• The University of Western Australia (M517), 35 Stirling Highway,

    6009 Perth

    Australia

  • 5740 Citations
  • 40 h-Index
20052019
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Research Output 2005 2019

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Article
2014
3 Citations (Scopus)

TLR4 polymorphism is not associated with biopsy proven giant cell arteritis

Dunstan, E., Lester, S. L., Rischmueller, M., Chan, H., Hewitt, A. & Hill, C. L., 2014, In : Clinical and Experimental Rheumatology. 32, SUPPL.82, p. S26-S29

Research output: Contribution to journalArticle

Giant Cell Arteritis
Biopsy
Single Nucleotide Polymorphism
Haplotypes
Meta-Analysis
1 Citation (Scopus)
174 Downloads (Pure)

Utility of temporal artery biopsy samples for genome-wide analysis of giant cell arteritis

Cremin, K., Leo, P. J., Harris, J. E., De Smit, E., Bradbury, L. A., Mckelvie, P. A., Hill, C. L., Brown, M. A. & Hewitt, A., Jul 2014, In : Genes and Immunity. 15, 5, p. 338-340

Research output: Contribution to journalArticle

Open Access
File
Temporal Arteries
Giant Cell Arteritis
Paraffin
Formaldehyde
Genome
28 Citations (Scopus)

What is the appropriate age cut-off for cycloplegia in refraction?

Sanfilippo, P. G., Chu, B., Bigault, O., Kearns, L. S., Boon, M. Y., Young, T. L., Hammond, C. J., Hewitt, A. & Mackey, D., Sep 2014, In : Acta Ophthalmologica. 92, 6, p. e458-e462

Research output: Contribution to journalArticle

Refractive Errors
Twin Studies
Young Adult
Cyclopentolate
Tropicamide
2013
3 Citations (Scopus)

A geometric morphometric assessment of hand shape and comparison to the 2D: 4D digit ratio as a marker of sexual dimorphism

Sanfilippo, P. G., Hewitt, A., Mountain, J. & Mackey, D., Apr 2013, In : Twin Research and Human Genetics. 16, 2, p. 590-600

Research output: Contribution to journalArticle

Open Access
Twin Studies
Learning Curve
Sex Characteristics
Internet
Software
7 Citations (Scopus)

Copy number variation at chromosome 5q21.2 is associated with intra-ocular pressure

Nag, A., Venturini, C., Hysi, PG., Arno, M., Aldecoa-Otalora Astarloa, E., Macgregor, S., Hewitt, A., Young, TL., Mitchell, P., Viswanathan, AC., Mackey, D. & Hammond, CJ., 2013, In : Investigative ophthalmology & visual science. 54, p. 3607-3612

Research output: Contribution to journalArticle

Open Access
12 Citations (Scopus)
252 Downloads (Pure)

Establishment and evolution of the Australian Inherited Retinal Disease Register and DNA Bank

De Roach, JN., Mclaren, TL., Paterson, RL., O'Brien, EC., Hoffman, L., Mackey, D., Hewitt, A. & Lamey, T., Jul 2013, In : Clinical and Experimental Ophthalmology. 41, 5, p. 476-483

Research output: Contribution to journalArticle

Open Access
File
Retinal Diseases
DNA
Usher Syndromes
Technology
Retinitis Pigmentosa
8 Citations (Scopus)

Genetic Loci for Retinal Arteriolar Microcirculation

Sim, X., Jensen, R. A., Ikram, M. K., Cotch, M. F., Li, X., Macgregor, S., Xie, J., Smith, A. V., Boerwinkle, E., Mitchell, P., Klein, R., Klein, B. E. K., Glazer, N. L., Lumley, T., Mcknight, B., Psaty, B. M., De Jong, P. T. V. M., Hofman, A., Rivadeneira, F., Uitterlinden, A. G. & 36 othersVan Duijn, C. M., Aspelund, T., Eiríksdóttir, G., Harris, T. B., Jónasson, F., Launer, L. J., Attia, J., Baird, P. N., Harrap, S., Holliday, E. G., Inouye, M., Rochtchina, E., Scott, R. J., Viswanathan, A., Li, G., Smith, N. L., Wiggins, K. L., Kuo, J. Z., Taylor, K. D., Hewitt, A., Martin, N. G., Montgomery, G. W., Sun, C., Young, T. L., Mackey, D., Van Zuydam, N. R., Doney, A. S. F., Palmer, C. N. A., Morris, A. D., Rotter, J. I., Tai, E. S., Gudnason, V., Vingerling, J. R., Siscovick, D. S., Wang, J. J. & Wong, T. Y., 2013, In : PLoS One. 8, 6, p. 12pp

