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Items where Author is "Craig, JE"

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Afshari, NA, Igo Jr, RP, Morris, NJ, Stambolian, D, Sharma, Shiwani, Pulagam, VL, Dunn, S, Stamler, JF, Truitt, BJ, Rimmler, J, Kuot, A, Croasdale, CR, Qin, X, Burdon, KP ORCID: 0000-0001-8217-1249, Riazuddin, SA, Mills, R, Klebe, S, Minear, MA, Zhao, J, Balajonda, E, Rosenwasser, GO, Baratz, KH, Mootha, VV, Patel, SV, Gregory, SG, Bailey-Wilson, JE, Price, MO, Price, FW, Craig, JE, Fingert, JH, Gottsch, JD, Aldave, AJ, Klintworth, GK, Lass, JH, Li, YJ and Iyengar, SK 2017 , 'Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy' , Nature Communications, vol. 8 , pp. 1-8 , doi: 10.1038/ncomms14898.

Bennett, SL, Hewitt, AW, Poulsen, JL, Kearns, LS, Morgan, JE, Craig, JE and Mackey, DA 2007 , 'Screening for glaucomatous disc changes prior to diagnosis of glaucoma in myocilin pedifrees' , Archives of Ophthalmology, vol. 125, no. 1 , pp. 112-116 .

Burdon, KP, McKay, JD, Wirth, MG, Russell-Eggit, IM, Bhatti, S, Ruddle, JB, Dimasi, D, Mackey, DA and Craig, JE 2006 , 'The PITX3 gene in posterior polar congenital cataract in Australia' , Molecular Vision, vol. 12 , pp. 367-371 .

Burdon, KP ORCID: 0000-0001-8217-1249, Awadalla, MS, Mitchell, P, Wang, JJ, White, A, Keane, MC, Souzeau, E, Graham, SL, Goldberg, I, Healey, PR, Landers, J, Mills, RAD, Best, S, Hewitt, AW ORCID: 0000-0002-5123-5999, Sharma, Shiwani and Craig, JE 2018 , 'DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma' , Ophthalmic Genetics, vol. 39, no. 2 , pp. 221-227 , doi: 10.1080/13816810.2017.1413659.

Charlesworth, JC, Stankovich, J, Mackey, DA, Craig, JE, Haybittel, M, Westmore, RN and Sale, MM 2006 , 'Confirmation of the Adult-Onset Primary Open Angle Glaucoma Locus GLC1B at 2cen-q13 in an Australian family' , Ophthalmologica, vol. 220, no. 1 , pp. 23-30 , doi: 10.1159/000089271.

Cohn, AC, Toomes, C, Potter, C, Towns, KV, Hewitt, AW, Inglehearn, CF, Craig, JE and Mackey, DA 2007 , 'Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations' , American Journal of Ophthalmology, vol. 143, no. 4 , pp. 656-662 , doi: 10.1016/j.ajo.2006.12.038.

Cooke Bailey, JN, Gharahkhani, P, Kang, JH, Butkiewicz, M, Sullivan, DA, Weinreb, RN, Aschard, H, Allingham, RR, Ashley-Koch, A, Lee, RK, Moroi, SE, Brilliant, MH, Wollstein, G, Schuman, JS, Fingert, JH, Budenz, DL, Realini, T, Gaasterland, T, Scott, WK, Singh, K, Sit, AJ, Igo Jr, RP, Song, YE, Hark, L, Ritch, R, Rhee, DJ, Vollrath, D, Zack, DJ, Medeiros, F, Vajaranant, TS, Chasman, DI, Christen, WG, Pericak-Vance, MA, Liu, Y, Kraft, P, Richards, JE, Rosner, BA, Hauser, MA, Craig, JE, Burdon, KP ORCID: 0000-0001-8217-1249, Hewitt, AW ORCID: 0000-0002-5123-5999, Mackey, DA, Haines, JL, MacGregor, S, Wiggs, JL and Pasquale, LR 2018 , 'Testosterone pathway genetic polymorphisms in relation to primary open-angle glaucoma: An analysis in two large datasets' , Investigative Ophthalmology and Visual Science, vol. 59, no. 2 , pp. 629-636 , doi: 10.1167/iovs.17-22708.

