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    Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants von Aragam, Krishna G., Jiang, Tao, Goel, Anuj, Kanoni, Stavroula, Wolford, Brooke N., Atri, Deepak S., Weeks, Elle M., Wang, Minxian, Hindy, George, Zhou, Wei, Grace, Christopher, Roselli, Carolina, Marston, Nicholas A., Kamanu, Frederick K., Surakka, Ida, Venegas, Loreto Muñoz, Sherliker, Paul, Koyama, Satoshi, Ishigaki, Kazuyoshi, Åsvold, Bjørn O., Brown, Michael R., Brumpton, Ben, de Vries, Paul S., Giannakopoulou, Olga, Giardoglou, Panagiota, Gudbjartsson, Daniel F., Güldener, Ulrich, Haider, Syed M. Ijlal, Helgadottir, Anna, Ibrahim, Maysson, Kastrati, Adnan, Kessler, Thorsten, Kyriakou, Theodosios, Konopka, Tomasz, Li, Ling, Ma, Lijiang, Meitinger, Thomas, Mucha, Sören, Munz, Matthias, Murgia, Federico, Nielsen, Jonas B., Nöthen, Markus M., Pang, Shichao, Reinberger, Tobias, Schnitzler, Gavin, Smedley, Damian, Thorleifsson, Gudmar, von Scheidt, Moritz, Ulirsch, Jacob C., Arnar, David O., Burtt, Noël P., Costanzo, Maria C., Flannick, Jason, Ito, Kaoru, Jang, Dong-Keun, Kamatani, Yoichiro, Khera, Amit V., Komuro, Issei, Kullo, Iftikhar J., Lotta, Luca A., Nelson, Christopher P., Roberts, Robert, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Webb, Thomas R., Baras, Aris, Björkegren, Johan L. M., Boerwinkle, Eric, Dedoussis, George, Holm, Hilma, Hveem, Kristian, Melander, Olle, Morrison, Alanna C., Orho-Melander, Marju, Rallidis, Loukianos S., Ruusalepp, Arno, Sabatine, Marc S., Stefansson, Kari, Zalloua, Pierre, Ellinor, Patrick T., Farrall, Martin, Danesh, John, Ruff, Christian T., Finucane, Hilary K., Hopewell, Jemma C., Clarke, Robert, Gupta, Rajat M., Erdmann, Jeanette, Samani, Nilesh J., Schunkert, Heribert, Watkins, Hugh, Willer, Cristen J., Deloukas, Panos, Kathiresan, Sekar, Butterworth, Adam S.

    Veröffentlicht in Nature genetics

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    Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries von Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C., Kamanu, Frederick K., Koido, Masaru, He, Yunye, Caro, Ilana, Krebs, Kristi, Liaw, Yi-Ching, Parodi, Livia, Bae, Hee-Joon, Chong, Michael R., Tomppo, Liisa, Akinyemi, Rufus, Roshchupkin, Gennady V., Habib, Naomi, Jee, Yon Ho, Thomassen, Jesper Qvist, Abedi, Vida, Cárcel-Márquez, Jara, Nygaard, Marianne, Yonova-Doing, Ekaterina, Knol, Maria J., Lewis, Adam J., Judy, Renae L., Amouyel, Philippe, Bakker, Mark K., Bennett, David A., Bis, Joshua C., Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M., Cho, Kelly, Chen, Zhengming, Cruchaga, Carlos, Cole, John W., de Cid, Rafael, Ferreira, Leslie E., He, Jing, Jeon, Christina E., Jern, Christina, Kamouchi, Masahiro, Keene, Keith L., Konuma, Takahiro, Kumar, Amit, Launer, Lenore J., Lee, Keon-Joo, Li, Jiang, Li, Liming, Manichaikul, Ani, Markus, Hugh S., Meitinger, Thomas, Mitchell, Braxton D., Morisaki, Takayuki, O’Donnell, Martin J., Onland-Moret, N. Charlotte, Ovbiagele, Bruce, Peters, Annette, Rosand, Jonathan, Sabatine, Marc S., Sacco, Ralph L., Saleheen, Danish, Schmidt, Carsten O., Smith, Nicholas L., Sloane, Kelly L., Sutoh, Yoichi, Tiwari, Hemant K., Wennberg, Patrik, Wilson, Peter W. F., Yang, Qiong, Yoon, Kyungheon, Gieger, Christian, Ninomiya, Toshiharu, Grabe, Hans J., Jukema, J. Wouter, Kim, Young Jin, Chen, Pei-Hsin, Mayerhofer, Ernst, Ikram, Mohammad A., Worrall, Bradford B., Lathrop, G. Mark, Riaz, Moeen, Simonsick, Eleanor M., Kõrv, Janika, Zand, Ramin, Prasad, Kameshwar, Frikke-Schmidt, Ruth, Liman, Thomas, Ruigrok, Ynte M., Bastarache, Lisa, Damrauer, Scott M., Rotter, Jerome I., Niiranen, Teemu J., Walters, Robin G., Owolabi, Mayowa O., Huffman, Jennifer E., Kamatani, Yoichiro, Dichgans, Martin, Debette, Stephanie

