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Open Access
Peer-reviewed
Research Article
Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness
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Yi Lu ,
Contributed equally to this work with: Yi Lu, David P. Dimasi
Affiliation Genetics and Population Health, Queensland Institute of Medical Research, Brisbane, Australia
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David P. Dimasi ,
Contributed equally to this work with: Yi Lu, David P. Dimasi
Affiliation Department of Ophthalmology, Flinders University, Adelaide, Australia
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Pirro G. Hysi,
Affiliation Department of Twin Research and Genetic Epidemiology, King's College London School of Medicine, St Thomas' Hospital, London, United Kingdom
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Alex W. Hewitt,
Affiliation Centre for Eye Research Australia, University of Melbourne, Royal Victorian Eye and Ear Hospital, Melbourne, Australia
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Kathryn P. Burdon,
Affiliation Department of Ophthalmology, Flinders University, Adelaide, Australia
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Tze'Yo Toh,
Affiliations Centre for Eye Research Australia, University of Melbourne, Royal Victorian Eye and Ear Hospital, Melbourne, Australia, University of Tasmania, the Eye Hospital, Launceston, Australia
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Jonathan B. Ruddle,
Affiliation Centre for Eye Research Australia, University of Melbourne, Royal Victorian Eye and Ear Hospital, Melbourne, Australia
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Yi Ju Li,
Affiliations Center for Human Genetics, Duke University Medical Center, Durham, North Carolina, United States of America, Department of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, North Carolina, United States of America
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Paul Mitchell,
Affiliation Centre for Vision Research, Westmead Millennium Institute, University of Sydney, Sydney, Australia
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Paul R. Healey,
Affiliation Centre for Vision Research, Westmead Millennium Institute, University of Sydney, Sydney, Australia
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Grant W. Montgomery,
Affiliation Genetics and Population Health, Queensland Institute of Medical Research, Brisbane, Australia
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Narelle Hansell,
Affiliation Genetics and Population Health, Queensland Institute of Medical Research, Brisbane, Australia
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Timothy D. Spector,
Affiliation Department of Twin Research and Genetic Epidemiology, King's College London School of Medicine, St Thomas' Hospital, London, United Kingdom
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Nicholas G. Martin,
Affiliation Genetics and Population Health, Queensland Institute of Medical Research, Brisbane, Australia
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Terri L. Young,
Affiliation Center for Human Genetics, Duke University Medical Center, Durham, North Carolina, United States of America
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Christopher J. Hammond,
Affiliation Department of Twin Research and Genetic Epidemiology, King's College London School of Medicine, St Thomas' Hospital, London, United Kingdom
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Stuart Macgregor ,
¶These authors also contributed equally to this work.
Affiliation Genetics and Population Health, Queensland Institute of Medical Research, Brisbane, Australia
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Jamie E. Craig ,
* E-mail: jamie.craig@flinders.edu.au
¶These authors also contributed equally to this work.
Affiliation Department of Ophthalmology, Flinders University, Adelaide, Australia
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David A. Mackey
¶These authors also contributed equally to this work.
Affiliations Centre for Eye Research Australia, University of Melbourne, Royal Victorian Eye and Ear Hospital, Melbourne, Australia, Lions Eye Institute, University of Western Australia, Centre for Ophthalmology and Visual Science, Perth, Australia
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Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness
- Yi Lu,
- David P. Dimasi,
- Pirro G. Hysi,
- Alex W. Hewitt,
- Kathryn P. Burdon,
- Tze'Yo Toh,
- Jonathan B. Ruddle,
- Yi Ju Li,
- Paul Mitchell,
- Paul R. Healey
- Published: May 13, 2010
- https://doi.org/10.1371/journal.pgen.1000947