Daniszewski, M, Nguyen, Q, Chy, HS, Singh, V, Crombie, DE, Kulkarni, T, Liang, HH, Sivakumaran, P, Lidgerwood, GE, Hernandez, D, Conquest, A, Rooney, LA, Chevalier, S, Andersen, SB, Senabouth, A, Vickers, JC ORCID: 0000-0001-5671-4879, Mackey, DA, Craig, JE, Laslett, AL, Hewitt, AW ORCID: 0000-0002-5123-5999, Powell, JE and Pebay, A 2018 , 'Single-cell profiling identifies key pathways expressed by iPSCs cultured in different commercial media' , iScience, vol. 7 , pp. 30-39 , doi: 10.1016/j.isci.2018.08.016.

Dave, A, Craig, JE, Skrzypiec, K, Quinn, S, Barnes, M, Di Girolamo, N, Mackey, DA, Burdon, KP ORCID: 0000-0001-8217-1249, de Iongh, RU and Sharma, S 2019 , 'Epha2 genotype influences ultraviolet radiation induced cataract in mice' , Experimental Eye Research, vol. 188 , pp. 1-10 , doi: 10.1016/j.exer.2019.107806.

Dickinson, JL, Sale, MM, Passmore, AJ, FitzGerald, LM, Wheatley, CM, Burdon, KP, Craig, JE, Tengtrisorn, S, Carden, SM, Franzco, HM and Mackey, DA 2006 , 'Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity' , Clinical and Experimental Ophthalmology, vol. 34, no. 7 , pp. 682-688 , doi: 10.1111/j.1442-9071.2006.01314.x.

Dimasi, DP, Hewitt, AW, Straga, T, Pater, J, MacKinnon, JR, Elder, JE, Casey, T, Mackey, DA and Craig, JE 2007 , 'Prevalence of CYP1B1 mutations in Australian patients with primary congenial glaucoma' , Clinical Genetics, vol. 72, no. 3 , pp. 255-260 , doi: 10.1111/j.1399-0004.2007.00864.x.

Gharahkhani, P, Burdon, KP ORCID: 0000-0001-8217-1249, Cooke Bailey, JN, Hewitt, AW ORCID: 0000-0002-5123-5999, Law, MH, Pasquale, LR, Kang, JH, Haines, JL, Souzeau, E, Zhou, T, Siggs, OM, Landers, J, Awadalla, M, Sharma, Shiwani, Mills, RA, Ridge, B, Lynn, D, Casson, R, Graham, SL, Goldberg, I, White, A, Healey, PR, Grigg, J, Lawlor, M, Mitchell, P, Ruddle, J, Coote, M, Walland, M, Best, S, Vincent, A, Gale, J, RadfordSmith, G, Whiteman, DC, Montgomery, GW, Martin, NG, Mackey, DA, Wiggs, JL, MacGregor, S and Craig, JE 2018 , 'Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma' , Scientific Reports, vol. 8, no. 1 , pp. 1-12 , doi: 10.1038/s41598-018-20435-9.

Graham, PS, Kaidonis, G, Abhary, S, Gillies, MC, Daniell, M, Essex, RW, Chang, JH, Lake, SR, Pal, B, Jenkins, AJ, Hewitt, AW ORCID: 0000-0002-5123-5999, Lamoureux, EL, Hykin, PG, Petrovsky, N, Brown, MA, Craig, JE and Burdon, KP ORCID: 0000-0001-8217-1249 2018 , 'Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy' , BMC Medical Genetics, vol. 19, no. 1 , pp. 1-8 , doi: 10.1186/s12881-018-0587-8.

Green, CM, Kearns, LS, Wu, F, Barbour, JM, Wilkinson, RM, Ring, M, Craig, JE, Wong, Tiffany L, Hewitt, AW and Mackey, DA 2007 , 'How significant is a family history of glaucoma? Experience from the Glaucoma Inheritance Study in Tasmania' , Clinical and Experimental Ophthalmology, vol. 35, no. 9 , pp. 793-799 , doi: 10.1111/j.1442-9071.2007.01612.x.

