Showing 1 - 19 results of 19 for search '"FOGARTY, Rhys"', query time: 2.33s Refine Results  

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

by Hysi, Pirro G, Cheng, Ching-Yu, Springelkamp, Henriët, Macgregor, Stuart, Bailey, Jessica N Cooke, Wojciechowski, Robert, Vitart, Veronique, Nag, Abhishek, Hewitt, Alex W, Höhn, René, Venturini, Cristina, Mirshahi, Alireza, Ramdas, Wishal D, Thorleifsson, Gudmar, Vithana, Eranga, Khor, Chiea-Chuen, Stefansson, Arni B, Liao, Jiemin, Haines, Jonathan L, Amin, Najaf, Wang, Ya Xing, Wild, Philipp S, Ozel, Ayse B, Li, Jun Z, Fleck, Brian W, Zeller, Tanja, Staffieri, Sandra E, Teo, Yik-Ying, Cuellar-Partida, Gabriel, Luo, Xiaoyan, Allingham, R Rand, Richards, Julia E, Senft, Andrea, Karssen, Lennart C, Zheng, Yingfeng, Bellenguez, Céline, Xu, Liang, Iglesias, Adriana I, Wilson, James F, Kang, Jae H, van Leeuwen, Elisabeth M, Jonsson, Vesteinn, Thorsteinsdottir, Unnur, Despriet, Dominiek D G, Ennis, Sarah, Moroi, Sayoko E, Martin, Nicholas G, Jansonius, Nomdo M, Yazar, Seyhan, Tai, E-Shyong, Amouyel, Philippe, Kirwan, James, van Koolwijk, Leonieke M E, Hauser, Michael A, Jonasson, Fridbert, Leo, Paul, Loomis, Stephanie J, Fogarty, Rhys, Rivadeneira, Fernando, Kearns, Lisa, Lackner, Karl J, de Jong, Paulus T V M, Simpson, Claire L, Pennell, Craig E, Oostra, Ben A, Uitterlinden, André G, Saw, Seang-Mei, Lotery, Andrew J, Bailey-Wilson, Joan E, Hofman, Albert, Vingerling, Johannes R, Maubaret, Cécilia, Pfeiffer, Norbert, Wolfs, Roger C W, Lemij, Hans G, Young, Terri L, Pasquale, Louis R, Delcourt, Cécile, Spector, Timothy D, Klaver, Caroline C W, Small, Kerrin S, Burdon, Kathryn P, Stefansson, Kari, Wong, Tien-Yin, Viswanathan, Ananth, Mackey, David A, Craig, Jamie E, Wiggs, Janey L, van Duijn, Cornelia M, Hammond, Christopher J, Aung, Tin
Published in Nature genetics (01.10.2014)

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Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error

by Ikram, M. Kamran, Barathi, Veluchamy A., Kemp, John P., Wang, Ya Xing, Wright, Alan F., Amin, Najaf, Tay, Wan-Ting, Hayward, Caroline, Polasek, Ozren, Vatavuk, Zoran, Pang, Chi Pui, Wegner, Aharon, Yip, Shea Ping, Murgia, Federico, Portas, Laura, Ang, Wei, Fan, Qiao, Zhou, Xin, Iyengar, Sudha K., Vital, Mark, Yoo, Sonia, Maguire, Leo, McCulley, James, Renucci, Ann, Oliva, Matt, Brown, Marlene, Reeves, Sherman, Hamilton, Stephen, Kelly, Kathleen, Shaughnessy, Michael, Steinemann, Thomas, Mifflin, Mark, Chodosh, James, Galentine, Paul G., Mannis, Mark, Varma, Rohit, Wedenoja, Juho, Mirshahi, Alireza, Brown, Matthew A., Corvin, Aiden, Duncanson, Audrey, Markus, Hugh S., Rautanen, Anna, Viswanathan, Ananth C., Giannoulatou, Eleni, Donnelly, Peter, Hammond, Naomi, McCann, Owen T., Ricketts, Michelle, Widaa, Sara, Yonova-Doing, Ekaterina, Klein, Ronald, Miller, D., Whitehouse, F., McLellan, M., Golden, E., Arrigg, P., Gauthier-Kelly, C., Lopes-Virella, M., Colwell, J., Farr, A., Elsing, S., Kaminski, L., Lorenzi, G., Johnsonbaugh, S., Liss, R., Gordon, J., Martin, C.L., Pop-Busui, R., Smith, A., Gothrup, J., Prosser, L., Schwartz, S., Maschak-Carey, B.J., Morrison, A., Meyer, D., Strowig, S., Gordon, A., Hokanson, J., Ginsberg, J., Van Ottingham, L., Harth, J., May, M., Adkins, T., White, N., Fradkin, J., Siebert, C., Danis, R., Dingledine, J., Chavers, B., Burzuk, B., Low, P., Wong, N., Fox, M., Clark, C., Zhang, L., Pang, Chi Pui, Inoko, Hidetoshi, Mitchell, Paul, Stambolian, Dwight
Published in American journal of human genetics (08.08.2013)

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

by 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, Susan, Paoli, Daniela, Schlottmann, Patricio G, Huang, Lulin, Sim, Kar Seng, Foo, Jia Nee, 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, Kenji, 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
Published in Nature genetics (27.05.2015)

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