Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohort

por Kuehn, Markus H., Wang, Kai, Roos, Ben, Stone, Edwin M., Kwon, Young H., Alward, Wallace L.M., Mullins, Robert F., Fingert, John H.
Publicado 2011

Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmos

por Khorram, David, Choi, Michael, Roos, Ben R., Stone, Edwin M., Kopel, Teresa, Allen, Richard, Alward, Wallace L.M., Scheetz, Todd E., Fingert, John H.
Publicado 2015

LADD syndrome with glaucoma is caused by a novel gene

por Simpson, Allie, Avdic, Armin, Roos, Ben R., DeLuca, Adam, Miller, Kathy, Schnieders, Michael J., Scheetz, Todd E., Alward, Wallace L.M., Fingert, John H.
Publicado 2017

SQSTM1 Mutations and Glaucoma

por Scheetz, Todd E., Roos, Ben R., Solivan-Timpe, Frances, Miller, Kathy, DeLuca, Adam P., Stone, Edwin M., Kwon, Young H., Alward, Wallace L. M., Wang, Kai, Fingert, John H.
Publicado 2016

Optical Coherence Tomography Analysis Based Prediction of Humphrey 24-2 Visual Field Thresholds in Patients With Glaucoma

por Guo, Zhihui, Kwon, Young H., Lee, Kyungmoo, Wang, Kai, Wahle, Andreas, Alward, Wallace L. M., Fingert, John H., Bettis, Daniel I., Johnson, Chris A., Garvin, Mona K., Sonka, Milan, Abràmoff, Michael D.
Publicado 2017

Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucoma

por Mao, Mao, Solivan-Timpe, Frances, Roos, Ben R., Mullins, Robert F., Oetting, Thomas A., Kwon, Young H., Brzeskiewicz, Peter M., Stone, Edwin M., Alward, Wallace L.M., Anderson, Michael G., Fingert, John H.
Publicado 2012

A Genome-Wide Association Study for Primary Open Angle Glaucoma and Macular Degeneration Reveals Novel Loci

por Scheetz, Todd E., Fingert, John H., Wang, Kai, Kuehn, Markus H., Knudtson, Kevin L., Alward, Wallace L. M., Boldt, H. Culver, Russell, Stephen R., Folk, James C., Casavant, Thomas L., Braun, Terry A., Clark, Abbot F., Stone, Edwin M., Sheffield, Val C.
Publicado 2013

Exome-based investigation of the genetic basis of human pigmentary glaucoma

por van der Heide, Carly, Goar, Wes, Meyer, Kacie J., Alward, Wallace L. M., Boese, Erin A., Sears, Nathan C., Roos, Ben R., Kwon, Young H., DeLuca, Adam P., Siggs, Owen M., Gonzaga-Jauregui, Claudia, Sheffield, Val C., Wang, Kai, Stone, Edwin M., Mullins, Robert F., Anderson, Michael G., Fan, Bao Jian, Ritch, Robert, Craig, Jamie E., Wiggs, Janey L., Scheetz, Todd E., Fingert, John H.
Publicado 2021