Research output: Contribution to journalArticle

Open Access
MEF2 Transcription Factors
flow resistance
Microcirculation
Retinal Vessels
vascular diseases
150 Citations (Scopus)

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Lu, Y., Vitart, V., Burdon, K. P., Khor, C. C., Bykhovskaya, Y., Mirshahi, A., Hewitt, A., Koehn, D., Hysi, P. G., Ramdas, W. D., Zeller, T., Vithana, E. N., Cornes, B. K., Tay, W-T., Tai, E. S., Cheng, C-Y., Liu, J., Foo, J-N., Saw, S. M., Thorleifsson, G. & 70 othersStefansson, K., Dimasi, D. P., Mills, R. A., Mountain, J., Ang, W., Hoehn, R., Verhoeven, V. J. M., Grus, F., Wolfs, R., Castagne, R., Lackner, K. J., Springelkamp, H., Yang, J., Jonasson, F., Leung, D. Y. L., Chen, L. J., Tham, C. C. Y., Rudan, I., Vatavuk, Z., Hayward, C., Gibson, J., Cree, A. J., Macleod, A., Ennis, S., Polasek, O., Campbell, H., Wilson, J. F., Viswanathan, A. C., Fleck, B., Li, X., Siscovick, D., Taylor, K. D., Rotter, J. I., Yazar, S., Ulmer, M., Li, J., Yaspan, B. L., Ozel, A. B., Richards, J. E., Moroi, S. E., Haines, J. L., Kang, J. H., Pasquale, L. R., Allingham, R. R., Ashley-Koch, A., Mitchell, P., Wang, J. J., Wright, A. F., Pennell, C., Spector, T. D., Young, T. L., Klaver, C. C. W., Martin, N. G., Montgomery, G. W., Anderson, M. G., Aung, T., Willoughby, C. E., Wiggs, J. L., Pang, C. P., Thorsteinsdottir, U., Lotery, A. J., Hammond, C. J., Van Duijn, C. M., Hauser, M. A., Rabinowitz, Y. S., Pfeiffer, N., Mackey, D., Craig, J. E., Macgregor, S. & Wong, T. Y., 2013, In : Nature Genetics. 45, p. 155

Research output: Contribution to journalArticle

220 Citations (Scopus)

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Verhoeven, V. J. M., Hysi, P. G., Wojciechowski, R., Fan, Q., Guggenheim, J. A., Höhn, R., Macgregor, S., Hewitt, A., Nag, A., Cheng, C., Yonova-Doing, E., Zhou, X., Ikram, M. K., Buitendijk, G. H. S., Mcmahon, G., Kemp, J. P., Pourcain, B. S., Simpson, C. L., Mäkelä, K. M., Lehtimäki, T. J. & 88 othersKähönen, M., Paterson, A. D., Hosseini, S. M. R. S., Wong, H., Xu, L., Jonas, J. B., Pärssinen, O., Wedenoja, J., Yip, S., Ho, D., Pang, C., Chen, L., Burdon, K. P., Craig, J. E., Klein, B. E. K., Klein, R. E., Haller, T., Metspalu, A. K., Khor, C. C., Tai, E. S. S., Aung, T., Vithana, E. N., Tay, W., Barathi, V. A., Chen, P., Li, R., Liao, J., Zheng, Y., Ong, R., Döring, A., Evans, D. M., Timpson, N. J., Verkerk, A. J. M. H., Meitinger, T. A., Raitakari, O. T., Hawthorne, F. A., Spector, T. D., Karssen, L. C., Pirastu, M., Murgia, F., Ang, W., Mishra, A., Montgomery, G. W., Pennell, C., Cumberland, P. M., Cotlarciuc, I., Mitchell, P., Wang, J., Schäche, M., Janmahasathian, S., Igo, R. P., Lass, J. H., Chew, E., Iyengar, S. K., Gorgels, T. G. M. F., Rudan, I., Hayward, C., Wright, A. F., Polašek, O., Vatavuk, Z., Wilson, J. F. F., Fleck, B. W., Zeller, T., Mirshahi, A., Mul̈ler, C., Uitterlinden, A. G., Rivadeneira, F. F., Vingerling, J. R., Hofman, A. F., Oostra, B. A., Amin, N., Bergen, A. A. B., Teo, Y. Y., Rahi, J. S., Vitart, V., Williams, C. E. C. S., Baird, P. N., Wong, T., Oexle, K., Pfeiffer, N., Mackey, D., Young, T., Van Duijn, C. M. A., Saw, S., Bailey-Wilson, J. E., Stambolian, D. E., Klaver, C. C. W. & Hammond, C. J., 2013, In : Nature Genetics. 45, 3, p. 314-318

