Items where Author is "Rietschel, Marcella"

2019

Schwarz, Emanuel and Doan, Nhat Trung and Pergola, Giulio and Westlye, Lars T. and Kaufmann, Tobias and Wolfers, Thomas and Brecheisen, Ralph and Quarto, Tiziana and Ing, Alex J. and Di Carlo, Pasquale and Gurholt, Tiril P. and Harms, Robbert L. and Noirhomme, Quentin and Moberget, Torgeir and Agartz, Ingrid and Andreassen, Ole A. and Bellani, Marcella and Bertolino, Alessandro and Blasi, Giuseppe and Brambilla, Paolo and Buitelaar, Jan K. and Cervenka, Simon and Flyckt, Lena and Frangou, Sophia and Franke, Barbara and Hall, Jeremy and Heslenfeld, Dirk J. and Kirsch, Peter and McIntosh, Andrew M. and Nöthen, Markus M. and Papassotiropoulos, Andreas and de Quervain, Dominique J.-F. and Rietschel, Marcella and Schumann, Gunter and Tost, Heike and Witt, Stephanie H. and Zink, Mathias and Meyer-Lindenberg, Andreas and Imagemend Consortium, Karolinska Schizophrenia Project Consortium. (2019) Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder. Translational Psychiatry, 9 (1). p. 12.

2016

Degenhardt, Franziska and Heinemann, Barbara and Strohmaier, Jana and Pfohl, Marvin A. and Giegling, Ina and Hofmann, Andrea and Ludwig, Kerstin U. and Witt, Stephanie H. and Ludwig, Michael and Forstner, Andreas J. and Albus, Margot and Schwab, Sibylle G. and Borrmann-Hassenbach, Margitta and Lennertz, Leonard and Wagner, Michael and Hoffmann, Per and Rujescu, Dan and Maier, Wolfgang and Cichon, Sven and Rietschel, Marcella and Nothen, Markus M.. (2016) Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. Psychiatric Genetics, 26 (6). pp. 293-296.

2015

Heilbronner, Urs and Malzahn, Dörthe and Strohmaier, Jana and Maier, Sandra and Frank, Josef and Treutlein, Jens and Muhleisen, Thomas W. and Forstner, Andreas J. and Witt, Stephanie H. and Cichon, Sven and Falkai, Peter and Nothen, Markus M. and Rietschel, Marcella and Schulze, Thomas G.. (2015) A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder. European Neuropsychopharmacology, 25 (12). pp. 2262-2270.

Buch, Stephan and Stickel, Felix and Trépo, Eric and Way, Michael and Herrmann, Alexander and Nischalke, Hans Dieter and Brosch, Mario and Rosendahl, Jonas and Berg, Thomas and Ridinger, Monika and Rietschel, Marcella and McQuillin, Andrew and Frank, Josef and Kiefer, Falk and Schreiber, Stefan and Lieb, Wolfgang and Soyka, Michael and Semmo, Nasser and Aigner, Elmar and Datz, Christian and Schmelz, Renate and Brückner, Stefan and Zeissig, Sebastian and Stephan, Anna-Magdalena and Wodarz, Norbert and Devière, Jacques and Clumeck, Nicolas and Sarrazin, Christoph and Lammert, Frank and Gustot, Thierry and Deltenre, Pierre and Völzke, Henry and Lerch, Markus M. and Mayerle, Julia and Eyer, Florian and Schafmayer, Clemens and Cichon, Sven and Nöthen, Markus M. and Nothnagel, Michael and Ellinghaus, David and Huse, Klaus and Franke, Andre and Zopf, Steffen and Hellerbrand, Claus and Moreno, Christophe and Franchimont, Denis and Morgan, Marsha Y. and Hampe, Jochen. (2015) A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis. Nature Genetics, 47 (12). pp. 1443-1448.