Han, X, Souzeau, E, Ong, J-S, An, J, Siggs, OM, Burdon, KP ORCID: 0000-0001-8217-1249, Best, S, Goldberg, I, Healey, PR, Graham, SL, Ruddle, JB, Mills, RA, Landers, J, Galanopoulos, A, White, AJR, Casson, R, Mackey, DA, Hewitt, AW ORCID: 0000-0002-5123-5999, Gharahkhani, P, Craig, JE and MacGregor, S 2018 , 'Myocilin gene Gln368Ter variant penetrance and association with glaucoma in population-based and registry-based studies' , JAMA Ophthalmology , E1-E8 , doi: 10.1001/jamaophthalmol.2018.4477.

Hewitt, AW, Bennett, SL, Fingert, JH, Cooper, RL, Stone, EM, Craig, JE and Mackey, DA 2007 , 'The optic nerve head in myocilin glaucoma' , Investigative Ophthalmology & Visual Science, vol. 48, no. 1 , pp. 238-243 , doi: 10.1167/iovs.06-0611.

Hewitt, AW, Garway-Heath, DF, Green, CM, Hammond, CJ, Hayreb, SS, Jonas, JB, Kaufman, PL, Miller, NR, Morgan, WH, Newman, NJ, Quigley, HA, Poulsen, JP, Samples, JR, Spaeth, GL, Pesudovs, K, Mackey, DA, Alward, WLM, Bennett, SL, Budde, WM, Cooper, RL, Craig, JE, Fingert, JH and Foster, PJ 2007 , 'Heritable features of the optic disc: a novel twin method for determining genetic significance' , Investigative Ophthalmology & Visual Science, vol. 48, no. 6 , pp. 2469-2475 , doi: 10.1167/iovs.06-1470.

Hewitt, AW, Heon, E, Craig, JE, Mackey, DA, Bennett, SL, Richards, JE, Dimasi, DP, Booth, AP, Inglehearn, CF, Anwar, R, Yamamoto, T and Fingert, JH 2007 , 'Myocilin Gly252Arg mutation and glaucoma of intermediate severity in caucasioan individuals' , Archives of Ophthalmology, vol. 125, no. 1 , pp. 98-104 .

Hewitt, AW, Mackey, DA and Craig, JE 2007 , 'Myocilin Allele-Specific Glaucoma Phenotype Database' , Human Mutation, vol. 29, no. 2 , pp. 207-211 , doi: 10.1002/humu.20634.

Hewitt, AW ORCID: 0000-0002-5123-5999, Januar, V, Sexton-Oates, A, Joo, JE, Franchina, M, Wang, JJ, Liang, H, Craig, JE and Saffery, R 2017 , 'DNA methylation landscape of ocular tissue relative to matched peripheral blood' , Scientific Reports, vol. 7 , pp. 1-8 , doi: 10.1038/srep46330.

Hewitt, AW, Sharma, Shiwani, Burdon, KP, Wang, JJ, Baird, PN, Dimasi, DP, Mackey, DA, Mitchell, P and Craig, JE 2007 , 'Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people' , Human Molecular Genetics, vol. 17, no. 5 , pp. 710-716 , doi: 10.1093/hmg/ddm342.

Iglesias, AI, Mishra, A, Vitart, V, Bykhovskaya, Y, Hohn, R, Springelkamp, H, Cuellar-Partida, G, Gharahkhani, P, Cooke Bailey, JN, Willoughby, CE, Li, Xiaohui, Yazar, S, Nag, A, Khawaja, AP, Polasek, O, Siscovick, D, Mitchell, P, Tham, YC, Haines, JL, Kearns, LS, Hayward, C, Shi, Y, van Leeuwen, EM, Taylor, KD, Bonnemaijer, P, Rotter, JI, Martin, NG, Zeller, T, Mills, RA, Staffieri, SE, Jonas, JB, Schmidtmann, I, Boutin, T, Kang, JH, Lucas, SEM, Wong, TY, Beutel, ME, Wilson, JF, Uitterlinden, AG, Vithana, EN, Foster, PJ, Hysi, PG, Hewitt, AW ORCID: 0000-0002-5123-5999, Khor, CC, Pasquale, LR, Montgomery, GW, Klaver, CCW, Aung, T, Pfeiffer, N, Mackey, DA, Hammond, CJ, Cheng, CY, Craig, JE, Rabinowitz, YS, Wiggs, JL, Burdon, KP ORCID: 0000-0001-8217-1249, van Duijn, CM and MacGregor, S 2018 , 'Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases' , Nature Communications, vol. 9, no. 1 , pp. 1-11 , doi: 10.1038/s41467-018-03646-6.