Research output: Contribution to journalArticle

Refractive Errors
Myopia
Meta-Analysis
Genome
Genetic Load
26 Citations (Scopus)

Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an australasian disease registry

Souzeau, E., Burdon, K. P., Dubowsky, A., Grist, S. A., Usher, B., Fitzgerald, J. T., Crawford, A. W., Hewitt, A., Goldberg, I., Mills, R. A. D., Ruddle, J. B., Landers, J. A., Mackey, D. & Craig, J. E., 2013, In : Ophthalmology. 120, 6, p. 1135-1143

Research output: Contribution to journalArticle

Glaucoma
Registries
Mutation
Age of Onset
Genetic Testing
28 Citations (Scopus)

Hypomethylation of the IL17RC Promoter in Peripheral Blood Leukocytes Is Not A Hallmark of Age-Related Macular Degeneration

Oliver, V. F., Franchina, M., Jaffe, A. E., Branham, K. E., Othman, M., Heckenlively, J. R., Swaroop, A., Campochiaro, B., Vote, B. J., Craig, J. E., Saffery, R., Mackey, D., Qian, J., Zack, D. J., Hewitt, A. & Merbs, S. L., 2013, In : Cell Reports. 5, 6, p. 1527-1535

Research output: Contribution to journalArticle

Open Access
Methylation
Macular Degeneration
Leukocytes
Blood
DNA Methylation
22 Citations (Scopus)

Identification of a candidate gene for astigmatism

Lopes, M. C., Hysi, P. G., Verhoeven, V. J. M., Macgregor, S., Hewitt, A., Montgomery, G. W., Cumberland, P. M., Vingerling, J. R., Young, T., Van Duijn, C. M. A., Oostra, B. A., Uitterlinden, A. G., Rahi, J. S., Mackey, D., Klaver, C. C. W., Andrew, T. & Hammond, C. J., 2013, In : Investigative Ophthalmology and Visual Science. 54, 2, p. 1260-1267

Research output: Contribution to journalArticle

Open Access
Astigmatism
Genetic Association Studies
Refractive Errors
Meta-Analysis
Meridians
6 Citations (Scopus)

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 study

Yazar, S., Mishra, A., Ang, W., Kearns, L. S., Mountain, J., Pennell, C., Montgomery, G. W., Young, T. L., Hammond, C. J., Macgregor, S., Mackey, D. & Hewitt, A., 2013, In : Molecular Vision. 19, p. 1238-1246

