Rachel M. Huckfeldt, Ph.D.
Affiliations: | Washington University, Saint Louis, St. Louis, MO |
Area:
visual neurophysiologyGoogle:
"Rachel Huckfeldt"Mean distance: 16.72 (cluster 6) | S | N | B | C | P |
Parents
Sign in to add mentor| Peter D. Lukasiewicz | grad student | 2009 | Washington University | |
| (Developmental mechanisms regulating the spatial organization of retinal horizontal cells.) | ||||
| Jean Bennett | post-doc | 2013-2014 | Penn (Cell & Gene Therapy Tree) | |
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Publications
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| Nano E, Baskin E, Greenberg PB, et al. (2023) Macular dystrophy with associated retinitis pigmentosa-1 like 1 genetic mutation. Clinical & Experimental Optometry. 1-3 |
| Raparia E, Ballios BG, Place EM, et al. (2022) RP2 X-LINKED RETINITIS PIGMENTOSA CARRIER STATE PRESENTING WITH VASCULAR LEAKAGE AND UNILATERAL MACULAR ATROPHY. Retinal Cases & Brief Reports. 17: 533-537 |
| Chorfi S, Place EM, Mallery RM, et al. (2022) Retinal Manifestations in Spinocerebellar Ataxia Type 3. Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society |
| Chorfi S, Place EM, Huckfeldt RM. (2022) Disparities in Inherited Retinal Degenerations. Seminars in Ophthalmology. 38: 201-206 |
| Girach A, Audo I, Birch DG, et al. (2022) RNA-based therapies in inherited retinal diseases. Therapeutic Advances in Ophthalmology. 14: 25158414221134602 |
| Aleman TS, Huckfeldt RM, Serrano LW, et al. (2022) AAV2-hCHM Subretinal Delivery to the Macula in Choroideremia: Two Year Interim Results of an Ongoing Phase I/II Gene Therapy Trial. Ophthalmology |
| Nikonov S, Aravand P, Lyubarsky A, et al. (2022) Restoration of Vision and Retinal Responses After Adeno-Associated Virus-Mediated Optogenetic Therapy in Blind Dogs. Translational Vision Science & Technology. 11: 24 |
| Catomeris AJ, Ballios BG, Sangermano R, et al. (2022) Novel variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophy. Ophthalmic Genetics. 1-8 |
| Ballios BG, Place EM, Martinez-Velazquez L, et al. (2021) 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 |
| Richard AJ, Huckfeldt RM, Reichel E, et al. (2021) Variants of Uncertain Significance: Twins With Identical Pathogenic Gene Mutations in Retinitis Punctata Albescens. Ophthalmic Surgery, Lasers & Imaging Retina. 52: 450-453 |