Javadiyan, S, Craig, JE, Sharma, Shiwani, Lower, KM, Casey, T, Haan, E, Souzeau, E and Burdon, KP ORCID: 0000-0001-8217-1249 2017 , 'Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)' , BMC Medical Genetics, vol. 18, no. 1 , pp. 1-6 , doi: 10.1186/s12881-017-0414-7.

Javadiyan, S, Craig, JE, Souzeau, E, Sharma, Shiwani, Lower, KM, Mackey, DA, Staffieri, SE, Elder, JE, Taranath, D, Straga, T, Black, J, Pater, J, Casey, T, Hewitt, AW ORCID: 0000-0002-5123-5999 and Burdon, KP ORCID: 0000-0001-8217-1249 2017 , 'High-throughput genetic screening of 51 pediatric cataract genes identifies causative mutations in inherited pediatric cataract in South Eastern Australia' , G3: Genes, Genomes, Genetics, vol. 7, no. 10 , pp. 3257-3268 , doi: 10.1534/g3.117.300109.

Javadiyan, S, Lucas, SEM, Wangmo, D, Ngy, M, Edussuriya, K, Craig, JE, Rudkin, A, Casson, R, Selva, D, Sharma, Shiwani, Lower, KM, Meucke, J and Burdon, KP ORCID: 0000-0001-8217-1249 2018 , 'Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri Lanka' , Molecular Genetics & Genomic Medicine , pp. 1-10 , doi: 10.1002/mgg3.406.

Kaidonis, G, Hassall, MM, Phillips, R, Raymond, G, Saha, N, Wong, GH, Gilhotra, JS, Liu, E, Burdon, KP ORCID: 0000-0001-8217-1249, Henderson, T, Newland, H, Lake, SR and Craig, JE 2017 , 'Visual outcomes following vitrectomy for diabetic retinopathy amongst Indigenous and non-Indigenous Australians in South Australia and the Northern Territory' , Clinical and Experimental Ophthalmology , pp. 1-7 , doi: 10.1111/ceo.13083.

Kuot, A, Hewitt, AW ORCID: 0000-0002-5123-5999, Snibson, GR, Souzeau, E, Mills, R, Craig, JE, Burdon, KP ORCID: 0000-0001-8217-1249 and Sharma, Shiwani 2017 , 'TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases' , PLoS One, vol. 12, no. 8 , pp. 1-13 , doi: 10.1371/journal.pone.0183719.

Kuot, A, Ronci, M, Mills, R, Klebe, S, Snibson, G, Wiffen, S, Loh, R, Corbett, M, Zhou, T, Chataway, T, Burdon, KP ORCID: 0000-0001-8217-1249, Craig, JE, Urbani, A and Sharma, Shiwani 2019 , 'Reduced expression of apolipoprotein E and immunoglobulin heavy constant gamma 1 proteins in Fuchs endothelial corneal dystrophy' , Clinical and Experimental Ophthalmology , pp. 1-15 , doi: 10.1111/ceo.13569.

Liu, E, Craig, JE and Burdon, K ORCID: 0000-0001-8217-1249 2017 , 'Diabetic macular oedema: clinical risk factors and emerging genetic influences' , Clinical and Experimental Optometry, vol. 100, no. 6 , pp. 569-576 , doi: 10.1111/cxo.12552.

