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Andzelm, Milena, Timothy Cherry, David Harmin, Annabel Boeke, Charlotte Lee, Martin Hemberg, Basil Pawlyk, et al. 2015. “MEF2D Drives Photoreceptor Development through a Genome-Wide Competition for Tissue-Specific Enhancers.”. Neuron 86 (1): 247-63.

Pundlik, Shrinivas, Matteo Tomasi, and Gang Luo. 2015. “Evaluation of a Portable Collision Warning Device for Patients With Peripheral Vision Loss in an Obstacle Course.”. Invest Ophthalmol Vis Sci.

Rubinfeld, Roy, William Trattler, Jonathan Talamo, Parag Majmudar, and Richard Lindstrom. 2015. “Screening of Refractive Surgery Candidates for LASIK and PRK.”. Cornea 34 (5): e13-4.

Uchiyama, Eduardo, Sepideh Faez, Humzah Nasir, Sebastian Unizony, Robert Plenge, George Papaliodis, and Lucia Sobrin. 2015. “Accuracy of the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) As a Research Tool for Identification of Patients With Uveitis and Scleritis.”. Ophthalmic Epidemiol 22 (2): 139-41.

Weis, Schmidt, Maamar, Raj, Lin, Tóth, Riedmann, et al. 2015. “Inhibition of Intestinal Tumor Formation by Deletion of the DNA Methyltransferase 3a”. Oncogene 34 (14): 1822-30.

Dohlman, Thomas, Masahiro Omoto, Jing Hua, William Stevenson, Sang-Mok Lee, Sunil Chauhan, and Reza Dana. 2015. “VEGF-Trap Aflibercept Significantly Improves Long-Term Graft Survival in High-Risk Corneal Transplantation.”. Transplantation 99 (4): 678-86.

Benaglio, Paola, Patricia Fernandez San Jose, Almudena Avila-Fernandez, Giulia Ascari, Shyana Harper, Gaël Manes, Carmen Ayuso, Christian Hamel, Eliot Berson, and Carlo Rivolta. 2014. “Mutational Screening of Splicing Factor Genes in Cases With Autosomal Dominant Retinitis Pigmentosa.”. Mol Vis 20: 843-51.

Venturini, Giulia, Hanna Koskiniemi-Kuendig, Shyana Harper, Eliot Berson, and Carlo Rivolta. 2015. “Two Specific Mutations Are Prevalent Causes of Recessive Retinitis Pigmentosa in North American Patients of Jewish Ancestry.”. Genet Med 17 (4): 285-90.