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Biorxiv : the Preprint Server for Biology|September 5, 2025
Leveraging Single-Cell Transcriptomics of Developing Rat Ocular Outflow Tissues for Prioritization of Congenital Glaucoma Candidate GenesSean M Martin, Kristina N Whisenhunt, Stuart W Tompson
Investigative Ophthalmology & Visual Science|June 24, 2022
Sonic Hedgehog Intron Variant Associated With an Unusual Pediatric Cortical CataractTerri L Young, Kristina N Whisenhunt, Sarah M LaMartina, et al.
Investigative Ophthalmology & Visual Science|April 7, 2017
Exome Sequence Analysis of 14 Families With High MyopiaBethany A Kloss, Stuart W Tompson, Kristina N Whisenhunt, et al.
Scientific Reports|July 1, 2026
Assessment of anti-VEGF intravitreal injection effects on murine neonatal Schlemm's canal morphologyGabriella D Hartman, Amirhesam Afsharpour, Sean M Martin, et al.
Ophthalmic Genetics|January 18, 2017
Reduced penetrance in a large Caucasian pedigree with Stickler syndromeStuart W Tompson, Charles Johnson, Diana Abbott, et al.
Plos One|May 18, 2019
In-utero epigenetic factors are associated with early-onset myopia in young childrenWei Jie Seow, Cheryl S Ngo, Hong Pan, et al.
The Journal of Clinical Investigation|November 7, 2017
Angiopoietin-1 is required for Schlemm's canal development in mice and humansBenjamin R Thomson, Tomokazu Souma, Stuart W Tompson, et al.
Plos One|October 11, 2019
Correction: Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM ConsortiumYee-Ling Wong, Pirro Hysi, Gemmy Cheung, et al.
Investigative Ophthalmology & Visual Science|October 7, 2020
SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital GlaucomaTerri L Young, Kristina N Whisenhunt, Jing Jin, et al.
Plos One|August 16, 2019
Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM ConsortiumYee-Ling Wong, Pirro Hysi, Gemmy Cheung, et al.
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