Hibar, Derrek P. and Stein, Jason L. and Renteria, Miguel E. and Arias-Vasquez, Alejandro and Desrivières, Sylvane and Jahanshad, Neda and Toro, Roberto and Wittfeld, Katharina and Abramovic, Lucija and Andersson, Micael and Aribisala, Benjamin S. and Armstrong, Nicola J. and Bernard, Manon and Bohlken, Marc M. and Boks, Marco P. and Bralten, Janita and Brown, Andrew A. and Chakravarty, M. Mallar and Chen, Qiang and Ching, Christopher R. K. and Cuellar-Partida, Gabriel and den Braber, Anouk and Giddaluru, Sudheer and Goldman, Aaron L. and Grimm, Oliver and Guadalupe, Tulio and Hass, Johanna and Woldehawariat, Girma and Holmes, Avram J. and Hoogman, Martine and Janowitz, Deborah and Jia, Tianye and Kim, Sungeun and Klein, Marieke and Kraemer, Bernd and Lee, Phil H. and Olde Loohuis, Loes M. and Luciano, Michelle and Macare, Christine and Mather, Karen A. and Mattheisen, Manuel and Milaneschi, Yuri and Nho, Kwangsik and Papmeyer, Martina and Ramasamy, Adaikalavan and Risacher, Shannon L. and Roiz-Santiañez, Roberto and Rose, Emma J. and Salami, Alireza and Sämann, Philipp G. and Schmaal, Lianne and Schork, Andrew J. and Shin, Jean and Strike, Lachlan T. and Teumer, Alexander and van Donkelaar, Marjolein M. J. and van Eijk, Kristel R. and Walters, Raymond K. and Westlye, Lars T. and Whelan, Christopher D. and Winkler, Anderson M. and Zwiers, Marcel P. and Alhusaini, Saud and Athanasiu, Lavinia and Ehrlich, Stefan and Hakobjan, Marina M. H. and Hartberg, Cecilie B. and Haukvik, Unn K. and Heister, Angelien J. G. A. M. and Hoehn, David and Kasperaviciute, Dalia and Liewald, David C. M. and Lopez, Lorna M. and Makkinje, Remco R. R. and Matarin, Mar and Naber, Marlies A. M. and McKay, D. Reese and Needham, Margaret and Nugent, Allison C. and Pütz, Benno and Royle, Natalie A. and Shen, Li and Sprooten, Emma and Trabzuni, Daniah and van der Marel, Saskia S. L. and van Hulzen, Kimm J. E. and Walton, Esther and Wolf, Christiane and Almasy, Laura and Ames, David and Arepalli, Sampath and Assareh, Amelia A. and Bastin, Mark E. and Brodaty, Henry and Bulayeva, Kazima B. and Carless, Melanie A. and Cichon, Sven and Corvin, Aiden and Curran, Joanne E. and Czisch, Michael and de Zubicaray, Greig I. and Dillman, Allissa and Duggirala, Ravi and Dyer, Thomas D. and Erk, Susanne and Fedko, Iryna O. and Ferrucci, Luigi and Foroud, Tatiana M. and Fox, Peter T. and Fukunaga, Masaki and Gibbs, J. Raphael and Göring, Harald H. H. and Green, Robert C. and Guelfi, Sebastian and Hansell, Narelle K. and Hartman, Catharina A. and Hegenscheid, Katrin and Heinz, Andreas and Hernandez, Dena G. and Heslenfeld, Dirk J. and Hoekstra, Pieter J. and Holsboer, Florian and Homuth, Georg and Hottenga, Jouke-Jan and Ikeda, Masashi and Jack Jr, Clifford R. and Jenkinson, Mark and Johnson, Robert and Kanai, Ryota and Keil, Maria and Kent Jr, Jack W. and Kochunov, Peter and Kwok, John B. and Lawrie, Stephen M. and Liu, Xinmin and Longo, Dan L. and McMahon, Katie L. and Meisenzahl, Eva and Melle, Ingrid and Mohnke, Sebastian and Montgomery, Grant W. and Mostert, Jeanette C. and Thomas W. Mühleisen, Thomas W. and Nalls, Michael A. and Nichols, Thomas E. and Nilsson, Lars G. and Nöthen, Markus M. and Ohi, Kazutaka