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Results 1-10 of 13 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2014Genetic study of diabetic retinopathy: recruitment methodology and analysis of baseline characteristicsKaidonis, G.; Abhary, S.; Daniell, M.; Gillies, M.; Fogarty, R.; Petrovsky, N.; Jenkins, A.; Essex, R.; Chang, J.; Pal, B.; Hewitt, A.; Burdon, K.; Craig, J.
2011Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1Burdon, K.; MacGregor, S.; Hewitt, A.; Sharma, S.; Chidlow, G.; Mills, R.; Danoy, P.; Casson, R.; Viswanathan, A.; Liu, J.; Landers, J.; Henders, A.; Wood, J.; Souzeau, E.; Crawford, A.; Leo, P.; Wang, J.; Rochtchina, E.; Nyholt, D.; Martin, N.; et al.
2016Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucomaZhou, T.; Souzeau, E.; Sharma, S.; Siggs, O.; Goldberg, I.; Healey, P.; Graham, S.; Hewitt, A.; Mackey, D.; Casson, R.; Landers, J.; Mills, R.; Ellis, J.; Leo, P.; Brown, M.; MacGregor, S.; Burdon, K.; Craig, J.
2013Ocular expression and distribution of products of the POAG-associated chromosome 9p21 gene regionChidlow, G.; Wood, J.; Sharma, S.; Dimasi, D.; Burdon, K.; Casson, R.; Craig, J.
2018PAX6 molecular analysis and genotype-phenotype correlations in families with aniridia from Australasia and Southeast AsiaSouzeau, E.; Rudkin, A.; Dubowsky, A.; Casson, R.; Muecke, J.; Mancel, E.; Whiting, M.; Mills, R.; Burdon, K.; Craig, J.
2012Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal-tension glaucoma, and advanced glaucomaBurdon, K.; Crawford, A.; Casson, R.; Hewitt, A.; Landers, J.; Danoy, P.; Mackey, D.; Mitchell, P.; Healey, P.; Craig, J.
2012Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eyeSharma, S.; Burdon, K.; Chidlow, G.; Klebe, S.; Crawford, A.; Dimasi, D.; Dave, A.; Martin, S.; Javadiyan, S.; Wood, J.; Casson, R.; Danoy, P.; Griggs, K.; Hewitt, A.; Landers, J.; Mitchell, P.; Mackey, D.; Craig, J.
2018Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri LankaJavadiyan, S.; Lucas, S.; Wangmo, D.; Ngy, M.; Edussuriya, K.; Craig, J.; Rudkin, A.; Casson, R.; Selva, D.; Sharma, S.; Lower, K.; Meucke, J.; Burdon, K.
2011Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucomaKhan, K.; Rudkin, A.; Parry, D.; Burdon, K.; McKibbin, M.; Logan, C.; Abdelhamed, Z.; Muecke, J.; Fernandez-Fuentes, N.; Laurie, K.; Shires, M.; Fogarty, R.; Carr, I.; Poulter, J.; Morgan, J.; Mohamed, M.; Jafri, H.; Raashid, Y.; Meng, N.; Piseth, H.; et al.
2009Common sequence variation in the VEGFA gene predicts risk of diabetic retinopathyAbhary, S.; Burdon, K.; Gupta, A.; Lake, S.; Selva-Nayagam, D.; Petrovsky, N.; Craig, J.