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    Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder von Demontis, Ditte, Walters, Raymond K., Martin, Joanna, Mattheisen, Manuel, Als, Thomas D., Agerbo, Esben, Baldursson, Gísli, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline I., Grasby, Katrina L., Grove, Jakob, Gudmundsson, Olafur O., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian B., Martin, Alicia R., Martin, Nicholas G., Moran, Jennifer, Pallesen, Jonatan, Palmer, Duncan S., Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Poterba, Timothy, Poulsen, Jesper Buchhave, Ripke, Stephan, Robinson, Elise B., Satterstrom, F. Kyle, Stefansson, Hreinn, Stevens, Christine, Turley, Patrick, Walters, G. Bragi, Won, Hyejung, Wright, Margaret J., Andreassen, Ole A., Asherson, Philip, Burton, Christie L., Boomsma, Dorret I., Cormand, Bru, Dalsgaard, Søren, Franke, Barbara, Gelernter, Joel, Geschwind, Daniel, Hakonarson, Hakon, Haavik, Jan, Kranzler, Henry R., Kuntsi, Jonna, Langley, Kate, Lesch, Klaus-Peter, Middeldorp, Christel, Reif, Andreas, Rohde, Luis Augusto, Roussos, Panos, Schachar, Russell, Sklar, Pamela, Sonuga-Barke, Edmund J. S., Sullivan, Patrick F., Thapar, Anita, Tung, Joyce Y., Waldman, Irwin D., Medland, Sarah E., Stefansson, Kari, Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Daly, Mark J., Faraone, Stephen V., Børglum, Anders D., Neale, Benjamin M.

    Veröffentlicht in Nature genetics

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    The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions von Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Møller, Peter L., Stefansdottir, Lilja, Galarneau, Geneviève, Turman, Constance, Danning, Rebecca, Law, Matthew H., Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Krassowski, Michal, Lepamets, Maarja, Marciniak, Błażej, Sobalska-Kwapis, Marta, Topbas-Selcuki, Nura F., Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S., Campbell, Archie, Cheuk, Cecilia S. K., DiVasta, Amy, Dorien, O., Donoghue, Jacqueline F., Fontanillas, Pierre, Geirsson, Reynir T., Girling, Jane E., Harkki, Paivi, Harris, Holly R., Heikinheimo, Oskari, Hostettler, Isabel C., Houlden, Henry, Houshdaran, Sahar, Jarvelin, Marjo-Riitta, Kamatani, Yoichiro, Kennedy, Stephen H., Kettunen, Johannes, Kubo, Michiaki, Kulig, Bartosz, Laivuori, Hannele, Laufer, Marc R., Lindgren, Cecilia M., MacGregor, Stuart, Mangino, Massimo, Martin, Nicholas G., Matalliotakis, Michail, Murray, Alison D., Ndungu, Anne, Nezhat, Camran, Opoku-Anane, Jessica, Padmanabhan, Sandosh, Peters, Maire, Polak, Grzegorz, Porteous, David J., Rexrode, Kathyrn M., Romanowicz, Hanna, Saare, Merli, Saavalainen, Liisu, Schork, Andrew J., Sen, Sushmita, Shafrir, Amy L., Siewierska-Górska, Anna, Smith, Blair H., Szaflik, Tomasz, Takahashi, Atsushi, Terry, Kathryn L., Tomassetti, Carla, Vanhie, Arne, Vincent, Katy, Vo, Kim C., Werring, David J., Zervou, Maria I., Adachi, Sosuke, Buring, Julie E., Ridker, Paul M., D’Hooghe, Thomas, Hapangama, Dharani K., Hayward, Caroline, Low, Siew-Kee, Martikainen, Hannu, Chasman, Daniel I., Saunders, Philippa T., Sirota, Marina, Spector, Tim, Strapagiel, Dominik, Tung, Joyce Y., Whiteman, David C., Velez-Edwards, Digna R., Uimari, Outi, Kraft, Peter, Salumets, Andres, Nyholt, Dale R., Stefansson, Kari, Becker, Christian M., Nyegaard, Mette, Missmer, Stacey A., Montgomery, Grant W., Morris, Andrew P.

    Veröffentlicht in Nature genetics

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