and Olvera, Rene L. and Perez-Iglesias, Rocio and Pike, G. Bruce and Potkin, Steven G. and Reinvang, Ivar and Reppermund, Simone and Rietschel, Marcella and Nina Romanczuk-Seiferth, Nina and Rosen, Glenn D. and Rujescu, Dan and Schnell, Knut and Schofield, Peter R. and Smith, Colin and Steen, Vidar M. and Sussmann, Jessika E. and Thalamuthu, Anbupalam and Toga, Arthur W. and Traynor, Bryan J. and Troncoso, Juan and Turner, Jessica A. and Valdés Hernández, Maria C. and van ’t Ent, Dennis and van der Brug, Marcel and Nvan der Wee, Nic J. A. and van Tol, Marie-Jose and Dick J., Veltman and Wassink, Thomas H. and Westman, Eric and Zielke, Ronald H. and Zonderman, Alan B. and Ashbrook, David G. and Hager, Reinmar and Lu, Lu and McMahon, Francis J. and Morris, Derek W. and Williams, Robert W. and Brunner, Han G. and Buckner, Randy L. and Buitelaar, Jan K. and Cahn, Wiepke and Calhoun, Vince D. and Cavalleri, Gianpiero L. and Crespo-Facorro, Benedicto and Dale, Anders M. and Davies, Gareth E. and Delanty, Norman and Depondt, Chantal and Djurovic, Srdjan and Drevets, Wayne C. and Espeseth, Thomas and Gollub, Randy L. and Ho, Beng-Choon and Hoffmann, Wolfgang and Hosten, Norbert and Kahn, René S. and Le Hellard, Stephanie and Meyer-Lindenberg, Andreas and Müller-Myhsok, Bertram and Nauck, Matthias and Nyberg, Lars and Pandolfo, Massimo and Penninx, Brenda W. J. H. and Roffman, Joshua L. and Sisodiya, Sanjay M. and Smoller, Jordan W. and van Bokhoven, Hans and van Haren, Neeltje E. M. and Völzke, Henry and Walter, Henrik and Weiner, Michael W. and Wen, Wei and White, Tonya and Agartz, Ingrid and Andreassen, Ole A. and Blangero, John and Boomsma, Dorret I. and Brouwer, Rachel M. and Cannon, Dara M. and Cookson, Mark R. and de Geus, Eco J. C. and Deary, Ian J. and Donohoe, Gary and Fernández, Guillén and Fisher, Simon E. and Francks, Clyde and Glahn, David C. and Grabe, Hans J. and Gruber, Oliver and Hardy, John and Hashimoto, Ryota and Hulshoff Pol, Hilleke E. and Jönsson, Erik G. and Kloszewska, Iwona and Lovestone, Simon and Mattay, Venkata S. and Mecocci, Patrizia and McDonald, Colm and McIntosh, Andrew M. and Ophoff, Roel A. and Paus, Tomas and Pausova, Zdenka and Ryten, Mina and Sachdev, Perminder and Saykin, Andrew J. and Simmons, Andy and Singleton, Andrew and Soininen, Hilkka and Wardlaw, Joanna M. and Weale, Michael E. and Weinberger, Daniel R. and Adams, Hieab H. H. and Launer, Lenore J. and Seiler, Stephan and Schmidt, Reinhold and Chauhan, Ganesh and Satizabal, Claudia L. and Becker, James T. and Yanek, Lisa and van der Lee, Sven J. and Ebling, Maritza and Fischl, Bruce and Longstreth Jr, W. T. and Greve, Douglas and Schmidt, Helena and Nyquist, Paul and Vinke, Louis N. and van Duijn, Cornelia M. and Xue, Luting and Mazoyer, Bernard and Bis, Joshua C. and Gudnason, Vilmundur and Seshadri, Sudha and Ikram, M. Arfan and The Alzheimer’s Disease Neuroimaging Initiative, and The CHARGE Consortium, and EPIGEN, and IMAGEN, and SYS, and Martin, Nicholas G. and Wright, Margaret J. and Schumann, Gunter and Franke, Barbara and Thompson, Paul M. and Medland, Sarah E.. (2015) Common genetic variants influence human subcortical brain structures. Nature, 520 (7546). pp. 224-229.

