Intersession test–retest variability of conventional and novel parameters using the MP-1 microperimeter

by Wong, Evan N, Mackey, David A, Morgan, William H, Chen, Fred Kuanfu
Published 2015

Benchmarking Undedicated Cloud Computing Providers for Analysis of Genomic Datasets

by Yazar, Seyhan, Gooden, George E. C., Mackey, David A., Hewitt, Alex W.
Published 2014

iPS Cells for Modelling and Treatment of Retinal Diseases

by Chen, Fred K., McLenachan, Samuel, Edel, Michael, Da Cruz, Lyndon, Coffey, Peter J., Mackey, David A.
Published 2014

Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research

by Souzeau, Emmanuelle, Burdon, Kathryn P., Mackey, David A., Hewitt, Alex W., Savarirayan, Ravi, Otlowski, Margaret, Craig, Jamie E.
Published 2016

Mitochondrial Oxidative Phosphorylation Compensation May Preserve Vision in Patients with OPA1-Linked Autosomal Dominant Optic Atrophy

by Van Bergen, Nicole J., Crowston, Jonathan G., Kearns, Lisa S., Staffieri, Sandra E., Hewitt, Alex W., Cohn, Amy C., Mackey, David A., Trounce, Ian A.
Published 2011

An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error

by Abbott, Diana, Li, Yi-Ju, Guggenheim, Jeremy A., Metlapally, Ravikanth, Malecaze, Francois, Calvas, Patrick, Rosenberg, Thomas, Paget, Sandrine, Zayats, Tetyana, Mackey, David A., Feng, Sheng, Young, Terri L.
Published 2012

Mutations in the EPHA2 Gene Are a Major Contributor to Inherited Cataracts in South-Eastern Australia

by Dave, Alpana, Laurie, Kate, Staffieri, Sandra E., Taranath, Deepa, Mackey, David A., Mitchell, Paul, Wang, Jie Jin, Craig, Jamie E., Burdon, Kathryn P., Sharma, Shiwani
Published 2013

Measurement of Systemic Mitochondrial Function in Advanced Primary Open-Angle Glaucoma and Leber Hereditary Optic Neuropathy

by 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.
Published 2015

Meta-analysis of human methylation data for evidence of sex-specific autosomal patterns

by McCarthy, Nina S, Melton, Phillip E, Cadby, Gemma, Yazar, Seyhan, Franchina, Maria, Moses, Eric K, Mackey, David A, Hewitt, Alex W
Published 2014

The role of toll-like receptor variants in acute anterior uveitis

by Pratap, Divya S., Lim, Lyndell L., Wang, Jie Jin, Mackey, David A., Kearns, Lisa S., Stawell, Richard J., Burdon, Kathryn P., Mitchell, Paul, Craig, Jamie E., Hall, Anthony J., Hewitt, Alex W.
Published 2011

Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: Results of a genome-wide association...

by Yazar, Seyhan, Mishra, Aniket, Ang, Wei, Kearns, Lisa S., Mountain, Jenny A., Pennell, Craig, Montgomery, Grant W., Young, Terri L., Hammond, Christopher J., Macgregor, Stuart, Mackey, David A., Hewitt, Alex W.
Published 2013

The p53 Codon 72 PRO/PRO Genotype May Be Associated with Initial Central Visual Field Defects in Caucasians with Primary Open Angle Glaucoma

by Wiggs, Janey L., Hewitt, Alex W., Fan, Bao Jian, Wang, Dan Yi, Figueiredo Sena, Dayse R., O’Brien, Colm, Realini, Anthony, Craig, Jamie E., Dimasi, David P., Mackey, David A., Haines, Jonathan L., Pasquale, Louis R.
Published 2012

Rationale, design and methods for a community-based study of clustering and cumulative effects of chronic disease processes and their effects on ageing: the Busselton healthy agein...

by James, Alan, Hunter, Michael, Straker, Leon, Beilby, John, Bucks, Romola, Davis, Tim, Eikelboom, Robert H, Hillman, David, Hui, Jennie, Hung, Joe, Knuiman, Matthew, Mackey, David A, Newton, Robert U, Palmer, Lyle J, Musk, AW Bill
Published 2013

CYP1B1 copy number variation is not a major contributor to primary congenital glaucoma

by Souzeau, Emmanuelle, Hayes, Melanie, Ruddle, Jonathan B., Elder, James E., Staffieri, Sandra E., Kearns, Lisa S., Mackey, David A., Zhou, Tiger, Ridge, Bronwyn, Burdon, Kathryn P., Dubowsky, Andrew, Craig, Jamie E.
Published 2015

Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration

by Cuellar-Partida, Gabriel, Craig, Jamie E., Burdon, Kathryn P., Wang, Jie Jin, Vote, Brendan J., Souzeau, Emmanuelle, McAllister, Ian L., Isaacs, Timothy, Lake, Stewart, Mackey, David A., Constable, Ian J., Mitchell, Paul, Hewitt, Alex W., MacGregor, Stuart
Published 2016

Study of mitochondrial respiratory defects on reprogramming to human induced pluripotent stem cells

by Hung, Sandy S.C., Van Bergen, Nicole J., Jackson, Stacey, Liang, Helena, Mackey, David A., Hernández, Damián, Lim, Shiang Y., Hewitt, Alex W., Trounce, Ian, Pébay, Alice, Wong, Raymond C.B.
Published 2016

Rare variants in optic disc area gene CARD10 enriched in primary open‐angle glaucoma

by Zhou, Tiger, Souzeau, Emmanuelle, Sharma, Shiwani, Siggs, Owen M., Goldberg, Ivan, Healey, Paul R., Graham, Stuart, Hewitt, Alex W., Mackey, David A., Casson, Robert J., Landers, John, Mills, Richard, Ellis, Jonathan, Leo, Paul, Brown, Matthew A., MacGregor, Stuart, Burdon, Kathryn P., Craig, Jamie E.
Published 2016

A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort

by Nag, Abhishek, Venturini, Cristina, Small, Kerrin S., Young, Terri L., Viswanathan, Ananth C., Mackey, David A., Hysi, Pirro G., Hammond, Christopher, Aung, Tin, Cheng, Ching-Yu, Fleck, Brian W, Gibson, Jane, Hewitt, Alex W, Hofman, Albert, Höhn, René, Jonas, Jost B, Khor, Chiea-Cheun, Klaver, Caroline CW, Lemij, Hans G, Liao, Jiemin, Lotery, Andrew J, Lu, Yi, Macgregor, Stuart, Mitchell, Paul, Ramdas, Wishal D, Springelkamp, Henriët, Tai, E-Shyong, Teo, Yik-Ying, Uitterlinden, André G, van Duijn, Cornelia M, van Koolwijk, Leonieke ME, Vingerling, Johannes R, Vitart, Veronique, Vithana, Eranga, Wang, Jie Jin, Williams, Katie M, Wojciechowski, Robert, Wong, Tien-Yin, Xu, Liang, Yonova-Doing, Ekaterina, Tanja, Zeller
Published 2014

Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

by Fan, Qiao, Guo, Xiaobo, Tideman, J. Willem L., Williams, Katie M., Yazar, Seyhan, Hosseini, S. Mohsen, Howe, Laura D., Pourcain, Beaté St, Evans, David M., Timpson, Nicholas J., McMahon, George, Hysi, Pirro G., Krapohl, Eva, Wang, Ya Xing, Jonas, Jost B., Baird, Paul Nigel, Wang, Jie Jin, Cheng, Ching-Yu, Teo, Yik-Ying, Wong, Tien-Yin, Ding, Xiaohu, Wojciechowski, Robert, Young, Terri L., Pärssinen, Olavi, Oexle, Konrad, Pfeiffer, Norbert, Bailey-Wilson, Joan E., Paterson, Andrew D., Klaver, Caroline C. W., Plomin, Robert, Hammond, Christopher J., Mackey, David A., He, Mingguang, Saw, Seang-Mei, Williams, Cathy, Guggenheim, Jeremy A.
Published 2016

Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma

by Gharahkhani, Puya, Burdon, Kathryn P, Fogarty, Rhys, Sharma, Shiwani, Hewitt, Alex W., Martin, Sarah, Law, Matthew H., Cremin, Katie, Bailey, Jessica N. Cooke, Loomis, Stephanie J., Pasquale, Louis R., Haines, Jonathan L., Hauser, Michael A., Viswanathan, Ananth C., McGuffin, Peter, Topouzis, Fotis, Foster, Paul J., Graham, Stuart L, Casson, Robert J, Chehade, Mark, White, Andrew J, Zhou, Tiger, Souzeau, Emmanuelle, Landers, John, Fitzgerald, Jude T, Klebe, Sonja, Ruddle, Jonathan B, Goldberg, Ivan, Healey, Paul R, Mills, Richard A., Wang, Jie Jin, Montgomery, Grant W., Martin, Nicholas G., RadfordSmith, Graham, Whiteman, David C., Brown, Matthew A., Wiggs, Janey L., Mackey, David A, Mitchell, Paul, MacGregor, Stuart, Craig, Jamie E.
Published 2014