Items where Author is "Reif, A."

2018

Hommers, L. G. and Richter, J. and Yang, Y. and Raab, A. and Baumann, C. and Lang, K. and Schiele, M. A. and Weber, H. and Wittmann, A. and Wolf, C. and Alpers, G. W. and Arolt, V. and Domschke, K. and Fehm, L. and Fydrich, T. and Gerlach, A. and Gloster, A. T. and Hamm, A. O. and Helbig-Lang, S. and Kircher, T. and Lang, T. and Pane-Farre, C. A. and Pauli, P. and Pfleiderer, B. and Reif, A. and Romanos, M. and Straube, B. and Stroehle, A. and Wittchen, H. -U. and Frantz, S. and Ertl, G. and Lohse, M. J. and Lueken, U. and Deckert, J.. (2018) A functional genetic variation of SLC6A2 repressor hsa-miR-579-3p upregulates sympathetic noradrenergic processes of fear and anxiety. Translational Psychiatry, 8. pp. 1-12.

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.

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.

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.

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.

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.

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.

Reif, A. and Richter, J. and Straube, B. and Höfler, M. and Lueken, U. and Gloster, A. T. and Weber, H. and Domschke, K. and Fehm, L. and Ströhle, A. and Jansen, A. and Gerlach, A. and Pyka, M. and Reinhardt, I. and Konrad, C. and Wittmann, A. and Pfleiderer, B. and Alpers, G. W. and Pauli, P. and Lang, T. and Arolt, V. and Wittchen, H.-U. and Hamm, A. and Kircher, T. and Deckert, J.. (2014) MAOA and mechanisms of panic disorder revisited: from bench to molecular psychotherapy. Molecular Psychiatry, 19 (1). pp. 122-128.

2013

Hamshere, M. L. and Langley, K. and Martin, J. and Agha, S. S. and Stergiakouli, E. and Anney, R. J. and Buitelaar, J. and Faraone, S. V. and Lesch, K. P. and Neale, B. M. and Franke, B. and Sonuga-Barke, E. and Asherson, P. and Merwood, A. and Kuntsi, J. and Medland, S. E. and Ripke, S. and Steinhausen, H. -C. and Freitag, C. and Reif, A. and Renner, T. J. and Romanos, M. and Romanos, J. and Warnke, A. and Meyer, J. and Palmason, H. and Vasquez, A. A. and Lambregts-Rommelse, N. and Roeyers, H. and Biederman, J. and Doyle, A. E. and Hakonarson, H. and Rothenberger, A. and Banaschewski, T. and Oades, R. D. and McGough, J. J. and Kent, L. and Williams, N. and Owen, M. J. and Holmans, P. and O'Donovan, M. C. and Thapar, A.. (2013) High loading of polygenic risk for ADHD in children comorbid for aggression. American Journal of Psychiatry, Vol. 170, H. 8. pp. 909-916.

2010

Domschke, K. and Reif, A. and Weber, H. and Richter, J. and Hohoff, C. and Ohrmann, P. and Pedersen, A. and Bauer, J. and Suslow, T. and Kugel, H. and Heindel, W. and Baumann, C. and Klauke, B. and Jacob, C. and Maier, W. and Fritze, J. and Bandelow, B. and Krakowitzky, P. and Rothermundt, M. and Erhardt, A. and Binder, E. and Holsboer, F. and Gerlach, A. L. and Kircher, T. and Lang, T. and Alpers, G. W. and Ströhle, A. and Fehm, L. and Gloster, A. T. and Wittchen, H. -U. and Arolt, V. and Pauli, P. and Hamm, A. and Deckert, J.. (2010) Neuropeptide S Receptor Gene-Converging Evidence for a Role in Panic Disorder. Molecular Psychiatry, 16 (9). pp. 938-948.

2008

Romanos, M. and Freitag, C. and Jacob, C. and Craig, D. W. and Dempfle, A. and Nguyen, T. T. and Halperin, R. and Walitza, S. and Renner, T. J. and Seitz, C. and Romanos, J. and Palmason, H. and Reif, A. and Heine, M. and Windemuth-Kieselbach, C. and Vogler, C. and Sigmund, J. and Warnke, A. and Schäfer, H. and Meyer, J. and Stephan, D. A. and Lesch, K. P.. (2008) Genome-wide linkage analysis of ADHD using high-density SNP arrays : novel loci at 5q13.1 and 14q12. Molecular psychiatry, 13 (5). pp. 522-530.