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Prevalence of Age-Related Macular Degeneration in Europe

by Colijn, Johanna M., Prokofyeva, Elena, Alves, Dalila, Cachulo, Maria L., Cougnard-Gregoire, Audrey, Korb, Christina, Erke, Maja G., Anastasopoulos, Eleftherios, Meester-Smoor, Magda A., Segato, Tatiana, de Jong, Paulus T.V.M., Creuzot-Garcher, Catherine, Pfeiffer, Norbert, Foster, Paul J., Korobelnik, Jean-François, Delcourt, Cécile, Klaver, Caroline C.W., Ajana, Soufiane, Arango-Gonzalez, Blanca, Bhatia, Vaibhav, Bhattacharya, Shomi S., Biarnés, Marc, Bühren, Sebastian, Colijn, Johanna M., Cougnard-Grégoire, Audrey, Dammeier, Sascha, De la Cerda, Berta, Delcourt, Cécile, Diaz-Corrales, Francisco J., Diether, Sigrid, Endermann, Tanja, Garcia, Míriam, Honisch, Sabina, Kersten, Eveline, Klaver, Caroline C.W., Langen, Hanno, Lengyel, Imre, Maugeais, Cyrille, Merle, Bénédicte M.J., Monés, Jordi, Rodríguez, Eduardo, Ueffing, Marius, Verzijden, Timo, Acar, Niyazi, Anastosopoulos, Eleftherios, Azuara-Blanco, Augusto, Bertelsen, Geir, Brétillon, Lionel, Buitendijk, Gabrielle, Cachulo, Maria Luz, Chakravarthy, Usha, Chan, Michelle, Cumberland, Philippa, Cunha-Vaz, José, Deak, Gabor, Dietzel, Martha, Finger, Robert, Fletcher, Astrid, Göbel, Arno, Gorgels, Theo, Grauslund, Jakob, Hammond, Christopher, Helmer, Catherine, Hense, Hans-Werner, Hermann, Manuel, Hoehn, René, Holz, Frank, Jansonius, Nomdo, Janssen, Sarah, Klaver, Caroline, Korobelnik, Jean-François, Lechanteur, Yara, Lotery, Andrew, Leung, Irene, Merle, Bénédicte, Meyer zu Westrup, Verena, Midena, Edoardo, Miotto, Stefania, Mirshahi, Alireza, Mohan-Saïd, Sadek, Mueller, Michael, Muldrew, Alyson, Nunes, Sandrina, Oexle, Konrad, Piermarocchi, Stefano, Prokofyeva, Elena, Raitakari, Olli, Ribeiro, Luisa, Salonikiou, Aggeliki, Shehata, Jasmin, Simader, Christian, Souied, Eric, Tapp, Robyn, Verhoeven, Virginie, Von Hanno, Therese, Vujosevic, Stela, Williams, Katie, Wolfram, Christian, Zerbib, Jennyfer, Zwiener, Isabella
Published in Ophthalmology (Rochester, Minn.) (01.12.2017)

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Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

by Thorleifsson, Gudmar, Haripriya, Aravind, Burdon, Kathryn P, Abu-Amero, Khaled, Hauser, Michael, Li, Zheng, Prakadeeswari, Gopalakrishnan, Inoue, Kenji, Park, Ki Ho, Perera, Shamira A, Vijaya, Lingam, Do, Tan, Edward, Deepak P, de Juan Marcos, Lourdes, Ideta, Ryuichi, Thomas, Samuel, Greer, Wenda L, Jia, Liyun, Qiao, Chunyan, Wang, Ya-Xing, Leruez, Stéphanie, Uebe, Steffen, Zenkel, Matthias, Hoja, Ursula, Mardin, Christian, Founti, Panayiota, Chatzikyriakidou, Anthi, Pappas, Theofanis, Sarangapani, Sripriya, Dallorto, Laura, Ishiko, Satoshi, Kiuchi, Yoshiaki, Ohashi, Tsutomu, Chuman, Hideki, Miyake, Masahiro, Matsuda, Fumihiko, Park, Kyu Hyung, Cruz-Aguilar, Marisa, Yong, Victor H K, Ashaye, Adeyinka O, Ugbede, Idakwo, Teekhasaenee, Chaiwat, Asimadu, Ifeoma, Kosior-Jarecka, Ewa, Roy, Sylvain, Dervan, Edward, Rao, Aparna, Sivori, Delia, Souzeau, Emmanuelle, Astakhov, Sergei Y, Emelyanov, Anton, Kazakbaeva, Gyulli, Fayzrakhmanov, Rinat, Chowbay, Balram, Peh, Su Qin, Heng, Khai Koon, Ho, Su-Ling, Hillmer, Axel M, Salas, Antonio, Kitnarong, Naris, Sakuntabhai, Anavaj, Nguyn, Giang T T, Zenz, Werner, Binder, Alexander, Hibberd, Martin L, Nöthen, Markus M, Rautenbach, Robyn M, Carmichael, Trevor R, Álvarez, Lydia, Fernández-Vega Cueto, Luis, Oguz, Çilingir, Atalay, Eray, Batu, Bilge, Aktas, Dilek, Kasım, Burcu, Coleman, Anne L, Challa, Pratap, Curtin, Karen, Chaya, Craig J, Zangwill, Linda M, Wong, Tien Yin, Kinoshita, Shigeru, Fingert, John H, Lee, Richard K, Sit, Arthur J, Kraft, Peter, Pericak-Vance, Margaret A, Kruse, Friedrich E, Weinreb, Robert N, Pasquale, Louis R, Haines, Jonathan L, Thorsteinsdottir, Unnur, Jonasson, Fridbert, Ritch, Robert, Kubota, Toshiaki, Micheal, Shazia, Topouzis, Fotis, Craig, Jamie E, Sundaresan, Periasamy, Stefansson, Kari
Published in Nature genetics (01.07.2017)

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