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Ophthalmic Genetics Volume 34, 2013 - Issue 1-2
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Research Reports

Confirmation of the association between the TCF4 risk allele and Fuchs endothelial corneal dystrophy in patients from the Midwestern United States

John F. StamlerDepartment of Ophthalmology and Visual Sciences, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA
,
Ben R. RoosDepartment of Ophthalmology and Visual Sciences, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA
,
Michael D. WagonerDepartment of Ophthalmology and Visual Sciences, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA
,
Ken M. GoinsDepartment of Ophthalmology and Visual Sciences, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA
,
Anna S. KitzmannDepartment of Ophthalmology and Visual Sciences, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA
,
Janet B. RileyDepartment of Ophthalmology and Visual Sciences, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA
,
Edwin M. Stone
&
John H. FingertDepartment of Ophthalmology and Visual Sciences, University of Iowa Carver College of Medicine, Iowa City, Iowa, USACorrespondence[email protected]
 show all
Pages 32-34 | Received 02 Aug 2012, Accepted 26 Aug 2012, Published online: 24 Sep 2012

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Ester Fernández López, Fook Chang Lam, Marieke Bruinsma, Lamis Baydoun, Isabel Dapena & Gerrit RJ Melles. (2015) Fuchs endothelial corneal dystrophy: current treatment recommendations and experimental surgical options. Expert Review of Ophthalmology 10:3, pages 301-312.
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Articles from other publishers (13)

Tatiana Romanovna Tsedilina, Elena Sharova, Valeriia Iakovets & Liubov Olegovna Skorodumova. (2023) Systematic review of SLC4A11, ZEB1, LOXHD1, and AGBL1 variants in the development of Fuchs’ endothelial corneal dystrophy. Frontiers in Medicine 10.
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Hironori Uehara, Xiaohui Zhang, Felipe Pereira, Siddharth Narendran, Susie Choi, Sai Bhuvanagiri, Jinlu Liu, Sangeetha Ravi Kumar, Austin Bohner, Lara Carroll, Bonnie Archer, Yue Zhang, Wei Liu, Guangping Gao, Jayakrishna Ambati, Albert S Jun & Balamurali K Ambati. (2021) Start codon disruption with CRISPR/Cas9 prevents murine Fuchs’ endothelial corneal dystrophy. eLife 10.
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Robert P. IgoJr.Jr. & Jessica N. Cooke Bailey. 2020. Genetics and Genomics of Eye Disease. Genetics and Genomics of Eye Disease 259 275 .
Jie Zhang, Charles N. J. McGhee & Dipika V. Patel. (2019) The Molecular Basis of Fuchs’ Endothelial Corneal Dystrophy. Molecular Diagnosis & Therapy 23:1, pages 97-112.
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Liubov O. Skorodumova, Alexandra V. Belodedova, Olga P. Antonova, Elena I. Sharova, Tatiana A. Akopian, Oksana V. Selezneva, Elena S. Kostryukova & Boris E. Malyugin. (2018) CTG18.1 Expansion is the Best Classifier of Late-Onset Fuchs' Corneal Dystrophy Among 10 Biomarkers in a Cohort From the European Part of Russia. Investigative Opthalmology & Visual Science 59:11, pages 4748.
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Michael D. Wagoner, Laura R. Bohrer, Benjamin T. Aldrich, Mark A. Greiner, Robert F. Mullins, Kristan S. Worthington, Budd A. Tucker & Luke A. Wiley. (2018) Feeder-free differentiation of cells exhibiting characteristics of corneal endothelium from human induced pluripotent stem cells. Biology Open.
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Sabine Foja, Mirjam Luther, Katrin Hoffmann, Andreas Rupprecht & Claudia Gruenauer-Kloevekorn. (2017) CTG18.1 repeat expansion may reduce TCF4 gene expression in corneal endothelial cells of German patients with Fuchs’ dystrophy. Graefe's Archive for Clinical and Experimental Ophthalmology 255:8, pages 1621-1631.
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Natalie A. Afshari, Robert P. IgoJrJr, Nathan J. Morris, Dwight Stambolian, Shiwani Sharma, V. Lakshmi Pulagam, Steven Dunn, John F. Stamler, Barbara J. Truitt, Jacqueline Rimmler, Abraham Kuot, Christopher R. Croasdale, Xuejun Qin, Kathryn P. Burdon, S. Amer Riazuddin, Richard Mills, Sonja Klebe, Mollie A. Minear, Jiagang Zhao, Elmer Balajonda, George O. Rosenwasser, Keith H Baratz, V. Vinod Mootha, Sanjay V. Patel, Simon G. Gregory, Joan E. Bailey-Wilson, Marianne O. Price, Francis W. PriceJrJr, Jamie E. Craig, John H. Fingert, John D. Gottsch, Anthony J. Aldave, Gordon K. Klintworth, Jonathan H. Lass, Yi-Ju Li & Sudha K. Iyengar. (2017) Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Nature Communications 8:1.
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Dan Li, XiaoYan Peng & HuiYu Sun. (2015) Association of TCF4 polymorphisms and fuchs’ endothelial dystrophy: a meta-analysis. BMC Ophthalmology 15:1.
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Monika Ołdak, Ewelina Ruszkowska, Monika Udziela, Dominika Oziębło, Ewelina Bińczyk, Aneta Ścieżyńska, Rafał Płoski & Jacek P. Szaflik. (2015) Fuchs Endothelial Corneal Dystrophy: Strong Association with rs613872 Not Paralleled by Changes in Corneal Endothelial TCF4 mRNA Level . BioMed Research International 2015, pages 1-6.
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Allen O. Eghrari, S. Amer Riazuddin & John D. Gottsch. 2015. Molecular Biology of Eye Disease. Molecular Biology of Eye Disease 79 97 .
Lawrence C. M. Lau, Li Ma, Alvin L. Young, Shi Song Rong, Vishal Jhanji, Marten E. Brelen, Chi Pui Pang & Li Jia Chen. (2014) Association of Common Variants in TCF4 and PTPRG with Fuchs' Corneal Dystrophy: A Systematic Review and Meta-Analysis. PLoS ONE 9:10, pages e109142.
Crossref
M Bruinsma, C M Tong & G R J Melles. (2013) What does the future hold for the treatment of Fuchs endothelial dystrophy; will ‘keratoplasty’ still be a valid procedure?. Eye 27:10, pages 1115-1122.
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