Measurement of Systemic Mitochondrial Function in Advanced Primary Open-Angle Glaucoma and Leber Hereditary Optic Neuropathy von Van Bergen, Nicole J, Crowston, Jonathan G, Craig, Jamie E, Burdon, Kathryn P, Kearns, Lisa S, Sharma, Shiwani, Hewitt, Alex W, Mackey, David A, Trounce, Ian A

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Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma von MacGregor, Stuart, Ong, Jue-Sheng, An, Jiyuan, Han, Xikun, Zhou, Tiger, Siggs, Owen M., Law, Matthew H., Souzeau, Emmanuelle, Sharma, Shiwani, Lynn, David J., Beesley, Jonathan, Sheldrick, Bronwyn, Mills, Richard A., Landers, John, Ruddle, Jonathan B., Graham, Stuart L., Healey, Paul R., White, Andrew J. R., Casson, Robert J., Best, Stephen, Grigg, John R, Goldberg, Ivan, Powell, Joseph E., Whiteman, David C., Radford-Smith, Graham L., Martin, Nicholas G., Montgomery, Grant W., Burdon, Kathryn P., Mackey, David A., Gharahkhani, Puya, Craig, Jamie E., Hewitt, Alex W.

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TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases von Kuot, Abraham, Hewitt, Alex W, Snibson, Grant R, Souzeau, Emmanuelle, Mills, Richard, Craig, Jamie E, Burdon, Kathryn P, Sharma, Shiwani

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Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1 von Burdon, Kathryn P, Macgregor, Stuart, Hewitt, Alex W, Sharma, Shiwani, Chidlow, Glyn, Mills, Richard A, Danoy, Patrick, Casson, Robert, Viswanathan, Ananth C, Liu, Jimmy Z, Landers, John, Henders, Anjali K, Wood, John, Souzeau, Emmanuelle, Crawford, April, Leo, Paul, Wang, Jie Jin, Rochtchina, Elena, Nyholt, Dale R, Martin, Nicholas G, Montgomery, Grant W, Mitchell, Paul, Brown, Matthew A, Mackey, David A, Craig, Jamie E

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A Systematic Meta-Analysis of Genetic Association Studies for Diabetic Retinopathy von ABHARY, Sotoodeh, HEWITT, Alex W, BURDON, Kathryn P, CRAIG, Jamie E

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Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy von Afshari, Natalie A., Igo, Robert P., Morris, Nathan J., Stambolian, Dwight, Sharma, Shiwani, Pulagam, V. Lakshmi, Dunn, Steven, Stamler, John F., Truitt, Barbara J., Rimmler, Jacqueline, Kuot, Abraham, Croasdale, Christopher R., Qin, Xuejun, Burdon, Kathryn P., Riazuddin, S. Amer, Mills, Richard, Klebe, Sonja, Minear, Mollie A., Zhao, Jiagang, Balajonda, Elmer, Rosenwasser, George O., Baratz, Keith H, Mootha, V. Vinod, Patel, Sanjay V., Gregory, Simon G., Bailey-Wilson, Joan E., Price, Marianne O., Price, Francis W., Craig, Jamie E., Fingert, John H., Gottsch, John D., Aldave, Anthony J., Klintworth, Gordon K., Lass, Jonathan H., Li, Yi-Ju, Iyengar, Sudha K.

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Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma von Siggs, Owen M., Souzeau, Emmanuelle, Taranath, Deepa A., Dubowsky, Andrew, Chappell, Angela, Zhou, Tiger, Javadiyan, Shari, Nicholl, Jillian, Kearns, Lisa S., Staffieri, Sandra E., Narita, Andrew, Smith, James E.H., Pater, John, Hewitt, Alex W., Ruddle, Jonathan B., Elder, James E., Mackey, David A., Burdon, Kathryn P., Craig, Jamie E.

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Uncovering genetic loci and biological pathways associated with age-related cataracts through GWAS meta-analysis von Diaz-Torres, Santiago, Lee, Samantha Sze-Yee, García-Marín, Luis M., Campos, Adrian I., Lingham, Garreth, Ong, Jue-Sheng, Mackey, David A., Burdon, Kathryn P., Hunter, Michael, Dong, Xianjun, MacGregor, Stuart, Gharahkhani, Puya, Rentería, Miguel E.

