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Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline von Li, Yong, Wuttke, Matthias, Winkler, Thomas W., Chai, Jin-Fang, Chu, Audrey Y., Cocca, Massimiliano, Feitosa, Mary F., Hoppmann, Anselm, Horn, Katrin, Li, Man, Nutile, Teresa, Tin, Adrienne, Tayo, Bamidele O., Bakker, Stephan J.L., Banas, Bernhard, Biggs, Mary L., Bottinger, Erwin P., Brenner, Hermann, Chalmers, John, Chee, Miao-Ling, Degenhardt, Frauke, Eckardt, Kai-Uwe, Ghanbari, Mohsen, Gieger, Christian, Hofer, Edith, Xian Foo, Valencia Hui, Hutri-Kähönen, Nina, Ikram, M. Arfan, Kähönen, Mika, Khor, Chiea-Chuen, Koenig, Wolfgang, Kramer, Holly, Krämer, Bernhard K., Kühnel, Brigitte, Lange, Leslie A., Franke, Lude, van der Harst, Pim, Navis, Gerjan, Snieder, Harold, Swertz, Morris, Wolffenbuttel, Bruce H.R., Wijmenga, Cisca, Abecasis, Goncalo, Baras, Aris, Coppola, Giovanni, Economides, Aris, Lotta, Luca A., Overton, John D., Reid, Jeffrey G., Beechert, Christina, Forsythe, Caitlin, Gu, Zhenhua, Lattari, Michael, Padilla, Maria Sotiropoulos, Toledo, Karina, Pradhan, Manasi, Manoochehri, Kia, Ulloa, Ricardo H., Bai, Xiaodong, Barnard, Leland, Blumenfeld, Andrew, Habegger, Lukas, Hawes, Alicia, Khalid, Shareef, Maxwell, Evan K., Salerno, William, Mitnaul, Lyndon J., Loos, Ruth J.F., Meisinger, Christa, Meitinger, Thomas, Melander, Olle, Milaneschi, Yuri, Mishra, Pashupati P., Mychaleckyj, Josyf C., Nikus, Kjell, Nolte, Ilja M., O’Donoghue, Michelle L., Pendergrass, Sarah A., Penninx, Brenda W.J.H., Preuss, Michael H., Psaty, Bruce M., Raitakari, Olli T., Rettig, Rainer, Rheinberger, Myriam, Rice, Kenneth M., Rosenkranz, Alexander R., Rossing, Peter, Sedaghat, Sanaz, Taylor, Kent D., Tremblay, Johanne, Völker, Uwe, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Wong, Tien-Yin, Snieder, Harold, Böger, Carsten A., Köttgen, Anna, Heid, Iris M.
Veröffentlicht in Kidney international
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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure von Lin, H.H., Hedman, A.K., Morley, M.P., Helgadottir, A., Dehghan, A., Almgren, P., Andersson, C., Brandimarto, J., Brown, M.R., Buckbinder, L., Chasman, D.I., Chung, J., Denaxas, S., Dunn, M.E., Engstrom, G., Felix, S.B., Finan, C., Ford, I., Ghasemi, S., Gottdiener, J.S., Gudbjartsson, D.F., Gutmann, R., Harst, P. van der, Ingelsson, E., Jukema, J.W., Lind, L., Lindgren, C.M., London, B., Lotta, L.A., Magnusson, P., Mahajan, A., Marz, W., Mordi, I.R., Morris, A.D., Morris, A.P., Morrison, A.C., Nagle, M.W., Niiranen, T., Owens, A.T., Perola, M., Portilla-Fernandez, E., Rice, K.M., Ridker, P.M., Rotter, J.I., Salomaa, V., Shalaby, A.A., Smith, N.L., Stender, S., Stott, D.J., Tammesoo, M.L., Thorgeirsson, G., Thorsteinsdottir, U., Uitterlinden, A.G., Volker, U., Voors, A.A., Wang, X.S., Waterworth, D., Weeke, P.E., Weiss, R., Wiggins, K.L., Yerges-Armstrong, L.M., Yu, B., Zhao, J.H., Hemingway, H., Samani, N.J., Newton-Cheh, C., Malarstig, A., Lubitz, S.A., Sattar, N., Cappola, T.P., Kuchenbaecker, K., Ellinor, P.T., Smith, J.G., Swerdlow, D.I., Lumbers, R.T., Abecasis, G., Bai, X.D., Balasubramanian, S., Banerjee, N., Barnard, L., Damask, A., Dewey, F., Fuller, E.D., Gurski, L., Hahn, Y., Hawes, A., Khalid, S., Li, A., Lin, N., Lopez, A., Manoochehri, K., Mitnaul, L.J., Overton, J.D., Paulding, C., Reid, J.G., Shuldiner, A., Ulloa, R.H., Widom, L., Yadav, A., Ye, B.
Veröffentlicht in Nature Communications
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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome von Ljungdahl, A, Stenton, S.L, Walker, S, Lord, J, Lemire, G, Martin-Geary, A.C, Ganesh, V.S, Ma, J, Delage, E, D’Souza, E.N, Dong, S, Adams, D.R, Allan, K, Bakshi, M, Berger, S.I, Bhatnagar, I, Blair, E, Burrage, L.C, Coman, D.J, Compton, A.G, Cunningham, C.A, D’Souza, P, Danecek, P, Délot, E.C, Dias, K.-R, Elias, E.R, Elmslie, F, Evans, C.-A, Ewans, L, Ezell, K, Fraser, J.L, Gallacher, L, Genetti, C.A, Goriely, A, Grant, C.L, Higgs, J.E, Hurles, M.E, Kuechler, A, Lachlan, K.L, Lalani, S.R, Lecoquierre, F, Leitão, E, Fevre, A.L, Leventer, R.J, Liebelt, J.E, Lindsay, S, Ma, A.S, Macnamara, E.F, Mansour, S, Maurer, T.M, Mendez, H.R, Metcalfe, K, Montgomery, S.B, Moosajee, M, Nassogne, M.-C, Neumann, S, O’Donoghue, M, O’Leary, M, Pattani, N, Phillips, J, Pitsava, G, Pysar, R, Rehm, H.L, Reuter, C.M, Revencu, N, Rius, R, Rodan, L, Roscioli, T, Rosenfeld, J.A, Sachdev, R, Shaw-Smith, C.J, Simons, C, Sisodiya, S.M, Snell, P, Stark, Z, Stewart, H.S, Tan, T.Y, Tan, N.B, Temple, S.E.L, Thorburn, D.R, Tifft, C.J, VanNoy, G.E, Vilain, E, Viskochil, D.H, Wedd, L, Wheeler, M.T, White, S.M, Wojcik, M, Wolfe, L.A, Wolfenson, Z, Wright, C.F, Xiao, C, Rubenstein, J.L, Fica, S.M, Baralle, D, Depienne, C, Howson, J.M.M, Sanders, S.J, O’Donnell-Luria, A, Whiffin, N
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