Landers, J.A., Henderson, T.R., Abhary, S., & Craig, J., 2012. Incidence of diabetic retinopathy in Indigenous Australians within Central Australia: the Central Australian ocular health study. Clinical and Experimental Ophthalmology, 40(1), 83-87.

Landers, J.A., Henderson, T.R., & Craig, J., 2012. The prevalence of glaucoma in Indigenous Australians within Central Australian: the Central Australian Ocular Health Study. British Journal of Ophthalmology, 96, 162-166.

Kuot, A., Hewitt, A.W., Griggs, K.M., Klebe, S., Mills, R.A., Jhanji, V., Craig, J., Sharma, S., & Burdon, K.P., 2012. Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process. European Journal of Human Genetics, 20, 632-638.

Dimasi, D.P., Hewitt, A.W., Kagame, K., Ruvama, S., Tindyebwa, L., Llamas, B., Kirk, K.A., Mitchell, P., Burdon, K.P., & Craig, J., 2011. Ethnic and mouse strain difference in central corneal thickness and association with pigment phenotype. PLoS One, 6(8).

Khan, K., Rudkin, A., Parry, D.A., Burdon, K.P., McKibbin, M., Logan, C., Abdelhamed, Z.I., Muecke, J.S., Fernandez-Fuentes, N., Laurie, K., et al., 2011. Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma. American Journal of Human Genetics, 89(3), 464-473.

Landers, J.A., Henderson, T.R., & Craig, J., 2011. The distribution and association of intraocular pressure in indigenous Australians within Central Australia: The Central Australian Ocular Health Study. Clinical and Experimental Ophthalmology, 39(7), 607-613.

Burdon, K.P., Macgregor, S., Hewitt, A.W., Sharma, S., Chidlow, G.R., Mills, R.A., Danoy, P., Casson, R.J., Viswanathan, A.C., Liu, J.Z., et al., 2011. Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nature Genetics, 43(6), 574-578.

Ronci, M., Sharma, S., Chataway, T.K., Burdon, K.P., Martin, S.M., Craig, J., & Voelcker, N.H., 2011. MALDI-MS-Imaging of Whole Human Lens Capsule. JOURNAL OF PROTEOME RESEARCH, 10(8), 3522-3529.

Awadalla, M.S., Burdon, K.P., Kuot, A., Hewitt, A.W., & Craig, J., 2011. Matrix metalloproteinase-9 genetic variation and primary angle closure glaucoma in a caucasian population. Molecular Vision, 17, 1420-1424.

Awadalla, M.S., Thapa, S.S., Burdon, K.P., Hewitt, A.W., & Craig, J., 2011. The association of hepatocyte growth factor (HGF) gene with primary angle closure glaucoma in the Nepalese population. Molecular Vision, 17, 2248-2254.

Mackey, D.A. & Craig, J., 2002. Glaucoma Inheritance study in Tasmania: An International Collaboration. In Basic And Clinical Science Course Section 13 2002-2003: International Ophthalmology. USA: American Academy of Ophthalmology.

Landers, J.A., Henderson, T.R., Abhary, S., & Craig, J., 2012. Incidence of diabetic retinopathy in Indigenous Australians within Central Australia: the Central Australian ocular health study. Clinical and Experimental Ophthalmology, 40(1), 83-87.

Landers, J.A., Henderson, T.R., & Craig, J., 2012. The prevalence of glaucoma in Indigenous Australians within Central Australian: the Central Australian Ocular Health Study. British Journal of Ophthalmology, 96, 162-166.

Kuot, A., Hewitt, A.W., Griggs, K.M., Klebe, S., Mills, R.A., Jhanji, V., Craig, J., Sharma, S., & Burdon, K.P., 2012. Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process. European Journal of Human Genetics, 20, 632-638.

Chang, J.H., Landers, J.A., Henderson, T.R., & Craig, J., 2011. Prevalence of uveitis in indigenous populations presenting to remote clinics of Central Australia: The Central Australian Ocular Health Study. Clinical and Experimental Ophthalmology.

Creasey, R., Sharma, S., Gibson, C., Craig, J., Ebner, A., Becker, T., Hinterdorfer, P., & Voelcker, N.H., 2011. Atomic force microscopy-based antibody recognition imaging of proteins in the pathological deposits in Pseudoexfoliation Syndrome. ULTRAMICROSCOPY, 111(8), 1055-1061.

