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Human Molecular Genetics|July 17, 2012
Analysis of ASB10 variants in open angle glaucomaJohn H Fingert, Ben R Roos, Frances Solivan-Timpe, et al.
American Journal of Ophthalmology|March 21, 2007
Familial cavitary optic disk anomalies: identification of a novel genetic locusJohn H Fingert, Robert A Honkanen, Suma P Shankar, et al.
Cornea|June 11, 2014
Graft survival versus glaucoma treatment after penetrating or Descemet stripping automated endothelial keratoplastyMatthew S Ward, Kenneth M Goins, Mark A Greiner, et al.
JAMA Ophthalmology|August 17, 2023
GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract SurgeryErin A Boese, Arlene V Drack, Benjamin R Roos, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
The New England Journal of Medicine|April 16, 1998
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)W L Alward, J H Fingert, M A Coote, et al.
Investigative Ophthalmology & Visual Science|August 11, 2017
Optical Coherence Tomography Analysis Based Prediction of Humphrey 24-2 Visual Field Thresholds in Patients With GlaucomaZhihui Guo, Young H Kwon, Kyungmoo Lee, et al.
Molecular Vision|April 18, 2012
Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucomaMao Mao, Frances Solivan-Timpe, Ben R Roos, et al.
Nature Genetics|December 1, 1996
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeE V Semina, R Reiter, N J Leysens, et al.
Ophthalmology. Glaucoma|March 26, 2019
Histochemical Analysis of Glaucoma Caused by a Myocilin Mutation in a Human Donor EyeCarly J van der Heide, Wallace L M Alward, Miles Flamme-Wiese, et al.
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