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PreviewIssue DateTitleAuthor(s)
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.
2018Genome-wide association study of intraocular pressure uncovers new pathways to glaucomaMacGregor, S.; Ong, J.; An, J.; Han, X.; Zhou, T.; Siggs, O.; Law, M.; Souzeau, E.; Sharma, S.; Lynn, D.; Beesley, J.; Sheldrick, B.; Mills, R.; Landers, J.; Ruddle, J.; Graham, S.; Healey, P.; White, A.; Casson, R.; Best, S.; et al.
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.
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.
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.
2016Role of the nucleolus in neurodegenerative diseases with particular reference to the retina: a reviewSia, P.; Wood, J.; Chidlow, G.; Sharma, S.; Craig, J.; Casson, R.
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.