Liu, E, Estevez, J, Kaidonis, G, Hassall, M, Phillips, R, Raymond, G, Saha, N, Wong, GHC, Gilhotra, J, Burdon, K ORCID: 0000-0001-8217-1249, Landers, J, Henderson, T, Newland, H, Lake, S and Craig, JE 2019 , 'Long-term survival rates of patients undergoing vitrectomy for diabetic retinopathy in an Australian population: a population-based audit' , Clinical and Experimental Ophthalmology, vol. 47, no. 5 , pp. 598-604 , doi: 10.1111/ceo.13466.

Liu, E, Kaidonis, G, Gillies, MC, Abhary, S, Essex, RW, Chang, JH, Pal, B, Daniell, M, Lake, S, Gilhotra, J, Petrovsky, N, Hewitt, AW, Jenkins, A, Lamoureux, EL, Gleadle, JM, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2019 , 'Mitochondrial haplogroups are not associated with diabetic retinopathy in a large Australian and British Caucasian sample' , Scientific Reports, vol. 9, no. 1 , pp. 1-7 , doi: 10.1038/s41598-018-37388-8.

Lucas, SEM, Zhou, T, Blackburn, NB, Mills, RA, Ellis, J, Leo, P, Souzeau, E, Ridge, B, Charlesworth, JC ORCID: 0000-0001-6201-3518, Brown, MA, Lindsay, RC, Craig, JE and Burdon, KP ORCID: 0000-0001-8217-1249 2017 , 'Rare, potentially pathogenic variants in ZNF469 are not enriched in keratoconus in a large Australian cohort of European descent' , Investigative Ophthalmology and Visual Science (Iovs), vol. 58, no. 14 , pp. 6248-6256 , doi: 10.1167/iovs.17-22417.

Lucas, SEM, Zhou, T, Blackburn, NB, Mills, RA, Ellis, J, Leo, P, Souzeau, E, Ridge, B, Charlesworth, JC ORCID: 0000-0001-6201-3518, Lindsay, R, Craig, JE and Burdon, KP ORCID: 0000-0001-8217-1249 2018 , 'Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent' , PLoS One, vol. 13, no. 6 , pp. 1-15 , doi: 10.1371/journal.pone.0199178.

MacGregor, S, Ong, J-S, An, J, Han, X, Zhou, T, Siggs, OM, Law, MH, Souzeau, E, Sharma, Shiwani, Lynn, DJ, Beesley, J, Sheldrick, B, Mills, RA, Landers, J, Ruddle, JB, Graham, SL, Healey, PR, White, AJR, Casson, RJ, Best, S, Grigg, JR, Goldberg, I, Powell, JE, Whiteman, DC, Radford-Smith, GL, Martin, NG, Montgomery, GW, Burdon, KP ORCID: 0000-0001-8217-1249, Mackey, DA, Gharahkhani, P, Craig, JE and Hewitt, AW ORCID: 0000-0002-5123-5999 2018 , 'Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma' , Nature Genetics, vol. 50, no. 8 , pp. 1067-1071 , doi: 10.1038/s41588-018-0176-y.

Marshall, HN, Andrew, NH, Hassall, M, Qassim, A, Souzeau, E, Ridge, B, Nguyen, T, Fitzgerald, J, Awadalla, MS, Burdon, KP ORCID: 0000-0001-8217-1249, Healey, PR, Agar, A, Galanopoulos, A, Hewitt, AW ORCID: 0000-0002-5123-5999, Graham, SL, Landers, J, Casson, RJ and Craig, JE 2019 , 'Macular ganglion cell-inner plexiform layer loss precedes peripapillary retinal nerve fiber layer loss in glaucoma with lower intraocular pressure' , Ophthalmology , pp. 1-12 , doi: 10.1016/j.ophtha.2019.03.016.

