Items where Author is "Nothen, M. M."

2016

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.

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.

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.

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.

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. 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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

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.

2014

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.

Witt, Stephanie H. and Juraeva, Dilafruz and Sticht, Carsten and Strohmaier, Jana and Meier, S. and Treutlein, J. and Dukal, Helene and Frank, Josef and Lang, Maren and Deuschle, Michael and Schulze, T. G. and Degenhardt, F. and Mattheisen, Manuel and Brors, B. and Cichon, Sven and Nothen, M. M. and Witt, Christian C. and Rietschel, Marcella. (2014) Investigation of manic and euthymic episodes identifies state- and trait-specific gene expression and STAB1 as a new candidate gene for bipolar disorder. Translational Psychiatry, 4. e426.