Khan, K., Rudkin, A., Parry, D.A., Burdon, K.P., McKibbin, M., Logan, C., Abdelhamed, Z.I., Muecke, J.S., Fernandez-Fuentes, N., Laurie, K., et al., 2011. Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma. American Journal of Human Genetics, 89(3), 464-473.

Landers, J.A., Henderson, T.R., & Craig, J., 2011. Prevalence of pterygium among indigenous Australians within central Australia: The Central Australian Ocular Health Study. Clinical and Experimental Ophthalmology, 39(7), 604-606.

Landers, J.A., Henderson, T.R., & Craig, J., 2011. The distribution and association of intraocular pressure in indigenous Australians within Central Australia: The Central Australian Ocular Health Study. Clinical and Experimental Ophthalmology, 39(7), 607-613.

Landers, J.A., Henderson, T.R., & Craig, J., 2011. The prevalence of pseudoexfoliation syndrome in Indigenous Australians within central Australia: The central Australian ocular health study. Clinical and Experimental Ophthalmology.

Pratap, D.S., Lim, L., Wang, J.J., Mackey, D.A., Kearns, L.A., Stawell, R., Burdon, K.P., Mitchell, P., Craig, J., Hall, A.J., et al., 2011. The role of toll-like receptor variants in acute anterior uveitis. Molecular Vision, 17, 2970-2977.

Ronci, M., Sharma, S., Chataway, T.K., Burdon, K.P., Martin, S.M., Craig, J., & Voelcker, N.H., 2011. MALDI-MS-Imaging of Whole Human Lens Capsule. JOURNAL OF PROTEOME RESEARCH, 10(8), 3522-3529.

Souzeau, E., Mills, R.A., Landers, J.A., Usher, B.J., Straga, T., Crawford, A.L., Hewitt, A.W., Mackey, D.A., Burdon, K.P., & Craig, J., 2011. The Australian and New Zealand Registry of Advanced Glaucome - Methodology and recruitment. Clinical and Experimental Ophthalmology.

Thapa, S.S., Rana, P.P., Twayana, S.N., Shrestha, M.K., Paudel, I., Paudyal, G., Gurung, R., Ruit, S., Hewitt, A.W., Craig, J., et al., 2011. Rationale, methods and baseline demographics of the Bhaktapur Glaucoma Study. Clinical and Experimental Ophthalmology, 39(2), 126-134.

Burdon, K.P., Macgregor, S., Hewitt, A.W., Sharma, S., Chidlow, G.R., Mills, R.A., Danoy, P., Casson, R.J., Viswanathan, A.C., Liu, J.Z., et al., 2011. Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nature Genetics, 43(6), 574-578.

Burdon, K.P., Macgregor, S., Bykhovskaya, Y., Javadiyan, S., Xiaohui, L., Laurie, K., Muszynska, D., Lindsay, R., Lechner, J., Haritunians, T., et al., 2011. Association of polymorphisms in the Hepatocyte Growth Factor (HGF) gene promoter with keratoconus. Investigative Ophthalmology and Visual Science, 52, 8514-8519.

Awadalla, M.S., Thapa, S.S., Burdon, K.P., Hewitt, A.W., & Craig, J., 2011. The association of hepatocyte growth factor (HGF) gene with primary angle closure glaucoma in the Nepalese population. Molecular Vision, 17, 2248-2254.

Awadalla, M.S., Burdon, K.P., Kuot, A., Hewitt, A.W., & Craig, J., 2011. Matrix metalloproteinase-9 genetic variation and primary angle closure glaucoma in a caucasian population. Molecular Vision, 17, 1420-1424.

Dimasi, D.P., Hewitt, A.W., Kagame, K., Ruvama, S., Tindyebwa, L., Llamas, B., Kirk, K.A., Mitchell, P., Burdon, K.P., & Craig, J., 2011. Ethnic and mouse strain difference in central corneal thickness and association with pigment phenotype. PLoS One, 6(8).

Abhary, S., Burdon, K.P., Casson, R.J., Goggin, M., Petrovsky, N., & Craig, J., 2010. Association between erythropoietin gene polymorphisms and diabetic retinopathy. Archives of Ophthalmology, 128(1), 102-106.