Meng, W, Shah, KP, Pollack, S, Toppila, I, Hebert, HL, McCarthy, MI, Groop, L, Ahlqvist, E, Lyssenko, V, Agardh, E, Daniell, M, Kaidonis, G, Craig, JE, Mitchell, P, Liew, G, Kifley, A, Wang, JJ, Christiansen, MW, Jensen, RA, Penman, A, Hancock, HA, Chen, CJ, Correa, A, Kuo, JZ, Li, Xiaohui, Chen, Y-der I, Rotter, JI, Klein, R, Klein, B, Wong, TY, Morris, AD, Doney, ASF, Colhoun, HM, Price, AL, Burdon, KP ORCID: 0000-0001-8217-1249, Groop, P-H, Sandholm, N, Grassi, MA, Sobrin, L and Palmer, CNA 2018 , 'A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes' , Acta Ophthalmologica, vol. 96, no. 7 , e811-e819 , doi: 10.1111/aos.13769.

Nguyen Tran, MT, Mohd Khalid, MKN, Pebay, A, Cook, AL ORCID: 0000-0003-1770-7910, Liang, HH, Wong, RCB, Craig, JE, Liu, G-S ORCID: 0000-0003-3379-724X, Hung, SS and Hewitt, AW ORCID: 0000-0002-5123-5999 2019 , 'Screening of CRISPR/Cas base editors to target the AMD high-risk Y402H complement factor H variant' , Molecular Vision, vol. 25 , pp. 174-182 .

Pollack, S, Igo Jr, RP, Jensen, RA, Christiansen, M, Li, X, Cheng, CY, Ng, MCY, Smith, AV, Rossin, EJ, Segre, AV, Davoudi, S, Tan, GS, Chen, Y-DI, Kuo, JZ, Dimitrov, LM, Stanwyck, LK, Meng, W, Hosseini, SM, Imamura, M, Nousome, D, Kim, J, Hai, Y, Jia, Y, Ahn, J, Leong, A, Shah, K, Park, KH, Guo, X, Ipp, E, Taylor, KD, Adler, SG, Sedor, JR, Freedman, BI, Lee, I-T, Sheu, WH-H, Kubo, M, Takahashi, A, Hadjadj, S, Marre, M, Tregouet, D-A, Mckean-Cowdin, R, Varma, R, McCarthy, MI, Groop, L, Ahlqvist, E, Lyssenko, V, Agardh, E, Morris, A, Doney, ASF, Colhoun, HM, Toppila, I, Sandholm, N, Groop, P-H, Maeda, S, Hanis, CL, Penman, A, Chen, CJ, Hancock, H, Mitchell, P, Craig, JE, Chew, EY, Paterson, AD, Grassi, MA, Palmer, C, Bowden, DW, Yaspan, BL, Siscovick, D, Cotch, MF, Wang, JJ, Burdon, KP ORCID: 0000-0001-8217-1249, Wong, TY, Klein, BEK, Klein, R, Rotter, JI, Iyengar, SK, Price, AL and Sobrin, L 2018 , 'Multiethnic genome-wide association study of diabetic retinopathy using liability threshold modeling of duration of diabetes and glycemic control' , Diabetes, vol. 68, no. 2 , pp. 441-456 , doi: 10.2337/db18-0567.

Shiga, Y, Akiyama, M, Nishiguchi, KM, Sato, K, Shimozawa, N, Takahashi, A, Momozawa, Y, Hirata, M, Matsuda, K, Yamaji, T, Iwasaki, M, Tsugane, S, Oze, I, Mikami, H, Naito, M, Wakai, K, Yoshikawa, M, Miyake, M, Yamashiro, K, Kashiwagi, K, Iwata, T, Mabuchi, F, Takamoto, M, Ozaki, M, Kawase, K, Aihara, M, Araie, M, Yamamoto, T, Kiuchi, Y, Nakamura, M, Ikeda, Y, Sonoda, KH, Ishibashi, T, Nitta, K, Iwase, A, Shirato, S, Oka, Y, Satoh, M, Sasaki, M, Fuse, N, Suzuki, Y, Cheng, CY, Khor, CC, Baskaran, M, Perera, S, Aung, T, Vithana, EN, Cooke Bailey, JN, Kang, JH, Pasquale, LR, Haines, JL, Wiggs, JL, Burdon, KP ORCID: 0000-0001-8217-1249, Gharahkhani, P, Hewitt, AW ORCID: 0000-0002-5123-5999, Mackey, DA, MacGregor, S, Craig, JE, Allingham, RR, Hauser, M, Ashaye, A, Budenz, DL, Akafo, S, Williams, SEI, Kamatani, Y, Nakazawa, T and Kubo, M 2018 , 'Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma' , Human Molecular Genetics, vol. 27, no. 8 , 1486–1496 , doi: 10.1093/hmg/ddy053.