Research output: Contribution to journalArticle

73 Citations (Scopus)

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

Cheng, C., Schäche, M., Ikram, M. K., Young, T., Guggenheim, J. A., Vitart, V., Macgregor, S., Verhoeven, V. J. M., Barathi, V. A., Liao, J., Hysi, P. G., Bailey-Wilson, J. E., St. Pourcain, B., Kemp, J. P., Mcmahon, G., Timpson, N. J., Evans, D. M., Montgomery, G. W., Mishra, A., Wang, Y. & 88 othersWang, J., Rochtchina, E., Polašek, O., Wright, A. F., Amin, N., Van Leeuwen, E. M., Wilson, J. F., Pennell, C., Van Duijn, C. M. A., De Jong, P. T. V. M., Vingerling, J. R., Zhou, X., Chen, P., Li, R., Tay, W., Zheng, Y., Chew, M., Burdon, K. P., Craig, J. E., Iyengar, S. K., Igo, R. P., Lass, J. H., Chew, E., Haller, T., Mihailov, E., Metspalu, A., Wedenoja, J., Simpson, C. L., Wojciechowski, R., Höhn, R., Mirshahi, A., Zeller, T., Pfeiffer, N., Lackner, K. J., Bettecken, T., Meitinger, T., Oexle, K., Pirastu, M., Portas, L., Nag, A., Williams, K. M., Yonova-Doing, E., Klein, R., Klein, B. E. K., Hosseini, S. M. R. S., Paterson, A. D., Mäkelä, K. M., Lehtimäki, T. J., Kähönen, M., Raitakari, O. T., Yoshimura, N., Matsuda, F., Chen, L., Pang, C., Yip, S., Yap, M., Meguro, A., Mizuki, N., Inoko, H., Foster, P. J. F., Zhao, J., Vithana, E. N., Tai, E. S. S., Fan, Q., Xu, L., Campbell, H., Fleck, B. W., Rudan, I., Aung, T., Hofman, A., Uitterlinden, A. G., Benčić, G., Khor, C. C., Forward, H., Pärssinen, O., Mitchell, P. B., Rivadeneira, F. F., Hewitt, A., Williams, C. E. C. S., Oostra, B. A., Teo, Y. Y., Hammond, C. J., Stambolian, D. E., Mackey, D., Klaver, C. C. W., Wong, T. Y., Saw, S. & Baird, P. N., 2013, In : American Journal of Human Genetics. 93, 2, p. 264-277

Research output: Contribution to journalArticle

Open Access
Eye Axial Length
Refractive Errors
Genome-Wide Association Study
Myopia
Hyperopia
19 Citations (Scopus)
286 Downloads (Pure)

Raine Eye Health Study: Design, Methodology and Baseline Prevalence of Ophthalmic Disease in a Birth-cohort Study of Young Adults

Yazar, S., Forward, H., Mcknight, C., Tan, A., Soloshenko, A., Oates, S. K., Ang, W., Sherwin, J., Wood, D., Mountain, J., Pennell, C., Hewitt, A. & Mackey, D., Dec 2013, In : Ophthalmic Genetics. 34, 4, p. 199-208

Research output: Contribution to journalArticle

Open Access
File
Eye Diseases
Young Adult
Cohort Studies
Parturition
Health
31 Citations (Scopus)

Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism

Poulter, J. A., Al-Araimi, M., Conte, I., Van Genderen, M. M., Sheridan, E., Carr, I. M., Parry, D. A., Shires, M., Carrella, S., Bradbury, J., Khan, K., Lakeman, P., Sergouniotis, P. I., Webster, A. R., Moore, A. T., Pal, B., Mohamed, M. D., Venkataramana, A., Ramprasad, V., Shetty, R. & 9 othersSaktivel, M., Kumaramanickavel, G., Tan, A., Mackey, D., Hewitt, A., Banfi, S., Ali, M., Inglehearn, C. F. & Toomes, C., 2013, In : American Journal of Human Genetics. 93, 6, p. 1143-1150

Research output: Contribution to journalArticle

Open Access
Albinism
Visual Pathways
Melanins
Optic Nerve
Oryzias
36 Citations (Scopus)

The association between pterygium and conjunctival ultraviolet autofluorescence: The Norfolk Island Eye Study

Sherwin, JC., Hewitt, AW., Kearns, LS., Griffiths, LR., Mackey, D. & Coroneo, MT., 2013, In : ACTA OPHTHALMOLOGICA SCANDINAVICA. 91, 4, p. 363-370

Research output: Contribution to journalArticle

2012

Application of a high-throughput genotyping method for loci exclusion in non-consanguineous Australian pedigrees with autosomal recessive retinitis pigmentosa

Paterson, R. L., De Roach, J. N., Mclaren, T. L., Hewitt, A., Hoffmann, L. & Lamey, T. M., 2012, In : Molecular Vision. 18, p. 2043

