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    Genetic variants associated with longitudinal changes in brain structure across the lifespan von Schnack, Hugo G., Jahanshad, Neda, Thomopoulos, Sophia I., Sprooten, Emma, Gogtay, Nitin, Whelan, Christopher D., Alloza, Clara, Artiges, Eric, Blok, Elisabet, Bright, Joanna K., Buimer, Elizabeth E. L., Cannon, Dara M., Ciufolini, Simone, Crossley, Nicolas A., Damatac, Christienne G., de Mol, Casper L., de Zwarte, Sonja M. C., Díaz-Caneja, Covadonga M., Doan, Nhat Trung, Dohm, Katharina, Fröhner, Juliane H., Goltermann, Janik, Grigis, Antoine, Han, Laura K. M., Hartman, Catharina A., Heindel, Walter, Janssen, Joost, Jiang, Jiyang, Jockwitz, Christiane, Lenroot, Rhoshel K., Mandl, René C. W., Medel, Vicente, de la Foz, Víctor Ortiz-García, Overs, Bronwyn J., Paillère Martinot, Marie-Laure, Repple, Jonathan, Roberts, Gloria, Setiaman, Nikita, Shumskaya, Elena, Wen, Wei, Westeneng, Henk-Jan, Wittfeld, Katharina, Zugman, Andre, Armstrong, Nicola J., Davies, Gail, Di Forti, Marta, Ding, Linda, Donohoe, Gary, Forstner, Andreas J., Guimaraes, Joao P. O. F. T., Knol, Maria J., Kwok, John B. J., Milaneschi, Yuri, Morris, Derek W., Rietschel, Marcella, Streit, Fabian, van ‘t Ent, Dennis, van der Meer, Dennis, van Eijk, Kristel R., Vázquez-Bourgon, Javier, Witt, Stephanie H., Agartz, Ingrid, Ames, David, Amunts, Katrin, Arango, Celso, Baune, Bernhard T., Belangero, Sintia I., Bokde, Arun L. W., Boomsma, Dorret I., Bressan, Rodrigo A., Brodaty, Henry, Cahn, Wiepke, Caspers, Svenja, Cox, Simon R., Fisher, Simon E., Flor, Herta, Grabe, Hans J., Hoekstra, Pieter J., Jackowski, Andrea P., Jansen, Andreas, Jönsson, Erik G., Kahn, Rene S., Kircher, Tilo, Krug, Axel, Lemaitre, Herve, Martinot, Jean-Luc, McDonald, Colm, Nenadić, Igor, Pan, Pedro M., Penninx, Brenda W. J. H., Poustka, Luise, Schofield, Peter R., Schumann, Gunter, Sim, Kang, Trollor, Julian N., Veldink, Jan H., Westlye, Lars T., Whelan, Robert, Medland, Sarah E., Thompson, Paul M.

    Veröffentlicht in Nature neuroscience

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    Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion von Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Johnston, H. Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A. S., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Warren, Stephen T., Chopra, Pankaj, Cutler, David J., Duncan, Richard, Mulle, Jennifer G., Voss, Anna J., Zwick, Michael E., Diacou, Alexander, Guo, Tingwei, Lin, Jhih-Rong, Wang, Tao, Zhang, Zhengdong, Zhao, Yingjie, Marshall, Christian, Jin, Andrea, Lilley, Brenna, Salmons, Harold I., Tran, Oanh, Pardinas, Antonio, Walters, James T. R., Demaerel, Wolfram, Boot, Erik, Butcher, Nancy J., Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese A. M. J., van Duin, Esther, Vingerhoets, Claudia, Breckpot, Jeroen, Devriendt, Koen, Vogels, Annick, Moss, Edward M., Sharkus, Robert J., Zackai, Elaine H., Calkins, Monica E., Gallagher, Robert S., Gur, Ruben C., Tang, Sunny X., Fritsch, Rosemarie, Ornstein, Claudia, Repetto, Gabriela M., Breetvelt, Elemi, Duijff, Sasja N., Fiksinski, Ania, Niarchou, Maria, Murphy, Kieran C., Prasad, Sarah E., Daly, Eileen M., Gudbrandsen, Maria, Murphy, Declan G., Buzzanca, Antonio, Digilio, Maria C., Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F., Ousley, Opal Y., Carmel, Miri, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stéphan, Sandini, Corrado, Béna, Frédérique Sloan, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Belzeaux, Raoul, Philip, Nicole, Campbell, Linda E., McCabe, Kathryn L., Hooper, Stephen R., Schoch, Kelly, Shashi, Vandana, Simon, Tony J., Tassone, Flora, Arango, Celso, García-Miñaúr, Sixto, Suñer, Damià H., Raventos-Simic, Jasna, Epstein, Michael P., Williams, Nigel M., Bassett, Anne S.

    Veröffentlicht in Molecular psychiatry

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