Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
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author: Kathryn P. Burdon, Sarah C Nelson, Martin L. Hibberd, André Reis, Mei-Chin Lee, Susan Eileen Isabella Williams, Michael A. Hauser, Zheng Li, Jessica N Cooke Bailey, Jae H Kang, Tomasz Żarnowski, Irma Järvelä, Mukharram Bikbov, Kenji Yamashiro, Jost B Jonas, Ronnie George, Per Kappelgaard, Pascal Reynier, Arkasubhra Ghosh, Shahin Yazdani, Masahiro Miyake, Jeeyun Ahn, V. Wee Yong, Muhammad I Khan, Aparna Rao, Emmanuelle Souzeau, Alex W. Hewitt, Evgeny L Akopov, Gyulli Kazakbaeva, Rinat R Fayzrakhmanov, Jia Nee Foo, Kar Seng Sim, Axel M Hillmer, Ching-Yu Cheng, Federico Martinón-Torres, Antonio Salas, Kessara Pathanapitoon, Linda Hansapinyo, Anavaj Sakuntabhai, Giang T T Nguyn, Michèle Ramsay, Lydia Álvarez, Montserrat García, Hector Gonzalez-Iglesias, Eray Atalay, Anne L. Coleman, John H. Fingert, Maria Grazia Cusi, Raheel Qamar, Soumya Raychaudhuri, Jonathan L Haines, Robert Ritch, Toshiaki Kubota, Fotis Topouzis, Jamie E Craig, Michael V Dubina, Chiea Chuen Khor, Rohit Shetty, Sonia Davila, Chie Sotozono, Shigeru Kinoshita, Ewa Kosior-Jarecka, Masakazu Nakano, Kei Tashiro, Morio Ueno, Paolo Manunta, Farah Akhtar, Shazia Micheal, Anneke den Hollander, R Rand Allingham, Eranga Nishanthie Vithana, Khaled K Abu-Amero, Satoko Nakano, Francesca Pasutto, John G. Kuchtey, Rachel Kuchtey, Margaret A. Pericak-Vance
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