Items where Author is "Degenhardt, F."

2016

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.

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.

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.

2014

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.

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.