    Veröffentlicht in Nature (London)

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    Genetic drivers of heterogeneity in type 2 diabetes pathophysiology von Southam, Lorraine, Yin, Xianyong, Melloni, Giorgio E. M., Rayner, Nigel W., Bocher, Ozvan, Namba, Shinichi, Lee, Simon S. K., Petty, Lauren E., Schroeder, Philip, Kals, Mart, Zhang, Weihua, Graff, Mariaelisa, Lamri, Amel, Parra, Esteban J., Bielak, Lawrence F., Hai, Yang, Sofer, Tamar, Nousome, Darryl, Sun, Meng, Noordam, Raymond, Lim, Victor J. Y., Yanek, Lisa R., An, Ping, Tan, Jingyi, Canouil, Mickaël, Chee, Miao-Li, Chen, Shyh-Huei, Chen, Yuan-Tsong, Dimitrov, Latchezar, Doumatey, Ayo P., Du, Shufa, Eckardt, Kai-Uwe, Gerstein, Hertzel C., Han, Sohee, Herder, Christian, Howard, Annie-Green, Hsueh, Willa, Ichihara, Sahoko, Ikram, Mohammad Arfan, Jang, Hye-Mi, Jonas, Jost B., Kandeel, Fouad R., Kaur, Varinderpal, Lange, Leslie A., Lee, Myung-Shik, Leong, Aaron, Liu, Ching-Ti, Louie, Tin, Luo, Xi, Maeda, Shiro, Mansuri, Sohail Rafik, Nalls, Michael A., Nayak, Uma, Okada, Yukinori, Patil, Snehal, Prasad, Gauri, Roden, Michael, Rohde, Rebecca, Sandow, Kevin, Sankareswaran, Alagu, So, Wing Yee, Stilp, Adrienne M., Taylor, Kent D., Thorand, Barbara, Valladares-Salgado, Adan, Wheeler, Eleanor, Raffel, Leslie J., Igase, Michiya, Province, Michael A., Rotimi, Charles N., Peyser, Patricia A., Pankow, James S., Wilson, James G., Sheu, Wayne H. H., Mook-Kanamori, Dennis O., Collins, Francis S., Paré, Guillaume, Shu, Xiao-Ou, Dupuis, Josee, Kato, Norihiro, Laakso, Markku, Wareham, Nicholas J., Kim, Bong-Jo, Stefansson, Kari, Goodarzi, Mark O., Mohlke, Karen L., Florez, Jose C., Zöllner, Sebastian, Mägi, Reedik, van Heel, David A., Finer, Sarah, Ng, Maggie C. Y., Sim, Xueling, Below, Jennifer E., Chang, Kyong-Mi, Meigs, James B., Mahajan, Anubha, Vujkovic, Marijana, Voight, Benjamin F., Morris, Andrew P.

    Veröffentlicht in Nature (London)

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    The genomics of heart failure: design and rationale of the HERMES consortium von Lumbers, R. Thomas, Shah, Sonia, Lin, Honghuang, Henry, Albert, Swerdlow, Daniel I., Holmes, Michael V., Ärnlöv, Johan, Sallah, Neneh, Asselin, Geraldine, Backman, Joshua D., Brandimarto, Jeffrey, Brunner‐La Rocca, Hans‐Peter, Chaffin, Mark D., Chazara, Olympe, Cleland, John G.F., Cook, James P., Denus, Simon, Dehghan, Abbas, Delgado, Graciela E., Denaxas, Spiros, Doney, Alexander S., Esko, Tõnu, Fatemifar, Ghazaleh, Ford, Ian, Ghasemi, Sahar, Giedraitis, Vilmantas, Giulianini, Franco, Gottdiener, John S., Gross, Stefan, Guðbjartsson, Daníel F., Hedman, Åsa K., Kamanu, Frederick, Khaw, Kay‐Tee, Kleber, Marcus E., Kuchenbaecker, Karoline, Lindgren, Cecilia M., Luan, Jian'an, Magnusson, Patrik, Mahajan, Anubha, Mann, Douglas, Margulies, Kenneth B., McMurray, John J.V., Melander, Olle, Mordi, Ify R., Morley, Michael P., Morris, Andrew D., Morris, Andrew P., Morrison, Alanna C., Nagle, Michael W., Nelson, Christopher P., Newton‐Cheh, Christopher, Niessner, Alexander, Niiranen, Teemu, Nowak, Christoph, O'Donoghue, Michelle L., Palmer, Colin N.A., Paré, Guillaume, Perreault, Louis‐Philippe Lemieux, Portilla‐Fernandez, Eliana, Rice, Kenneth M., Ridker, Paul M., Romaine, Simon P.R., Roselli, Carolina, Rotter, Jerome I., Ruff, Christian T., Sabatine, Marc S., Salomaa, Veikko, Setten, Jessica, Smelser, Diane T., Smith, Nicholas L., Stott, David J., Sveinbjörnsson, Garðar, Taylor, Kent D., Teder‐Laving, Maris, Teumer, Alexander, Thorsteinsdottir, Unnur, Torp‐Pedersen, Christian, Trompet, Stella, Tuckwell, Danny, Uitterlinden, Andre G., Vaura, Felix, Veluchamy, Abirami, Visscher, Peter M., Wareham, Nicholas J., Weiss, Raul, Xing, Heming, Yang, Jian, Yang, Yifan, Yerges‐Armstrong, Laura M., Zannad, Faiez, Holm, Hilma, Lanfear, David E., Dunn, Michael E., Wells, Quinn S., Asselbergs, Folkert W., Hingorani, Aroon D., Samani, Nilesh J., Lang, Chim C., Cappola, Thomas P., Smith, J. Gustav

