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Issue Date
Title
Author(s)
2018
PAX6 molecular analysis and genotype-phenotype correlations in families with aniridia from Australasia and Southeast Asia
Souzeau, E.
;
Rudkin, A.
;
Dubowsky, A.
;
Casson, R.
;
Muecke, J.
;
Mancel, E.
;
Whiting, M.
;
Mills, R.
;
Burdon, K.
;
Craig, J.
2014
Genetic study of diabetic retinopathy: recruitment methodology and analysis of baseline characteristics
Kaidonis, 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.
2016
Association of polymorphisms in MACRO domain containing 2 with thyroid-associated orbitopathy
Khong, 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)
2010
Association between erythropoietin gene polymorphisms and diabetic retinopathy
Abhary, S.
;
Burdon, K.
;
Casson, R.
;
Goggin, M.
;
Petrovsky, N.
;
Craig, J.
2013
Ocular expression and distribution of products of the POAG-associated chromosome 9p21 gene region
Chidlow, G.
;
Wood, J.
;
Sharma, S.
;
Dimasi, D.
;
Burdon, K.
;
Casson, R.
;
Craig, J.
;
Mittal, B.
2011
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma
Khan, 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.
2011
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1
Burdon, 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.
2012
Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal-tension glaucoma, and advanced glaucoma
Burdon, K.
;
Crawford, A.
;
Casson, R.
;
Hewitt, A.
;
Landers, J.
;
Danoy, P.
;
Mackey, D.
;
Mitchell, P.
;
Healey, P.
;
Craig, J.
2012
The Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitment
Souzeau, 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.
2018
Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri Lanka
Javadiyan, 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.
Discover
Author
9
Craig, J.
8
Casson, R.
5
Hewitt, A.
4
Crawford, A.
4
Landers, J.
4
Sharma, S.
3
Chidlow, G.
3
Danoy, P.
3
Mackey, D.
3
Mills, R.
.
next >
Subject
6
Humans
4
Female
4
Glaucoma, Open-Angle
4
Male
4
Middle Aged
4
Polymorphism, Single Nucleotide
3
Animals
3
Genetic Predisposition to Disease
3
Risk Factors
2
Aged
.
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Date issued
2
2018
1
2016
1
2014
1
2013
3
2012
2
2011
1
2010