Treffer 1 - 20 von 22 für Suche 'Weston, Raymond Eric', Suchdauer: 0,92s Treffer weiter einschränken
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    Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes von Ruderfer, Douglas M., Boocock, James, Stahl, Eli A., Charney, Alexander W., Ori, Anil P.S., Alliey-Rodriguez, Ney, Anjorin, Adebayo, Badner, Judith A., Band, Gavin, Bruggeman, Richard, Buccola, Nancy G., Bumpstead, Suzannah J., Casas, Juan P., Chan, Raymond C.K., Chen, Ronald Y.L., Collier, David A., Cormican, Paul, Craddock, Nicholas, Crowley, James J., Curtis, David, Dannlowski, Udo, Davidson, Michael, Demontis, Ditte, Dronov, Serge, Elvsashagen, Torbjorn, Etain, Bruno, Fan, Chun Chieh, Forty, Liz, Fraser, Christine, Garnham, Julie, Gill, Michael, Gillman, Matthew, Gratten, Jacob, Gwilliam, Rhian, Hammer, Christian, Hansen, Thomas, Henskens, Frans A., Jamain, Stephane, Jankowski, Janusz, Joa, Inge, Julia, Antonio, Kandaswamy, Radhika, Kavanagh, David, Keller, Matthew C., Khrunin, Andrey, Lee, Phil H., Legge, Sophie E., Lencz, Todd, Levinson, Douglas F., Levy, Shawn E., Li, Tao, Lin, Kuang, Macek, Milan, McCarley, Robert W., McGuffin, Peter, McInnis, Melvin G., Meijer, Carin J., Melegh, Bela, Mesholam-Gately, Raquelle I., Myin-Germeys, Inez, Nicodemus, Kristin K., Nimgaonkar, Vishwajit, Nordin, Annelie, Nöthen, Markus M., Van Os, Jim, Owen, Michael J., Palmer, Colin N.A., Palotie, Aarno, Papadimitriou, George N., Pato, Michele T., Perlis, Roy H., Petryshen, Tracey L., Plomin, Robert, Potash, James B., Powell, John, Ramos-Quiroga, Josep Antoni, Rautanen, Anna, Reichenberg, Abraham, Ribases, Marta, Rice, John P., Richards, Alexander L., Ricketts, Michelle, Sanchez-Mora, Cristina, Sanders, Alan R., Schall, Ulrich, Serretti, Alessandro, Sham, Pak C., Straub, Richard E., Strauss, John S., Szatkiewicz, Jin P., Thompson, Robert C., Thorgeirsson, Thorgeir E., Treutlein, Jens, Vedder, Helmut, Wang, Qiang, Wu, Jing Qin, Sullivan, Patrick F., Wray, Naomi R., Sklar, Pamela, Kendler, Kenneth S.

    Veröffentlicht in Cell

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    Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia von Kendler, Kenneth S., Walters, James, Blackwell, Jenefer M., Bramon, Elvira, Markus, Hugh S., Rautanen, Anna, Freeman, Colin, Hopkins, Lucinda, Edkins, Sarah, Bumpstead, Suzannah J., Dronov, Serge, Gillman, Matthew, Gray, Emma, Liddle, Jennifer, Potter, Simon C., Weston, Paul, Ripke, Stephan, Farh, Kai‐How, Holmans, Peter A., Lee, Phil, Huang, Hailiang, Bacanu, Silviu A., Belliveau, Richard A., Bene, Judit, Bigdeli, Tim B., Bruggeman, Richard, Cahn, Wiepke, Carrera, Noa, Cheung, Eric F. C., Cohen, David, Craddock, Nick, Davis, Kenneth L., Dinan, Timothy, Drapeau, Elodie, Dudbridge, Frank, Durmishi, Naser, Eichhammer, Peter, Farrell, Martilias S., Franke, Lude, Freimer, Nelson B., Friedman, Joseph I., Fromer, Menachem, Gratten, Jacob, Haroutunian, Vahram, Hartmann, Annette M., Henskens, Frans A., Hofman, Andrea, Hollegaard, Mads V., Joa, Inge, Keller, Matthew C., Klovins, Janis, Konte, Bettina, Kucinskiene, Zita Ausrele, Laurent, Claudine, Loughland, Carmel M., Mallet, Jacques, Mattheisen, Manuel, McCarley, Robert W., McDonald, Colm, Meier, Sandra, Meijer, Carin J., Metspalu, Andres, Milani, Lili, Milanova, Vihra, Mokrab, Younes, Myin‐Germeys, Inez, Nenadic, Igor, Nikitina‐Zake, Liene, O'Callaghan, Eadbhard, O'Neill, F. Anthony, Paunio, Tiina, Pejovic‐Milovancevic, Milica, Perkins, Diana O., Pietiläinen, Olli, Quested, Digby, Reichenberg, Abraham, Salomaa, Veikko, Scolnick, Edward M., Silagadze, Teimuraz, So, Hon‐Cheong, Spencer, Chris C. A., Suvisaari, Jaana, Szatkiewicz, Jin P., Thirumalai, Srinivas, Tosato, Sarah, Waddington, John, Wang, Qiang, Williams, Nigel M., Witt, Stephanie H., Wormley, Brandon K., Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R., Buxbaum, Joseph D., Jablensky, Assen V., Knight, Jo, Levinson, Douglas F., Malhotra, Anil K., Weinberger, Daniel R., Werge, Thomas


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