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2016

Adams, H. H. and Hibar, D. P. and Chouraki, V. and Stein, J. L. and Nyquist, P. A. and Renteria, M. E. and Trompet, S. and Arias-Vasquez, A. and Seshadri, S. and Desrivieres, S. and Beecham, A. H. and Jahanshad, N. and Wittfeld, K. and Van der Lee, S. J. and Abramovic, L. and Alhusaini, S. and Amin, N. and Andersson, M. and Arfanakis, K. and Aribisala, B. S. and Armstrong, N. J. and Athanasiu, L. and Axelsson, T. and Beiser, A. and Bernard, M. and Bis, J. C. and Blanken, L. M. and Blanton, S. H. and Bohlken, M. M. and Boks, M. P. and Bralten, J. and Brickman, A. M. and Carmichael, O. and Chakravarty, M. M. and Chauhan, G. and Chen, Q. and Ching, C. R. and Cuellar-Partida, G. and Braber, A. D. and Doan, N. T. and Ehrlich, S. and Filippi, I. and Ge, T. and Giddaluru, S. and Goldman, A. L. and Gottesman, R. F. and Greven, C. U. and Grimm, O. and Griswold, M. E. and Guadalupe, T. and Hass, J. and Haukvik, U. K. and Hilal, S. and Hofer, E. and Hoehn, D. and Holmes, A. J. and Hoogman, M. and Janowitz, D. and Jia, T. and Kasperaviciute, D. and Kim, S. and Klein, M. and Kraemer, B. and Lee, P. H. and Liao, J. and Liewald, D. C. and Lopez, L. M. and Luciano, M. and Macare, C. and Marquand, A. and Matarin, M. and Mather, K. A. and Mattheisen, M. and Mazoyer, B. and McKay, D. R. and McWhirter, R. and Milaneschi, Y. and Mirza-Schreiber, N. and Muetzel, R. L. and Maniega, S. M. and Nho, K. and Nugent, A. C. and Loohuis, L. M. and Oosterlaan, J. and Papmeyer, M. and Pappa, I. and Pirpamer, L. and Pudas, S. and Putz, B. and Rajan, K. B. and Ramasamy, A. and Richards, J. S. and Risacher, S. L. and Roiz-Santianez, R. and Rommelse, N. and Rose, E. J. and Royle, N. A. and Rundek, T. and Samann, P. G. and Satizabal, C. L. and Schmaal, L. and Schork, A. J. and Shen, L. and Shin, J. and Shumskaya, E. and Smith, A. V. and Sprooten, E. and Strike, L. T. and Teumer, A. and Thomson, R. and Tordesillas-Gutierrez, D. and Toro, R. and Trabzuni, D. and Vaidya, D. and Van der Grond, J. and Van der Meer, D. and Van Donkelaar, M. M. and Van Eijk, K. R. and Van Erp, T. G. and Van Rooij, D. and Walton, E. and Westlye, L. T. and Whelan, C. D. and Windham, B. G. and Winkler, A. M. and Woldehawariat, G. and Wolf, C. and Wolfers, T. and Xu, B. and Yanek, L. R. and Yang, J. and Zijdenbos, A. and Zwiers, M. P. and Agartz, I. and Aggarwal, N. T. and Almasy, L. and Ames, D. and Amouyel, P. and Andreassen, O. A. and Arepalli, S. and Assareh, A. A. and Barral, S. and Bastin, M. E. and Becker, D. M. and Becker, J. T. and Bennett, D. A. and Blangero, J. and van Bokhoven, H. and Boomsma, D. I. and Brodaty, H. and Brouwer, R. M. and Brunner, H. G. and Buckner, R. L. and Buitelaar, J. K. and Bulayeva, K. B. and Cahn, W. and Calhoun, V. D. and Cannon, D. M. and Cavalleri, G. L. and Chen, C. and Cheng, C. Y. and Cichon, S. and Cookson, M. R. and Corvin, A. and Crespo-Facorro, B. and Curran, J. E. and Czisch, M. and Dale, A. M. and Davies, G. E. and De Geus, E. J. and De Jager, P. L. and de Zubicaray, G. I. and Delanty, N. and Depondt, C. and DeStefano, A. L. and Dillman, A. and Djurovic, S. and Donohoe, G. and Drevets, W. C. and Duggirala, R. and Dyer, T. D. and Erk, S. and Espeseth, T. and Evans, D. A. and Fedko, I. O. and Fernandez, G. and Ferrucci, L. and Fisher, S. E. and Fleischman, D. A. and Ford, I. and Foroud, T. M. and Fox, P. T. and Francks, C. and Fukunaga, M. and Gibbs, J. R. and Glahn, D. C. and Gollub, R. L. and Goring, H. H. and Grabe, H. J. and Green, R. C. and Gruber, O. and Gudnason, V. and Guelfi, S. and Hansell, N. K. and Hardy, J. and Hartman, C. A. and Hashimoto, R. and Hegenscheid, K. and Heinz, A. and Le Hellard, S. and Hernandez, D. G. and Heslenfeld, D. J. and Ho, B. C. and Hoekstra, P. J. and Hoffmann, W. and Hofman, A. and Holsboer, F. and Homuth, G. and Hosten, N. and Hottenga, J. J. and Pol, H. E. and Ikeda, M. and Ikram, M. K. and Jack, C. R. and Jr., and Jenkinson, M. and Johnson, R. and Jonsson, E. G. and Jukema, J. W. and Kahn, R. S. and Kanai, R. and Kloszewska, I. and Knopman, D. S. and Kochunov, P. and Kwok, J. B. and Lawrie, S. M. and Lemaitre, H. and Liu, X. and Longo, D. L. and Longstreth, W. T. and Jr., and Lopez, O. L. and Lovestone, S. and Martinez, O. and Martinot, J. L. and Mattay, V. S. and McDonald, C. and McIntosh, A. M. and McMahon, K. L. and McMahon, F. J. and Mecocci, P. and Melle, I. and Meyer-Lindenberg, A. and Mohnke, S. and Montgomery, G. W. and Morris, D. W. and Mosley, T. H. and Muhleisen, T. W. and Muller-Myhsok, B. and Nalls, M. A. and Nauck, M. and Nichols, T. E. and Niessen, W. J. and Nothen, M. M. and Nyberg, L. and Ohi, K. and Olvera, R. L. and Ophoff, R. A. and Pandolfo, M. and Paus, T. and Pausova, Z. and Penninx, B. W. and Pike, G. B. and Potkin, S. G. and Psaty, B. M. and Reppermund, S. and Rietschel, M. and Roffman, J. L. and Romanczuk-Seiferth, N. and Rotter, J. I. and Ryten, M. and Sacco, R. L. and Sachdev, P. S. and Saykin, A. J. and Schmidt, R. and Schofield, P. R. and Sigurdsson, S. and Simmons, A. and Singleton, A. and Sisodiya, S. M. and Smith, C. and Smoller, J. W. and Soininen, H. and Srikanth, V. and Steen, V. M. and Stott, D. J. and Sussmann, J. E. and Thalamuthu, A. and Tiemeier, H. and Toga, A. W. and Traynor, B. J. and Troncoso, J. and Turner, J. A. and Tzourio, C. and Uitterlinden, A. G. and Hernandez, M. C. and Van der Brug, M. and Van der Lugt, A. and Van der Wee, N. J. and Van Duijn, C. M. and Van Haren, N. E. and Van, T. Ent D. and Van Tol, M. J. and Vardarajan, B. N. and Veltman, D. J. and Vernooij, M. W. and Volzke, H. and Walter, H. and Wardlaw, J. M. and Wassink, T. H. and Weale, M. E. and Weinberger, D. R. and Weiner, M. W. and Wen, W. and Westman, E. and White, T. and Wong, T. Y. and Wright, C. B. and Zielke, H. R. and Zonderman, A. B. and Deary, I. J. and DeCarli, C. and Schmidt, H. and Martin, N. G. and De Craen, A. J. and Wright, M. J. and Launer, L. J. and Schumann, G. and Fornage, M. and Franke, B. and Debette, S. and Medland, S. E. and Ikram, M. A. and Thompson, P. M.. (2016) Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, 19 (12). pp. 1569-1582.

