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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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    Genome-wide association analysis identifies 13 new risk loci for schizophrenia von Chambert, Kimberly, Akterin, Susanne, Collins, Ann L, Fromer, Menachem, Kim, Yunjung, Lee, Sang Hong, Magnusson, Patrik KE, Sanchez, Nick, Stahl, Eli A, Williams, Stephanie, Wray, Naomi R, Xia, Kai, Borglum, Anders D, Bulik-Sullivan, Brendan K, Craddock, Nick, de Leeuw, Christiaan, Durmishi, Naser, Gill, Michael, Hamshere, Marian L, Morris, Derek W, Mors, Ole, Neale, Benjamin M, Owen, Michael J, Posthuma, Danielle, Powell, John, Richards, Alexander L, Ruderfer, Douglas, Rujescu, Dan, Suvisaari, Jaana, Tosato, Sarah, Verhage, Matthijs, Walters, James T, Multicenter Genetic Studies of Schizophrenia Consortium, Levinson, Douglas F, O'Donovan, Michael C, Dudbridge, Frank, Shi, Jianxin, Albus, Margot, Cohen, David, Duan, Jubao, Eichhammer, Peter, Godard, Stephanie, Hansen, Mark, Papadimitriou, George N, Ribble, Robert, Sanders, Alan R, Silverman, Jeremy M, Walsh, Dermot, Williams, Nigel M, Psychosis Endophenotypes International Consortium, Arranz, Maria J, Bramon, Elvira, Collier, David, Iyegbe, Conrad, Jablensky, Assen, Kahn, Rene S, Kalaydjieva, Luba, Lawrie, Stephen, McIntosh, Andrew, Ophoff, Roel A, Van Os, Jim, Wiersma, Durk, Wellcome Trust Case Control Consortium 2, Donnelly, Peter, Barroso, Ines, Blackwell, Jenefer M, Casas, Juan P, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Palmer, Colin NA, Rautanen, Anna, Trembath, Richard C, Viswanathan, Ananth C, Spencer, Chris CA, Giannoulatou, Eleni, Pirinen, Matti, Pearson, Richard D, Vukcevic, Damjan, Langford, Cordelia, Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J, Dronov, Serge, Gray, Emma, Jayakumar, Alagurevathi, Liddle, Jennifer, Ricketts, Michelle, Waller, Matthew J, Weston, Paul, Widaa, Sara, Whittaker, Pamela, McCarthy, Mark I, Scolnick, Edward, Purcell, Shaun, McCarroll, Steven A, Sklar, Pamela, Hultman, Christina M, Sullivan, Patrick F

    Veröffentlicht in Nature genetics

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