Glaucoma Cascade Screening in a High-risk Afro-Caribbean Haitian Population: A Pilot Study.
Feb 08 2022
PubMed ID: 35131981 Author(s): Chang TC, Celestin L, Hodapp EA, Grajewski AL, Junk A, Rothman AL, Duerr ERH, Swaminathan SS, Gedde SJ, Young TL, Wiggs J, Olivier MMG, Quintanilla R, Arrieta E, Savatovsky EJ, Vanner…
Read MoreCellular crosstalk regulates the aqueous humor outflow pathway and provides new targets for glaucoma therapies.
Oct 18 2021
PubMed ID: 34663817 Author(s): Thomson BR, Liu P, Onay T, Du J, Tompson SW, Misener S, Purohit RR, Young TL, Jin J, Quaggin SE. Cellular crosstalk regulates the aqueous humor outflow pathway and provides new…
Read MoreOphthalmic manifestations in Costello syndrome caused by Ras pathway dysregulation during development.
Oct 06 2021
PubMed ID: 34612139 Author(s): Shankar SP, Fallurin R, Watson T, Shankar PR, Young TL, Orel-Bixler D, Rauen KA. Ophthalmic manifestations in Costello syndrome caused by Ras pathway dysregulation during development. Ophthalmic Genet. 2021 Oct 6:1-10.…
Read MoreGenetic Variants Associated With Human Eye Size Are Distinct From Those Conferring Susceptibility to Myopia.
Oct 04 2021
PubMed ID: 34698770 Author(s): Plotnikov D, Cui J, Clark R, Wedenoja J, Pärssinen O, Tideman JWL, Jonas JB, Wang Y, Rudan I, Young TL, Mackey DA, Terry L, Williams C, Guggenheim JA; UK Biobank Eye…
Read MoreEvaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia.
Jun 01 2021
PubMed ID: 33830181 Author(s): Tideman JWL, Pärssinen O, Haarman AEG, Khawaja AP, Wedenoja J, Williams KM, Biino G, Ding X, Kähönen M, Lehtimäki T, Raitakari OT, Cheng CY, Jonas JB, Young TL, Bailey-Wilson JE, Rahi…
Read MoreGenome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.
Feb 24 2021
PubMed ID: 33627673 Author(s): Gharahkhani P, Jorgenson E, Hysi P, Khawaja AP, Pendergrass S, Han X, Ong JS, Hewitt AW, Segrè AV, Rouhana JM, Hamel AR, Igo RP Jr, Choquet H, Qassim A, Josyula NS,…
Read MoreMYOPIA
Dec 01 2020
To identify genes that are involved in eye growth specifically in individuals and families with nearsightedness (myopia).
Read MoreGENETIC EYE DISORDERS
Dec 01 2020
To identify the gene or genes responsible for developmental causes of blindness in the world, and to establish a Pediatric Ophthalmic Genetics and Research Program at the University of Wisconsin – Madison.
Read MoreSVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma.
Oct 01 2020
PubMed ID: 33027505 Author(s): Young TL, Whisenhunt KN, Jin J, LaMartina SM, Martin SM, Souma T, Limviphuvadh V, Suri F, Souzeau E, Zhang X, Dan Y, Anagnos E, Carmona S, Jody NM, Stangel N, Higuchi…
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