Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

- Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yin Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Wang, Jie Jin, Rochtchina, Elena, Attia, John, Scott, Rodney, Holliday, Elizabeth G., Baird, Paul N., Xie, Jing, Inouye, Michael, Viswanathan, Ananth, Sim, Xueling, Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A., Staffieri, Sandra E., Jonas, Jost B., Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H., Lucas, Sionne E. M., Wong, Tien Yin, Beutel, Manfred E., Wilson, James F., Allingham, R. Rand, Brilliant, Murray H., Budenz, Donald L., Christen, William G., Fingert, John, Friedman, David S., Gaasterland, Douglas, Gaasterland, Terry, Hauser, Michael A., Kraft, Peter, Lee, Richard K., Lichter, Paul R., Liu, Yutao, Loomis, Stephanie J., Moroi, Sayoko E., Pericak-Vance, Margaret A., Realini, Anthony, Richards, Julia E., Schuman, Joel S., Scott, William K., Singh, Kuldev, Sit, Arthur J., Vollrath, Douglas, Weinreb, Robert N., Wollstein, Gadi, Zack, Donald J., Zhang, Kang

Genetic loci for retinal arteriolar microcirculation

- Sim, Xueling, Jensen, Richard A., Klein, Ronald, Klein, Barbara E. K., Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., de Jong, Paulus T. V. M., Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G., Ikram, M. Kamran, van Duijn, Cornelia M., Aspelund, Thor, Eiriksdottir, Gudny, Harris, Tamara B., Jonasson, Fridbert, Launer, Lenore J., The Wellcome Trust Case Control Consortium, Attia, John, Baird, Paul N., Harrap, Stephen, Cotch, Mary Frances, Holliday, Elizabeth G., Inouye, Michael, Rochtchina, Elena, Scott, Rodney J., Viswanathan, Ananth, Global BPGen Consortium, Li, Guo, Smith, Nicholas L., Wiggins, Kerri L., Kuo, Jane Z., Li, Xiaohui, Taylor, Kent D., Hewitt, Alex W., Martin, Nicholas G., Montgomery, Grant W., Sun, Cong, Young, Terri L., Mackey, David A., van Zuydam, Natalie R., Doney, Alex S. F., Palmer, Colin N. A., MacGregor, Stuart, Morris, Andrew D., Rotter, Jerome I., Tai, E. Shyong, Gudnason, Vilmundur, Vingerling, Johannes R., Siscovick, David S., Wang, Jie Jin, Wong, Tien Y., Xie, Jing, Smith, Albert Vernon, Boerwinkle, Eric, Mitchell, Paul

Genome-wide association study of retinopathy in individuals without diabetes

- Jensen, Richard A., Sim, Xueling, Launer, Lenore J., Smith, Albert Vernon, Boerwinkle, Eric, Cheung, Ning, Hewitt, Alex W., Liew, Gerald, Mitchell, Paul, Wang, Jie Jin, Attia, John, Scott, Rodney, Li, Xiaohui, Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., Taylor, Kent, Hofman, Albert, de Jong, Paulus T. V. M., Rivadeneira, Fernando, Uitterlinden, Andre G., Tay, Wan-Ting, Cotch, Mary Frances, Teo, Yik Ying, Seielstad, Mark, Liu, Jianjun, Cheng, Ching-Yu, Saw, Seang-Mei, Aung, Tin, Ganesh, Santhi K., O'Donnell, Christopher J., Nalls, Mike A., Wiggins, Kerri L., Ikram, M. Kamran, Kuo, Jane Z., The Blue Mountains Eye Study GWAS Team, CKDGen Consortium, Klein, Cornelia M., van Duijn, Cornelia M., Gudnason, Vilmundur, Klein, Ronald, Siscovick, David S., Rotter, Jerome I., Tai, E. Shong, Holliday, Elizabeth G., Vingerling, Johannes, Wong, Tien Y., Eiriksdottir, Gudny, Harris, Tamara B., Jonasson, Fridbert, Klein, Barbara E. K.

Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis

- Holliday, Elizabeth G., Smith, Albert V., Cheng, Ching Yu, Van Duijn, Cornelia M., Eiriksdottir, Gudny, Gudnason, Vilmundur, Harris, Tamara, Hewitt, Alex W., Inouye, Michael, Jonasson, Fridbert, Klein, Barbara E. K., Launer, Lenore, Cornes, Belinda K., Li, Xiaohui, Liew, Gerald, Lumley, Thomas, McElduff, Patrick, McKnight, Barbara, Mitchell, Paul, Psaty, Bruce M., Rochtchina, Elena, Rotter, Jerome I., Scott, Rodney J., Buitendijk, Gabrielle H. S., Tay, Wanting, Taylor, Kent, Teo, Yik Ying, Uitterlinden, Andre G., Viswanathan, Ananth, Xie, Sophia, Wellcome Trust Case Control Consortium, Vingerling, Johannes R., Klaver, Caroline C. W., Tai, E. Shyong, Jensen, Richard A., Siscovick, David, Klein, Ronald, Cotch, Mary Frances, Wong, Tien Y., Attia, John, Wang, Jie Jin, Sim, Xueling, Aspelund, Thor, Aung, Tin, Baird, Paul N., Boerwinkle, Eric

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

- Stambolian, Dwight, Wojciechowski, Robert, Wong, Tien Y., Simpson, Claire L., Klaver, Caroline C. W., van Duijn, Cornelia M., Verhoeven, Virginie J. M., Baird, Paul N., Vitart, Veronique, Paterson, Andrew D., Mitchell, Paul, Saw, Seang Mei, Oexle, Konrad, Holliday, Elizabeth G., Attia, John, Scott, Rodney J., Pirastu, Mario, Li, Xiaohui, Raffel, Leslie J., Cotch, Mary Frances, Chew, Emily Y., Klein, Barbara, Klein, Ronald