Bigdeli, T. B. and Ripke, S. and Bacanu, S. A. and Lee, S. H. and Wray, N. R. and Gejman, P. V. and Rietschel, M. and Cichon, S. and St Clair, D. and Corvin, A. and Kirov, G. and McQuillin, A. and Gurling, H. and Rujescu, D. and Andreassen, O. A. and Werge, T. and Blackwood, D. H. and Pato, C. N. and Pato, M. T. and Malhotra, A. K. and O'Donovan, M. C. and Kendler, K. S. and Fanous, A. H. and Schizophrenia Working Group of the Psychiatric Genomics, Consortium. (2016) Genome‐wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. American Journal of Medical Genetics; Part B: Neuropsychiatric Genetics, 171B (2). pp. 276-289.

Cao, H. and Bertolino, A. and Walter, H. and Schneider, M. and Schafer, A. and Taurisano, P. and Blasi, G. and Haddad, L. and Grimm, O. and Otto, K. and Dixson, L. and Erk, S. and Mohnke, S. and Heinz, A. and Romanczuk-Seiferth, N. and Muhleisen, T. W. and Mattheisen, M. and Witt, S. H. and Cichon, S. and Noethen, M. and Rietschel, M. and Tost, H. and Meyer-Lindenberg, A.. (2016) Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia. JAMA Psychiatry, 73 (6). pp. 598-605.

Chang, H. and Li, L. and Peng, T. and Grigoroiu-Serbanescu, M. and Bergen, S. E. and Landen, M. and Hultman, C. M. and Forstner, A. J. and Strohmaier, J. and Hecker, J. and Schulze, T. G. and Muller-Myhsok, B. and Reif, A. and Mitchell, P. B. and Martin, N. G. and Cichon, S. and Nothen, M. M. and Jamain, S. and Leboyer, M. and Bellivier, F. and Etain, B. and Kahn, J. P. and Henry, C. and Rietschel, M. and Swedish Bipolar Study, Group and Moo, D. S. Consortium and Xiao, X. and Li, M.. (2016) Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1. Molecular Neurobiology, 54 (7). pp. 5166-5176.

Direk, N. and Williams, S. and Smith, J. A. and Ripke, S. and Air, T. and Amare, A. T. and Amin, N. and Baune, B. T. and Bennett, D. A. and Blackwood, D. H. and Boomsma, D. and Breen, G. and Buttenschon, H. N. and Byrne, E. M. and Borglum, A. D. and Castelao, E. and Cichon, S. and Clarke, T. K. and Cornelis, M. C. and Dannlowski, U. and De Jager, P. L. and Demirkan, A. and Domenici, E. and van Duijn, C. M. and Dunn, E. C. and Eriksson, J. G. and Esko, T. and Faul, J. D. and Ferrucci, L. and Fornage, M. and de Geus, E. and Gill, M. and Gordon, S. D. and Grabe, H. J. and van Grootheest, G. and Hamilton, S. P. and Hartman, C. A. and Heath, A. C. and Hek, K. and Hofman, A. and Homuth, G. and Horn, C. and Jan Hottenga, J. and Kardia, S. L. and Kloiber, S. and Koenen, K. and Kutalik, Z. and Ladwig, K. H. and Lahti, J. and Levinson, D. F. and Lewis, C. M. and Lewis, G. and Li, Q. S. and Llewellyn, D. J. and Lucae, S. and Lunetta, K. L. and MacIntyre, D. J. and Madden, P. and Martin, N. G. and McIntosh, A. M. and Metspalu, A. and Milaneschi, Y. and Montgomery, G. W. and Mors, O. and Mosley, T. H. and Jr., and Murabito, J. M. and Muller-Myhsok, B. and Nothen, M. M. and Nyholt, D. R. and O'Donovan, M. C. and Penninx, B. W. and Pergadia, M. L. and Perlis, R. and Potash, J. B. and Preisig, M. and Purcell, S. M. and Quiroz, J. A. and Raikkonen, K. and Rice, J. P. and Rietschel, M. and Rivera, M. and Schulze, T. G. and Shi, J. and Shyn, S. and Sinnamon, G. C. and Smit, J. H. and Smoller, J. W. and Snieder, H. and Tanaka, T. and Tansey, K. E. and Teumer, A. and Uher, R. and Umbricht, D. and Van der Auwera, S. and Ware, E. B. and Weir, D. R. and Weissman, M. M. and Willemsen, G. and Yang, J. and Zhao, W. and Tiemeier, H. and Sullivan, P. F.. (2016) An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype. Biological Psychiatry, 83 (5). pp. 322-329.

Giddaluru, S. and Espeseth, T. and Salami, A. and Westlye, L. T. and Lundquist, A. and Christoforou, A. and Cichon, S. and Adolfsson, R. and Steen, V. M. and Reinvang, I. and Nilsson, L. G. and Le Hellard, S. and Nyberg, L.. (2016) Genetics of structural connectivity and information processing in the brain. Brain Structure and Function, 221 (9). pp. 4643-4661.

Grumach, A. S. and Stieber, C. and Veronez, C. L. and Cagini, N. and Constantino-Silva, R. N. and Cordeiro, E. and Nothen, M. M. and Pesquero, J. B. and Cichon, S.. (2016) Homozygosity for a factor XII mutation in one female and one male patient with hereditary angio-oedema. Allergy, 71 (1). pp. 119-123.

Hou, L. and Bergen, S. E. and Akula, N. and Song, J. and Hultman, C. M. and Landen, M. and Adli, M. and Alda, M. and Ardau, R. and Arias, B. and Aubry, J. M. and Backlund, L. and Badner, J. A. and Barrett, T. B. and Bauer, M. and Baune, B. T. and Bellivier, F. and Benabarre, A. and Bengesser, S. and Berrettini, W. H. and Bhattacharjee, A. K. and Biernacka, J. M. and Birner, A. and Bloss, C. S. and Brichant-Petitjean, C. and Bui, E. T. and Byerley, W. and Cervantes, P. and Chillotti, C. and Cichon, S. and Colom, F. and Coryell, W. and Craig, D. W. and Cruceanu, C. and Czerski, P. M. and Davis, T. and Dayer, A. and Degenhardt, F. and Del Zompo, M. and DePaulo, J. R. and Edenberg, H. J. and Etain, B. and Falkai, P. and Foroud, T. and Forstner, A. J. and Frisen, L. and Frye, M. A. and Fullerton, J. M. and Gard, S. and Garnham, J. S. and Gershon, E. S. and Goes, F. S. and Greenwood, T. A. and Grigoroiu-Serbanescu, M. and Hauser, J. and Heilbronner, U. and Heilmann-Heimbach, S. and Herms, S. and Hipolito, M. and Hitturlingappa, S. and Hoffmann, P. and Hofmann, A. and Jamain, S. and Jimenez, E. and Kahn, J. P. and Kassem, L. and Kelsoe, J. R. and Kittel-Schneider, S. and Kliwicki, S. and Koller, D. L. and Konig, B. and Lackner, N. and Laje, G. and Lang, M. and Lavebratt, C. and Lawson, W. B. and Leboyer, M. and Leckband, S. G. and Liu, C. and Maaser, A. and Mahon, P. B. and Maier, W. and Maj, M. and Manchia, M. and Martinsson, L. and McCarthy, M. J. and McElroy, S. L. and McInnis, M. G. and McKinney, R. and Mitchell, P. B. and Mitjans, M. and Mondimore, F. M. and Monteleone, P. and Muhleisen, T. W. and Nievergelt, C. M. and Nothen, M. M. and Novak, T. and Nurnberger, J. I. and Jr., and Nwulia, E. A. and Osby, U. and Pfennig, A. and Potash, J. B. and Propping, P. and Reif, A. and Reininghaus, E. and Rice, J. and Rietschel, M. and Rouleau, G. A. and Rybakowski, J. K. and Schalling, M. and Scheftner, W. A. and Schofield, P. R. and Schork, N. J. and Schulze, T. G. and Schumacher, J. and Schweizer, B. W. and Severino, G. and Shekhtman, T. and Shilling, P. D. and Simhandl, C. and Slaney, C. M. and Smith, E. N. and Squassina, A. and Stamm, T. and Stopkova, P. and Streit, F. and Strohmaier, J. and Szelinger, S. and Tighe, S. K. and Tortorella, A. and Turecki, G. and Vieta, E. and Volkert, J. and Witt, S. H. and Wright, A. and Zandi, P. P. and Zhang, P. and Zollner, S. and McMahon, F. J.. (2016) Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. Human Molecular Genetics, 25 (15). pp. 3383-3394.

