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Items where Author is "Cichon, S."

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2016

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.

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.

Schwantes-An, T. H. and Zhang, J. and Chen, L. S. and Hartz, S. M. and Culverhouse, R. C. and Chen, X. and Coon, H. and Frank, J. and Kamens, H. M. and Konte, B. and Kovanen, L. and Latvala, A. and Legrand, L. N. and Maher, B. S. and Melroy, W. E. and Nelson, E. C. and Reid, M. W. and Robinson, J. D. and Shen, P. H. and Yang, B. Z. and Andrews, J. A. and Aveyard, P. and Beltcheva, O. and Brown, S. A. and Cannon, D. S. and Cichon, S. and Corley, R. P. and Dahmen, N. and Degenhardt, L. and Foroud, T. and Gaebel, W. and Giegling, I. and Glatt, S. J. and Grucza, R. A. and Hardin, J. and Hartmann, A. M. and Heath, A. C. and Herms, S. and Hodgkinson, C. A. and Hoffmann, P. and Hops, H. and Huizinga, D. and Ising, M. and Johnson, E. O. and Johnstone, E. and Kaneva, R. P. and Kendler, K. S. and Kiefer, F. and Kranzler, H. R. and Krauter, K. S. and Levran, O. and Lucae, S. and Lynskey, M. T. and Maier, W. and Mann, K. and Martin, N. G. and Mattheisen, M. and Montgomery, G. W. and Muller-Myhsok, B. and Murphy, M. F. and Neale, M. C. and Nikolov, M. A. and Nishita, D. and Nothen, M. M. and Nurnberger, J. and Partonen, T. and Pergadia, M. L. and Reynolds, M. and Ridinger, M. and Rose, R. J. and Rouvinen-Lagerstrom, N. and Scherbaum, N. and Schmal, C. and Soyka, M. and Stallings, M. C. and Steffens, M. and Treutlein, J. and Tsuang, M. and Wall, T. L. and Wodarz, N. and Yuferov, V. and Zill, P. and Bergen, A. W. and Chen, J. and Cinciripini, P. M. and Edenberg, H. J. and Ehringer, M. A. and Ferrell, R. E. and Gelernter, J. and Goldman, D. and Hewitt, J. K. and Hopfer, C. J. and Iacono, W. G. and Kaprio, J. and Kreek, M. J. and Kremensky, I. M. and Madden, P. A. and McGue, M. and Munafo, M. R. and Philibert, R. A. and Rietschel, M. and Roy, A. and Rujescu, D. and Saarikoski, S. T. and Swan, G. E. and Todorov, A. A. and Vanyukov, M. M. and Weiss, R. B. and Bierut, L. J. and Saccone, N. L.. (2016) Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics, 46 (2). pp. 151-169.

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.

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.

Zayats, T. and Jacobsen, K. K. and Kleppe, R. and Jacob, C. P. and Kittel-Schneider, S. and Ribases, M. and Ramos-Quiroga, J. A. and Richarte, V. and Casas, M. and Mota, N. R. and Grevet, E. H. and Klein, M. and Corominas, J. and Bralten, J. and Galesloot, T. and Vasquez, A. A. and Herms, S. and Forstner, A. J. and Larsson, H. and Breen, G. and Asherson, P. and Gross-Lesch, S. and Lesch, K. P. and Cichon, S. and Gabrielsen, M. B. and Holmen, O. L. and Bau, C. H. and Buitelaar, J. and Kiemeney, L. and Faraone, S. V. and Cormand, B. and Franke, B. and Reif, A. and Haavik, J. and Johansson, S.. (2016) Exome chip analyses in adult attention deficit hyperactivity disorder. Translational Psychiatry, 6 (10). e923.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

2015

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.

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.

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.

2014

Li, M. and Luo, X.-J. and Rietschel, M. and Lewis, C. M. and Mattheisen, M. and Müller-Myhsok, B. and Jamain, S. and Leboyer, M. and Landén, M. and Thompson, P. M. and Cichon, S. and Nöthen, M. M. and Schulze, T. G. and Sullivan, P. F. and Bergen, S. E. and Donohoe, G. and Morris, D. W. and Hargreaves, A. and Gill, M. and Corvin, A. and Hultman, C. and Toga, A. W. and Shi, L. and Lin, Q. and Shi, H. and Gan, L. and Meyer-Lindenberg, A. and Czamara, D. and Henry, C. and Etain, B. and Bis, J. C. and Ikram, M. A. and Fornage, M. and Debette, S. and Launer, L. J. and Seshadri, S. and Erk, S. and Walter, H. and Heinz, A. and Bellivier, F. and Stein, J. L. and Medland, S. E. and Arias Vasquez, A. and Hibar, D. P. and Franke, B. and Martin, N. G. and Wright, M. J. and MooDS Bipolar Consortium, and Swedish Bipolar Study Group, and Alzheimer's Disease Neuroimaging Initiative, and Enigma Consortium, and Charge Consortium, and Su, B.. (2014) Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry, 19 (4). pp. 452-461.

