Studies
A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD)
A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD)
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Overview
Selected Publications (6)
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.
S. Riazuddin, N. Zaghloul, A. Al-Saif, et al.. (2010). American journal of human genetics. Cited 188 times.
https://doi.org/10.1016/j.ajhg.2009.12.001
A Multicenter Study to Map Genes for Fuchs Endothelial Corneal Dystrophy: Baseline Characteristics and Heritability
M. Louttit, Laura J. Kopplin, R. Igo, et al.. (2012). Cornea. Cited 110 times.
https://doi.org/10.1097/ICO.0b013e31821c9b8f
A Multicenter Study to Map Genes for Fuchs Endothelial Corneal Dystrophy: Baseline Characteristics and Heritability
M. Louttit, Laura J. Kopplin, R. Igo, et al.. (2012). Cornea. Cited 110 times.
https://doi.org/10.1097/ICO.0b013e31821c9b8f
Clinical study of Fuchs corneal endothelial dystrophy leading to penetrating keratoplasty: a 30-year experience.
N. Afshari, A. Pittard, Adnan Siddiqui, et al.. (2006). Archives of ophthalmology. Cited 100 times.
https://doi.org/10.1001/ARCHOPHT.124.6.777
Replication of TCF4 through Association and Linkage Studies in Late-Onset Fuchs Endothelial Corneal Dystrophy
Yi-Ju Li, Mollie A Minear, J. Rimmler, et al.. (2011). PLoS ONE. Cited 79 times.
https://doi.org/10.1371/journal.pone.0018044
Genome-wide linkage scan in fuchs endothelial corneal dystrophy.
N. Afshari, Yi-Ju Li, M. Pericak-Vance, et al.. (2009). Investigative ophthalmology & visual science. Cited 51 times.
https://doi.org/10.1167/iovs.08-1839
