Last Updated: 09/26/2026
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Found 10 publications
Orbital and Intracranial Imaging Abnormalities in Herpes Zoster Ophthalmicus.
Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society
Published: November 08, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Journal: Nature genetics
Published: March 17, 2021
DDX58(RIG-I)-related disease is associated with tissue-specific interferon pathway activation.
Journal: Journal of medical genetics
Published: September 08, 2020
Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort.
Journal: Scientific reports
Published: August 12, 2020
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice.
Journal: PLoS genetics
Published: December 11, 2018
A Triple Mutation of BetaB2-Crystallin is Necessary to Develop Cataract and Glaucoma.
Journal: Journal of clinical & experimental ophthalmology
Published: May 29, 2018
BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons.
Journal: Experimental eye research
Published: May 31, 2016
Congenital cataracts: de novo gene conversion event in CRYBB2.
Journal: Molecular vision
Published: May 27, 2014
Genome-wide association study and meta-analysis of intraocular pressure.
Journal: Human genetics
Published: April 07, 2013
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Last Updated: 09/26/2026