Research output: Contribution to journalArticle

23 Citations (Scopus)

Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eye

Sharma, S., Burdon, K. P., Chidlow, G., Klebe, S., Crawford, A., Dimasi, D. P., Dave, A., Martin, S., Javadiyan, S., Wood, J. P., Casson, R., Danoy, P., Griggs, K., Hewitt, A., Landers, J., Mitchell, P., Mackey, D. & Craig, J. E., 2012, In : Investigative ophthalmology & visual science. 53, 8, p. 4917-4925

Research output: Contribution to journalArticle

107 Citations (Scopus)

Common genetic determinants of intraocular pressure and primary open-angle Glaucoma

Van Koolwijk, L. M. E., Ramdas, W. D., Ikram, M. K., Jansonius, N. M., Pasutto, F., Hysi, P. G., Macgregor, S., Janssen, S. F., Hewitt, A., Viswanathan, A. C., Ten Brink, J. B., Hosseini, S. M., Amin, N., Despriet, D. D. G., Willemse-Assink, J. J. M., Kramer, R., Rivadeneira, F., Struchalin, M., Aulchenko, Y. S., Weisschuh, N. & 29 othersZenkel, M., Mardin, C. Y., Gramer, E., Welge-Lüssen, U., Montgomery, G. W., Carbonaro, F., Young, T. L., Bellenguez, C., Mcguffin, P., Foster, P. J., Topouzis, F., Mitchell, P., Wang, J. J., Wong, T. Y., Czudowska, M. A., Hofman, A., Uitterlinden, A. G., Wolfs, R. C. W., De Jong, P. T. V. M., Oostra, B. A., Paterson, A. D., Mackey, D., Bergen, A. A. B., Reis, A., Hammond, C. J., Vingerling, J. R., Lemij, H. G., Klaver, C. C. W. & Van Duijn, C. M., 2012, In : PLoS Genetics. 8, 5, p. 14pp

Research output: Contribution to journalArticle

Open Access
21 Citations (Scopus)

Genetic investigation into the endophenotypic status of central corneal thickness and optic disc parameters in relation to open-angle glaucoma

Dimasi, DP., Burdon, KP., Hewitt, A., Fitzgerald, J., Wang, JJ., Healey, PR., Mitchell, P., Mackey, D. & Craig, JE., 2012, In : American Journal of Ophthalmology. 154, p. 833-842.e2

Research output: Contribution to journalArticle

21 Citations (Scopus)

Genetic variants near PDGFRA are associated with corneal curvature in Australians

Mishra, A., Yazar, S., Hewitt, A., Mountain, J. A., Ang, W., Pennell, C., Martin, N. G., Montgomery, G. W., Hammond, C. J., Young, T. L., Macgregor, S. & Mackey, D., 2012, In : Investigative ophthalmology & visual science. 53, p. 7131

Research output: Contribution to journalArticle

Open Access
50 Citations (Scopus)

Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal-tension glaucoma, and advanced glaucoma

Burdon, K. P., Crawford, A., Casson, R. J., Hewitt, A., Landers, J., Danoy, P., Mackey, D., Mitchell, P., Healey, P. R. & Craig, J. E., 2012, In : Ophthalmology. 119, p. 1539-1545

Research output: Contribution to journalArticle

11 Citations (Scopus)

Heritability of Strabismus: Genetic influence is specific to eso-deviation and independent of refractive error

Sanfilippo, PG., Hammond, CJ., Staffieri, SE., Kearns, LS., Melissa Liew, SH., Barbour, JM., Hewitt, A., Ge, D., Snieder, H., Mackinnon, JR., Brown, SA., Lorenz, B., Spector, TD., Martin, NG., Wilmer, JB. & Mackey, D., 2012, In : Twin Research and Human Genetics. 15, 5, p. 624-630