Abhary, S., Burdon, K.P., Kuot, A., Javadiyan, S., Whiting, M.J., Kasmeridis, N., Petrovsky, N., & Craig, J., 2010. Sequence variation in DDAH1 and DDAH2 genes is strongly and additively associated with serum ADMA concentrations in individuals with type 2 diabetes. PLoS One, 5(3).

Abhary, S., Burdon, K.P., Laurie, K., Thorpe, S., Landers, J.A., Goold, L., Lake, S., Petrovsky, N., & Craig, J., 2010. Aldose reductase gene polymorphisms and diabetic retinopathy susceptibility. Diabetes Care, 33(8), 1834-1836.

Burdon, K.P., Hewitt, A.W., Mackey, D.A., Mitchell, P., & Craig, J., 2010. Tag SNPs detect association of teh CYP1B1 gene with primary open angle glaucoma. Molecular Vision, 2286-2293.

Charlesworth, J.C., Kramer, P.L., Dyer, T.D., Diego, V., Samples, J.R., Craig, J., Mackey, D.A., Hewitt, A.W., Blangero, J., & Wirtz, M.K., 2010. The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ration, and central corneal thickness. Investigative Ophthalmology and Visual Science, 51(7), 3509-3514.

Creasey, R., Sharma, S., Craig, J., Gibson, C., Ebner, A., Hinterdorfer, P., & Voelcker, N.H., 2010. Detecting Protein Aggregates on Untreated Human Tissue Samples by Atomic Force Microscopy Recognition Imaging. Biophysical Journal, 99(5), 1660-1667.

Dimasi, D.P., Burdon, K.P., & Craig, J., 2010. The genetics of central corneal thickness. British Journal of Ophthalmology, 94(8), 971-976.

Dimasi, D.P., Burdon, K.P., Hewitt, A.W., Savarirayan, R., Healey, P.R., Mitchell, P., Mackey, D.A., & Craig, J., 2010. Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness. Molecular Vision, 16, 562-569.

Dimasi, D.P., Chen, J., Hewitt, A.W., Klebe, S., Davey, R., Stirling, J.W., Thompson, E., Forbes, R., Tan, T.Y., Savarirayan, R., et al., 2010. Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes. Human Genetics, (1), 33-44.

Hattersely, K., Laurie, K., Leibelt, J.E., Gezc, J., Durkin, S., Craig, J., & Burdon, K.P., 2010. A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian aboriginal family maps to 1p35.3-p36.32. BMC MEDICAL GENETICS, 11, 1-6.

Hewitt, A.W., Green, C.M., Wu, J., Lai, T., Kearns, L.A., Craig, J., & Mackey, D.A., 2010. Systemic disease association of familial and sporadic glaucome: the glaucoma inheritance study inTasmania. Acta Ophthalmologica Scandinavica, 88(1), 70-74.

Hewitt, A.W., Sanfilippo, P.G., Ring, M.A., Craig, J., & Mackey, D.A., 2010. Mortality in primary open-angle glaucoma: 'two cupped discs and a funeral'. Eye, 24(1), 59-63.

Landers, J.A., Henderson, T.R., & Craig, J., 2010. Central Australian ocular health study: design and baseline description of participants. Clinical and Experimental Ophthalmology, 38(3), 375-380.

Landers, J.A., Henderson, T.R., & Craig, J., 2010. Prevalence and associations of blinding trachoma in indigenous Australians within central Australia: the Central Australian ocular Health Study. Clinical and Experimental Ophthalmology, 38(4), 398-404.

Landers, J.A., Henderson, T.R., & Craig, J., 2010. Prevalence and associations of cataract in indigenous Australians within central Australia: the Central Australian ocular health study. Clinical and Experimental Ophthalmology, 38(4), 387-392.

Landers, J.A., Henderson, T.R., & Craig, J., 2010. Prevalence and associations of refractive error in indigenous Australians within central Australia: the central Australian ocular health study. Clinical and Experimental Ophthalmology, 38(4), 381-386.

Landers, J.A., Henderson, T.R., & Craig, J., 2010. The prevalence and causes of visual impairment in indigenous Australians within central Australia: the central Australian ocular health study. British Journal of Ophthalmology, 94, 1140-1144.