    Veröffentlicht in ESC Heart Failure

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    Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants von Aragam, Krishna G, Jiang, Tao, Goel, Anuj, Kanoni, Stavroula, Wolford, Brooke N, Atri, Deepak S, Weeks, Elle M, Wang, Minxian, Hindy, George, Zhou, Wei, Grace, Christopher, Roselli, Carolina, Marston, Nicholas A, Kamanu, Frederick K, Surakka, Ida, Venegas, Loreto Muñoz, Sherliker, Paul, Koyama, Satoshi, Ishigaki, Kazuyoshi, Åsvold, Bjørn O, Brown, Michael R, Brumpton, Ben, de Vries, Paul S, Giannakopoulou, Olga, Giardoglou, Panagiota, Gudbjartsson, Daniel F, Güldener, Ulrich, Haider, Syed M Ijlal, Helgadottir, Anna, Ibrahim, Maysson, Kastrati, Adnan, Kessler, Thorsten, Kyriakou, Theodosios, Konopka, Tomasz, Li, Ling, Ma, Lijiang, Meitinger, Thomas, Mucha, Sören, Munz, Matthias, Murgia, Federico, Nielsen, Jonas B, Nöthen, Markus M, Pang, Shichao, Reinberger, Tobias, Schnitzler, Gavin, Smedley, Damian, Thorleifsson, Gudmar, von Scheidt, Moritz, Ulirsch, Jacob C, Biobank Japan, EPIC-CVD, Arnar, David O, Burtt, Noël P, Costanzo, Maria C, Flannick, Jason, Ito, Kaoru, Jang, Dong-Keun, Kamatani, Yoichiro, Khera, Amit V, Komuro, Issei, Kullo, Iftikhar J, Lotta, Luca A, Nelson, Christopher P, Roberts, Robert, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Webb, Thomas R, Baras, Aris, Björkegren, Johan LM, Boerwinkle, Eric, Dedoussis, George, Holm, Hilma, Hveem, Kristian, Melander, Olle, Morrison, Alanna C, Orho-Melander, Marju, Rallidis, Loukianos S, Ruusalepp, Arno, Sabatine, Marc S, Stefansson, Kari, Zalloua, Pierre, Ellinor, Patrick T, Farrall, Martin, Danesh, John, Ruff, Christian T, Finucane, Hilary K, Hopewell, Jemma C, Clarke, Robert, Gupta, Rajat M, Erdmann, Jeanette, Samani, Nilesh J, Schunkert, Heribert, Watkins, Hugh, Willer, Cristen J, Deloukas, Panos, Kathiresan, Sekar, Butterworth, Adam S, CARDIoGRAMplusC4D Consortium

