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Pflugfelder, Stephen, Mina Massaro-Giordano, Victor Perez, Pedram Hamrah, Sophie Deng, Ladan Espandar, Stephen Foster, et al. 2020. “Topical Recombinant Human Nerve Growth Factor (Cenegermin) for Neurotrophic Keratopathy: A Multicenter Randomized Vehicle-Controlled Pivotal Trial”. Ophthalmology 127 (1): 14-26.

Lambert, Scott, Deborah VanderVeen, Vinay Aakalu, and Stephen Kim. 2020. “Reply”. Ophthalmology 127 (1): e8-e9.

Lambert, Scott, Deborah VanderVeen, and Stephen Kim. 2020. “Reply”. Ophthalmology 127 (1): e6-e7.

Brydon, Elizabeth, Revital Bronstein, Adriana Buskin, Majlinda Lako, Eric Pierce, and Rosario Fernandez-Godino. 2019. “AAV-Mediated Gene Augmentation Therapy Restores Critical Functions in Mutant PRPF31 IPSC-Derived RPE Cells”. Mol Ther Methods Clin Dev 15: 392-402.

Miyajima, Taiga, Geetha Melangath, Shan Zhu, Neha Deshpande, Shivakumar Vasanth, Bodhisattwa Mondal, Varun Kumar, et al. 2020. “Loss of NQO1 Generates Genotoxic Estrogen-DNA Adducts in Fuchs Endothelial Corneal Dystrophy”. Free Radic Biol Med 147: 69-79.

Elhusseiny, Abdelrahman, Elisah Huynh, and Linda Dagi. 2019. “Evaluation and Management of V Pattern Strabismus in Craniosynostosis”. J Binocul Vis Ocul Motil, 1-6.

Liu, Cailing, Taiga Miyajima, Geetha Melangath, Takashi Miyai, Shivakumar Vasanth, Neha Deshpande, Varun Kumar, et al. 2020. “Ultraviolet A Light Induces DNA Damage and Estrogen-DNA Adducts in Fuchs Endothelial Corneal Dystrophy Causing Females to Be More Affected”. Proc Natl Acad Sci U S A 117 (1): 573-83.

Gaier, Eric, and Gena Heidary. 2019. “Pediatric Idiopathic Intracranial Hypertension”. Semin Neurol 39 (6): 704-10.

Gauthier, Angela, and Janey Wiggs. 2020. “Childhood Glaucoma Genes and Phenotypes: Focus on FOXC1 Mutations Causing Anterior Segment Dysgenesis and Hearing Loss”. Exp Eye Res 190: 107893.

Modjtahedi, Bobeck, Deborah Jacobs, and Donald Fong. 2020. “A New Patient-Centered Approach to Ocular Surface Discomfort”. Ocul Surf 18 (2): 196-98.