Landers, J.A., Henderson, T.R., Abhary, S., & Craig, J., 2010. Prevalence and associations of diabetic retinopathy in indigenous Australians within central Australia: the Central Australian Ocular Health Study. Clinical and Experimental Ophthalmology, 38(4), 393-397.

Lu, Y., Dimasi, D.P., Hysi, P.G., Hewitt, A.W., Burdon, K.P., Toh, T., Ruddle, J., Li, Y.J., Mitchell, P., Healey, P.R., et al., 2010. Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness Publication. PloS Genetics, 6(5).

Macgregor, S., Hewitt, A.W., Hysi, P.G., Ruddle, J., Medland, S.E., Henders, A.K., Gordon, S.D., Andrew, T., McEvoy, B., Sanfilippo, P.G., et al., 2010. Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Human Molecular Genetics, 19(13), 2716-2724.

Poulter, J.A., Ali, M., Gilmour, D.E., Rice, A., Kondo, H., Hayashi, K., Mackey, D.A., Kearns, L.A., Ruddle, J., Craig, J., et al., 2010. Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy. American Journal of Human Genetics, 86, 248-253.

Rudkin, A., Gray, T.L., Awadalla, M.S., & Craig, J., 2010. Bilateral simultaneous acute angle closure glaucoma precipitated by non-presciption cold and flue medication. Emergency Medicine Australasia, 22(5), 477-479.

Thorleifsson, G., Walters, G.B., Hewitt, A.W., Masson, G., Helgason, A., DeWan, A., Sigurdsson, A., Jonasdottir, A., Gudjonsson, S., Magnusson, K.P., et al., 2010. Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nature Genetics, 42(10), 906-909.

Xu, J., Ishikawa, H., Wollstein, G., Bilonick, R.A., Kagemann, L., Craig, J., Mackey, D.A., Hewitt, A.W., & Schuman, J., 2010. Automated volumetric evaluation of stereoscopic disc photography. Optics Express, 18(11), 1137-1159.

Abhary, S., Burdon, K.P., Gupta, A., Petrovsky, N., & Craig, J., 2009. Diabetic retinopathy is not associated with carbonic anhydrase gene polymorphisms. Molecular Vision, 15, 1179-1184.

Abhary, S., Burdon, K.P., Gupta, A., Lake, S., Selva, D., Petrovsky, N., & Craig, J., 2009. Common sequence variation in the VEGFA gene predicts risk of diabetic retinopathy. Investigative Ophthalmology and Visual Science, 50(12), 5552-5558.

Zhang, T., Hau, R., Xiao, W., Burdon, K.P., Bhattacharya, S.S., Craig, J., Shang, D., Zhao, X., Mackey, D.A., Moore, A.T., et al., 2009. Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract. Human Mutation, 30(5), E603-E611.

Sun, C., Zhu, G., Wong, T.Y., Hewitt, A.W., Ruddle, J., Hodgson, L., Montgomery, G., Young, T.L., Hammond, C.J., Craig, J., et al., 2009. Quantitative genetic analysis of the retinal vascular caliber: the Australian twins eye study. Hypertension, 54(4), 788-795.

Sherwin, J.C., Hewitt, A.W., Bennett, S.L., Baird, P.N., Craig, J., & Mackey, D.A., 2009. Primary open angle glaucoma in subjects harbouring the predicted GLC1L haplotype reveals a normotensive phenotype. Clinical and Experimental Ophthalmology, 37(2), 201-207.

Sharma, S., Koh, K., Collin, C., Dave, A., McMellon, A.E., Sugiyama, Y., McAvoy, J., Voss, A.K., Gecz, J., & Craig, J., 2009. NHS-A isoform of the NHS gene is a novel interactor of ZO-1. Experimental Cell Research, 315(14), 2358-2372.

Sharma, S., Chataway, T.K., Burdon, K.P., Jonavicius, L., Klebe, S., Hewitt, A.W., Mills, R.A., & Craig, J., 2009. Identification of LOXL1 protein and Apolipoprotein E as components of surgically isolated pseudoexfoliation material by direct mass spectrometry. Experimental Eye Research, 89(4), 479-485.

Landers, J.A., Hewitt, A.W., Dimasi, D.P., Charlesworth, J.C., Straga, T., Mills, R.A., Savarirayan, R., Mackey, D.A., Burdon, K.P., & Craig, J., 2009. Heritability of central corneal thickness in nuclear families. Investigative Ophthalmology and Visual Science, 50(9), 4087-4090.

