L. Peripheral Leakage on Ultra-Widefield Fluorescein Angiography in Patients With Inherited Retinal Degeneration. Journal of Vitreoretinal Diseases. 5: 147-156. PMID 37009079 DOI: 10.1177/2474126420951988 |
0.357 |
|
2020 |
Fan NW, Li J, Mittal SK, Foulsham W, Elbasiony E, Huckfeldt RM, Chauhan SK, Chen Y. Characterization of clinical and immune responses in an experimental chronic autoimmune uveitis model. The American Journal of Pathology. PMID 32966818 DOI: 10.1016/j.ajpath.2020.09.004 |
0.337 |
|
2020 |
Huckfeldt RM, Grigorian F, Place E, Comander JI, Vavvas D, Young LH, Yang P, Shurygina M, Pierce EA, Pennesi ME. Biallelic -associated retinal dystrophies: Expanding the mutational and clinical spectrum. Molecular Vision. 26: 423-433. PMID 32565670 |
0.389 |
|
2020 |
Scott HA, Place EM, Ferenchak K, Zampaglione E, Wagner NE, Chao KR, DiTroia SP, Navarro-Gomez D, Mukai S, Huckfeldt RM, Pierce EA, Bujakowska KM. Expanding the phenotypic spectrum in RDH12-associated retinal disease. Cold Spring Harbor Molecular Case Studies. 6. PMID 32014858 DOI: 10.1101/mcs.a004754 |
0.413 |
|
2019 |
Stanwyck LK, Place EM, Comander J, Huckfeldt RM, Sobrin L. Predictive value of genetic testing for inherited retinal diseases in patients with suspected atypical autoimmune retinopathy. American Journal of Ophthalmology Case Reports. 15: 100461. PMID 31193260 DOI: 10.1016/J.Ajoc.2019.100461 |
0.385 |
|
2017 |
Gupta PR, Huckfeldt RM. Gene therapy for inherited retinal degenerations: initial successes and future challenges. Journal of Neural Engineering. 14: 051002. PMID 28829759 DOI: 10.1088/1741-2552/Aa7A27 |
0.512 |
|
2016 |
Ramachandran P, Lee V, Wei Z, Song JY, Casal G, Cronin T, Willett K, Huckfeldt R, Morgan JI, Aleman TS, Maguire AM, Bennett J. Evaluation of dose and safety of AAV7m8 and AAV8BP2 in the non-human primate retina. Human Gene Therapy. PMID 27750461 DOI: 10.1089/hum.2016.111 |
0.6 |
|
2016 |
Huckfeldt RM, Comander J. Management of Cystoid Macular Edema in Retinitis Pigmentosa. Seminars in Ophthalmology. 1-9. PMID 27748628 DOI: 10.1080/08820538.2016.1228404 |
0.532 |
|
2016 |
Roybal CN, Kucukevcilioglu M, Huckfeldt R, Elshatory Y, Thurtell MJ, Folk JC. TREATMENT OF RETINOPATHY AND MACULAR EDEMA SECONDARY TO A CAROTID-CAVERNOUS FISTULA. Retinal Cases & Brief Reports. 10: 225-8. PMID 26536012 DOI: 10.1097/Icb.0000000000000234 |
0.408 |
|
2016 |
Ramachandran PS, Nikonov S, Willett K, Huckfeldt R, Lyubarsky A, Morgan J, Aleman T, Maguire A, Bennett J. 270. Optogenetic Activation of Remnant Cone Cells Can Restore Ganglion Cell Light Responses in a Canine Model of Retinitis Pigmentosa Molecular Therapy. 24: S107. DOI: 10.1016/S1525-0016(16)33079-9 |
0.74 |
|
2014 |
Cronin T, Vandenberghe LH, Hantz P, Juttner J, Reimann A, Kacsó AE, Huckfeldt RM, Busskamp V, Kohler H, Lagali PS, Roska B, Bennett J. Efficient transduction and optogenetic stimulation of retinal bipolar cells by a synthetic adeno-associated virus capsid and promoter. Embo Molecular Medicine. 6: 1175-90. PMID 25092770 DOI: 10.15252/Emmm.201404077 |
0.719 |
|
2014 |
Huckfeldt RM, Bennett J. Promising first steps in gene therapy for choroideremia. Human Gene Therapy. 25: 96-7. PMID 24502407 DOI: 10.1089/hum.2014.2503 |
0.426 |
|
2014 |
Nikonov S, Huckfeldt R, Willett K, Bennett J. Expression of halorhodopsin in bipolar cells can restore ganglion cell light responses in a large animal (canine) model of cone-rod dystrophy. Journal of Vision. 14: 37-37. DOI: 10.1167/14.15.37 |
0.651 |
|
2013 |
Huckfeldt RM, Vavvas DG. Neuroprotection for retinal detachment. International Ophthalmology Clinics. 53: 105-17. PMID 24088937 DOI: 10.1097/Iio.0B013E31829Cf08D |
0.577 |
|
2010 |
Schubert T, Huckfeldt RM, Parker E, Campbell JE, Wong RO. Assembly of the outer retina in the absence of GABA synthesis in horizontal cells. Neural Development. 5: 15. PMID 20565821 DOI: 10.1186/1749-8104-5-15 |
0.465 |
|
2009 |
Huckfeldt RM, Schubert T, Morgan JL, Godinho L, Di Cristo G, Huang ZJ, Wong RO. Transient neurites of retinal horizontal cells exhibit columnar tiling via homotypic interactions. Nature Neuroscience. 12: 35-43. PMID 19060895 DOI: 10.1038/Nn.2236 |
0.428 |
|
2005 |
Morgan J, Huckfeldt R, Wong RO. Imaging techniques in retinal research. Experimental Eye Research. 80: 297-306. PMID 15721612 DOI: 10.1016/J.Exer.2004.12.010 |
0.551 |
|
Show low-probability matches. |