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Proceedings of the National Academy of Sciences of the United States of America|January 10, 2018
<i>CFH</i> and <i>ARMS2</i> genetic risk determines progression to neovascular age-related macular degeneration after antioxidant and zinc supplementationDemetrios G Vavvas, Kent W Small, Carl C Awh, et al.
Ophthalmology. Retina|February 13, 2022
North Carolina Macular Dystrophy: Long-term Follow-up of the Original FamilyKent W Small, Robert Wiggins, Nitin Udar, et al.
Ophthalmology. Retina|April 25, 2019
Fungal Endophthalmitis after Intravitreal Injections of Triamcinolone Contaminated by a Compounding Pharmacy: Five-Year Follow-up of 23 PatientsKent W Small, Elaine M Tran, Christine A Garabetian, et al.
Journal of Vitreoretinal Diseases|April 3, 2023
New Noncoding Base Pair Mutation at the Identical Locus as the Original NCMD/MCDR1 in a Mexican Family, Suggesting a Mutational HotspotKent W Small, Stijn Van de Sompele, Jessica Avetisjan, et al.
Retina (Philadelphia, Pa.)|August 25, 2022
CONGENITAL POSTERIOR POLAR CHORIORETINAL HYPOPLASIA: Expansion of the Clinical Spectrum, Mutation, and Its Association With PRDM13Kent W Small, Caroline A Tawfik, Nitin Udar, et al.
Cornea|February 24, 2005
Candidate gene screening for posterior polymorphous dystrophyAnthony J Aldave, Vivek S Yellore, Alexandre H Principe, et al.
Ophthalmology|February 12, 2011
Thirty-Year follow-up of an African American family with macular dystrophy of the retina, locus 1 (North Carolina macular dystrophy)Daniel F Kiernan, Rohan J Shah, Seenu M Hariprasad, et al.
Human Mutation|January 29, 2003
Identification of GUCY2D gene mutations in CORD5 families and evidence of incomplete penetranceNitin Udar, Svetlana Yelchits, Meenal Chalukya, et al.
Ophthalmic Genetics|December 13, 2021
Best Vitelliform Macular Dystrophy (BVMD) is a phenocopy of North Carolina Macular Dystrophy (NCMD/MCDR1)Kent W Small, Lee M Jampol, Benjamin Bakall, et al.
Molecular Vision|April 11, 2024
Two novel non-coding single nucleotide variants in the DNase1 hypersensitivity site of <i>PRDM13</i> causing North Carolina macular dystrophy in KoreaYuri Seo, Kwangsic Joo, Junwon Lee, et al.
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