Steinberg, S. and de Jong, S. and Mattheisen, M. and Costas, J. and Demontis, D. and Jamain, S. and Pietiläinen, O. P. H. and Lin, K. and Papiol, S. and Huttenlocher, J. and Sigurdsson, E. and Vassos, E. and Giegling, I. and Breuer, R. and Fraser, G. and Walker, N. and Melle, I. and Djurovic, S. and Agartz, I. and Tuulio-Henriksson, A. and Suvisaari, J. and Lönnqvist, J. and Paunio, T. and Olsen, L. and Hansen, T. and Ingason, A. and Pirinen, M. and Strengman, E. and Group, and Hougaard, D. M. and Ørntoft, T. and Didriksen, M. and Hollegaard, M. V. and Nordentoft, M. and Abramova, L. and Kaleda, V. and Arrojo, M. and Sanjuán, J. and Arango, C. and Etain, B. and Bellivier, F. and Méary, A. and Schürhoff, F. and Szoke, A. and Ribolsi, M. and Magni, V. and Siracusano, A. and Sperling, S. and Rossner, M. and Christiansen, C. and Kiemeney, L. A. and Franke, B. and van den Berg, L. H. and Veldink, J. and Curran, S. and Bolton, P. and Poot, M. and Staal, W. and Rehnstrom, K. and Kilpinen, H. and Freitag, C. M. and Meyer, J. and Magnusson, P. and Saemundsen, E. and Martsenkovsky, I. and Bikshaieva, I. and Martsenkovska, I. and Vashchenko, O. and Raleva, M. and Paketchieva, K. and Stefanovski, B. and Durmishi, N. and Pejovic Milovancevic, M. and Lecic Tosevski, D. and Silagadze, T. and Naneishvili, N. and Mikeladze, N. and Surguladze, S. and Vincent, J. B. and Farmer, A. and Mitchell, P. B. and Wright, A. and Schofield, P. R. and Fullerton, J. M. and Montgomery, G. W. and Martin, N. G. and Rubino, I. A. and van Winkel, R. and Kenis, G. and De Hert, M. and Réthelyi, J. M. and Bitter, I. and Terenius, L. and Jönsson, E. G. and Bakker, S. and van Os, J. and Jablensky, A. and Leboyer, M. and Bramon, E. and Powell, J. and Murray, R. and Corvin, A. and Gill, M. and Morris, D. and O'Neill, F. A. and Kendler, K. and Riley, B. and Wellcome Trust Case Control Consortium, and Craddock, N. and Owen, M. J. and O'Donovan, M. C. and Thorsteinsdottir, U. and Kong, A. and Ehrenreich, H. and Carracedo, A. and Golimbet, V. and Andreassen, O. A. and Børglum, A. D. and Mors, O. and Mortensen, P. B. and Werge, T. and Ophoff, R. A. and Nöthen, M. M. and Rietschel, M. and Cichon, S. and Ruggeri, M. and Tosato, S. and Palotie, A. and St Clair, D. and Rujescu, D. and Collier, D. A. and Stefansson, H. and Stefansson, K.. (2014) Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19 (1). pp. 108-114.

Luo, X.-J. and Li, M. and Huang, L. and Steinberg, S. and Mattheisen, M. and Liang, G. and Donohoe, G. and Shi, Y. and Chen, C. and Yue, W. and Alkelai, A. and Lerer, B. and Li, Z. and Yi, Q. and Rietschel, M. and Cichon, S. and Collier, D. A. and Tosato, S. and Suvisaari, J. and Rujescu, Dan and Golimbet, V. and Silagadze, T. and Durmishi, N. and Milovancevic, M. P. and Stefansson, H. and Schulze, T. G. and Nöthen, M. M. and Chen, C. and Lyne, R. and Morris, D. W. and Gill, M. and Corvin, A. and Zhang, D. and Dong, Q. and Moyzis, R. K. and Stefansson, K. and Sigurdsson, E. and Hu, F. and MooDS SCZ Consortium, and Su, B. and Gan, L.. (2014) Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene. Molecular Psychiatry, 19 (7). pp. 774-783.

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.

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.

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.

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.

2011

Erhardt, A. and Czibere, L. and Roeske, D. and Lucae, S. and Unschuld, P. G. and Ripke, S. and Specht, M. and Kohli, M. A. and Kloiber, S. and Ising, M. and Heck, A. and Pfister, H. and Zimmermann, P. and Lieb, R. and Pütz, B. and Uhr, M. and Weber, P. and Deussing, J. M. and Gonik, M. and Bunck, M. and Kebler, M. S. and Frank, E. and Hohoff, C. and Domschke, K. and Krakowitzky, P. and Maier, W. and Bandelow, B. and Jacob, C. and Deckert, J. and Schreiber, S. and Strohmaier, J. and Nöthen, M. and Cichon, S. and Rietschel, M. and Bettecken, T. and Keck, M. E. and Landgraf, R. and Müller-Myhsok, B. and Holsboer, F. and Binder, E. B.. (2011) TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies. Molecular Psychiatry, 16 (6). pp. 647-663.

This list was generated on Fri Mar 29 13:12:45 2024 CET.