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Items where Author is "Strohmaier, J."

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Number of items: 7.

2016

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.

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.

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.

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.

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.

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.

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