Research output: Contribution to journalArticle

50 Citations (Scopus)

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

Verhoeven, V. J. M., Hysi, P. G., Saw, S-M., Vitart, V., Mirshahi, A., Guggenheim, J. A., Cotch, M. F., Yamashiro, K., Baird, P. N., Mackey, D., Wojciechowski, R., Ikram, M. K., Hewitt, A., Duggal, P., Janmahasatian, S., Khor, C-C., Fan, Q., Zhou, X., Young, T. L., Tai, E-S. & 75 othersGoh, L-K., Li, Y-J., Aung, T., Vithana, E., Teo, Y-Y., Tay, W., Sim, X., Rudan, I., Hayward, C., Wright, A. F., Polasek, O., Campbell, H., Wilson, J. F., Fleck, B. W., Nakata, I., Yoshimura, N., Yamada, R., Matsuda, F., Ohno-Matsui, K., Nag, A., Mcmahon, G., Pourcain, B. S., Lu, Y., Rahi, J. S., Cumberland, P. M., Bhattacharya, S., Simpson, C. L., Atwood, L. D., Li, X., Raffel, L. J., Murgia, F., Portas, L., Despriet, D. D. G., Van Koolwijk, L. M. E., Wolfram, C., Lackner, K. J., Tönjes, A., Mägi, R., Lehtimäki, T., Kähönen, M., Esko, T., Metspalu, A., Rantanen, T., Pärssinen, O., Klein, B. E., Meitinger, T., Spector, T. D., Oostra, B. A., Smith, A. V., De Jong, P. T. V. M., Hofman, A., Amin, N., Karssen, L. C., Rivadeneira, F., Vingerling, J. R., Eiríksdóttir, G., Gudnason, V., Döring, A., Bettecken, T., Uitterlinden, A. G., Williams, C., Zeller, T., Castagné, R., Oexle, K., Van Duijn, C. M., Iyengar, S. K., Mitchell, P., Wang, J. J., Höhn, R., Pfeiffer, N., Bailey-Wilson, J. E., Stambolian, D., Wong, T-Y., Hammond, C. J. & Klaver, C. C. W., 2012, In : Human Genetics. 131, p. 1467-1480

Research output: Contribution to journalArticle

Open Access
6 Citations (Scopus)

Missing X and Y: a review of participant ages in population-based eye studies

Forward, H., Hewitt, AW. & Mackey, D., 2012, In : Clinical and Experimental Ophthalmology. 40, p. 305–319

Research output: Contribution to journalArticle

28 Citations (Scopus)

Reliability and validity of conjunctival ultraviolet autofluorescence measurement

Sherwin, JC., Mcknight, C. M., Hewitt, A., Griffiths, LR., Coroneo, MT. & Mackey, D., 2012, In : British Journal of Ophthalmology. 96, p. 801-805

Research output: Contribution to journalArticle

7 Citations (Scopus)

Role of the TCF4 Gene Intronic Variant in Normal Variation of Corneal Endothelium

Mackey, D., Warrington, N., Hewitt, AW., Oates, SK., Yazar, S., Soloshenko, A., Crawford, G., Mountain, JA. & Pennell, C., 2012, In : Cornea. 31, 2, p. 162-166

Research output: Contribution to journalArticle

50 Citations (Scopus)

The association between time spent outdoors and myopia using a novel biomarker of outdoor light exposure

Sherwin, JC., Hewitt, A., Coroneo, MT., Kearns, LS., Griffiths, LR. & Mackey, D., 2012, In : Investigative ophthalmology & visual science. 53, 8, p. 4363-4370

Research output: Contribution to journalArticle

15 Citations (Scopus)

The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucoma.

Wiggs, JL., Hewitt, A., Fan, BJ., Wang, DY., Figueiredo Sena, DR., O'Brien, C., Realini, A., Craig, JE., Dimasi, DP., Mackey, D., Haines, JL. & Pasquale, LR., 26 Sep 2012, In : PLoS One. 7, 9, p. 7pp

Research output: Contribution to journalArticle

Open Access
glaucoma
Visual Fields
codons
Codon
Genotype
2011
10 Citations (Scopus)

Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutation

Cohn, A. C., Turnbull, C., Ruddle, J. B., Guymer, R. H., Kearns, L. S., Staffieri, S., Daggett, H. T., Hewitt, A. W. & Mackey, D., 2011, In : Eye. PMID: 21109774, 26 November 2010, p. 208-217

Research output: Contribution to journalArticle

19 Citations (Scopus)

Classification of iris colour: review and refinement of a classification schema

Mackey, D., Wilkinson, C. H., Kearns, L. S. & Hewitt, A. W., 2011, In : Clinical and Experimental Ophthalmology. 39, p. 462-471

