Journal article
Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian population.
S Sahebjada, M Schache, AJ Richardson, G Snibson, S MacGregor, M Daniell, PN Baird
Investigative Ophthalmology Visual Science | ASSOC RESEARCH VISION OPHTHALMOLOGY INC | Published : 2013
Abstract
A recent genome-wide association study (GWAS) identified six loci associated with central corneal thickness that also conferred associated risk of keratoconus (KC). We aimed to assess whether genetic associations existed for these loci with KC or corneal curvature in an independent cohort of European ancestry. In total, 157 patients with KC were recruited from public and private clinics in Melbourne, Australia, and 673 individuals without KC were identified through the Genes in Myopia study from Australia. The following six single-nucleotide polymorphisms (SNPs) that showed a statistically significant association with KC in a recent GWAS study were selected for genotyping in our cohort: rs48..
View full abstractGrants
Awarded by Australian National Health and Medical Research Council (NHMRC) Clinical Research Excellence Grant "Translational Clinical Research in Major Eye Diseases,''
Awarded by NHMRC Senior Research Fellowship
Funding Acknowledgements
Supported by Australian National Health and Medical Research Council (NHMRC) Clinical Research Excellence Grant 529923 "Translational Clinical Research in Major Eye Diseases,'' NHMRC Senior Research Fellowship 1028444 (PNB), NHMRC Career Development Award (SM), The Royal Victorian Eye and Ear Hospital Small Research Grants, and the Angior Family Foundation. The Centre for Eye Research Australia receives operational infrastructure support from the Victorian government. The authors