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Khan, Arif, Mohammed Almutlaq, Darren Oystreck, Elizabeth Engle, Khaled Abu-Amero, and Thomas Bosley. 2016. “Retinal Dysfunction in Patients With Congenital Fibrosis of the Extraocular Muscles Type 2.”. Ophthalmic Genet 37 (2): 130-6.

Ma, Jie, Yu Sun, Francisco López, Peter Adamson, Edit Kurali, and Kameran Lashkari. 2016. “Blockage of PI3K/MTOR Pathways Inhibits Laser-Induced Choroidal Neovascularization and Improves Outcomes Relative to VEGF-A Suppression Alone.”. Invest Ophthalmol Vis Sci 57 (7): 3138-44.

Park, Jong, Max Tischfield, Alicia Nugent, Long Cheng, Silvio Alessandro Di Gioia, Wai-Man Chan, Gail Maconachie, et al. 2016. “Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects.”. Am J Hum Genet 98 (6): 1220-7.

Wan, Michael, Nicole Ullrich, Peter Manley, Mark Kieran, Liliana Goumnerova, and Gena Heidary. 2016. “Long-Term Visual Outcomes of Optic Pathway Gliomas in Pediatric Patients Without Neurofibromatosis Type 1.”. J Neurooncol 129 (1): 173-8.

Ebrahimiadib, Nazanin, Bobeck Modjtahedi, Ramak Roohipoor, Stephen Anesi, and Stephen Foster. 2016. “Successful Treatment Strategies in Granulomatosis With Polyangiitis-Associated Peripheral Ulcerative Keratitis.”. Cornea 35 (11): 1459-65.

Eliott, Dean, George Papaliodis, Marlene Durand, and Sarah Turbett. 2016. “CASE RECORDS of the MASSACHUSETTS GENERAL HOSPITAL. Case 20-2016. A 50-Year-Old Man With Cloudy Vision, Hearing Loss, and Unsteadiness.”. N Engl J Med 374 (26): 2586-93.

Cai, Sophie, Tobias Elze, Peter Bex, Janey Wiggs, Louis Pasquale, and Lucy Shen. 2017. “Clinical Correlates of Computationally Derived Visual Field Defect Archetypes in Patients from a Glaucoma Clinic”. Curr Eye Res 42 (4): 568-74.

Choi, Catherine, Anna Stagner, Suzanne Freitag, Frederick Jakobiec, and Nahyoung Grace Lee. 2016. “Atypical Location of Primary Orbital Conjunctival Epithelial Cysts: A Case Series.”. Clin Experiment Ophthalmol 44 (6): 524-6.

Greenwald, Scott, Jeremy Charette, Magdalena Staniszewska, Lan Ying Shi, Steve Brown, Lisa Stone, Qin Liu, et al. 2016. “Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease.”. Am J Pathol 186 (7): 1925-38.

Igo, Robert, Jessica Cooke Bailey, Jane Romm, Jonathan Haines, and Janey Wiggs. 2016. “Quality Control for the Illumina HumanExome BeadChip.”. Curr Protoc Hum Genet 90: 2.14.1-2.14.16.