John H Fingert

Automated segmentation of the optic disc from stereo color photographs using physiologically plausible features.

Young H. Kwon, Michael D Abràmoff, Lesya Shuba, 2007, Investigative ophthalmology & visual science.

North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13.

Adam P. DeLuca, S Scott Whitmore, Adam P DeLuca, 2016, Ophthalmology.

Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutation.

Edwin M Stone, David A Mackey, Jamie E Craig, 2003, Archives of ophthalmology.

Copy number variations and primary open-angle glaucoma.

Young H. Kwon, Edwin M Stone, Todd E Scheetz, 2011, Investigative ophthalmology & visual science.

Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open angle glaucoma

Robert N Weinreb, Peter Kraft, Terry Gaasterland, 2015, Nature Genetics.

Guidelines for the use and interpretation of assays formonitoring autophagy (3rd edition)

Sangeeta Khare, Xin Qi, Ying Wang, 2016 .

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy

Nathan J Morris, Xuejun Qin, Joan E Bailey-Wilson, 2017, Nature Communications.

Increased expression of the WNT antagonist sFRP-1 in glaucoma elevates intraocular pressure.

Edwin M Stone, Val C Sheffield, Abbot F Clark, 2008, The Journal of clinical investigation.

Automated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shape.

Young H. Kwon, Michael D Abràmoff, Li Tang, 2010, Investigative ophthalmology & visual science.