Showing 61 - 80 results of 86 for search '"Muller-Nurasyid, Martina"', query time: 2.74s Refine Results  

Genetic variants in RBFOX3 are associated with sleep latency

by Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Müller-Myhsok, Bertram, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tõnu, van Mill, Josine G, Mbarek, Hamdi, Watson, Nathaniel F, Melville, Scott A, Del Greco, Fabiola M, Byrne, Enda M, Oole, Edwin, Kolcic, Ivana, Chen, Ting-Hsu, Evans, Daniel S, Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A, Zgaga, Lina, Mihailov, Evelin, Stone, Katie L, Campbell, Harry, Brouwer, Rutger Ww, Demirkan, Ayse, Isaacs, Aaron, Dogas, Zoran, Marciante, Kristin D, Campbell, Susan, Borovecki, Fran, Luik, Annemarie I, Li, Man, Hottenga, Jouke Jan, Huffman, Jennifer E, van den Hout, Mirjam Cgn, Cummings, Steven R, Aulchenko, Yurii S, Gehrman, Philip R, Uitterlinden, André G, Wichmann, Heinz-Erich, Müller-Nurasyid, Martina, Fehrmann, Rudolf Sn, Montgomery, Grant W, Hofman, Albert, Kao, Wen Hong Linda, Oostra, Ben A, Wright, Alan F, Vink, Jacqueline M, Wilson, James F, Pramstaller, Peter P, Hicks, Andrew A, Polasek, Ozren, Punjabi, Naresh M, Redline, Susan, Psaty, Bruce M, Heath, Andrew C, Merrow, Martha, Tranah, Gregory J, Gottlieb, Daniel J, Boomsma, Dorret I, Martin, Nicholas G, Rudan, Igor, Tiemeier, Henning, van IJcken, Wilfred Fj, Penninx, Brenda W, Metspalu, Andres, Meitinger, Thomas, Franke, Lude, Roenneberg, Till, van Duijn, Cornelia M
Published in European journal of human genetics : EJHG (01.10.2016)

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Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium

by Weng, Lu-Chen, Lunetta, Kathryn L., Müller-Nurasyid, Martina, Smith, Albert Vernon, Thériault, Sébastien, Weeke, Peter E., Barnard, John, Bis, Joshua C., Lyytikäinen, Leo-Pekka, Kleber, Marcus E., Martinsson, Andreas, Lin, Henry J., Rienstra, Michiel, Trompet, Stella, Krijthe, Bouwe P., Dörr, Marcus, Klarin, Derek, Chasman, Daniel I., Sinner, Moritz F., Waldenberger, Melanie, Launer, Lenore J., Harris, Tamara B., Soliman, Elsayed Z., Alonso, Alvaro, Paré, Guillaume, Teixeira, Pedro L., Denny, Joshua C., Shoemaker, M. Benjamin, Van Wagoner, David R., Smith, Jonathan D., Psaty, Bruce M., Sotoodehnia, Nona, Taylor, Kent D., Kähönen, Mika, Nikus, Kjell, Delgado, Graciela E., Melander, Olle, Engström, Gunnar, Yao, Jie, Guo, Xiuqing, Christophersen, Ingrid E., Ellinor, Patrick T., Geelhoed, Bastiaan, Verweij, Niek, Macfarlane, Peter, Ford, Ian, Heeringa, Jan, Franco, Oscar H., Uitterlinden, André G., Völker, Uwe, Teumer, Alexander, Rose, Lynda M., Kääb, Stefan, Gudnason, Vilmundur, Arking, Dan E., Conen, David, Roden, Dan M., Chung, Mina K., Heckbert, Susan R., Benjamin, Emelia J., Lehtimäki, Terho, März, Winfried, Smith, J. Gustav, Rotter, Jerome I., van der Harst, Pim, Jukema, J. Wouter, Stricker, Bruno H., Felix, Stephan B., Albert, Christine M., Lubitz, Steven A.
Published in Scientific reports (12.09.2017)

