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Lee, JuKyung, SuRyon Shin, Anna Desalvo, Geonhui Lee, Jeong Yoon Lee, Alessandro Polini, Sukyoung Chae, et al. 2017. “Nonmediated, Label-Free Based Detection of Cardiovascular Biomarker in a Biological Sample”. Adv Healthc Mater 6 (17).

Sun, Ye, Chi-Hsiu Liu, Zhongxiao Wang, Steven Meng, Samuel Burnim, John Paul SanGiovanni, Theodore Kamenecka, Laura Solt, and Jing Chen. 2017. “RORα Modulates Semaphorin 3E Transcription and Neurovascular Interaction in Pathological Retinal Angiogenesis”. FASEB J 31 (10): 4492-4502.

Xie, Hua-Tao, Dan Zhao, Yang Liu, and Ming-Chang Zhang. 2017. “Umbilical Cord Patch Transplantation for Corneal Perforations and Descemetoceles”. J Ophthalmol 2017: 2767053.

Kurreeman, Fina, Eli Stahl, Yukinori Okada, Katherine Liao, Dorothee Diogo, Soumya Raychaudhuri, Jan Freudenberg, et al. 2012. “Use of a Multiethnic Approach to Identify Rheumatoid- Arthritis-Susceptibility Loci, 1p36 and 17q12”. Am J Hum Genet 90 (3): 524-32.

Kurreeman, Fina, Katherine Liao, Lori Chibnik, Brendan Hickey, Eli Stahl, Vivian Gainer, Gang Li, et al. 2011. “Genetic Basis of Autoantibody Positive and Negative Rheumatoid Arthritis Risk in a Multi-Ethnic Cohort Derived from Electronic Health Records”. Am J Hum Genet 88 (1): 57-69.

Lee, Yvonne, Soumya Raychaudhuri, Jing Cui, Immaculata De Vivo, Bo Ding, Lars Alfredsson, Leonid Padyukov, et al. 2009. “The PRL -1149 G/T Polymorphism and Rheumatoid Arthritis Susceptibility”. Arthritis Rheum 60 (5): 1250-4.

Qazi, Yureeda, Shelley Hurwitz, Sarosh Khan, Ula Jurkunas, Reza Dana, and Pedram Hamrah. 2016. “Validity and Reliability of a Novel Ocular Pain Assessment Survey (OPAS) in Quantifying and Monitoring Corneal and Ocular Surface Pain”. Ophthalmology 123 (7): 1458-68.

Saboo, Ujwala, Francisco Amparo, Hasanain Shikari, Ula Jurkunas, and Reza Dana. 2015. “Outcomes of Phacoemulsification in Patients With Chronic Ocular Graft-versus-Host Disease”. Graefes Arch Clin Exp Ophthalmol 253 (6): 901-7.

Hamill, Cecily, Thore Schmedt, and Ula Jurkunas. 2013. “Fuchs Endothelial Cornea Dystrophy: A Review of the Genetics Behind Disease Development”. Semin Ophthalmol 28 (5-6): 281-6.

Di Gioia, Silvio Alessandro, Samantha Connors, Norisada Matsunami, Jessica Cannavino, Matthew Rose, Nicole Gilette, Pietro Artoni, et al. 2017. “A Defect in Myoblast Fusion Underlies Carey-Fineman-Ziter Syndrome”. Nat Commun 8: 16077.