| Role of oxidative stress in ocular diseases associated with retinal ganglion cells degeneration EYC Kang, PK Liu, YT Wen, PMJ Quinn, SR Levi, NK Wang, RK Tsai Antioxidants 10 (12), 1948, 2021 | 44 | 2021 |
| Prime editing for inherited retinal diseases BL Costa, SR Levi, E Eulau, YT Tsai, PMJ Quinn Frontiers in Genome Editing 3, 775330, 2021 | 24 | 2021 |
| Ocular complications of obstructive sleep apnea PK Liu, TY Chiu, NK Wang, SR Levi, MJ Tsai Journal of Clinical Medicine 10 (15), 3422, 2021 | 18 | 2021 |
| Do people with hereditary cancer syndromes inform their at-risk relatives? A systematic review and meta-analysis MD Ahsan, SR Levi, EM Webster, H Bergeron, J Lin, P Narayan, ... PEC innovation 2, 100138, 2023 | 11 | 2023 |
| Fundoscopy-directed genetic testing to re-evaluate negative whole exome sequencing results A Cho, JR Lima de Carvalho, AJ Tanaka, R Jauregui, SR Levi, AG Bassuk, ... Orphanet journal of rare diseases 15, 1-11, 2020 | 11 | 2020 |
| Quantitative autofluorescence following gene therapy with voretigene neparvovec SR Levi, JK Oh, JRL de Carvalho, VB Mahajan, SH Tsang, JR Sparrow JAMA ophthalmology 138 (8), 919-921, 2020 | 10 | 2020 |
| PKM2 ablation enhanced retinal function and survival in a preclinical model of retinitis pigmentosa E Zhang, J Ryu, SR Levi, JK Oh, CW Hsu, X Cui, TT Lee, NK Wang, ... Mammalian Genome 31, 77-85, 2020 | 10 | 2020 |
| What happens in the long term: Uptake of cancer surveillance and prevention strategies among at‐risk relatives with pathogenic variants detected via cascade testing MK Frey, MD Ahsan, N Badiner, J Lin, P Narayan, R Nitecki, ... Cancer 128 (24), 4241-4250, 2022 | 9 | 2022 |
| Patient perspectives on risk-reducing salpingectomy with delayed oophorectomy for ovarian cancer risk-reduction: A systematic review of the literature L Perez, E Webster, L Bull, JT Brewer, MD Ahsan, J Lin, SR Levi, ... Gynecologic oncology 173, 106-113, 2023 | 8 | 2023 |
| Web-based tool for cancer family history collection: A prospective randomized controlled trial MK Frey, MD Ahsan, E Webster, SR Levi, JT Brewer, J Lin, SV Blank, ... Gynecologic oncology 173, 22-30, 2023 | 8 | 2023 |
| Photoreceptor manifestations of primary mitochondrial optic nerve disorders YH Chang, EYC Kang, PK Liu, SR Levi, HH Wang, YJ Tseng, GH Seo, ... Investigative Ophthalmology & Visual Science 63 (5), 5-5, 2022 | 8 | 2022 |
| Optical gap biomarker in cone-dominant retinal dystrophy JK Oh, J Ryu, JRL de Carvalho Jr, SR Levi, W Lee, E Tsamis, ... American journal of ophthalmology 218, 40-53, 2020 | 8 | 2020 |
| Prime editing for the installation and correction of mutations causing inherited retinal disease: a brief methodology YT Tsai, BL da Costa, ND Nolan, SM Caruso, LA Jenny, SR Levi, ... Retinitis Pigmentosa, 313-331, 2022 | 6 | 2022 |
| Precision medicine trials in retinal degenerations SR Levi, J Ryu, PK Liu, SH Tsang Annual Review of Vision Science 7 (1), 851-865, 2021 | 6 | 2021 |
| Comparative analysis of functional and structural decline in retinitis pigmentosas T Cabral, JR Lima de Carvalho Jr, J Kim, JK Oh, SR Levi, KS Park, ... International Journal of Molecular Sciences 21 (8), 2730, 2020 | 6 | 2020 |
| Generation of CRB1 RP Patient-Derived iPSCs and a CRISPR/Cas9-Mediated Homology-Directed Repair Strategy for the CRB1 c.2480G>T Mutation BL da Costa, Y Li, SR Levi, SH Tsang, PMJ Quinn Retinal Degenerative Diseases XIX: Mechanisms and Experimental Therapy, 571-576, 2023 | 5 | 2023 |
| Clinical and Therapeutic Evaluation of the Ten Most Prevalent CRB1 Mutations B Lopes da Costa, M Kolesnikova, SR Levi, T Cabral, SH Tsang, ... Biomedicines 11 (2), 385, 2023 | 5 | 2023 |
| Generation of human ipsc-derived retinal organoids for assessment of aav-mediated gene delivery A Tso, BL da Costa, A Fehnel, SR Levi, LA Jenny, SD Ragi, Y Li, ... Retinitis Pigmentosa, 287-302, 2022 | 5 | 2022 |
| Differences in intraretinal pigment migration across inherited retinal dystrophies JK Oh, SR Levi, J Kim, JRL de Carvalho Jr, J Ryu, JR Sparrow, SH Tsang American journal of ophthalmology 217, 252-260, 2020 | 5 | 2020 |
| Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa JK Oh, JR Lima de Carvalho, YJ Sun, S Ragi, J Yang, SR Levi, J Ryu, ... Orphanet journal of rare diseases 14, 1-10, 2019 | 5 | 2019 |
