A common variant near TGFBR3 is associated with primary open angle glaucoma

Autor: Li, Zheng, Allingham, Rand, Nakano, Masakazu, Jia, Liyun, Chen, Yuhong, Ikeda, Yoko, Mani, Baskaran, Chen, Li-Jia, Kee, Changwon, Garway-Heath, David, Sripriya, Sarangapani, Fuse, Nobuo, Abu-Amero, Khaled, Huang, Chukai, Namburi, Prasanthi, Burdon, Kathryn, Perera, Shamira, Gharahkhani, Puya, Lin, Ying, Ueno, Morio, Ozaki, Mineo, Mizoguchi, Takanori, Krishnadas, Subbiah, Osman, Essam, Lee, Mei, S Y Chan, Anita, Tajudin, Liza-Sharmini, Do, Tan, Goncalves, Aurelien, Reynier, Pascal, Zhang, Hong, Bourne, Rupert, Goh, David, Broadway, David, Husain, Rahat, Negi, Anil, Su, Daniel, Ho, Ching-Lin, Blanco, Augusto, Leung, Christopher, Wong, Tina, Yakub, Azhany, Liu, Yutao, Nongpiur, Monisha, Han, Jong, Hon, Do, Shantha, Balekudaru, Zhao, Bowen, Sang, Jinghong, Zhang, NiHong, Sato, Ryuichi, Yoshii, Kengo, Panda-Jonas, Songhomita, Koch, Allison, Herndon, Leon, Moroi, Sayoko, Challa, Pratap, Foo, Jia, Bei, Jin-Xin, Zeng, Yi-Xin, Simmons, Cameron, Chau, Tran, Sharmila, Philomenadin, Chew, Merwyn, Lim, Blanche, Tam, Pansy, Chua, Elaine, Ng, Xiao, Yong, Victor, Chong, Yaan, Meah, Wee, Vijayan, Saravanan, Seongsoo, Sohn, Xu, Wang, Teo, Yik, Bailey, Jessica, Kang, Jae, Haines, Jonathan, Cheng, Ching, Saw, Seang-Mei, Tai, E-Shyong, Consortium, ICAARE-Glaucoma, Consortium, NEIGHBORHOOD, Richards, Julia, Ritch, Robert, Gaasterland, Douglas, Pasquale, Louis, Liu, Jianjun, Jonas, Jost, Milea, Dan, George, Ronnie, Al-Obeidan, Saleh, Mori, Kazuhiko, Macgregor, Stuart, Hewitt, Alex, Girkin, Christopher, Zhang, Mingzhi, Sundaresan, Periasamy, Vijaya, Lingam, Mackey, David, Wong, Tien, Craig, Jamie, Sun, Xinghuai, Kinoshita, Shigeru, Wiggs, Janey, Khor, Chiea-Chuen, Yang, Zhenglin, Pang, Chi, Wang, Ningli, Hauser, Michael, Tashiro, Kei, Aung, Tin, Vithana, Eranga

Publikováno v: Human molecular genetics
Human molecular genetics online, 2015, 24, pp.3880-92

International audience; Primary open angle glaucoma (POAG), a major cause of blindness worldwide, is a complex disease with a significant genetic contribution. We performed Exome Array (Illumina) analysis on 3504 POAG cases and 9746 controls with rep

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::824e74e7122a4642f607fc1afd2ab5bb
https://hal.archives-ouvertes.fr/hal-02104536