Hou, L. and Heilbronner, U. and Degenhardt, F. and Adli, M. and Akiyama, K. and Akula, N. and Ardau, R. and Arias, B. and Backlund, L. and Banzato, C. E. and Benabarre, A. and Bengesser, S. and Bhattacharjee, A. K. and Biernacka, J. M. and Birner, A. and Brichant-Petitjean, C. and Bui, E. T. and Cervantes, P. and Chen, G. B. and Chen, H. C. and Chillotti, C. and Cichon, S. and Clark, S. R. and Colom, F. and Cousins, D. A. and Cruceanu, C. and Czerski, P. M. and Dantas, C. R. and Dayer, A. and Etain, B. and Falkai, P. and Forstner, A. J. and Frisen, L. and Fullerton, J. M. and Gard, S. and Garnham, J. S. and Goes, F. S. and Grof, P. and Gruber, O. and Hashimoto, R. and Hauser, J. and Herms, S. and Hoffmann, P. and Hofmann, A. and Jamain, S. and Jimenez, E. and Kahn, J. P. and Kassem, L. and Kittel-Schneider, S. and Kliwicki, S. and Konig, B. and Kusumi, I. and Lackner, N. and Laje, G. and Landen, M. and Lavebratt, C. and Leboyer, M. and Leckband, S. G. and Jaramillo, C. A. and MacQueen, G. and Manchia, M. and Martinsson, L. and Mattheisen, M. and McCarthy, M. J. and McElroy, S. L. and Mitjans, M. and Mondimore, F. M. and Monteleone, P. and Nievergelt, C. M. and Nothen, M. M. and Osby, U. and Ozaki, N. and Perlis, R. H. and Pfennig, A. and Reich-Erkelenz, D. and Rouleau, G. A. and Schofield, P. R. and Schubert, K. O. and Schweizer, B. W. and Seemuller, F. and Severino, G. and Shekhtman, T. and Shilling, P. D. and Shimoda, K. and Simhandl, C. and Slaney, C. M. and Smoller, J. W. and Squassina, A. and Stamm, T. and Stopkova, P. and Tighe, S. K. and Tortorella, A. and Turecki, G. and Volkert, J. and Witt, S. and Wright, A. and Young, L. T. and Zandi, P. P. and Potash, J. B. and DePaulo, J. R. and Bauer, M. and Reininghaus, E. Z. and Novak, T. and Aubry, J. M. and Maj, M. and Baune, B. T. and Mitchell, P. B. and Vieta, E. and Frye, M. A. and Rybakowski, J. K. and Kuo, P. H. and Kato, T. and Grigoroiu-Serbanescu, M. and Reif, A. and Del Zompo, M. and Bellivier, F. and Schalling, M. and Wray, N. R. and Kelsoe, J. R. and Alda, M. and Rietschel, M. and McMahon, F. J. and Schulze, T. G.. (2016) Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. The Lancet, 387 (10023). pp. 1085-1093.

Ibrahim-Verbaas, C. A. and Bressler, J. and Debette, S. and Schuur, M. and Smith, A. V. and Bis, J. C. and Davies, G. and Trompet, S. and Smith, J. A. and Wolf, C. and Chibnik, L. B. and Liu, Y. and Vitart, V. and Kirin, M. and Petrovic, K. and Polasek, O. and Zgaga, L. and Fawns-Ritchie, C. and Hoffmann, P. and Karjalainen, J. and Lahti, J. and Llewellyn, D. J. and Schmidt, C. O. and Mather, K. A. and Chouraki, V. and Sun, Q. and Resnick, S. M. and Rose, L. M. and Oldmeadow, C. and Stewart, M. and Smith, B. H. and Gudnason, V. and Yang, Q. and Mirza, S. S. and Jukema, J. W. and deJager, P. L. and Harris, T. B. and Liewald, D. C. and Amin, N. and Coker, L. H. and Stegle, O. and Lopez, O. L. and Schmidt, R. and Teumer, A. and Ford, I. and Karbalai, N. and Becker, J. T. and Jonsdottir, M. K. and Au, R. and Fehrmann, R. S. and Herms, S. and Nalls, M. and Zhao, W. and Turner, S. T. and Yaffe, K. and Lohman, K. and van Swieten, J. C. and Kardia, S. L. and Knopman, D. S. and Meeks, W. M. and Heiss, G. and Holliday, E. G. and Schofield, P. W. and Tanaka, T. and Stott, D. J. and Wang, J. and Ridker, P. and Gow, A. J. and Pattie, A. and Starr, J. M. and Hocking, L. J. and Armstrong, N. J. and McLachlan, S. and Shulman, J. M. and Pilling, L. C. and Eiriksdottir, G. and Scott, R. J. and Kochan, N. A. and Palotie, A. and Hsieh, Y. C. and Eriksson, J. G. and Penman, A. and Gottesman, R. F. and Oostra, B. A. and Yu, L. and DeStefano, A. L. and Beiser, A. and Garcia, M. and Rotter, J. I. and Nothen, M. M. and Hofman, A. and Slagboom, P. E. and Westendorp, R. G. and Buckley, B. M. and Wolf, P. A. and Uitterlinden, A. G. and Psaty, B. M. and Grabe, H. J. and Bandinelli, S. and Chasman, D. I. and Grodstein, F. and Raikkonen, K. and Lambert, J. C. and Porteous, D. J. and Generation, Scotland and Price, J. F. and Sachdev, P. S. and Ferrucci, L. and Attia, J. R. and Rudan, I. and Hayward, C. and Wright, A. F. and Wilson, J. F. and Cichon, S. and Franke, L. and Schmidt, H. and Ding, J. and de Craen, A. J. and Fornage, M. and Bennett, D. A. and Deary, I. J. and Ikram, M. A. and Launer, L. J. and Fitzpatrick, A. L. and Seshadri, S. and van Duijn, C. M. and Mosley, T. H.. (2016) GWAS for executive function and processing speed suggests involvement of the CADM2 gene. Molecular Psychiatry, 21 (2). pp. 189-197.

Johnson, E. C. and Bjelland, D. W. and Howrigan, D. P. and Abdellaoui, A. and Breen, G. and Borglum, A. and Cichon, S. and Degenhardt, F. and Forstner, A. J. and Frank, J. and Genovese, G. and Heilmann-Heimbach, S. and Herms, S. and Hoffman, P. and Maier, W. and Mattheisen, M. and Morris, D. and Mowry, B. and Muller-Mhysok, B. and Neale, B. and Nenadic, I. and Nothen, M. M. and O'Dushlaine, C. and Rietschel, M. and Ruderfer, D. M. and Rujescu, D. and Schulze, T. G. and Simonson, M. A. and Stahl, E. and Strohmaier, J. and Witt, S. H. and Schizophrenia Working Group of the Psychiatric Genomics, Consortium and Sullivan, P. F. and Keller, M. C.. (2016) No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. PLoS Genetics, 12 (10). e1006343.

Li, M. and Huang, L. and Grigoroiu-Serbanescu, M. and Bergen, S. E. and Landen, M. and Hultman, C. M. and Forstner, A. J. and Strohmaier, J. and Hecker, J. and Schulze, T. G. and Muller-Myhsok, B. and Reif, A. and Mitchell, P. B. and Martin, N. G. and Cichon, S. and Nothen, M. M. and Alkelai, A. and Lerer, B. and Jamain, S. and Leboyer, M. and Bellivier, F. and Etain, B. and Kahn, J. P. and Henry, C. and Rietschel, M. and Moo, D. S. Consortium and Swedish Bipolar Study, Group. (2016) Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis. Molecular Neurobiology, 53 (10). pp. 6608-6619.

