A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

被引：0

作者：

Tin Aung

Mineo Ozaki

Takanori Mizoguchi

R Rand Allingham

Zheng Li

Aravind Haripriya

Satoko Nakano

Steffen Uebe

Jeffrey M Harder

Anita S Y Chan

Mei Chin Lee

Kathryn P Burdon

Yury S Astakhov

Khaled K Abu-Amero

Juan C Zenteno

Yildirim Nilgün

Tomasz Zarnowski

Mohammad Pakravan

Leen Abu Safieh

Liyun Jia

Ya Xing Wang

Susan Williams

Daniela Paoli

Patricio G Schlottmann

Lulin Huang

Kar Seng Sim

Jia Nee Foo

Masakazu Nakano

Yoko Ikeda

Rajesh S Kumar

Morio Ueno

Shin-ichi Manabe

Ken Hayashi

Shigeyasu Kazama

Ryuichi Ideta

Yosai Mori

Kazunori Miyata

Kazuhisa Sugiyama

Tomomi Higashide

Etsuo Chihara

Kenji Inoue

Satoshi Ishiko

Akitoshi Yoshida

Masahide Yanagi

Yoshiaki Kiuchi

Makoto Aihara

Tsutomu Ohashi

Toshiya Sakurai

Takako Sugimoto

Hideki Chuman

机构：

[1] Singapore Eye Research Institute,Department of Ophthalmology

[2] Singapore National Eye Center,Department of Ophthalmology

[3] Yong Loo Lin School of Medicine,Department of Ophthalmology

[4] National University of Singapore,Department of Ophthalmology

[5] Division of Human Genetics,Department of Ophthalmology

[6] Duke University–National University of Singapore Graduate Medical School,Department of Ophthalmology

[7] Ozaki Eye Hospital,Department of Ophthalmology

[8] Hayashi Eye Hospital,Department of Genetics

[9] Mizoguchi Eye Hospital,Department of Biochemistry

[10] Duke University Eye Center,Department of Ophthalmology

[11] Intraocular Lens and Cataract Clinic,Department of Diagnostics and Microsurgery of Glaucoma

[12] Aravind Eye Hospital,Department of Ophthalmology

[13] Oita University Faculty of Medicine,Division of Ophthalmology, Department of Neurosciences

[14] Institute of Human Genetics,Department of Ophthalmology

[15] Friedrich Alexander Universität Erlangen-Nürnberg,Department of Genomic Medical Sciences

[16] Howard Hughes Medical Institute,Department of Ophthalmology

[17] Jackson Laboratory,Department of Ophthalmology

[18] Flinders University,Department of Ophthalmology and Visual Science

[19] Menzies Institute for Medical Research,Department of Medicine and Engineering Combined Research Institute

[20] University of Tasmania,Department of Ophthalmology

[21] First Pavlov State Medical University of St. Petersburg,Department of Ophthalmology and Visual Science

[22] College of Medicine,Department of Ophthalmology and Visual Sciences

[23] King Saud University,Department of Ophthalmology and Visual Sciences

[24] College of Medicine,Department of Medicine

[25] University of Florida,Department of Cellular Biology and Anatomy

[26] Institute of Ophthalmology Conde de Valenciana,Division of Ophthalmology

[27] Faculty of Medicine,Department of Ophthalmology and Westmead Millennium Institute

[28] Universidad Nacional Autónoma de México,Department of Genetics

[29] Eskisehir Osmangazi University,Department of Ophthalmology

[30] Medical University,Department of Ophthalmology

[31] Ophthalmic Research Center,Department of Ophthalmology

[32] Labbafinejad Medical Center,Department of Genomics

[33] Shahid Beheshti University of Medical Sciences,Division of Medical Genetics

[34] King Khaled Eye Specialist Hospital,Department of Biomedicine

[35] Beijing Ophthalmology and Visual Sciences Key Laboratory,Department of Ophthalmology

[36] Beijing Tongren Eye Centre,Department of Ophthalmology

[37] Beijing Tongren Hospital,Department of Ophthalmology

[38] Capital Medical University,Department of Biology and Genetics

[39] Beijing Institute of Ophthalmology,Department of Ophthalmology

[40] Beijing Tongren Hospital,Channing Division of Network Medicine

[41] Capital University of Medical Science,Department of Ophthalmology

[42] University of the Witwatersrand,Department of Neuroscience and Pharmacology

[43] Monfalcone Hospital,Department of Ophthalmology

[44] Organización Médica de Investigación,Department of Ophthalmology and Visual Sciences

[45] Sichuan Provincial Key Laboratory for Human Disease Gene Study,Department of Ophthalmology

[46] Hospital of the University of Electronic Science and Technology of China and Sichuan Provincial People's Hospital,Division of Medical Sciences

[47] School of Medicine,Department of Clinical Pharmacology

[48] University of Electronic Science and Technology of China,Department of Surgery

[49] Sichuan Translational Medicine Hospital,Department of Ophthalmology

[50] Chinese Academy of Sciences,undefined

来源：

Nature Genetics | 2015年 / 47卷

关键词：

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Tin Aung, Chiea-Chuen Khor and colleagues report the results of a genome-wide association study of exfoliation syndrome. They replicate a known association at LOXL1 and identify a previously unreported association at CACNA1A.

引用

页码：387 / 392

页数：5

共 50 条

[1] Correction: Corrigendum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Tin Aung
Mineo Ozaki
Takanori Mizoguchi
R Rand Allingham
Zheng Li
Aravind Haripriya
Satoko Nakano
Steffen Uebe
Jeffrey M Harder
Anita S Y Chan
Mei Chin Lee
Kathryn P Burdon
Yury S Astakhov
Khaled K Abu-Amero
Juan C Zenteno
Yildirim Nilgün
Tomasz Zarnowski
Mohammad Pakravan
Leen Abu Safieh
Liyun Jia
Ya Xing Wang
Susan Williams
Daniela Paoli
Patricio G Schlottmann
Lulin Huang
Kar Seng Sim
Jia Nee Foo
Masakazu Nakano
Yoko Ikeda
Rajesh S Kumar
Morio Ueno
Shin-ichi Manabe
Ken Hayashi
Shigeyasu Kazama
Ryuichi Ideta
Yosai Mori
Kazunori Miyata
Kazuhisa Sugiyama
Tomomi Higashide
Etsuo Chihara
Kenji Inoue
Satoshi Ishiko
Akitoshi Yoshida
Masahide Yanagi
Yoshiaki Kiuchi
Makoto Aihara
Tsutomu Ohashi
Toshiya Sakurai
Takako Sugimoto
Hideki Chuman
Nature Genetics, 2015, 47 : 689 - 689
[2] A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome (vol 47, pg 387, 2015)
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Sugimoto, Takako
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[3] A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome (vol 47, pg 387, 2015)
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NATURE GENETICS, 2015, 47 (04) : 387 - U145
[4] LOXL1 and CACNA1A SNPs associated with exfoliation syndrome susceptibility in a sample of Northern Spanish population
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[5] CACNA1A variant associated with generalized dystonia
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[6] CACNA1A variant can be associated with generalized dystonia
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[7] LOXL1 and CACNA1A SNPs associated with exfoliation syndrome susceptibility in a sample of Northern Spanish population, revealed by high-resolution melting analysis.
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[8] Hypertension and CACNA1A locus in relation to exfoliation glaucoma/glaucoma suspect
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[9] Expression of CACNA1A in Patients with Pseudoexfoliation Syndrome
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[10] Novel CACNA1A variant may cause cervical dystonia and cerebellar ataxia syndrome
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