Basmanav, F. Buket and Forstner, Andreas J. and Fier, Heide and Herms, Stefan and Meier, Sandra and Degenhardt, Franziska and Hoffmann, Per and Barth, Sandra and Fricker, Nadine and Strohmaier, Jana and Witt, Stephanie H. and Ludwig, Michael and Schmael, Christine and Moebus, Susanne and Maier, Wolfgang and Mössner, Rainald and Rujescu, Dan and Rietschel, Marcella and Lange, Christoph and Nöthen, Markus M. and Cichon, Sven. (2015) Investigation of the Role of TCF4 Rare Sequence Variants in Schizophrenia. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 168B (5). pp. 354-362.

Luo, Xiong-Jian and Mattheisen, Manuel and Li, Ming and Huang, Liang and Rietschel, Marcella and Børglum, Anders D. and Als, Thomas D. and van den Oord, Edwin J. and Aberg, Karolina A. and Mors, Ole and Mortensen, Preben Bo and Luo, Zhenwu and Degenhardt, Franziska and Cichon, Sven and Schulze, Thomas G. and Nöthen, Markus M. and iPSYCH-GEMS, SCZ working group and MooDS, SCZ Consortium and Su, Bing and Zhao, Zhongming and Gan, Lin and Yao, Yong-Gang. (2015) Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function. Schizophrenia Bulletin, 41 (6). pp. 1294-1308.

Juraeva, Dilafruz and Treutlein, Jens and Scholz, Henrike and Frank, Josef and Degenhardt, Franziska and Cichon, Sven and Ridinger, Monika and Mattheisen, Manuel and Witt, Stephanie H. and Lang, Maren and Sommer, Wolfgang H. and Hoffmann, Per and Herms, Stefan and Wodarz, Norbert and Soyka, Michael and Zill, Peter and Maier, Wolfgang and Jünger, Elisabeth and Gaebel, Wolfgang and Dahmen, Norbert and Scherbaum, Norbert and Schmäl, Christine and Steffens, Michael and Lucae, Susanne and Ising, Marcus and Smolka, Michael N. and Zimmermann, Ulrich S. and Müller-Myhsok, Bertram and Nöthen, Markus M. and Mann, Karl and Kiefer, Falk and Spanagel, Rainer and Brors, Benedikt and Rietschel, Marcella. (2015) XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans. Neuropsychopharmacology, 40 (2). pp. 361-371.

2014

Hammer, Christian and Degenhardt, Franziska and Priebe, Lutz and Stutz, Adrian M. and Heilmann, Stefanie and Waszak, Sebastian M. and Schlattl, Andreas and Mangold, Elisabeth and Hoffmann, Per and MooDS Consortium, and Nöthen, Markus M. and Rietschel, Marcella and Rappold, Gudrun and Korbel, Jan O. and Cichon, Sven and Niesler, Beate. (2014) A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders. Bipolar disorders, 16 (7). pp. 764-768.

Witt, Stephanie H. and Kleindienst, Nikolaus and Frank, Josef and Treutlein, Jens and Muhleisen, Thomas W. and Degenhardt, Franziska and Jungkunz, Martin and Krumm, Bertram and Cichon, Sven and Tadic, André and Dahmen, Norbert and Schwarze, Cornelia E. and Schott, Björn H. and Dietl, Lydia and Nöthen, Markus M. and Mobascher, Arian and Lieb, Klaus and Roepke, Stefan and Rujescu, Dan and Rietschel, Marcella and Schmahl, Christian and Bohus, Martin. (2014) Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder. Psychiatric Genetics, 24 (6). pp. 262-265.

Jamain, Stéphane and Cichon, Sven and Etain, Bruno and Muhleisen, Thomas W. and Georgi, Alexander and Zidane, Nora and Chevallier, Lucie and Deshommes, Jasmine and Nicolas, Aude and Henrion, Annabelle and Degenhardt, Franziska and Mattheisen, Manuel and Priebe, Lutz and Mathieu, Flavie and Kahn, Jean-Pierre and Henry, Chantal and Boland, Anne and Zelenika, Diana and Gut, Ivo and Heath, Simon and Lathrop, Mark and Maier, Wolfgang and Albus, Margot and Rietschel, Marcella and Schulze, Thomas G. and McMahon, Francis J. and Kelsoe, John R. and Hamshere, Marian and Craddock, Nicholas and Nothen, Markus M. and Bellivier, Frank and Leboyer, Marion. (2014) Common and rare variant analysis in early-onset bipolar disorder vulnerability. PLoS ONE, 9 (8). e104326.