Li, M. and Luo, X. J. and Landen, M. and Bergen, S. E. and Hultman, C. M. and Li, X. and Zhang, W. and Yao, Y. G. and Zhang, C. and Liu, J. and Mattheisen, M. and Cichon, S. and Muhleisen, T. W. and Degenhardt, F. A. and Nothen, M. M. and Schulze, T. G. and Grigoroiu-Serbanescu, M. and Li, H. and Fuller, C. K. and Chen, C. and Dong, Q. and Chen, C. and Jamain, S. and Leboyer, M. and Bellivier, F. and Etain, B. and Kahn, J. P. and Henry, C. and Preisig, M. and Kutalik, Z. and Castelao, E. and Wright, A. and Mitchell, P. B. and Fullerton, J. M. and Schofield, P. R. and Montgomery, G. W. and Medland, S. E. and Gordon, S. D. and Martin, N. G. and Moo, D. S. Consortium and Swedish Bipolar Study, Group and Rietschel, M. and Liu, C. and Kleinman, J. E. and Hyde, T. M. and Weinberger, D. R. and Su, B.. (2016) Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. The British Journal of Psychiatry, 208 (2). pp. 128-137.

Plauth, A. and Geikowski, A. and Cichon, S. and Wowro, S. J. and Liedgens, L. and Rousseau, M. and Weidner, C. and Fuhr, L. and Kliem, M. and Jenkins, G. and Lotito, S. and Wainwright, L. J. and Sauer, S.. (2016) Hormetic shifting of redox environment by pro-oxidative resveratrol protects cells against stress. Free Radical Biology and Medicine, 99. pp. 608-622.

Plauth, A. and Geikowski, A. and Cichon, S. and Wowro, S. J. and Liedgens, L. and Rousseau, M. and Weidner, C. and Fuhr, L. and Kliem, M. and Jenkins, G. and Lotito, S. and Wainwright, L. J. and Sauer, S.. (2016) Data of oxygen- and pH-dependent oxidation of resveratrol. Data in Brief, 9. pp. 433-437.

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van Rheenen, W. and Shatunov, A. and Dekker, A. M. and McLaughlin, R. L. and Diekstra, F. P. and Pulit, S. L. and van der Spek, R. A. and Vosa, U. and de Jong, S. and Robinson, M. R. and Yang, J. and Fogh, I. and van Doormaal, P. T. and Tazelaar, G. H. and Koppers, M. and Blokhuis, A. M. and Sproviero, W. and Jones, A. R. and Kenna, K. P. and van Eijk, K. R. and Harschnitz, O. and Schellevis, R. D. and Brands, W. J. and Medic, J. and Menelaou, A. and Vajda, A. and Ticozzi, N. and Lin, K. and Rogelj, B. and Vrabec, K. and Ravnik-Glavac, M. and Koritnik, B. and Zidar, J. and Leonardis, L. and Groselj, L. D. and Millecamps, S. and Salachas, F. and Meininger, V. and de Carvalho, M. and Pinto, S. and Mora, J. S. and Rojas-Garcia, R. and Polak, M. and Chandran, S. and Colville, S. and Swingler, R. and Morrison, K. E. and Shaw, P. J. and Hardy, J. and Orrell, R. W. and Pittman, A. and Sidle, K. and Fratta, P. and Malaspina, A. and Topp, S. and Petri, S. and Abdulla, S. and Drepper, C. and Sendtner, M. and Meyer, T. and Ophoff, R. A. and Staats, K. A. and Wiedau-Pazos, M. and Lomen-Hoerth, C. and Van Deerlin, V. M. and Trojanowski, J. Q. and Elman, L. and McCluskey, L. and Basak, A. N. and Tunca, C. and Hamzeiy, H. and Parman, Y. and Meitinger, T. and Lichtner, P. and Radivojkov-Blagojevic, M. and Andres, C. R. and Maurel, C. and Bensimon, G. and Landwehrmeyer, B. and Brice, A. and Payan, C. A. and Saker-Delye, S. and Durr, A. and Wood, N. W. and Tittmann, L. and Lieb, W. and Franke, A. and Rietschel, M. and Cichon, S. and Nothen, M. M. and Amouyel, P. and Tzourio, C. and Dartigues, J. F. and Uitterlinden, A. G. and Rivadeneira, F. and Estrada, K. and Hofman, A. and Curtis, C. and Blauw, H. M. and van der Kooi, A. J. and de Visser, M. and Goris, A. and Weber, M. and Shaw, C. E. and Smith, B. N. and Pansarasa, O. and Cereda, C. and Del Bo, R. and Comi, G. P. and D'Alfonso, S. and Bertolin, C. and Soraru, G. and Mazzini, L. and Pensato, V. and Gellera, C. and Tiloca, C. and Ratti, A. and Calvo, A. and Moglia, C. and Brunetti, M. and Arcuti, S. and Capozzo, R. and Zecca, C. and Lunetta, C. and Penco, S. and Riva, N. and Padovani, A. and Filosto, M. and Muller, B. and Stuit, R. J. and Parals Registry, and Slalom Group, and Slap Registry, and Fals Sequencing Consortium, and Slagen Consortium, and Nnipps Study Group, and Blair, I. and Zhang, K. and McCann, E. P. and Fifita, J. A. and Nicholson, G. A. and Rowe, D. B. and Pamphlett, R. and Kiernan, M. C. and Grosskreutz, J. and Witte, O. W. and Ringer, T. and Prell, T. and Stubendorff, B. and Kurth, I. and Hubner, C. A. and Leigh, P. N. and Casale, F. and Chio, A. and Beghi, E. and Pupillo, E. and Tortelli, R. and Logroscino, G. and Powell, J. and Ludolph, A. C. and Weishaupt, J. H. and Robberecht, W. and Van Damme, P. and Franke, L. and Pers, T. H. and Brown, R. H. and Glass, J. D. and Landers, J. E. and Hardiman, O. and Andersen, P. M. and Corcia, P. and Vourc'h, P. and Silani, V. and Wray, N. R. and Visscher, P. M. and de Bakker, P. I. and van Es, M. A. and Pasterkamp, R. J. and Lewis, C. M. and Breen, G. and Al-Chalabi, A. and van den Berg, L. H. and Veldink, J. H.. (2016) Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nature Genetics, 48 (9). pp. 1043-1048.

Wang, Y. and Thompson, W. K. and Schork, A. J. and Holland, D. and Chen, C. H. and Bettella, F. and Desikan, R. S. and Li, W. and Witoelar, A. and Zuber, V. and Devor, A. and Bipolar, Disorder and Schizophrenia Working Group of the Psychiatric Genomics, Consortium and Enhancing Neuro Imaging Genetics through Meta Analysis, Consortium and Nothen, M. M. and Rietschel, M. and Chen, Q. and Werge, T. and Cichon, S. and Weinberger, D. R. and Djurovic, S. and O'Donovan, M. and Visscher, P. M. and Andreassen, O. A. and Dale, A. M.. (2016) Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS. PLoS Genetics, 12 (1). e1005803.

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2015

Basmanav, F. Buket and Forstner, Andreas J. and Fier, Heide and Herms, Stefan and Meier, Sandra and Degenhardt, Franziska and Hoffmann, Per and Barth, Sandra and Fricker, Nadine and Strohmaier, Jana and Witt, Stephanie H. and Ludwig, Michael and Schmael, Christine and Moebus, Susanne and Maier, Wolfgang and Mössner, Rainald and Rujescu, Dan and Rietschel, Marcella and Lange, Christoph and Nöthen, Markus M. and Cichon, Sven. (2015) Investigation of the Role of TCF4 Rare Sequence Variants in Schizophrenia. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 168B (5). pp. 354-362.

