Alpha-gal syndrome (AGS) in a glaucoma suspect with narrow iridocorneal angles

por Tejan-Kamara, Aminatta Z., Murhammer, Joan M., Fingert, John H.
Publicado 2023

Assessment of SNPs associated with the human glucocorticoid receptor in primary open-angle glaucoma and steroid responders

por Fingert, John H., Alward, Wallace L., Wang, Kai, Yorio, Thomas, Clark, Abbot F.
Publicado 2010

Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in Southern India

por Sundaresan, Periasamy, Vijayalakshmi, P., Thompson, Stewart, Ko, Audrey C., Fingert, John H., Stone, Edwin M.
Publicado 2009

Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy

por Rosenberg, Thomas, Roos, Ben, Johnsen, Thorkild, Bech, Niels, Scheetz, Todd E., Larsen, Michael, Stone, Edwin M., Fingert, John H.
Publicado 2010

Progressive optic nerve changes in cavitary optic disc anomaly: integration of copy number alteration and cis-expression quantitative trait loci to assess disease etiology

por Hwang, Eileen S., Morgan, Denise J., Pennington, Katie L., Owen, Leah A., Fingert, John H., Bernstein, Paul S., DeAngelis, Margaret M.
Publicado 2019

Recombinant adenovirus causes prolonged mobilization of macrophages in the anterior chambers of mice

por Meyer, Kacie J., Pellack, Danielle, Hedberg-Buenz, Adam, Pomernackas, Nicholas, Soukup, Dana, Wang, Kai, Fingert, John H., Anderson, Michael G.
Publicado 2021

Nanophthalmos patient with a THR518MET mutation in MYRF, a case report

por Hagedorn, Joshua, Avdic, Armin, Schnieders, Michael J., Roos, Benjamin R., Kwon, Young H., Drack, Arlene V., Boese, Erin A., Fingert, John H.
Publicado 2020

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

Automated Axon Counting in Rodent Optic Nerve Sections with AxonJ

por Zarei, Kasra, Scheetz, Todd E., Christopher, Mark, Miller, Kathy, Hedberg-Buenz, Adam, Tandon, Anamika, Anderson, Michael G., Fingert, John H., Abràmoff, Michael David
Publicado 2016

Corrigendum: Automated Axon Counting in Rodent Optic Nerve Sections with AxonJ

por Zarei, Kasra, Scheetz, Todd E., Christopher, Mark, Miller, Kathy, Hedberg-Buenz, Adam, Tandon, Anamika, Anderson, Michael G., Fingert, John H., Abràmoff, Michael David
Publicado 2016

Duplication of TBK1 Stimulates Autophagy in iPSC-derived Retinal Cells from a Patient with Normal Tension Glaucoma

por Tucker, Budd A., Solivan-Timpe, Frances, Roos, Ben R., Anfinson, Kristin R., Robin, Alan L., Wiley, Luke A., Mullins, Robert F., Fingert, John H.
Publicado 2014

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

MMP19 expression in the human optic nerve

por Chirco, Kathleen R., Hazlewood, Ralph J., Miller, Kathy, Workalemahu, Grefachew, Jampol, Lee M., Lesser, G. Robert, Mullins, Robert F., Kuehn, Markus H., Fingert, John H.
Publicado 2016

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

Evaluation of variants in the selectin genes in age-related macular degeneration

por Mullins, Robert F, Skeie, Jessica M, Folk, James C, Solivan-Timpe, Frances M, Oetting, Thomas A, Huang, Jian, Wang, Kai, Stone, Edwin M, Fingert, John H
Publicado 2011

Calpain-5 Mutations Cause Autoimmune Uveitis, Retinal Neovascularization, and Photoreceptor Degeneration

por Mahajan, Vinit B., Skeie, Jessica M., Bassuk, Alexander G., Fingert, John H., Braun, Terry A., Daggett, Heather T., Folk, James C., Sheffield, Val C., Stone, Edwin M.
Publicado 2012

Cell–Matrix Interactions in the Eye: From Cornea to Choroid

por Pouw, Andrew E., Greiner, Mark A., Coussa, Razek G., Jiao, Chunhua, Han, Ian C., Skeie, Jessica M., Fingert, John H., Mullins, Robert F., Sohn, Elliott H.
Publicado 2021

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