A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
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Published:2015-02-23
Issue:4
Volume:47
Page:387-392
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ISSN:1061-4036
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Container-title:Nature Genetics
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language:en
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Short-container-title:Nat Genet
Author:
Aung Tin, , Ozaki Mineo, Mizoguchi Takanori, Allingham R Rand, Li Zheng, Haripriya Aravind, Nakano Satoko, Uebe Steffen, Harder Jeffrey M, Chan Anita S Y, Lee Mei Chin, Burdon Kathryn P, Astakhov Yury S, Abu-Amero Khaled K, Zenteno Juan C, Nilgün Yildirim, Zarnowski Tomasz, Pakravan Mohammad, Safieh Leen Abu, Jia Liyun, Wang Ya Xing, Williams SusanORCID, Paoli Daniela, Schlottmann Patricio G, Huang Lulin, Sim Kar SengORCID, Foo Jia NeeORCID, Nakano Masakazu, Ikeda Yoko, Kumar Rajesh S, Ueno Morio, Manabe Shin-ichi, Hayashi Ken, Kazama Shigeyasu, Ideta Ryuichi, Mori Yosai, Miyata Kazunori, Sugiyama Kazuhisa, Higashide Tomomi, Chihara Etsuo, Inoue Kenji, Ishiko Satoshi, Yoshida Akitoshi, Yanagi Masahide, Kiuchi Yoshiaki, Aihara Makoto, Ohashi Tsutomu, Sakurai Toshiya, Sugimoto Takako, Chuman Hideki, Matsuda Fumihiko, Yamashiro KenjiORCID, Gotoh Norimoto, Miyake Masahiro, Astakhov Sergei Y, Osman Essam A, Al-Obeidan Saleh A, Owaidhah Ohoud, Al-Jasim Leyla, Shahwan Sami Al, Fogarty Rhys A, Leo Paul, Yetkin Yaz, Oğuz Çilingir, Kanavi Mozhgan Rezaei, Beni Afsaneh Naderi, Yazdani Shahin, Akopov Evgeny L, Toh Kai-Yee, Howell Gareth R, Orr Andrew C, Goh Yufen, Meah Wee Yang, Peh Su Qin, Kosior-Jarecka Ewa, Lukasik Urszula, Krumbiegel Mandy, Vithana Eranga N, Wong Tien Yin, Liu Yutao, Koch Allison E Ashley, Challa Pratap, Rautenbach Robyn M, Mackey David A, Hewitt Alex W, Mitchell Paul, Wang Jie Jin, Ziskind Ari, Carmichael Trevor, Ramakrishnan Rangappa, Narendran Kalpana, Venkatesh Rangaraj, Vijayan Saravanan, Zhao Peiquan, Chen Xueyi, Guadarrama-Vallejo Dalia, Cheng Ching Yu, Perera Shamira A, Husain Rahat, Ho Su-Ling, Welge-Luessen Ulrich-Christoph, Mardin Christian, Schloetzer-Schrehardt Ursula, Hillmer Axel M, Herms Stefan, Moebus Susanne, Nöthen Markus M, Weisschuh Nicole, Shetty Rohit, Ghosh Arkasubhra, Teo Yik Ying, Brown Matthew A, Lischinsky Ignacio, Crowston Jonathan G, Coote Michael, Zhao Bowen, Sang Jinghong, Zhang Nihong, You QishengORCID, Vysochinskaya Vera, Founti Panayiota, Chatzikyriakidou Anthoula, Lambropoulos Alexandros, Anastasopoulos Eleftherios, Coleman Anne L, Wilson M Roy, Rhee Douglas J, Kang Jae Hee, May-Bolchakova Inna, Heegaard Steffen, Mori Kazuhiko, Alward Wallace L M, Jonas Jost BORCID, Xu Liang, Liebmann Jeffrey M, Chowbay Balram, Schaeffeler Elke, Schwab Matthias, Lerner Fabian, Wang Ningli, Yang Zhenglin, Frezzotti Paolo, Kinoshita Shigeru, Fingert John H, Inatani Masaru, Tashiro Kei, Reis AndréORCID, Edward Deepak P, Pasquale Louis R, Kubota Toshiaki, Wiggs Janey L, Pasutto Francesca, Topouzis Fotis, Dubina Michael, Craig Jamie E, Yoshimura Nagahisa, Sundaresan Periasamy, John Simon W M, Ritch Robert, Hauser Michael A, Khor Chiea-Chuen,
Publisher
Springer Science and Business Media LLC
Reference34 articles.
1. Schlötzer-Schrehardt, U. & Naumann, G.O. Ocular and systemic pseudoexfoliation syndrome. Am. J. Ophthalmol. 141, 921–937 (2006). 2. Ritch, R. & Schlotzer-Schrehardt, U. Exfoliation syndrome. Surv. Ophthalmol. 45, 265–315 (2001). 3. Thorleifsson, G. et al. Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science 317, 1397–1400 (2007). 4. Chen, H. et al. Ethnicity-based subgroup meta-analysis of the association of LOXL1 polymorphisms with glaucoma. Mol. Vis. 16, 167–177 (2010). 5. Fingert, J.H. et al. LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States. Am. J. Ophthalmol. 144, 974–975 (2007).
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