Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

by Gorski, Mathias, Jung, Bettina, Li, Yong, Matias-Garcia, Pamela R., Wuttke, Matthias, Coassin, Stefan, Thio, Chris H. L., Kleber, Marcus E., Winkler, Thomas W., Wanner, Veronika, Chai, Jin-Fang, Chu, Audrey Y., Cocca, Massimiliano, Feitosa, Mary F., Ghasemi, Sahar, Hoppmann, Anselm, Horn, Katrin, Li, Man, Nutile, Teresa, Scholz, Markus, Sieber, Karsten B., Teumer, Alexander, Tin, Adrienne, Wang, Judy, Tayo, Bamidele O., Ahluwalia, Tarunveer S., Almgren, Peter, Bakker, Stephan J. L., Banas, Bernhard, Bansal, Nisha, Biggs, Mary L., Boerwinkle, Eric, Bottinger, Erwin P., Brenner, Hermann, Carroll, Robert J., Chalmers, John, Chee, Miao-Li, Chee, Miao-Ling, Cheng, Ching-Yu, Coresh, Josef, de Borst, Martin H., Degenhardt, Frauke, Eckardt, Kai-Uwe, Endlich, Karlhans, Franke, Andre, Freitag-Wolf, Sandra, Gampawar, Piyush, Gansevoort, Ron T., Ghanbari, Mohsen, Gieger, Christian, Hamet, Pavel, Ho, Kevin, Hofer, Edith, Holleczek, Bernd, Xian Foo, V.H., Hutri-Kähönen, N., Hwang, Shih-Jen, Ikram, M. Arfan, Josyula, Navya Shilpa, Kähönen, M., Khor, Chiea-Chuen, Koenig, Wolfgang, Kramer, Holly, Krämer, B.K., Kühnel, B., Lange, Leslie A., Lehtimäki, T., Lieb, Wolfgang, Alizadeh, B.Z., Boezen, H.M., Franke, L., van der Harst, Pim, Navis, G., Rots, M., Snieder, Harold, Swertz, M., Wolffenbuttel, B.H.R., Wijmenga, C., Abecasis, G., Baras, A., Cantor, M., Coppola, G., Economides, A., Lotta, L.A., Overton, J.D., Reid, J.G., Shuldiner, A., Beechert, C., Forsythe, C., Fuller, E.D., Gu, Z., Lattari, M., Lopez, A., Schleicher, T.D., Padilla, M.S., Toledo, K., Widom, L., Wolf, S.E., Pradhan, M., Manoochehri, K., Ulloa, R.H., Bai, X., Balasubramanian, S., Barnard, L., Blumenfeld, A., Eom, G., Habegger, L., Hawes, A., Khalid, S., Maxwell, E.K., Salerno, W., Staples, J.C., Jones, M.B., Mitnaul, L.J., Loos, Ruth J. F., Lukas, Mary Ann, Lyytikäinen, L.-P., Meisinger, Christa, Meitinger, Thomas, Melander, Olle, Milaneschi, Yuri, Mishra, Pashupati P., Mononen, Nina, Mychaleckyj, Josyf C., Nadkarni, Girish N., Nauck, Matthias, Nikus, Kjell, Ning, Boting, Nolte, Ilja M., O'Donoghue, Michelle L., Orho-Melander, Marju, Pendergrass, Sarah A., Penninx, Brenda W. J. H., Preuss, Michael H., Psaty, Bruce M., Raffield, Laura M., Raitakari, Olli T., Rettig, Rainer, Rheinberger, Myriam, Rice, Kenneth M., Rosenkranz, Alexander R., Rossing, Peter, Rotter, Jerome, I, Sabanayagam, Charumathi, Schmidt, Helena, Schmidt, Reinhold, Schöttker, B., Schulz, Christina-Alexandra, Sedaghat, Sanaz, Shaffer, Christian M., Strauch, Konstantin, Szymczak, Silke, Taylor, Kent D., Tremblay, Johanne, Chaker, Layal, van der Most, Peter J., Verweij, Niek, Völker, U., Waldenberger, Melanie, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Wong, Tien-Yin, Woodward, Mark, Yang, Qiong, Yasuda, Masayuki, Yerges-Armstrong, Laura M., Zhang, Yan, Wanner, Christoph, Böger, C.A., Köttgen, A., Kronenberg, Florian, Pattaro, Cristian, Heid, Iris M., Lifelines Cohort Study., Regeneron Genetics Center.
Published 2022