Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy

Fuchs endothelial corneal dystrophy (FECD) is one of the most common reasons for corneal transplantation, and is known to cluster in families. Here, the authors discover new genetic loci associated with FECD with sex-specific effects and implications for disease mechanism.

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Autores principales: Natalie A. Afshari, Robert P. Igo, 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. Price, Jamie E. Craig, John H. Fingert, John D. Gottsch, Anthony J. Aldave, Gordon K. Klintworth, Jonathan H. Lass, Yi-Ju Li, Sudha K. Iyengar
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/d1c65f3362014583bd22c5188abefc76
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spelling oai:doaj.org-article:d1c65f3362014583bd22c5188abefc762021-12-02T14:40:21ZGenome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy10.1038/ncomms148982041-1723https://doaj.org/article/d1c65f3362014583bd22c5188abefc762017-03-01T00:00:00Zhttps://doi.org/10.1038/ncomms14898https://doaj.org/toc/2041-1723Fuchs endothelial corneal dystrophy (FECD) is one of the most common reasons for corneal transplantation, and is known to cluster in families. Here, the authors discover new genetic loci associated with FECD with sex-specific effects and implications for disease mechanism.Natalie A. AfshariRobert P. IgoNathan J. MorrisDwight StambolianShiwani SharmaV. Lakshmi PulagamSteven DunnJohn F. StamlerBarbara J. TruittJacqueline RimmlerAbraham KuotChristopher R. CroasdaleXuejun QinKathryn P. BurdonS. Amer RiazuddinRichard MillsSonja KlebeMollie A. MinearJiagang ZhaoElmer BalajondaGeorge O. RosenwasserKeith H BaratzV. Vinod MoothaSanjay V. PatelSimon G. GregoryJoan E. Bailey-WilsonMarianne O. PriceFrancis W. PriceJamie E. CraigJohn H. FingertJohn D. GottschAnthony J. AldaveGordon K. KlintworthJonathan H. LassYi-Ju LiSudha K. IyengarNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Natalie A. Afshari
Robert P. Igo
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. Price
Jamie E. Craig
John H. Fingert
John D. Gottsch
Anthony J. Aldave
Gordon K. Klintworth
Jonathan H. Lass
Yi-Ju Li
Sudha K. Iyengar
Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy
description Fuchs endothelial corneal dystrophy (FECD) is one of the most common reasons for corneal transplantation, and is known to cluster in families. Here, the authors discover new genetic loci associated with FECD with sex-specific effects and implications for disease mechanism.
format article
author Natalie A. Afshari
Robert P. Igo
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. Price
Jamie E. Craig
John H. Fingert
John D. Gottsch
Anthony J. Aldave
Gordon K. Klintworth
Jonathan H. Lass
Yi-Ju Li
Sudha K. Iyengar
author_facet Natalie A. Afshari
Robert P. Igo
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. Price
Jamie E. Craig
John H. Fingert
John D. Gottsch
Anthony J. Aldave
Gordon K. Klintworth
Jonathan H. Lass
Yi-Ju Li
Sudha K. Iyengar
author_sort Natalie A. Afshari
title Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy
title_short Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy
title_full Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy
title_fullStr Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy
title_full_unstemmed Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy
title_sort genome-wide association study identifies three novel loci in fuchs endothelial corneal dystrophy
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/d1c65f3362014583bd22c5188abefc76
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