Siggs, OM, Javadiyan, S, Sharma, Shiwani, Souzeau, E, Lower, KM, Taranath, DA, Black, J, Pater, J, Willoughby, JG, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2017 , 'Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataract' , European Journal of Human Genetics, vol. 25, no. 6 , pp. 711-718 , doi: 10.1038/ejhg.2017.33.

Siggs, OM, Souzeau, E, Pasutto, F, Dubowsky, A, Smith, JEH, Taranath, D, Pater, J, Rait, JL, Narita, A, Mauri, L, Del Longo, A, Reis, A, Chappell, A, Kearns, LS, Staffieri, SE, Elder, JE, Ruddle, JB, Hewitt, AW ORCID: 0000-0002-5123-5999, Burdon, KP ORCID: 0000-0001-8217-1249, Mackey, DA and Craig, JE 2019 , 'Prevalence of FOXC1 variants in individuals with a suspected diagnosis of primary congenital glaucoma' , JAMA Ophthalmology, no. Januar , E1-E8 , doi: 10.1001/jamaophthalmol.2018.5646.

Sobrin, L, Chong, YH, Fan, Q, Gan, A, Stanwyck, LK, Kaidonis, G, Craig, JE, Kim, J, Liao, WL, Huang, YC, Lee, WJ, Hung, YJ, Guo, X, Hai, Y, Ipp, E, Pollack, S, Hancock, H, Price, A, Penman, A, Mitchell, P, Liew, G, Smith, AV, Gudnason, V, Tan, G, Klein, BEK, Kuo, J, Li, Xiaohui, Christiansen, MW, Psaty, BM, Sandow, K, Jensen, RA, Klein, R, Cotch, MF, Wang, JJ, Jia, Y, Chen, CJ, Chen, YDI, Rotter, JL, Tsai, FJ, Hanis, CL, Burdon, KP ORCID: 0000-0001-8217-1249, Wong, TY and Cheng, CY 2017 , 'Genetically determined plasma lipid levels and risk of diabetic retinopathy: A mendelian randomization study' , Diabetes, vol. 66, no. 12 , pp. 3130-3141 , doi: 10.2337/db17-0398.

Souzeau, E, Rudkin, AK, Dubowsky, A, Casson, RJ, Muecke, JS, Mancel, E, Whiting, M, Mills, RAD, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2018 , 'PAX6 molecular analysis and genotype-phenotype correlations in families with aniridia from Australasia and Southeast Asia' , Molecular Vision, vol. 24 , pp. 261-273 .

Souzeau, E, Siggs, OM, Zhou, T, Galanopoulos, A, Hodson, T, Taranath, D, Mills, RA, Landers, J, Pater, J, Smith, JE, Elder, JE, Rait, JL, Giles, P, Phakey, V, Staffieri, SE, Kearns, LS, Dubowsky, A, Mackey, DA, Hewitt, AW ORCID: 0000-0002-5123-5999, Ruddle, JB, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2017 , 'Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants' , European Journal of Human Genetics, vol. 25, no. 7 , pp. 839-847 , doi: 10.1038/ejhg.2017.59.

Souzeau, E, Tram, KH, Witney, M, Ruddle, JB, Graham, SL, Healey, PR, Goldberg, I, Mackey, DA, Hewitt, AW ORCID: 0000-0002-5123-5999, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2017 , 'Myocilin predictive genetic testing for primary open-angle glaucoma leads to early identification of at-risk individuals' , Ophthalmology, vol. 124, no. 3 , pp. 303-309 , doi: 10.1016/j.ophtha.2016.11.011.

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This list was generated on Thu Feb 27 01:40:01 2020 AEDT.
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