Primary Open-Angle Glaucoma

Por Kwon, Young H., Fingert, John H., Kuehn, Markus H., Alward, Wallace L.M.
Publicado em 2009

Robust Multiscale Stereo Matching from Fundus Images with Radiometric Differences

Por Tang, Li, Garvin, Mona K., Lee, Kyungmoo, Alward, Wallace L.M., Kwon, Young H., Abràmoff, Michael D.
Publicado em 2011

Circumferential iris trans-illumination defects in exfoliation syndrome

Por Fingert, John H., Burden, James H., Wang, Kai, Kwon, Young H., Alward, Wallace L.M., Anderson, Michael G.
Publicado em 2013

Primary congenital and developmental glaucomas

Por Lewis, Carly J., Hedberg-Buenz, Adam, DeLuca, Adam P., Stone, Edwin M., Alward, Wallace L.M., Fingert, John H.
Publicado no Hum Mol Genet (2017)

Lyst Mutation in Mice Recapitulates Iris Defects of Human Exfoliation Syndrome

Por Trantow, Colleen M., Mao, Mao, Petersen, Greg E., Alward, Erin M., Alward, Wallace L. M., Fingert, John H., Anderson, Michael G.
Publicado em 2008

Automated segmentation of the optic nerve head from stereo color photographs using physiologically plausible feature detectors

Por Abràmoff, Michael D., Alward, Wallace L. M., Greenlee, Emily C., Shuba, Lesya, Kim, Chan Y., Fingert, John H., Kwon, Young H.
Publicado em 2007

Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)

Por Fingert, John H., Robin, Alan L., Scheetz, Todd E., Kwon, Young H., Liebmann, Jeffrey M., Ritch, Robert, Alward, Wallace L.M.
Publicado no Trans Am Ophthalmol Soc (2016)

Automated Segmentation of the Cup and Rim from Spectral Domain OCT of the Optic Nerve Head

Por Abràmoff, Michael D., Lee, Kyungmoo, Niemeijer, Meindert, Alward, Wallace L. M., Greenlee, Emily C., Garvin, Mona K., Sonka, Milan, Kwon, Young H.
Publicado em 2009

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 em 2011

Characterization and Comparison of the Human and Mouse GLC1A Glaucoma Genes

Por Fingert, John H., Ying, Lihua, Swiderski, Ruth E., Nystuen, Arne M., Arbour, Nancy C., Alward, Wallace L.M., Sheffield, Val C., Stone, Edwin M.
Publicado em 1998

Identification of Proteins that Interact with TANK Binding Kinase 1 and Testing for Mutations Associated with Glaucoma

Por Seo, Seongjin, Solivan-Timpe, Frances, Roos, Ben R., Robin, Alan L., Stone, Edwin M., Kwon, Young H., Alward, Wallace L.M., Fingert, John H.
Publicado em 2013

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 no Mol Vis (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 no Mol Vis (2017)

Genomic organization of TBK1 copy number variations in glaucoma patients

Por DeLuca, Adam P., Alward, Wallace, L.M., Liebmann, Jeffrey, Ritch, Robert, Kawase, Kazuhide, Kwon, Young H., Robin, Alan L., Stone, Edwin M., Scheetz, Todd E., Fingert, John H.
Publicado no J Glaucoma (2017)

Analysis of ASB10 variants in open angle glaucoma

Por Fingert, John H., Roos, Ben R., Solivan-Timpe, Frances, Miller, Kathy A., Oetting, Thomas A., Wang, Kai, Kwon, Young H., Scheetz, Todd E., Stone, Edwin M., Alward, Wallace L.M.
Publicado em 2012

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 no PLoS One (2016)

Familial cavitary optic disc anomalies: Identification of a novel genetic locus

Por Fingert, John H., Honkanen, Robert A., Shankar, Suma P., Affatigato, Louisa M., Ehlinger, Mary A., Moore, Michael D., Jampol, Lee M., Sheffield, Val C., Stone, Edwin M., Alward, Wallace L.M.
Publicado em 2007

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 no Invest Ophthalmol Vis Sci (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 em 2012

Copy number variations on chromosome 12q14 in patients with normal tension glaucoma

Por Fingert, John H., Robin, Alan L., Stone, Jennifer L., Roos, Ben R., Davis, Lea K., Scheetz, Todd E., Bennett, Steve R., Wassink, Thomas H., Kwon, Young H., Alward, Wallace L.M., Mullins, Robert F., Sheffield, Val C., Stone, Edwin M.
Publicado em 2011