Kakaday, T., Hewitt, A.W., Voelcker, N.H., Li, J.S., & Craig, J., 2009. Advances in telemetric continuous intraocular pressure assessment. British Journal of Ophthalmology, 93(8), 992-996.

Hewitt, A.W., Chappell, A.J., Straga, T., Landers, J.A., Mills, R.A., & Craig, J., 2009. Sensitivity of confocal laser tomography versus optical coherence tomography in detecting advanced glaucoma. Clinical and Experimental Ophthalmology, 37(9), 836-841.

Craig, J., Hewitt, A.W., McMellon, A.E., Henders, A.K., Ma, L., Wallace, L., Sharma, S., Burdon, K.P., Visscher, P., Montgomery, G., et al., 2009. Rapid inexpensive genome-wide association using pooled whole blood. Genome Research, 19(11), 2075-2080.

Burdon, K.P., Durkin, S., Burke, M., Edwards, M., Pater, J.B., Straga, T., Gecz, J., Liebelt, J.E., & Craig, J., 2009. A novel genetic syndrome characterized by pediatric cataract, dysmorphism, ectodermal features, and developmental delay in an indigenous Australian family. American Journal of Medical Genetics Part A, 149A(4), 633-639.

Abhary, S., Hewitt, A.W., Burdon, K.P., & Craig, J., 2009. A systematic meta-analysis of genetic association studies for diabetic retinopathy. Diabetes, 58(9), 2137-2147.

Abhary, S., Kasmeridis, N., Burdon, K.P., Kuot, A., Whiting, M.J., Yew, W.P., Petrovsky, N., & Craig, J., 2009. Diabetic retinopathy is associated with elevated serum asymmetric and symmetric dimethylarginines. Diabetes Care, 32(11), 2084-2086.

Ali, M., McKibbin, M., Booth, A.P., Parry, D.A., Jain, P., Riazuddin, A., Hejtmancik, J.F., Khan, S.N., Firasat, S., Shires, M., et al., 2009. Null mutations in LTBP2 cause primary congenital glaucoma. American Journal of Human Genetics, 84(5), 664-671.

Hewitt, A.W., Sharma, S., Burdon, K.P., Wang, J.J., Baird, P.N., Dimasi, D.P., Mackey, D.A., Mitchell, P., & Craig, J., 2008. Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people. Human Molecular Genetics, 17(5), 710-716.

Hewitt, A.W., Mackey, D.A., & Craig, J., 2008. Myocilin allele-specific glaucoma phenotype database. Human Mutation, 29(2), 207-211.

Craig, J., Friend, K., Gecz, J., Rattray, K.M., Troski, M., Mackey, D.A., & Burdon, K.P., 2008. A novel locus for X-lined congenital cataract on Xq24. Molecular Vision, 14, 721-726.

Cohn, A., Toomes, C., Hewitt, A.W., Kearns, L.A., Inglehearn, C.F., Craig, J., & Mackey, D.A., 2008. The natural history of OPA1-related autosomal dominant optic atrophy. British Journal of Ophthalmology, 92(10), 1333-1336.

Burdon, K.P., Sharma, S., Hewitt, A.W., McMellon, A.E., JJ, W., DA, M., P, M., & Craig, J., 2008. Genetic analysis of the clusterin gene in pseudoexfoliation syndrome. Molecular Vision, 14, 1727-1736.

Zhu, G., Hewitt, A.W., Ruddle, J., Kearns, L.A., Brown, S.A., MacKinnon, J.R., Chen, C.Y., Hammond, C.J., Craig, J., Montgomery, G.W., et al., 2008. Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5q. Ophthalmology, 115(6), 1053-1057.e2.

Burdon, K.P., Coster, D.J., Charlesworth, J.C., Mills, R.A., Laurie, K., Giunta, C., Hewitt, A.W., Latimer, P., & Craig, J., 2008. Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci. Human Genetics, 124(4), 379-386.

Sharma, S., Burdon, K.P., Dave, A., Jamieson, R., Yaron, Y., Billson, F., Maldergem, L., Lorenz, B., Gecz, J., & Craig, J., 2008. Novel causative mutations in patients with Nance-Horan Syndrome and altered localization of the mutant NHS-A protein isoform. Molecular Vision, 14, 1856-1864.

