Alpha-gal syndrome (AGS) in a glaucoma suspect with narrow iridocorneal angles by Aminatta Z. Tejan-Kamara, Joan M. Murhammer, John H. Fingert

Get full text

Nanophthalmos patient with a THR518MET mutation in MYRF, a case report by Joshua Hagedorn, Armin Avdic, Michael J. Schnieders, Benjamin R. Roos, Young H. Kwon, Arlene V. Drack, Erin A. Boese, John H. Fingert

Get full text

Cell–Matrix Interactions in the Eye: From Cornea to Choroid by Andrew E. Pouw, Mark A. Greiner, Razek G. Coussa, Chunhua Jiao, Ian C. Han, Jessica M. Skeie, John H. Fingert, Robert F. Mullins, Elliott H. Sohn

Get full text

SQSTM1 Mutations and Glaucoma. by Todd E Scheetz, Ben R Roos, Frances Solivan-Timpe, Kathy Miller, Adam P DeLuca, Edwin M Stone, Young H Kwon, Wallace L M Alward, Kai Wang, John H Fingert

Get full text

A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci. by Todd E Scheetz, John H Fingert, Kai Wang, Markus H Kuehn, Kevin L Knudtson, Wallace L M Alward, H Culver Boldt, Stephen R Russell, James C Folk, Thomas L Casavant, Terry A Braun, Abbot F Clark, Edwin M Stone, Val C Sheffield

Get full text

Genetic Association between MMP9 and Choroidal Neovascularization in Age-Related Macular Degeneration by Elliott H. Sohn, MD, Ian C. Han, MD, Benjamin R. Roos, BS, Benjamin Faga, BS, Meagan A. Luse, BS, Elaine M. Binkley, MD, H. Culver Boldt, MD, James C. Folk, MD, Stephen R. Russell, MD, Robert F. Mullins, PhD, John H. Fingert, MD, PhD, Edwin M. Stone, MD, PhD, Todd E. Scheetz, PhD

Get full text

Exome-based investigation of the genetic basis of human pigmentary glaucoma by Carly van der Heide, Wes Goar, Kacie J. Meyer, Wallace L. M. Alward, Erin A. Boese, Nathan C. Sears, Ben R. Roos, Young H. Kwon, Adam P. DeLuca, Owen M. Siggs, Claudia Gonzaga-Jauregui, Val C. Sheffield, Kai Wang, Edwin M. Stone, Robert F. Mullins, Michael G. Anderson, Bao Jian Fan, Robert Ritch, Jamie E. Craig, Janey L. Wiggs, Todd E. Scheetz, John H. Fingert

Get full text

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy by Natalie A. Afshari, Robert P. Igo, Nathan J. Morris, Dwight Stambolian, Shiwani Sharma, V. Lakshmi Pulagam, Steven Dunn, John F. Stamler, Barbara J. Truitt, Jacqueline Rimmler, Abraham Kuot, Christopher R. Croasdale, Xuejun Qin, Kathryn P. Burdon, S. Amer Riazuddin, Richard Mills, Sonja Klebe, Mollie A. Minear, Jiagang Zhao, Elmer Balajonda, George O. Rosenwasser, Keith H Baratz, V. Vinod Mootha, Sanjay V. Patel, Simon G. Gregory, Joan E. Bailey-Wilson, Marianne O. Price, Francis W. Price, Jamie E. Craig, John H. Fingert, John D. Gottsch, Anthony J. Aldave, Gordon K. Klintworth, Jonathan H. Lass, Yi-Ju Li, Sudha K. Iyengar

Get full text