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    Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants von Aragam, Krishna G, Jiang, Tao, Goel, Anuj, Kanoni, Stavroula, Wolford, Brooke N, Atri, Deepak S, Weeks, Elle M, Wang, Minxian, Hindy, George, Zhou, Wei, Grace, Christopher, Roselli, Carolina, Marston, Nicholas A, Kamanu, Frederick K, Surakka, Ida, Venegas, Loreto Muñoz, Sherliker, Paul, Koyama, Satoshi, Ishigaki, Kazuyoshi, Åsvold, Bjørn O, Brown, Michael R, Brumpton, Ben, de Vries, Paul S, Giannakopoulou, Olga, Giardoglou, Panagiota, Gudbjartsson, Daniel F, Güldener, Ulrich, Haider, Syed M Ijlal, Helgadottir, Anna, Ibrahim, Maysson, Kastrati, Adnan, Kessler, Thorsten, Kyriakou, Theodosios, Konopka, Tomasz, Li, Ling, Ma, Lijiang, Meitinger, Thomas, Mucha, Sören, Munz, Matthias, Murgia, Federico, Nielsen, Jonas B, Nöthen, Markus M, Pang, Shichao, Reinberger, Tobias, Schnitzler, Gavin, Smedley, Damian, Thorleifsson, Gudmar, von Scheidt, Moritz, Ulirsch, Jacob C, Biobank Japan, EPIC-CVD, Arnar, David O, Burtt, Noël P, Costanzo, Maria C, Flannick, Jason, Ito, Kaoru, Jang, Dong-Keun, Kamatani, Yoichiro, Khera, Amit V, Komuro, Issei, Kullo, Iftikhar J, Lotta, Luca A, Nelson, Christopher P, Roberts, Robert, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Webb, Thomas R, Baras, Aris, Björkegren, Johan LM, Boerwinkle, Eric, Dedoussis, George, Holm, Hilma, Hveem, Kristian, Melander, Olle, Morrison, Alanna C, Orho-Melander, Marju, Rallidis, Loukianos S, Ruusalepp, Arno, Sabatine, Marc S, Stefansson, Kari, Zalloua, Pierre, Ellinor, Patrick T, Farrall, Martin, Danesh, John, Ruff, Christian T, Finucane, Hilary K, Hopewell, Jemma C, Clarke, Robert, Gupta, Rajat M, Erdmann, Jeanette, Samani, Nilesh J, Schunkert, Heribert, Watkins, Hugh, Willer, Cristen J, Deloukas, Panos, Kathiresan, Sekar, Butterworth, Adam S, CARDIoGRAMplusC4D Consortium

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    Stroke genetics informs drug discovery and risk prediction across ancestries von Jürgenson, Tuuli, Krebs, Kristi, Lin, Kuang, Srinivasasainagendra, Vinodh, Bae, Hee-Joon, Jee, Yon Ho, Abedi, Vida, Armstrong, Nicole D, Bartz, Traci M, Bennett, David A, Bis, Joshua C, Bordes, Constance, Cho, Kelly, Jager, Phil L. de, Kitazono, Takanari, Lee, Keon-Joo, Lepik, Kaido, Marston, Nicholas A, Nordestgaard, Borge G, Tiwari, Hemant K, Wennberg, Patrik, Wilson, James G, Furie, Karen L, Peddareddygari, Leema Reddy, Lindstrom, Sara, Pattee, Jack W, Suchon, Pierre, Reiner, Alexander P, O'Donnell, Chris J, Dijk, Ewoud J. van, Luijckx, Gert-Jan, Levi, Christopher R, Schmidt, Reinhold, Slowik, Agnieszka, Johnson, Julie A, Heitsch, Laura, Lemmons, Robin, Lopez, Oscar L, Lioutas, Vasileios, Roquer, Jaume, Sibolt, Gerli, Rutten-Jacobs, Loes, Kanai, Masahiro, Holliday, Elizabeth G, Ingelsson, Erik, Kissela, Brett M, Lin, Wei-Yu, Walters, Matthew, Amin, Najaf, Berr, Claudine, Chowhan, Ayesha, Kaffashian, Sara, Kalra, Lalit, Kloss, Manja, Labovitz, Daniel L, Li, Linxin, Lindgren, Cecilia M, Pedersen, Nancy L, Jousilahti, Pekka, Riba-Llena, Iolanda, Sarin, Antti-Pekka, Stine, O. Colin, Strauch, Konstantin, Tsugane, Shoichiro, Valdimarsson, Einar M, Wahab, Kolawole, Olalere, Abimbola, Chen, Junshi, Chen, Yiping, Pozarickij, Alfred, Schmidt, Dan, de Jager, Phil L, de Laat, Karlijn F, Norden, Anouk G. W. van, den Heijer, Tom, Rooij, Frank G. W. van, Ellekjaer, Hanne, Thomas, Laurent F, Kleinschnitz, Christoph, Lledos, Miquel, Sobrino, Tomas, Ribo, Marc, Lopez-Cancio, Elena, Prats-Sanchez, Luis, Sumoy, Lauro, Marti-Fabregas, Joan, Benn, Marianne, Tiainen, Marjaana, Kinnunen, Janne, Kim, Young Jin, Mayerhofer, Ernst, Howson, Joanna M. M, Rundek, Tatjana, Worrall, Bradford B, Lathrop, G. Mark, Liman, Thomas, Jung, Keum Ji, Damrauer, Scott M, Fornage, Myriam, Fernandez-Cadenas, Israel

    Veröffentlicht in Nature
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