Research output: Contribution to journalArticle

16 Citations (Scopus)

Distribution of conjunctival ultraviolet autofluorescence in a population-based study: the Norfolk Island Eye Study

Sherwin, JC., Hewitt, AW., Kearns, LS., Coroneo, MT., Griffiths, LR. & Mackey, D., 2011, In : Eye. 25, p. 893-900

Research output: Contribution to journalArticle

263 Citations (Scopus)

Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1

Burdon, KP., Macgregor, S., Hewitt, AW., Sharma, S., Chidlow, G., Mills, RA., Danoy, P., Casson, R., Viswanathan, AC., Liu, J. Z., Landers, J., Henders, AK., Wood, J., Souzeau, E., Crawford, A., Leo, P., Wang, JJ., Rochtchina, E., Nyholt, DR., Martin, NG. & 5 othersMontgomery, GW., Mitchell, P., Brown, MA., Mackey, D. & Craig, JE., 2011, In : Nature Genetics. 43, 6, p. 574-578

Research output: Contribution to journalArticle

33 Citations (Scopus)

Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophy

Van Bergen, NJ., Crowston, JG., Kearns, LS., Staffieri, SE., Hewitt, AW., Cohn, AC., Mackey, D. & Trounce, IA., 2011, In : PLoS One. 6, 6, p. e21347

Research output: Contribution to journalArticle

Open Access
11 Citations (Scopus)

Ophthalmic Phenotypes and the Representativeness of Twin Data for the General Population

Sanfilippo, PG., Medland, SE., Hewitt, AW., Kearns, LS., Ruddle, JB., Sun, C., Hammond, CJ., Young, TL., Martin, NG. & Mackey, D., 2011, In : Investigative ophthalmology & visual science. 52, p. 5565-5572

Research output: Contribution to journalArticle

13 Citations (Scopus)

Optic disc evaluation in optic neuropathies: the optic disc assessment project

O'Neill, E. C., Danesh-Meyer, H. V., Kong, G. X. Y., Hewitt, A. W., Coote, M. A., Mackey, D. & Crowston, J. G., 2011, In : Ophthalmology. PMID: 21126771, 30 November 2010, p. N/A

Research output: Contribution to journalArticle

3 Citations (Scopus)

Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family

Mackey, D., Hewitt, AW., Ruddle, JB., Vote, B., Buttery, RG., Toomes, C., Metlapally, R., Li, YJ., Tran-Viet, KN., Malecaze, F., Calvas, P., Rosenberg, T., Guggenheim, JA. & Young, TL., 2011, In : Molecular Vision. 17, p. 2118-2128

Research output: Contribution to journalArticle

13 Citations (Scopus)

Prevalence and predictors of refractive error in a genetically isolated population: the Norfolk Island Eye Study

Sherwin, JC., Kelly, J., Hewitt, AW., Kearns, LS., Griffiths, LR. & Mackey, D., 2011, In : Clinical and Experimental Ophthalmology. 39, p. 734-742

Research output: Contribution to journalArticle

9 Citations (Scopus)

Prevalence of chronic ocular diseases in a genetic isolate: the Norfolk Island Eye Study (NIES)

Sherwin, JC., Kearns, LS., Hewitt, AW., Ma, Y., Kelly, J., Griffiths, LR. & Mackey, D., 2011, In : Ophthalmic Epidemiology. 18, 2, p. 61-71

Research output: Contribution to journalArticle

38 Citations (Scopus)

The Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitment

Souzeau, E., Goldberg, I., Healey, PR., Mills, RA., Landers, J., Graham, SL., Grigg, JR., Usher, B., Straga, T., Crawford, A., Casson, RJ., Morgan, W., Ruddle, JB., Coote, MA., White, A., Stewart, J., Hewitt, AW., Mackey, D., Burdon, KP. & Craig, JE., 2011, In : Clinical and Experimental Ophthalmology. EPub 15 December 2011, p. 1-22

Research output: Contribution to journalArticle

10 Citations (Scopus)

The Norfolk Island Study (NIES): Rationale, Methodology and Distribution of Ocular Biometry (Biometry of the Bounty)

