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Hecht, Heiko, Jenny Hörichs, Sarah Sheldon, Jessilin Quint, and Alex Bowers. 2015. “The Effects of Simulated Vision Impairments on the Cone of Gaze.”. Atten Percept Psychophys 77 (7): 2399-408.

DeLoss, Karen, Hong-Gam Le, Anisa Gire, Gloria Chiu, Deborah Jacobs, and Karen Carrasquillo. 2016. “PROSE Treatment for Ocular Chronic Graft-Versus-Host Disease As a Clinical Network Expands.”. Eye Contact Lens 42 (4): 262-6.

White, Michelle, James Chodosh, Jisun Jang, and Claes Dohlman. 2015. “Incidence of Stevens-Johnson Syndrome and Chemical Burns to the Eye.”. Cornea 34 (12): 1527-33.

Patel, Avni, Anne Marie Lane, Margaux Morrison, Alexei Trofimov, Helen Shih, Evangelos Gragoudas, and Ivana Kim. 2016. “Visual Outcomes After Proton Beam Irradiation for Choroidal Melanomas Involving the Fovea.”. Ophthalmology 123 (2): 369-77.

Duncker, Tobias, Gregory Stein, Winston Lee, Stephen Tsang, Jana Zernant, Srilaxmi Bearelly, Donald Hood, et al. 2015. “Quantitative Fundus Autofluorescence and Optical Coherence Tomography in ABCA4 Carriers.”. Invest Ophthalmol Vis Sci 56 (12): 7274-85.

Pasquale, Louis, Akiko Hanyuda, Ai Ren, Michael Giovingo, Scott Greenstein, Clara Cousins, Thomas Patrianakos, et al. 2015. “Nailfold Capillary Abnormalities in Primary Open-Angle Glaucoma: A Multisite Study.”. Invest Ophthalmol Vis Sci 56 (12): 7021-8.

Dagi Glass, Lora, Catherine Choi, and Nahyoung Grace Lee. 2015. “Orbital Complication Following Calcium Hydroxylapatite Filler Injection.”. Ophthal Plast Reconstr Surg.

Aggarwal, Shruti, Takefumi Yamaguchi, Reza Dana, and Pedram Hamrah. 2017. “Exophiala Phaeomuriformis Fungal Keratitis: Case Report and In Vivo Confocal Microscopy Findings”. Eye Contact Lens 43 (2): e4-e6.

Sparrow, Janet, Tobias Duncker, Russell Woods, and François Delori. 2016. “Quantitative Fundus Autofluorescence in Best Vitelliform Macular Dystrophy: RPE Lipofuscin Is Not Increased in Non-Lesion Areas of Retina.”. Adv Exp Med Biol 854: 285-90.

Whitman, Mary, Caroline Andrews, Wai-Man Chan, Max Tischfield, Steven Stasheff, Francesco Brancati, Xilma Ortiz-Gonzalez, et al. 2016. “Two Unique TUBB3 Mutations Cause Both CFEOM3 and Malformations of Cortical Development.”. Am J Med Genet A 170 (2): 297-305.