Buch, Stephan and Stickel, Felix and Trépo, Eric and Way, Michael and Herrmann, Alexander and Nischalke, Hans Dieter and Brosch, Mario and Rosendahl, Jonas and Berg, Thomas and Ridinger, Monika and Rietschel, Marcella and McQuillin, Andrew and Frank, Josef and Kiefer, Falk and Schreiber, Stefan and Lieb, Wolfgang and Soyka, Michael and Semmo, Nasser and Aigner, Elmar and Datz, Christian and Schmelz, Renate and Brückner, Stefan and Zeissig, Sebastian and Stephan, Anna-Magdalena and Wodarz, Norbert and Devière, Jacques and Clumeck, Nicolas and Sarrazin, Christoph and Lammert, Frank and Gustot, Thierry and Deltenre, Pierre and Völzke, Henry and Lerch, Markus M. and Mayerle, Julia and Eyer, Florian and Schafmayer, Clemens and Cichon, Sven and Nöthen, Markus M. and Nothnagel, Michael and Ellinghaus, David and Huse, Klaus and Franke, Andre and Zopf, Steffen and Hellerbrand, Claus and Moreno, Christophe and Franchimont, Denis and Morgan, Marsha Y. and Hampe, Jochen. (2015) A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis. Nature Genetics, 47 (12). pp. 1443-1448.

Dessart, P. and Defendi, F. and Humeau, H. and Nicolie, B. and Sarre, M. E. and Charignon, D. and Ponard, D. and Cichon, S. and Drouet, C. and Martin, L.. (2015) Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema. Dermatology, 230 (4). pp. 324-331.

Farrell, M. S. and Werge, T. and Sklar, P. and Owen, M. J. and Ophoff, R. A. and O'Donovan, M. C. and Corvin, A. and Cichon, S. and Sullivan, P. F.. (2015) Evaluating historical candidate genes for schizophrenia. Molecular Psychiatry, 20 (5). pp. 555-562.

Forstner, A. J. and Hofmann, A. and Maaser, A. and Sumer, S. and Khudayberdiev, S. and Muhleisen, T. W. and Leber, M. and Schulze, T. G. and Strohmaier, J. and Degenhardt, F. and Treutlein, J. and Mattheisen, M. and Schumacher, J. and Breuer, R. and Meier, S. and Herms, S. and Hoffmann, P. and Lacour, A. and Witt, S. H. and Reif, A. and Muller-Myhsok, B. and Lucae, S. and Maier, W. and Schwarz, M. and Vedder, H. and Kammerer-Ciernioch, J. and Pfennig, A. and Bauer, M. and Hautzinger, M. and Moebus, S. and Priebe, L. and Sivalingam, S. and Verhaert, A. and Schulz, H. and Czerski, P. M. and Hauser, J. and Lissowska, J. and Szeszenia-Dabrowska, N. and Brennan, P. and McKay, J. D. and Wright, A. and Mitchell, P. B. and Fullerton, J. M. and Schofield, P. R. and Montgomery, G. W. and Medland, S. E. and Gordon, S. D. and Martin, N. G. and Krasnov, V. and Chuchalin, A. and Babadjanova, G. and Pantelejeva, G. and Abramova, L. I. and Tiganov, A. S. and Polonikov, A. and Khusnutdinova, E. and Alda, M. and Cruceanu, C. and Rouleau, G. A. and Turecki, G. and Laprise, C. and Rivas, F. and Mayoral, F. and Kogevinas, M. and Grigoroiu-Serbanescu, M. and Propping, P. and Becker, T. and Rietschel, M. and Cichon, S. and Schratt, G. and Nothen, M. M.. (2015) Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Translational Psychiatry , 5. e678.

Frank, J. and Lang, M. and Witt, S. H. and Strohmaier, J. and Rujescu, D. and Cichon, S. and Degenhardt, F. and Nothen, M. M. and Collier, D. A. and Ripke, S. and Naber, D. and Rietschel, M.. (2015) Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients. Molecular Psychiatry , 20 (7). p. 913.

Heilbronner, Urs and Malzahn, Dörthe and Strohmaier, Jana and Maier, Sandra and Frank, Josef and Treutlein, Jens and Muhleisen, Thomas W. and Forstner, Andreas J. and Witt, Stephanie H. and Cichon, Sven and Falkai, Peter and Nothen, Markus M. and Rietschel, Marcella and Schulze, Thomas G.. (2015) A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder. European Neuropsychopharmacology, 25 (12). pp. 2262-2270.

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H. and Launer, Lenore J. and Seiler, Stephan and Schmidt, Reinhold and Chauhan, Ganesh and Satizabal, Claudia L. and Becker, James T. and Yanek, Lisa and van der Lee, Sven J. and Ebling, Maritza and Fischl, Bruce and Longstreth Jr, W. T. and Greve, Douglas and Schmidt, Helena and Nyquist, Paul and Vinke, Louis N. and van Duijn, Cornelia M. and Xue, Luting and Mazoyer, Bernard and Bis, Joshua C. and Gudnason, Vilmundur and Seshadri, Sudha and Ikram, M. Arfan and The Alzheimer’s Disease Neuroimaging Initiative, and The CHARGE Consortium, and EPIGEN, and IMAGEN, and SYS, and Martin, Nicholas G. and Wright, Margaret J. and Schumann, Gunter and Franke, Barbara and Thompson, Paul M. and Medland, Sarah E.. (2015) Common genetic variants influence human subcortical brain structures. Nature, 520 (7546). pp. 224-229.

Hommers, Leif and Raab, Annette and Bohl, Alexandra and Weber, Heike and Scholz, Claus-Jürgen and Erhardt, Angelika and Binder, Elisabeth and Arolt, Volker and Gerlach, Alexander and Gloster, Andrew and Kalisch, Raffael and Kircher, Tilo and Lonsdorf, Tina and Ströhle, Andreas and Zwanzger, Peter and Mattheisen, Manuel and Cichon, Sven and Lesch, Klaus-Peter and Domschke, Katharina and Reif, Andreas and Lohse, Martin J. and Deckert, Jürgen. (2015) MicroRNA hsa-miR-4717-5p Regulates RGS2 and May Be a Risk Factor for Anxiety-Related Traits. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics , 168B (4). pp. 296-306.

Johnson, Michael R. and Behmoaras, Jacques and Bottolo, Leonardo and Krishnan, Michelle L. and Pernhorst, Katharina and Meza Santoscoy, Paola L. and Rossetti, Tiziana and Speed, Doug and Srivastava, Prashant K. and Chadeau-Hyam, Marc and Hajji, Nabil and Dabrowska, Dabrowska and Rotival, Maxime and Razzaghi, Banafsheh and Kovac, Stjepana and Wanisch, Klaus and Grillo, Federico W. and Slaviero, Anna and Langley, Sarah R. and Shkura, Kirill and Roncon, Paolo and De, Tisham and Mattheisen, Manuel and Niehusmann, Pitt and O'Brien, Terence J. and Petrovski, Slave and von Lehe, Marec and Hoffmann, Per and Eriksson, Johan and Coffey, Alison J. and Cichon, Sven and Walker, Matthew and Simonato, Michele and Danis, Bénédicte and Mazzuferi, Manuela and Foerch, Patrik and Schoch, Susanne and De Paola, Vincenzo and Kaminski, Rafal M. and Cunliffe, Vincent T. and Becker, Albert J. and Petretto, Enrico. (2015) Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus. Nature Communications, 6. p. 6031.

Juraeva, Dilafruz and Treutlein, Jens and Scholz, Henrike and Frank, Josef and Degenhardt, Franziska and Cichon, Sven and Ridinger, Monika and Mattheisen, Manuel and Witt, Stephanie H. and Lang, Maren and Sommer, Wolfgang H. and Hoffmann, Per and Herms, Stefan and Wodarz, Norbert and Soyka, Michael and Zill, Peter and Maier, Wolfgang and Jünger, Elisabeth and Gaebel, Wolfgang and Dahmen, Norbert and Scherbaum, Norbert and Schmäl, Christine and Steffens, Michael and Lucae, Susanne and Ising, Marcus and Smolka, Michael N. and Zimmermann, Ulrich S. and Müller-Myhsok, Bertram and Nöthen, Markus M. and Mann, Karl and Kiefer, Falk and Spanagel, Rainer and Brors, Benedikt and Rietschel, Marcella. (2015) XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans. Neuropsychopharmacology, 40 (2). pp. 361-371.