Pakrou, N., Gray, T., Mills, R.A., Landers, J.A., & Craig, J., 2008. Clinical comparison of the Icare tonometer and Goldmann applanation tonometry. Journal of Glaucoma, 17(1), 43-47.

Ormsby, R.J., Ranganathan, S., Tong, J.C., Griggs, K.M., Dimasi, D.P., Hewitt, A.W., Burdon, K.P., Craig, J., Hoh, J., & Gordon, D.L., 2008. Functional and structural implications of the complement factor H Y402H polymorphism associated with age-related macular degeneration. Investigative Ophthalmology and Visual Science, 49(5), 1763-1770.

Burdon, K.P., Hattersely, K., Lachke, S.A., Laurie, K., Maas, R.L., Mackey, D.A., & Craig, J., 2008. Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract. Molecular Vision, 14, 1799-1804.

Bennett, S.L., Hewitt, A.W., Poulsen, J.L., Kearns, L.A., Morgan, J.E., Craig, J., & Mackey, D.A., 2007. Screening for glaucomatous disc changes prior to diagnosis of glaucoma in myocilin pedigrees. Archives of Ophthalmology, 125(1), 112-116.

Andrew Symons, R., Turakulov, R., Foote, S.J., Craig, J., Mccartney, P.J., & Mackey, D.A., 2007. No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma. Ophthalmic Genetics, 28(1), 39-41.

Burdon, K.P., Sharma, S., Chen, C.S., Mackey, D.A., Dimasi, D.P., & Craig, J., 2007. A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site. Human Mutation, 28(7), 742-751.

Hewitt, A.W., Poulsen, J.L., Alward, W.L., Bennett, S.L., Budde, W.M., Cooper, R.L., Craig, J., Fingert, J.H., Foster, P.J., Garway-Heath, D.F., et al., 2007. Heritable features of the optic disc: a novel twin method for determining genetic significance. Investigative Ophthalmology and Visual Science, 48(6), 2469-2475.

Hewitt, A.W., Bennett, S.L., Richards, J.E., Dimasi, D.P., Booth, A.P., Inglehearn, C., Anwar, R., Yamamoto, T., Fingert, J.H., Heon, E., et al., 2007. Myocilin Gly252Arg mutation and glaucoma of intermediate severity in caucasian individuals. Archives of Ophthalmology, 125(1), 98-104.

Hewitt, A.W., Bennett, S.L., Fingert, J.H., Cooper, R.L., Stone, E.M., Craig, J., & Mackey, D.A., 2007. The optic nerve head in myocilin glaucoma. Investigative Ophthalmology and Visual Science, 48(1), 238-243.

Green, C.M., Kearns, L.A., Wu, J., Barbour, J.M., Wilkinson, R.M., Ring, M.A., Craig, J., Wong, T.L., Hewitt, A.W., & Mackey, D.A., 2007. How significant is a family history of glaucoma? Experience from the glaucoma inheritance study in Tasmania. Clinical and Experimental Ophthalmology, 35(9), 793-799.

Dimasi, D.P., Hewitt, A.W., Straga, T., Pater, J.B., MacKinnon, J.R., Elder, J.E., Casey, T., Mackey, D.A., & Craig, J., 2007. Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma. Clinical Genetics, 72(3), 255-260.

Cohn, A., Toomes, C., Potter, C., Towns, K.V., Hewitt, A.W., Inglehearn, C.F., Craig, J., & Mackey, D.A., 2007. Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations. American Journal of Ophthalmology, 143(4), 656-662.

Burdon, K.P., McKay, J.D., Wirth, M., Russell-Eggit, I., Bhatti, S., Ruddle, J., Dimasi, D.P., Mackey, D.A., & Craig, J., 2006. The PITX3 gene in posterior polar congenital cataract in Australia. Molecular Vision, 12, 367-371.

Charlesworth, J.C., Stankovich, J.M., Mackey, D.A., Craig, J., Haybittel, M., Westmore, R.N., & Sale, M.M., 2006. Confirmation of the adult-onset primary open angle glaucoma locus GLC1B at 2cen-q13 in an Australian family. Ophthalmologica, 220(1), 23-30.