Schultz, Carl Christoph and Muhleisen, Thomas W. and Nenadic, I. and Koch, Kathrin and Wagner, Gerd and Schachtzabel, C. and Siedek, Florian and Nöthen, Markus M. and Rietschel, Marcella and Deufel, Thomas and Kiehntopf, M. and Cichon, Sven and Reichenbach, Jürgen and Sauer, Heinrich and Schlosser, Ralf G.. (2014) Common variation in NCAN, a risk factor for bipolar disorder and schizophrenia, influences local cortical folding in schizophrenia. Psychological medicine, 44 (4). pp. 811-820.

Won, Sungho and Kwon, Min-Seok and Mattheisen, Manuel and Park, Suyeon and Park, Changsoon and Kihara, Daisuke and Cichon, Sven and Ophoff, Roel and Nöthen, Markus M. and Rietschel, Marcella and Baur, Max and Uitterlinden, Andre G. and Hofmann, A. and Group Investigators, and Lange, Christoph. (2014) Efficient strategy for detecting gene x gene joint action and its application in schizophrenia. Genetic Epidemiology, 38 (1). pp. 60-71.

Nieratschker, Vanessa and Grosshans, Martin and Frank, Josef and Strohmaier, Jana and von der Goltz, Christoph and El-Maarri, Osman and Witt, Stephanie H. and Cichon, Sven and Nöthen, Markus M. and Kiefer, Falk and Rietschel, Marcella. (2014) Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age. Addiction Biology, 19 (2). pp. 305-311.

Schott, Björn H. and Assmann, Anne and Schmierer, Phöbe and Soch, Joram and Erk, Susanne and Garbusow, Maria and Mohnke, Sebastian and Pohland, Lydia and Romanczuk-Seiferth, Nina and Barman, Adrian and Wustenberg, Torsten and Haddad, Linda and Grimm, Oliver and Witt, Stephanie H. and Richter, Sylvia and Klein, Marieke and Schutze, Hartmut and Muhleisen, Thomas W. and Cichon, Sven and Rietschel, Marcella and Noethen, Markus M. and Tost, H. and Gundelfinger, Eckart D. and Duzel, Emrah and Heinz, Andreas and Meyer-Lindenberg, Andreas and Seidenbecher, Constanze I. and Walter, Henrik . (2014) Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding. Translational Psychiatry, 4. e372.

Mohnke, Sebastian and Erk, Susanne and Schnell, Knut and Schütz, Claudia and Romanczuk-Seiferth, Nina and Grimm, Oliver and Haddad, Leila and Pohland, Lydia and Garbusow, Maria and Schmitgen, Mike M. and Kirsch, Peter and Esslinger, Christine and Rietschel, Marcella and Witt, Stephanie H. and Nöthen, Markus M. and Cichon, Sven and Mattheisen, Manuel and Mühleisen, Thomas and Jensen, Jimmy and Schott, Björn H. and Maier, Wolfgang and Heinz, Andreas and Meyer-Lindenberg, Andreas and Walter, Henrik . (2014) Further evidence for the impact of a genome-wide-supported psychosis risk variant in ZNF804A on the Theory of Mind Network. Neuropsychopharmacology, 39 (5). pp. 1196-1205.

Muhleisen, Thomas W. and Leber, Markus and Schulze, Thomas G. and Strohmaier, Jana and Degenhardt, Franziska and Treutlein, Jens and Mattheisen, Manuel and Forstner, Andreas J. and Schumacher, Johannes and Breuer, René and Meier, Sandra and Herms, Stefan and Hoffmann, Per and Lacour, André and Witt, Stephanie H. and Reif, Andreas and Müller-Myhsok, Bertram and Lucae, Susanne and Maier, Wolfgang and Schwarz, Markus and Vedder, Helmut and Kammerer-Ciernioch, Jutta and Pfennig, Andrea and Bauer, Michael and Hautzinger, Martin and Moebus, Susanne and Priebe, Lutz and Czerski, Piotr M. and Hauser, Joanna and Lissowska, Jolanta and Szeszenia-Dabrowska, Neonila and Brennan, Paul and McKay, James and Wright, Adam and Mitchell, Philip B and Fullerton, Janice M. and Schofield, Peter R. and Montgomery, Grant W. and Medland, Sarah E. and Gordon, Scott D. and Martin, Nicolas G. and Krasnow, Valery and Chuchalin, Alexander and Babadjanova, Gulja and Pantelejeva, Galina and Abramova, Lilia I. and Tiganov, Alexander S. and Polonikov, Alexey and Khusnutdinova, Elza and Alda, Martin and Grof, Paul and Rouleau, Guy A. and Turecki, Gustavo and Laprise, Catherine and Rivas, Fabio and Mayoral, Fermin and Kogevinas, Manolis and Grigoroiu-Serbanescu, Maria and Propping, Peter and Becker, Tim and Rietschel, Marcella and Nöthen, Markus M. and Cichon, Sven. (2014) Genome-wide association study reveals two new risk loci for bipolar disorder. Nat Commun, 5. p. 3339.