Mackey, D., Sherwin, JC., Kearns, LS., Ma, Y., Kelly, J., Chu, B-S., Macmillan, R., Barbour, JM., Wilkinson, CH., Matovinovic, E., Cox, HC., Bellis, C., Lea, RA., Quinlan, S., Griffiths, LR. & Hewitt, AW., 2011, In : Twin Research and Human Genetics. 14, 1, p. 42-52

Research output: Contribution to journalArticle

Open Access
8 Citations (Scopus)

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

Pratap, DS., Lim, LL., Wang, JJ., Mackey, D., Kearns, LS., Stawell, RJ., Burdon, KP., Mitchell, P., Craig, JE., Hall, AJ. & Hewitt, AW., 2011, In : Molecular Vision. 17, p. 2970-2977

Research output: Contribution to journalArticle

2010
149 Citations (Scopus)

A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25

Hysi, P. G., Young, T. L., Mackey, D., Andrew, T., Fernandez-Medarde, A., Solouki, A. M., Hewitt, A. W., Macgregor, S., Vingerling, J. R., Li, Y. J., Ikram, M. K., Fai, L. Y., Sham, P. C., Manyes, L., Porteros, A., Lopes, M. C., Carbonaro, F., Fahy, S. J., Martin, N. G., Van Duijn, C. M. & 5 othersSpector, T. D., Rahi, J. S., Santos, E., Klaver, C. C. W. & Hammond, C. J., 2010, In : Nature Genetics. 42, p. 902-+

Research output: Contribution to journalArticle

12 Citations (Scopus)

A geometric morphometric assessment of the optic cup in glaucoma

Sanfilippo, P. G., Cardini, A., Sigal, I. A., Ruddle, J. B., Chua, B. E., Hewitt, A. W. & Mackey, D., 2010, In : Experimental Eye Research. 91, p. 405-414

Research output: Contribution to journalArticle

12 Citations (Scopus)

Associations of birth weight with ocular biometry, refraction, and glaucomatous endophenotypes: the Australian Twin Eye Study

Sun, C., Ponsonby, A-L., Brown, S. A., Kearns, L. S., Mackinnon, J. R., Barbour, J. R., Ruddle, J. B., Hewitt, A. W., Wright, M. J., Martin, N. G., Dwyer, T. & Mackey, D., 2010, In : American Journal of Ophthalmology. 150, 6, p. 909-916

Research output: Contribution to journalArticle

7 Citations (Scopus)

Automated Quantification of Inherited Phenotypes from Color Images: A Twin Study of the Variability of Optic Nerve Head Shape

Tang, L., Scheetz, T. E., Mackey, D., Hewitt, A. W., Fingert, J. H., Kwon, Y. H., Quellec, G., Reinhardt, J. M. & Abramoff, M. D., 2010, In : Investigative ophthalmology & visual science. 51, p. 5870-5877

Research output: Contribution to journalArticle

6 Citations (Scopus)

Automated volumetric evaluation of stereoscopic disc photography

Xu, J., Ishikawa, H., Wollstein, G., Bilonick, R. A., Kagemann, L., Craig, J. E., Mackey, D. A., Hewitt, A. W. & Schuman, J. S., 24 May 2010, In : Optics Express. 18, 11, p. 11347-11359 13 p.

Research output: Contribution to journalArticle

photography
evaluation
optics
photogrammetry
nerves
11 Citations (Scopus)

Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness

Dimasi, D. P., Burdon, K. P., Hewitt, A. W., Savarirayan, R., Healey, P. R., Mitchell, P., Mackey, D. & Craig, J. E., 2010, In : Molecular Vision. 16, p. 562-569

Research output: Contribution to journalArticle

88 Citations (Scopus)

Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness

Lu, Y., Dimasi, D. P., Hysi, P. G., Hewitt, A. W., Burdon, K. P., Toh, T., Ruddle, J. B., Li, Y. J., Mitchell, P., Healey, P. R., Montgomery, G. W., Hansell, N., Spector, T. D., Martin, N. G., Young, T. L., Hammond, C. J., Macgregor, S., Craig, J. E. & Mackey, D., 2010, In : PLoS Genetics. 6, p. -

Research output: Contribution to journalArticle

Open Access