Libin, Alexander V. and Scholten, Joel and Schladen, Manon Maitland and Danford, Ellen and Shara, Nawar and Penk, Walter and Grafman, Jordan and Resnik, Linda and Bruner, Dwan and Cichon, Samantha and Philmon, Miriam and Tsai, Brenda and Blackman, Marc and Dromerick, Alexander. (2015) Executive functioning in TBI from rehabilitation to social reintegration: COMPASS (goal,) a randomized controlled trial (grant: 1I01RX000637-01A3 by the VA ORD RR&D, 2013-2016). Military Medical Research, 2. p. 32.

Luo, Xiong-Jian and Mattheisen, Manuel and Li, Ming and Huang, Liang and Rietschel, Marcella and Børglum, Anders D. and Als, Thomas D. and van den Oord, Edwin J. and Aberg, Karolina A. and Mors, Ole and Mortensen, Preben Bo and Luo, Zhenwu and Degenhardt, Franziska and Cichon, Sven and Schulze, Thomas G. and Nöthen, Markus M. and iPSYCH-GEMS, SCZ working group and MooDS, SCZ Consortium and Su, Bing and Zhao, Zhongming and Gan, Lin and Yao, Yong-Gang. (2015) Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function. Schizophrenia Bulletin, 41 (6). pp. 1294-1308.

Mansi, M. and Zanichelli, A. and Coerezza, A. and Suffritti, C. and Wu, M. A. and Vacchini, R. and Stieber, C. and Cichon, S. and Cicardi, M.. (2015) Presentation, diagnosis and treatment of angioedema without wheals: a retrospective analysis of a cohort of 1058 patients. Journal of Internal Medicine, 277 (5). pp. 585-593.

Nenadic, I. and Maitra, R. and Basmanav, F. B. and Schultz, C. C. and Lorenz, C. and Schachtzabel, C. and Smesny, S. and Nöthen, M. M. and Cichon, S. and Reichenbach, J. R. and Sauer, H. and Schlösser, R. G. M. and Gaser, C.. (2015) ZNF804A genetic variation (rs1344706) affects brain grey but not white matter in schizophrenia and healthy subjects. Psychological Medicine, 45 (1). pp. 143-152.

Paternoster, Lavinia and Standl, Marie and Waage, Johannes and Baurecht, Hansjörg and Hotze, Melanie and Strachan, David P. and Curtin, John A. and Bønnelykke, Klaus and Tian, Chao and Takahashi, Atsushi and Esparza-Gordillo, Jorge and Alves, Alexessander Couto and Thyssen, Jacob P. and den Dekker, Herman T. and Ferreira, Manuel A. and Altmaier, Elisabeth and Sleiman, Patrick M. and Xiao, Feng Li and Gonzalez, Juan R. and Marenholz, Ingo and Kalb, Birgit and Pino-Yanes, Maria and Xu, Cheng Jian and Carstensen, Lisbeth and Groen-Blokhuis, Maria M. and Venturini, Cristina and Pennell, Craig E. and Barton, Sheila J. and Levin, Arbet M. and Curjuric, Ivan and Bustamante, Mariona and Kreiner-Møller, Eskil and Lockett, Gabrielle A. and Bacelis, Jonas and Bunyavanich, Supinda and Myers, Rachel A. and Matanovic, Anja and Kumar, Ashish and Tung, Joyce Y and Hirota, Tomomitsu and Kubo, Michiaki and McArdle, Wendy L. and Henderson, A. John and Kemp, John P. and Zheng, Jie and Smith, George Davey and Rüschendorf, Franz and Bauerfeind, Anja and Lee-Kirsch, Min Ae and Arnold, Andreas and Homuth, Georg and Schmidt, Carsten O. and Mangold, Elisabeth and Cichon, Sven and Keil, Thomas and Rodríguez, Elke and Peters, Annette and Franke, Andre and Lieb, Wolfgang and Novak, Natalija and Fölster-Holst, Regina and Horikoshi, Momoko and Pekkanen, Juha and Sebert, Sylvain and Husemoen, Lise L. and Grarup, Niels and de Jongste, Johan C. and Rivadeneira, Fernando and Hofman, Albert and Jaddoe, Vincent W. V. and Pasmans, Suzanne G. M. A. and Elbert, Niels J. and Uitterlinden, André G. and Marks, Guy B. and Thompson, Philip J. and Matheson, Melanie C. and Robertson, Colin F. and Australian Asthma Genetics, Consortium (AAGC) and Ried, Janina S. and Li, Jin and Zuo, Xian Bo and Zheng, Xiao Dong and Yin, Xian Yong Yin and Sun, Liang Dan and McAleer, Maeve A. and O'Regan, Grainne M. and Fahy, Caoimhe M. R. and Campbell, Linda E. and Macek, Milan and Kurek, Michael and Hu, Donglei and Eng, Celeste and Postma, Dirkje S. and Feenstra, Bjarke and Geller, Frank and Hottenga, Jouke Jan and Middeldorp, Christel M. and Hysi, Pirro and Bataille, Veronique and Spector, Tim and Tiesler, Carla M. T. and Thiering, Elisabeth and Pahukasahasram, Badri and Yang, James J. and Imboden, Madea and Huntsman, Scott and Vilor-Tejedor, Natàlia and Relton, Caroline L. and Myhre, Ronny and Nystad, Wenche and Custovic, Adnan and Weiss, Scott T. and Meyers, Deborah A. and Soderhall, Cilla and Melén, Erik and Ober, Carole and Raby, Benjamin A. and Simpson, Angela and Jacobsson, Bo and Holloway, John W. and Bisgaard, Hans and Sunyer, Jordi and Probst-Hensch, Nicole M. and Williams, L. Keoki and Godfrey, Keith M. and Wang, Carol A. and Boomsma, Dorret I. and Melbye, Mads and Koppelman, Gerard H. and Jarvis, Deborah and McLean, W. H. Irwin and Irvine, Alan D. and Zhang, Xue Jun and Hakonarson, Hakon and Gieger, Christian and Burchard, Esteban G. and Martin, Nicholas G. and Duijts, Liesbeth and Linneberg, Allan and Jarvelin, Marjo-Riitta and Noethen, Markus M. and Lau, Susanne and Hübner, Norbert and Lee, Young-Ae and Tamari, Mayum and Hinds, David A. and Glass, Daniel and Brown, Sara J. and Heinrich, Joachim and Evans, David M. and Weidinger, Stephan and EArly Genetics, and Lifecourse Epidemiology (EAGLE) Eczema Consortium, . (2015) Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nature Genetics, 47 (12). pp. 1449-1456.