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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

by Mahajan, Anubha, Wessel, Jennifer, Willems, Sara, Zhao, Wei, Robertson, Neil, Chu, Audrey, Gan, Wei, Kitajima, Hidetoshi, Taliun, Daniel, Rayner, N. William, Guo, Xiuqing, Lu, Yingchang, Li, Man, Jensen, Richard, Hu, Yao, Huo, Shaofeng, Lohman, Kurt, Zhang, Weihua, Cook, James, Prins, Bram Peter, Flannick, Jason, Grarup, Niels, Trubetskoy, Vassily Vladimirovich, Kravic, Jasmina, Kim, Young Jin, Rybin, Denis, Yaghootkar, Hanieh, Müller-Nurasyid, Martina, Meidtner, Karina, Li-Gao, Ruifang, Varga, Tibor, Marten, Jonathan, Li, Jin, Smith, Albert Vernon, An, Ping, Ligthart, Symen, Gustafsson, Stefan, Malerba, Giovanni, Demirkan, Ayse, Tajes, Juan Fernandez, Steinthorsdottir, Valgerdur, Wuttke, Matthias, Lecoeur, Cécile, Preuss, Michael, Bielak, Lawrence, Graff, Marielisa, Highland, Heather, Justice, Anne, Liu, Dajiang, Marouli, Eirini, Peloso, Gina Marie, Warren, Helen, Afaq, Saima, Afzal, Shoaib, Ahlqvist, Emma, Almgren, Peter, Amin, Najaf, Bang, Lia, Bertoni, Alain, Bombieri, Cristina, Bork-Jensen, Jette, Brandslund, Ivan, Brody, Jennifer, Burtt, Noël, Canouil, Mickaël, Chen, Yii-Der Ida, Cho, Yoon Shin, Christensen, Cramer, Eastwood, Sophie, Eckardt, Kai-Uwe, Fischer, Krista, Gambaro, Giovanni, Giedraitis, Vilmantas, Grove, Megan, de Haan, Hugoline, Hackinger, Sophie, Hai, Yang, Han, Sohee, Tybjærg-Hansen, Anne, Hivert, Marie-France, Isomaa, Bo, Jäger, Susanne, Jørgensen, Marit, Jørgensen, Torben, Käräjämäki, Annemari, Kim, Bong-Jo, Kim, Sung Soo, Koistinen, Heikki, Kovacs, Peter, Kriebel, Jennifer, Kronenberg, Florian, Läll, Kristi, Lange, Leslie, Lee, Jung-Jin, Lehne, Benjamin, Li, Huaixing, Lin, Keng-Hung, Linneberg, Allan, Liu, Ching-Ti, Liu, Jun
Published in Nature genetics (09.04.2018)

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Simulation of Finnish Population History, Guided by Empirical Genetic Data, to Assess Power of Rare-Variant Tests in Finland

by Wang, Sophie R., Agarwala, Vineeta, Flannick, Jason, Chiang, Charleston W.K., Altshuler, David, Flannick, Jason, Manning, Alisa, Hartl, Christopher, Agarwala, Vineeta, Fontanillas, Pierre, Green, Todd, Banks, Eric, DePristo, Mark, Poplin, Ryan, Shakir, Khalid, Fennell, Timothy, Murphy, Jacquelyn, Burtt, Noël, Gabriel, Stacey, Altshuler, David, Fuchsberger, Christian, Kang, Hyun Min, Sim, Xueling, Ma, Clement, Locke, Adam, Blackwell, Thomas, Jackson, Anne, Teslovich, Tanya, Stringham, Heather, Chines, Peter, Kwan, Phoenix, Huyghe, Jeroen, Tan, Adrian, Jun, Goo, Stitzel, Michael, Bergman, Richard N., Bonnycastle, Lori, Tuomilehto, Jaakko, Collins, Francis S., Scott, Laura, Mohlke, Karen, Abecasis, Gonçalo, Boehnke, Michael, Strom, Tim, Gieger, Christian, Müller-Nurasyid, Martina, Grallert, Harald, Kriebel, Jennifer, Ried, Janina, Hrabé de Angelis, Martin, Huth, Cornelia, Meisinger, Christa, Peters, Annette, Rathmann, Wolfgang, Strauch, Konstantin, Meitinger, Thomas, Kravic, Jasmina, Ladenvall, Claes, Toumi, Tiinamaija, Isomaa, Bo, Groop, Leif, Gaulton, Kyle, Moutsianas, Loukas, Rivas, Manny, Pearson, Richard, Mahajan, Anubha, Prokopenko, Inga, Kumar, Ashish, Perry, John, Chen, Jeff, Howie, Bryan, van de Bunt, Martijn, Small, Kerrin, Lindgren, Cecilia, Lunter, Gerton, Robertson, Neil, Rayner, Will, Morris, Andrew, Buck, David, Hattersley, Andrew, Spector, Tim, McVean, Gil, Frayling, Tim, Donnelly, Peter, McCarthy, Mark, Hirschhorn, Joel N.
Published in American journal of human genetics (01.05.2014)

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