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Ocular Oncology and Pathology|October 30, 2020
An Online Application for Retinoblastoma SurveillanceNakul Singh, Meghan J DeBenedictis, Arun D SinghOphthalmic Genetics|September 26, 2017
A novel dominant CRX mutation causes adult-onset macular dystrophyJoseph F Griffith, Meghan J DeBenedictis, Elias I TraboulsiOphthalmic Genetics|July 28, 2020
A novel TIMP3 mutation associated with a retinitis pigmentosa-like phenotypeMeghan J DeBenedictis, Yosef Gindzin, Enrico Glaab, et al.Retina (Philadelphia, Pa.)|August 18, 2022
TOPICAL CARBONIC ANHYDRASE INHIBITORS IN THE LONG-TERM TREATMENT OF JUVENILE X-LINKED RETINOSCHISISMelanie A Schmitt, Kevin Wang, Meghan J DeBenedictis, et al.Ophthalmic Genetics|March 2, 2023
A novel ocular phenotype associated with pathogenic variants in MFSD8 leading to macular dystrophyMadeline Beckman, Leanne Clevenger, Meghan J DeBenedictis, et al.Ophthalmic Genetics|July 8, 2025
An USH2A variant leading to isolated maculopathy: a novel phenotypeParam Bhatter, Gabrielle Hallai, Meghan J Debenedictis, et al.Retinal Cases & Brief Reports|December 18, 2024
BEST1 VARIANT ASSOCIATED WITH AN ATYPICAL MACULAR AND PERIPHERAL RETINAL PHENOTYPESrinidhi Singuri, Meghan J DeBenedictis, Elias I Traboulsi, et al.Ophthalmic Genetics|November 20, 2025
A novel TSPAN12 mutation causing retinitis pigmentosa-like appearance of familial exudative vitreoretinopathyJoseph R Abraham, Alison Zhao, Meghan J Debenedictis, et al.Ophthalmic Genetics|February 11, 2020
Novel mutation in CTNNB1 causes familial exudative vitreoretinopathy (FEVR) and microcephaly: case report and review of the literatureRazek Georges Coussa, Yue Zhao, Meghan J DeBenedictis, et al.European Journal of Ophthalmology|November 5, 2019
Correlation between Argus II array-retina distance and electrical thresholds of stimulation is improved by measuring the entire arrayLucy T Xu, Aleksandra V Rachitskaya, Meghan J DeBenedictis, et al.Pageof 2