Lee, S. H. and Byrne, E. M. and Hultman, C. M. and Kahler, A. and Vinkhuyzen, A. A. and Ripke, S. and Andreassen, O. A. and Frisell, T. and Gusev, A. and Hu, X. and Karlsson, R. and Mantzioris, V. X. and McGrath, J. J. and Mehta, D. and Stahl, E. A. and Zhao, Q. and Kendler, K. S. and Sullivan, P. F. and Price, A. L. and O'Donovan, M. and Okada, Y. and Mowry, B. J. and Raychaudhuri, S. and Wray, N. R. and Schizophrenia Working Group of the Psychiatric Genomics, Consortium and Rheumatoid Arthritis Consortium, International and Schizophrenia Working Group of the Psychiatric Genomics Consorti, Authors and Byerley, W. and Cahn, W. and Cantor, R. M. and Cichon, S. and Cormican, P. and Curtis, D. and Djurovic, S. and Escott-Price, V. and Gejman, P. V. and Georgieva, L. and Giegling, I. and Hansen, T. F. and Ingason, A. and Kim, Y. and Konte, B. and Lee, P. H. and McIntosh, A. and McQuillin, A. and Morris, D. W. and Nothen, M. M. and O'Dushlaine, C. and Olincy, A. and Olsen, L. and Pato, C. N. and Pato, M. T. and Pickard, B. S. and Posthuma, D. and Rasmussen, H. B. and Rietschel, M. and Rujescu, D. and Schulze, T. G. and Silverman, J. M. and Thirumalai, S. and Werge, T. and Agartz, I. and Amin, F. and Azevedo, M. H. and Bass, N. and Black, D. W. and Blackwood, D. H. and Bruggeman, R. and Buccola, N. G. and Choudhury, K. and Cloninger, R. C. and Corvin, A. and Craddock, N. and Daly, M. J. and Datta, S. and Donohoe, G. J. and Duan, J. and Dudbridge, F. and Fanous, A. and Freedman, R. and Freimer, N. B. and Friedl, M. and Gill, M. and Gurling, H. and De Haan, L. and Hamshere, M. L. and Hartmann, A. M. and Holmans, P. A. and Kahn, R. S. and Keller, M. C. and Kenny, E. and Kirov, G. K. and Krabbendam, L. and Krasucki, R. and Lawrence, J. and Lencz, T. and Levinson, D. F. and Lieberman, J. A. and Lin, D. Y. and Linszen, D. H. and Magnusson, P. K. and Maier, W. and Malhotra, A. K. and Mattheisen, M. and Mattingsdal, M. and McCarroll, S. A. and Medeiros, H. and Melle, I. and Milanova, V. and Myin-Germeys, I. and Neale, B. M. and Ophoff, R. A. and Owen, M. J. and Pimm, J. and Purcell, S. M. and Puri, V. and Quested, D. J. and Rossin, L. and Ruderfer, D. and Sanders, A. R. and Shi, J. and Sklar, P. and St Clair, D. and Stroup, T. S. and Van Os, J. and Visscher, P. M. and Wiersma, D. and Zammit, S. and Rheumatoid Arthritis Consortium International, Authors and Bridges, S. L. and Jr., and Choi, H. K. and Coenen, M. J. and de Vries, N. and Dieud, P. and Greenberg, J. D. and Huizinga, T. W. and Padyukov, L. and Siminovitch, K. A. and Tak, P. P. and Worthington, J. and De Jager, P. L. and Denny, J. C. and Gregersen, P. K. and Klareskog, L. and Mariette, X. and Plenge, R. M. and van Laar, M. and van Riel, P.. (2015) New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology, 44 (5). pp. 1706-1721.

2014

Boraska, Vesna and Franklin, Christopher S. and Floyd, James A.B. and Thornton, Laura M. and Huckins, Laura M. and Southam, Lorraine and Rayner, N. William and Tachmazidou, Ioanna and Klumpp, Kelly and Treasure, Janet and Lewis, Cathryn M. and Schmidt, Ulrike and Tozzi, Federica and Kiezebrink, Kirsty and Hebebrand, Johannes and Gorwood, Philip and Adan, Roger A. H. and Kas, Martin J. H. and Favaro, Angela and Santonastaso, Paolo and Fernández-Aranda, Fernando and Gratacòs, Mònica and Rybakowski, Filip and Dmitrzak-Weglarz, Monika and Kaprio, Jaakko and Keski-Rahkonen, Anna and Raevuori, Anu and Van Furth, Eric F. and Slof-Op 't Landt, Margarita and Hudson, James I. and Reichborn-Kjennerud, Ted and Knudsen, Gun Peggy S. and Monteleone, Palmiero and Kaplan, Allan S. and Karwautz, Andreas and Hakonarson, Hakon and Berrettini, Wade H. and Guo, Yiran and Li, Dong and Schork, Nicholas and Komaki, Gen and Ando, Tetsuya and Inoko, Hidetoshi and Esko, Tõnu and Fischer, Krista and Männik, Katrin and Metspalu, Andres and Baker, Jessica H. and Cone, Roger D. and Dackor, Jennifer and DeSocio, Janiece E. and Hilliard, Christopher E. and O'Toole, Julie K. and Pantel, Jacques and Szatkiewicz, Jin P. and Taico, Chrysecolla and Zerwas, Stephanie and Trace, Sara E. and Davis, Oliver S. P. and Helder, Sietske and Buhren, Katherina and Burghardt, Roland and de Zwaan, Martina and Egberts, Karin and Ehrlich, Stefan and Herpertz-Dahlmann, Beate and Herzog, Wolfgang and Imgart, Hartmut and Scherag, André and Scherag, Susann and Zipfel, Stephan and Boni, Claudette and Ramoz, Nicolas and Versini, Audrey and Brandys, Marek K. and Danner, Unna N. and de Kovel, Carolien and Hendriks, Judith and Koeleman, Bobby P. C. and Ophoff, Roel A. and Strengman, Eric and van Elburg, Annemarie A. and Bruson, Alice and Clementi, Maurizio and Degortes, Daniela and Forzan, Monica and Tenconi, Elena and Docampo, Elisa and Escaramis, Georgia and Jiménez-Murcia, Susana and Lissowska, Jolanta and Rajewski, Andrzej and Szeszenia-Dabrowska, Neonila and Slopien, Agnieszka and Hauser, Joanna and Karhunen, Leila and Meulenbelt, Ingrid and Slagboom, P. Eline and Tortorella, Alfonso and Maj, Mario and Dedoussis, George and Dikeos, Dimitris and Gonidakis, Fragiskos and Tziouvas, Konstantinos and Tsitsika, Artemis and Papezova, Hana and Slachtova, Lenka and Martaskova, Debora and Kennedy, James L. and Levitan, Robert D. and Yilmaz, Zeynep and Huemer, Julia and Koubek, Doris and Merler, Elisabeth and Wagner, Gudrun and Lichtenstein, Paul and Breen, Gerome and Cohen-Woods, Sarah and Farmer, Ann and McGuffin, Peter and Cichon, Sven and Giegling, Ina and Herms, Stefan and Rujescu, Dan and Schreiber, Stefan and Wichmann, H-Erich and Dina, Christian and Sladek, Rob and Gambaro, Giovanni and Soranzo, Nicole and Julia, Antonio and Marsal, Sara and Rabionet, Raquel and Gaborieau, Valerie and Dick, Danielle M. and Palotie, Aarno and Ripatti, Samuli and Widen, Elisabeth and Andreassen, Ole A. and Espeseth, Thomas and Lundervold, Astri J. and Reinvang, Ivar and Steen, Vidar M. and Le Hellard, Stephanie and Mattingsdal, Morten and Ntalla, Ioanna and Bencko, Vladimir and Foretova, Lenka and Janout, Vladimir and Navratilova, Marie and Gallinger, Steven and Pinto, Dalila and Scherer, Stephen W. and Aschauer, Harald and Carlberg, Laura and Schosser, Alexandra and Alfredsson, Lars and Ding, Bo and Klareskog, Lars and Padyukov, Leonid and Finan, Chris and Guillaume, Phillippe and Kalsi, Gursharan and Roberts, Marion and Logan, Darren W. and Peltonen, Leena and Ritchie, Graham R. S. and Barrett, Jeffrey C. and Wellcome Trust Case Control Consortium, and Estivill, Xavier and Hinney, Anke and Sullivan, Patrik F. and Collier, David A. and Zeggini, Eleftheria and Bulik, Cynthia M.. (2014) A genome-wide association study of anorexia nervosa. Molecular Psychiatry, 19 (10). pp. 1085-1094.

Børglum, A. D. and Demontis, D. and Grove, J. and Pallesen, J. and Hollegaard, M. V. and Pedersen, C. B. and Hedemand, A. and Mattheisen, M. and Group investigators, and Uitterlinden, A. and Nyegaard, M. and Ørntoft, T. and Wiuf, C. and Didriksen, M. and Nordentoft, M. and Nöthen, M. M. and Rietschel, M. and Ophoff, R. A. and Cichon, S. and Yolken, R. H. and Hougaard, D. M. and Mortensen, P. B. and Mors, O.. (2014) Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. Molecular Psychiatry, 19 (3). pp. 325-333.

Caspers, Svenja and Moebus, Susanne and Lux, Silke and Pundt, Noreen and Schutz, Holger and Muhleisen, Thomas W. and Gras, Vincent and Eickhoff, Simon B. and Romanzetti, Sandro and Stocker, Tony and Stirnberg, Rüdiger and Kirlangic, Mehmet E. and Minnerop, Martina and Pieperhoff, Peter and Modder, Ulrich and Das, Samir and Evans, Alan C. and Jöckel, Karl-Heinz and Erbel, Raimund and Cichon, Sven and Nöthen, Markus M. and Sturma, Dieter and Bauer, Andreas and Shah, N. Jon and Zilles, Karl and Amunts, Katrin. (2014) Studying variability in human brain aging in a population-based German cohort-rationale and design of 1000BRAINS. Frontiers in Aging Neuroscience, 6. p. 149.

