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Results 1-10 of 12 (Search time: 0.001 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
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.
2016Association of polymorphisms in MACRO domain containing 2 with thyroid-associated orbitopathyKhong, J.J.; Burdon, K.; Lu, Y.; Leonardos, L.; Laurie, K.; Walsh, J.; Gajdatsy, A.; Ebeling, P.; Mcnab, A.; Hardy, T.; Stawell, R.; Davis, G.; Selva, D.; Tsirbas, A.; Montgomery, G.; Macgregor, S.; Craig, J.; The Royal Australian and New Zealand College of Ophthalmologists, Annual Scientific Congress (19 Nov 2016 - 23 Nov 2016 : Melbourne, Vic)
2010Association between erythropoietin gene polymorphisms and diabetic retinopathyAbhary, S.; Burdon, K.; Casson, R.; Goggin, M.; Petrovsky, N.; 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.; Mittal, B.
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.
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.
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.
2012The Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitmentSouzeau, E.; Goldberg, I.; Healey, P.; Mills, R.; Landers, J.; Graham, S.; Grigg, J.; Usher, B.; Straga, T.; Crawford, A.; Casson, R.; Morgan, W.; Ruddle, J.; Coote, M.; White, A.; Stewart, J.; Hewitt, A.; Mackey, D.; Burdon, K.; Craig, J.
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.

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