Wu, J., Hewitt, A.W., Green, C.M., Mccartney, P.J., Craig, J., & Mackey, D.A., 2006. Disease severity of familial glaucoma compared with sporadic glaucoma. Archives of Ophthalmology, 124(7), 950-954.

Sharma, S., Ang, S., Shaw, M., Mackey, D.A., Gecz, J., McAvoy, J., & Craig, J., 2006. Nance-Horan syndrome protein, NHS, associates with epithelial cell junctions. Human Molecular Genetics, 15(12), 1972-1983.

Petersen, M.B., Kitsos, G., Samples, J.R., Gaudette, D., Economou-Petersen, E., Sykes, R., Rust, K., Grigoriadou, M., Aperis, G., Choi, D., et al., 2006. A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variability. Investigative Ophthalmology and Visual Science, 47(2), 620-625.

Mimiwati, Z., Mackey, D.A., Craig, J., MacKinnon, J.R., Rait, J., Liebelt, J.E., Ayala-Lugo, R., Vollrath, D., & Richards, J.E., 2006. Nail-patella syndrome and its association with glaucoma: a review of eight families. British Journal of Ophthalmology, 90(12), 1505-1509.

Landers, J.A., Henderson, T.R., & Craig, J., 2006. Optic nerve head parameters of an indigenous population living within Central Australia. Clinical and Experimental Ophthalmology, 34(9), 852-856.

Landers, J.A., Billing, K.J., Mills, R.A., Henderson, T.R., & Craig, J., 2006. Central corneal thickness of Indigenous Australians within Central Australia. American Journal of Ophthalmology, 143(2), 360-362.

Hewitt, A.W., MacKinnon, J.R., Giubilato, A., Elder, J.E., Craig, J., & Mackey, D.A., 2006. Familial transmission risk of infantile glaucoma in Australia. Ophthalmic Genetics, 27(3), 93-97.

Chen, C.S., Phillips, K.D., Grist, S.A., Bennet, G., Craig, J., Muecke, J.S., & Suthers, G.K., 2006. Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancer. Familial Cancer, 5(4), 397-404.

Craig, J., Hewitt, A.W., Dimasi, D.P., Howell, N., Toomes, C., Cohn, A., & Mackey, D.A., 2006. The role of the Met98Lys optineurin variant in inherited optic nerve diseases. British Journal of Ophthalmology, 90(11), 1420-1424.

Dickinson, J.L., Sale, M.M., Passmore, A., Fitzgerald, L.M., Wheatley, C.M., Burdon, K.P., Craig, J., Tengtrisorn, S., Carden, S.M., Maclean, H., et al., 2006. Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity. Clinical and Experimental Ophthalmology, 34(7), 682-688.

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Hewitt, A.W., Craig, J., & Mackey, D.A., 2006. Complex genetics of complex traits: the case of primary open-angle glaucoma. Clinical and Experimental Ophthalmology, 34(5), 472-484.

Hewitt, A.W., Dimasi, D.P., Mackey, D., & Craig, J., 2006. A glaucoma case-control study of the WDR36 gene D658G sequence variant. American Journal of Ophthalmology, 142(2), 324-325.

Baird, P., Foote, S.J., Mackey, D., Craig, J., & Speed, T.P., 2005. Evidence for a novel glaucoma locus at chromosome 3p21-22. Human Genetics, 117(2-3), 249-257.

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Charlesworth, J.C., Dyer, T.D., Stankovich, J.M., Blangero, J., Mackey, D., Craig, J., Green, C., Foote, S.J., Baird, P., & Sale, M.M., 2005. Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree. Investigative Ophthalmology and Visual Science, 46(10), 3723-3729.

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Burdon, K.P., Wirth, M., Mackey, D.A., Russell-Eggit, I., Craig, J., Elder, J.E., Dickinson, J.L., & Sale, M.M., 2004. A novel mutation in the Connexin 46 Gene causes autosomal dominant congenital cataract with incomplete penetrance. Journal of Medical Genetics, 41(8).

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Toomes, C., Bottomley, H.M., Jackson, R.M., Towns, K.V., Scott, S., Mackay, D., Craig, J., Jiang, L., Yang, Z., Trembath, R., et al., 2004. Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinotherapy locus on chromosome 11q. American Journal of Human Genetics, 74(4), 721-730.