Charignon, Delphine and Ghannam, Arije and Defendi, Federica and Ponard, Denise and Monnier, Nicole and Lopez Trascasa, Margarita and Launay, David and Caballero, Teresa and Djenouhat, K. and Fain, Olivier and Cichon, Sven and Martin, Ludovic and Drouet, Christian. (2014) Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype. Allergy, 69 (12). pp. 1659-1665.

Choi, S. and Lee, S. and Cichon, S. and Nothen, M. M. and Lange, C. and Park, T. and Won, S.. (2014) FARVAT: a family-based rare variant association test. Bioinformatics, 30 (22). pp. 3197-3205.

Christoforou, Andrea and Espeseth, Thomas and Davies, Gail and Fernandes, Carla P. D. and Giddaluru, Sudheer and Mattheisen, Manuel and Tenesa, Albert and Harris, Sarah E. and McLachlan Liewald, David Cherry and Payton, Antony and Ollier, William and Horan, Michael A. and Pendleton, Neil and Haggarty, Paul and Djurovic, Srdjan and Herms, Stefan and Hoffmann, Per and Cichon, Sven and Starr, John M. and Lundervold, Astri J. and Reinvang, Ivar and Steen, Vidar M. and Deary, Ian J. and Le Hellard, Stephanie. (2014) GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. Genes, Brain and Behavior, 13 (7). pp. 663-674.

Erk, Susanne and Meyer-Lindenberg, Andreas and Linden, David E. and Lancaster, Thomas and Mohnke, Sebastian and Grimm, Oliver and Degenhardt, Franziska and Holmans, Peter and Pocklington, Andrew and Schmierer, Phöbe and Haddad, Leila and Muhleisen, Thomas W. and Mattheisen, Manuel and Witt, Stephanie H. and Romanczuk-Seiferth, Nina and Tost, Heike and Schott, Björn H. and Cichon, Sven and Nothen, Markus M. and Rietschel, Marcella and Heinz, Andreas and Walter, Henrik . (2014) Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects. NeuroImage, 94. pp. 147-154.

Erk, Susanne and Meyer-Lindenberg, Andreas and Schmierer, Phöbe and Mohnke, Sebastian and Grimm, Oliver and Garbusow, Maria and Haddad, Leila and Poehland, Lydia and Muhleisen, Thomas W. and Witt, Stephanie H. and Tost, Heike and Kirsch, Peter and Romanczuk-Seiferth, Nina and Schott, Björn H. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Heinz, Andreas and Walter, Henrik . (2014) Hippocampal and frontolimbic function as intermediate phenotype for psychosis: evidence from healthy relatives and a common risk variant in CACNA1C. Biological Psychiatry, 76 (6). pp. 466-475.

Forstner, Andreas J. and Basmanav, F. Buket and Mattheisen, Manuel and Böhmer, Anne Christin and Hollegaard, Mads V. and Janson, Esther and Strengman, Eric and Priebe, Lutz and Degenhardt, Franziska and Hoffmann, Per and Herms, Stefan and Maier, Wolfgang and Mössner, Rainald and Rujescu, Dan and Ophoff, Roel A. and Moebus, Susanne and Mortensen, Preben Bo and Borglum, A. D. and Hougaard, David M. and Frank, Josef and Witt, Stephanie H. and Rietschel, Marcella and Zimmermann, Andrea and Nöthen, Markus M. and Miro, Xavier and Cichon, Sven. (2014) Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia. Journal of psychiatry & neuroscience, 39 (6). pp. 386-396.

Grimm, Oliver and Heinz, Andreas and Walter, Henrik and Kirsch, Peter and Erk, Susanne and Haddad, Leila and Plichta, Michael M. and Romanczuk-Seiferth, Nina and Pohland, Lydia and Mohnke, Sebastian and Muhleisen, Thoomas W. and Mattheisen, Manuel and Witt, Stephanie H. and Schafer, Axel and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Tost, Heike and Meyer-Lindenberg, Andreas. (2014) Striatal response to reward anticipation: evidence for a systems-level intermediate phenotype for schizophrenia. JAMA Psychiatry, 71 (5). pp. 531-539.

Hammer, Christian and Degenhardt, Franziska and Priebe, Lutz and Stutz, Adrian M. and Heilmann, Stefanie and Waszak, Sebastian M. and Schlattl, Andreas and Mangold, Elisabeth and Hoffmann, Per and MooDS Consortium, and Nöthen, Markus M. and Rietschel, Marcella and Rappold, Gudrun and Korbel, Jan O. and Cichon, Sven and Niesler, Beate. (2014) A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders. Bipolar disorders, 16 (7). pp. 764-768.

Jamain, Stéphane and Cichon, Sven and Etain, Bruno and Muhleisen, Thomas W. and Georgi, Alexander and Zidane, Nora and Chevallier, Lucie and Deshommes, Jasmine and Nicolas, Aude and Henrion, Annabelle and Degenhardt, Franziska and Mattheisen, Manuel and Priebe, Lutz and Mathieu, Flavie and Kahn, Jean-Pierre and Henry, Chantal and Boland, Anne and Zelenika, Diana and Gut, Ivo and Heath, Simon and Lathrop, Mark and Maier, Wolfgang and Albus, Margot and Rietschel, Marcella and Schulze, Thomas G. and McMahon, Francis J. and Kelsoe, John R. and Hamshere, Marian and Craddock, Nicholas and Nothen, Markus M. and Bellivier, Frank and Leboyer, Marion. (2014) Common and rare variant analysis in early-onset bipolar disorder vulnerability. PLoS ONE, 9 (8). e104326.

Jarick, I. and Volckmar, A. L. and Pütter, C. and Pechlivanis, S. and Nguyen, T. T. and Dauvermann, M. R. and Beck, S. and Albayrak, Ö. and Scherag, S. and Gilsbach, S. and Cichon, S. and Hoffmann, P. and Degenhardt, F. and Nöthen, M. M. and Schreiber, S. and Wichmann, H.-E. and Jöckel, K.-H. and Heinrich, J. and Tiesler, C. M. T. and Faraone, S. V. and Walitza, S. and Sinzig, J. and Freitag, C. and Meyer, J. and Herpertz-Dahlmann, B. and Lehmkuhl, G. and Renner, T. J. and Warnke, A. and Romanos, M. and Lesch, K.-P. and Reif, A. and Schimmelmann, B. G. and Hebebrand, J. and Scherag, A. and Hinney, A.. (2014) Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular Psychiatry, 19 (1). pp. 115-121.

Juraeva, Dilafruz and Haenisch, Britta and Zapatka, Marc and Frank, Josef and Group Investigators, and Psych-Gems Scz Working Group, and Witt, Stephanie H. and Muhleisen, Thomas W. and Treutlein, Jens and Strohmaier, Jana and Meier, Sandra and Degenhardt, Franziska and Giegling, Ina and Ripke, Stephan and Leber, Markus and Lange, Christoph and Schulze, Thomas G. and Mössner, Rainald and Nenadic, Igor and Sauer, Heinrich and Rujescu, Dan and Maier, Wolfgang and Borglum, Anders and Ophoff, Roel A. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Mattheisen, Manuel and Brors, Benedikt. (2014) Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. PLoS Genetics, 10 (6). e1004345.

Lavebratt, C. and Olsson, S. and Backlund, L. and Frisén, L. and Sellgren, C. and Priebe, L. and Nikamo, P. and Träskman-Bendz, L. and Cichon, S. and Vawter, M. P. and Ösby, U. and Engberg, G. and Landén, M. and Erhardt, S. and Schalling, M.. (2014) The KMO allele encoding Arg452 is associated with psychotic features in bipolar disorder type 1, and with increased CSF KYNA level and reduced KMO expression. Molecular Psychiatry, 19 (3). pp. 334-341.

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