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Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness von Lu, Yi, Dimasi, David P, Hysi, Pirro G, Hewitt, Alex W, Burdon, Kathryn P, Toh, Tze'Yo, Ruddle, Jonathan B, Li, Yi Ju, Mitchell, Paul, Healey, Paul R, Montgomery, Grant W, Hansell, Narelle, Spector, Timothy D, Martin, Nicholas G, Young, Terri L, Hammond, Christopher J, Macgregor, Stuart, Craig, Jamie E, Mackey, David A

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The Association Between Vitamin D and Multiple Sclerosis Risk: 1,25(OH)2D3 Induces Super-Enhancers Bound by VDR von Lu, Ming, McComish, Bennet J., Burdon, Kathryn P., Taylor, Bruce V., Körner, Heinrich

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Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression von Craig, Jamie E., Han, Xikun, Qassim, Ayub, Hassall, Mark, Cooke Bailey, Jessica N., Kinzy, Tyler G., Khawaja, Anthony P., An, Jiyuan, Marshall, Henry, Gharahkhani, Puya, Igo, Robert P., Graham, Stuart L., Healey, Paul R., Ong, Jue-Sheng, Zhou, Tiger, Siggs, Owen, Law, Matthew H., Souzeau, Emmanuelle, Ridge, Bronwyn, Hysi, Pirro G., Burdon, Kathryn P., Mills, Richard A., Landers, John, Ruddle, Jonathan B., Agar, Ashish, Galanopoulos, Anna, White, Andrew J. R., Willoughby, Colin E., Andrew, Nicholas H., Best, Stephen, Vincent, Andrea L., Goldberg, Ivan, Radford-Smith, Graham, Martin, Nicholas G., Montgomery, Grant W., Vitart, Veronique, Hoehn, Rene, Wojciechowski, Robert, Jonas, Jost B., Aung, Tin, Pasquale, Louis R., Cree, Angela Jane, Sivaprasad, Sobha, Vallabh, Neeru A., Viswanathan, Ananth C., Pasutto, Francesca, Haines, Jonathan L., Klaver, Caroline C. W., van Duijn, Cornelia M., Casson, Robert J., Foster, Paul J., Khaw, Peng Tee, Hammond, Christopher J., Mackey, David A., Mitchell, Paul, Lotery, Andrew J., Wiggs, Janey L., Hewitt, Alex W., MacGregor, Stuart

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Identifying Genetic Biomarkers Predicting Response to Anti-Vascular Endothelial Growth Factor Injections in Diabetic Macular Edema von Gurung, Rajya L, FitzGerald, Liesel M, Liu, Ebony, McComish, Bennet J, Kaidonis, Georgia, Ridge, Bronwyn, Hewitt, Alex W, Vote, Brendan J, Verma, Nitin, Craig, Jamie E, Burdon, Kathryn P

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Generation of MNZTASi001-A, a human pluripotent stem cell line from a person with primary progressive multiple sclerosis von Mehta, Ashish, Lu, Peter, Taylor, Bruce V., Charlesworth, Jac, Cook, Anthony L., Burdon, Kathryn P., Hewitt, Alex W., Young, Kaylene M.

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Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent von Lucas, Sionne E M, Zhou, Tiger, Blackburn, Nicholas B, Mills, Richard A, Ellis, Jonathan, Leo, Paul, Souzeau, Emmanuelle, Ridge, Bronwyn, Charlesworth, Jac C, Lindsay, Richard, Craig, Jamie E, Burdon, Kathryn P

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Association of genetic variants with primary angle closure glaucoma in two different populations von Awadalla, Mona S, Thapa, Suman S, Hewitt, Alex W, Burdon, Kathryn P, Craig, Jamie E

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Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy von Graham, Patricia S, Kaidonis, Georgia, Abhary, Sotoodeh, Gillies, Mark C, Daniell, Mark, Essex, Rohan W, Chang, John H, Lake, Stewart R, Pal, Bishwanath, Jenkins, Alicia J, Hewitt, Alex W, Lamoureux, Ecosse L, Hykin, Philip G, Petrovsky, Nikolai, Brown, Matthew A, Craig, Jamie E, Burdon, Kathryn P

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The genetics of central corneal thickness von Dimasi, D P, Burdon, K P, Craig, J E

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The utility of genomic testing in the ophthalmology clinic: A review von Burdon, Kathryn P.

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Genome-wide association studies in the hunt for genes causing primary open-angle glaucoma: a review von Burdon, Kathryn P

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High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia von Javadiyan, Shari, Craig, Jamie E, Souzeau, Emmanuelle, Sharma, Shiwani, Lower, Karen M, Mackey, David A, Staffieri, Sandra E, Elder, James E, Taranath, Deepa, Straga, Tania, Black, Joanna, Pater, John, Casey, Theresa, Hewitt, Alex W, Burdon, Kathryn P

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