
Last Updated: 09/26/2026
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Found 85 publications
ClinGen Glaucoma Variant Curation Expert Panel recommendations enhance classification of myocilin variants.
Journal: medRxiv : the preprint server for health sciences
Published: August 20, 2026
Forging Ahead: The Need for Improved Representation in Academic Ophthalmology.
Journal: American journal of ophthalmology
Published: April 16, 2026
Assessment of anti-VEGF intravitreal injection effects on murine neonatal Schlemm's canal morphology.
Journal: Scientific reports
Published: March 11, 2026
Uncovering the Genetic Architecture of Optic Nerve Integrity Estimates through Genome-wide Association Study Meta-analyses.
Journal: medRxiv : the preprint server for health sciences
Published: February 12, 2026
Using Adjustable-Focus Spectacles in Young Children to Meet Increasing Eyecare Needs.
Journal: JAMA ophthalmology
Published: August 24, 2023
Disparities in Promotion and Retention Rates Among Underrepresented in Medicine Faculty in U.S. Ophthalmology Departments.
Journal: American journal of ophthalmology
Published: June 05, 2023
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.
Journal: American journal of medical genetics. Part A
Published: March 23, 2023
Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panel.
Journal: Human mutation
Published: June 27, 2022
Sonic Hedgehog Intron Variant Associated With an Unusual Pediatric Cortical Cataract.
Journal: Investigative ophthalmology & visual science
Published: June 24, 2022
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci.
Journal: Nature genetics
Published: March 09, 2022
Genetic Variants Associated With Human Eye Size Are Distinct From Those Conferring Susceptibility to Myopia.
Journal: Investigative ophthalmology & visual science
Published: October 26, 2021
Ophthalmic manifestations in Costello syndrome caused by Ras pathway dysregulation during development.
Journal: Ophthalmic genetics
Published: October 06, 2021
Last Updated: 09/26/2026