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53 results found

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

Publication: Journal Article

Cheng, Ching-Yu, Maria Schache, Kamran Ikram, Terri Young, Jeremy Guggenheim, Veronique Vitart, Stuart Macgregor, et al. 2013. “Nine Loci for Ocular Axial Length Identified through Genome-Wide Association Studies, Including Shared Loci With Refractive Error”. Am J Hum Genet 93 (2): 264-77.

Shivakumar Vasanth, PhD Title: Investigator, Mass Eye and Ear & Instructor of Ophthalmology, Harvard Medical School Current position: Sr. Staff Scientist / Study director at Covance Google Scholar Reena Gupta, MD Title: Clinical Research Fellow / Cornea Fellow, Mass Eye and Ear Yuming Chen, MD Years...

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Publication: Journal Article

Verhoeven, Virginie, Pirro Hysi, Robert Wojciechowski, Qiao Fan, Jeremy Guggenheim, René Höhn, Stuart Macgregor, et al. 2013. “Genome-Wide Meta-Analyses of Multiancestry Cohorts Identify Multiple New Susceptibility Loci for Refractive Error and Myopia”. Nat Genet 45 (3): 314-8.

Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy

Publication: Journal Article

Riazuddin, Amer, David Parker, Elyse McGlumphy, Edwin Oh, Benjamin Iliff, Thore Schmedt, Ula Jurkunas, Robert Schleif, Nicholas Katsanis, and John Gottsch. 2012. “Mutations in LOXHD1, a Recessive-Deafness Locus, Cause Dominant Late-Onset Fuchs Corneal Dystrophy”. Am J Hum Genet 90 (3): 533-9.

A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability

Publication: Journal Article

Louttit, Megan, Laura Kopplin, Robert Igo, Jeremy Fondran, Angela Tagliaferri, David Bardenstein, Anthony Aldave, et al. 2012. “A Multicenter Study to Map Genes for Fuchs Endothelial Corneal Dystrophy: Baseline Characteristics and Heritability”. Cornea 31 (1): 26-35.

Molecular bases of corneal endothelial dystrophies

Publication: Journal Article

Schmedt, Thore, Mariana Mazzini Silva, Alireza Ziaei, and Ula Jurkunas. 2012. “Molecular Bases of Corneal Endothelial Dystrophies”. Exp Eye Res 95 (1): 24-34.

The culture and transplantation of human limbal stem cells

Publication: Journal Article

Ahmad, Sajjad, Charles Osei-Bempong, Reza Dana, and Ula Jurkunas. 2010. “The Culture and Transplantation of Human Limbal Stem Cells”. J Cell Physiol 225 (1): 15-9.

Topical bevacizumab in the treatment of corneal neovascularization: results of a prospective, open-label, noncomparative study

Publication: Journal Article

Dastjerdi, Mohammad, Khalid Al-Arfaj, Nambi Nallasamy, Pedram Hamrah, Ula Jurkunas, Roberto Pineda, Deborah Pavan-Langston, and Reza Dana. 2009. “Topical Bevacizumab in the Treatment of Corneal Neovascularization: Results of a Prospective, Open-Label, Noncomparative Study”. Arch Ophthalmol 127 (4): 381-9.

Keratoglobus in association with posterior polymorphous dystrophy

Publication: Journal Article

Harissi-Dagher, Mona, Reza Dana, and Ula Jurkunas. 2007. “Keratoglobus in Association With Posterior Polymorphous Dystrophy”. Cornea 26 (10): 1288-91.

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Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

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Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy

A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability

Molecular bases of corneal endothelial dystrophies

The culture and transplantation of human limbal stem cells

Topical bevacizumab in the treatment of corneal neovascularization: results of a prospective, open-label, noncomparative study

Keratoglobus in association with posterior polymorphous dystrophy