Erk, Susanne and Meyer-Lindenberg, Andreas and Schmierer, Phöbe and Mohnke, Sebastian and Grimm, Oliver and Garbusow, Maria and Haddad, Leila and Poehland, Lydia and Muhleisen, Thomas W. and Witt, Stephanie H. and Tost, Heike and Kirsch, Peter and Romanczuk-Seiferth, Nina and Schott, Björn H. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Heinz, Andreas and Walter, Henrik . (2014) Hippocampal and frontolimbic function as intermediate phenotype for psychosis: evidence from healthy relatives and a common risk variant in CACNA1C. Biological Psychiatry, 76 (6). pp. 466-475.

Juraeva, Dilafruz and Haenisch, Britta and Zapatka, Marc and Frank, Josef and Group Investigators, and Psych-Gems Scz Working Group, and Witt, Stephanie H. and Muhleisen, Thomas W. and Treutlein, Jens and Strohmaier, Jana and Meier, Sandra and Degenhardt, Franziska and Giegling, Ina and Ripke, Stephan and Leber, Markus and Lange, Christoph and Schulze, Thomas G. and Mössner, Rainald and Nenadic, Igor and Sauer, Heinrich and Rujescu, Dan and Maier, Wolfgang and Borglum, Anders and Ophoff, Roel A. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Mattheisen, Manuel and Brors, Benedikt. (2014) Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. PLoS Genetics, 10 (6). e1004345.

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.

Forstner, Andreas J. and Basmanav, F. Buket and Mattheisen, Manuel and Böhmer, Anne Christin and Hollegaard, Mads V. and Janson, Esther and Strengman, Eric and Priebe, Lutz and Degenhardt, Franziska and Hoffmann, Per and Herms, Stefan and Maier, Wolfgang and Mössner, Rainald and Rujescu, Dan and Ophoff, Roel A. and Moebus, Susanne and Mortensen, Preben Bo and Borglum, A. D. and Hougaard, David M. and Frank, Josef and Witt, Stephanie H. and Rietschel, Marcella and Zimmermann, Andrea and Nöthen, Markus M. and Miro, Xavier and Cichon, Sven. (2014) Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia. Journal of psychiatry & neuroscience, 39 (6). pp. 386-396.

Schulze, Thomas G. and Akula, Nirmala and Breuer, René and Steele, Jo and Nalls, Michael A. and Singleton, Andrew B. and Degenhardt, Franziska A. and Nöthen, Markus M. and Cichon, Sven and Rietschel, Marcella and The Bipolar Genome Study, and McMahon, Francis J.. (2014) Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder. The World Journal of Biological Psychiatry, 15 (3). pp. 200-208.

Erk, Susanne and Meyer-Lindenberg, Andreas and Linden, David E. and Lancaster, Thomas and Mohnke, Sebastian and Grimm, Oliver and Degenhardt, Franziska and Holmans, Peter and Pocklington, Andrew and Schmierer, Phöbe and Haddad, Leila and Muhleisen, Thomas W. and Mattheisen, Manuel and Witt, Stephanie H. and Romanczuk-Seiferth, Nina and Tost, Heike and Schott, Björn H. and Cichon, Sven and Nothen, Markus M. and Rietschel, Marcella and Heinz, Andreas and Walter, Henrik . (2014) Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects. NeuroImage, 94. pp. 147-154.

Treutlein, Jens and Strohmaier, Jana and Frank, Josef and Muhleisen, Thomas W. and Degenhardt, Franziska and Witt, Stephanie H. and Schulze, Thomas G. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella. (2014) Smoking behaviour: investigation of the coaction of environmental and genetic risk factors. Psychiatric Genetics, 24 (6). pp. 279-280.

Grimm, Oliver and Heinz, Andreas and Walter, Henrik and Kirsch, Peter and Erk, Susanne and Haddad, Leila and Plichta, Michael M. and Romanczuk-Seiferth, Nina and Pohland, Lydia and Mohnke, Sebastian and Muhleisen, Thoomas W. and Mattheisen, Manuel and Witt, Stephanie H. and Schafer, Axel and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Tost, Heike and Meyer-Lindenberg, Andreas. (2014) Striatal response to reward anticipation: evidence for a systems-level intermediate phenotype for schizophrenia. JAMA Psychiatry, 71 (5). pp. 531-539.

Thompson, Paul M. and Stein, Jason L. and Medland, Sarah E. and Hibar, Derrek P. and Vasquez, Alejandro Arias and Renteria, Miguel E. and Toro, Roberto and Jahanshad, Neda and Schumann, Gunter and Franke, Barbara and Wright, Margaret J. and Martin, Nicholas G. and Agartz, Ingrid and Alda, Martin and Alhusaini, Saud and Almasy, Laura and Almeida, Jorge and Alpert, Kathryn and Andreasen, Nancy C. and Andreassen, Ole A. and Apostolova, Liana G. and Appel, Katja and Armstrong, Nicola J. and Aribisala, Benjamin S. and Bastin, Mark E. and Bauer, Michael and Bearden, Carrie E. and Bergmann, Orjan and Binder, Elisabeth B. and Blangero, John and Bockholt, Henry J. and Boen, Erlend and Bois, Catherine and Boomsma, Dorette I. and Booth, Tom and Bowman, Ian J. and Bralten, Janita and Brouwer, Rachel M. and Brunner, Han G. and Brohawn, David G. and Buckner, Randy L. and Buitelaar, Jan and Bulayeva, Kazima B. and Bustillo, Juan R. and Calhoun, Vince D. and Cannon, Dara M. and Cantor, Rita M. and Carless, Melanie A. and Caseras, Xavier and Cavalleri, Gianpiero L. and Chakravarty, M. Mallar and Chang, Kiki D. and Ching, Christopher R. K. and Christoforou, Andrea and Cichon, Sven and Clark, Vincent P. and Conrod, Patricia and Coppola, Giovanni and Crespo-Facorro, Benedicto and Curran, Joanne E. and Czisch, Michael and Deary, Ian J. and de Geus, Eco J. C. and den Braber, Anouk and Delvecchio, Giuseppe and Depondt, Chantal and de Haan, Lieuwe and de Zubicaray, Greig I. and Dima, Danai and Dimitrova, Rali and Djurovic, Srdjan and Dong, Hongping and Donohoe, Gary and Duggirala, Ravindranath and Dyer, Thomas D. and Ehrlich, Stefan and Ekman, Carl Johan and Elvsåshagen, Torbjørn and Emsell, Louise and Erk, Susanne and Espeseth, Thomas and Fagerness, Jesen and Fears, Scott and Fedko, Iryna O. and Fernández, Guillén and Fisher, Simon E. and Foroud, Tatiana M. and Fox, Peter T. and Francks, Clyde and Frangou, Sophia and Frey, Eva Maria and Frodl, Thomas and Frouin, Vincent and Garavan, Hugh and Giddaluru, Sudheer and Glahn, David C. and Godlewska, Beata and Goldstein, Rita Z. and Gollub, Randy L. and Grabe, Hans J. and Grimm, Oliver and Gruber, Oliver and Guadalupe, Tulio and Gur, Raquel E. and Gur, Ruben C. and Göring, Harald H. H. and Hagenaars, Saskia and Hajek, Tomas and Hall, Geoffrey B. and Hall, Jeremy and Hardy, John and Hartman, Catharina A. and Hass, Johanna and Hatton, Sean N. and Haukvik, Unn K. and Hegenscheid, Katrin and Heinz, Andreas and Hickie, Ian B. and Ho, Beng-Choon and Hoehn, David and Hoekstra, Pieter J. and Hollinshead, Marisa and Holmes, Avram J. and Homuth, Georg and Hoogman, Martine and Hong, L. Elliot and Hosten, Norbert and Hottenga, Jouke-Jan and Hulshoff Pol, Hilleke E. and Hwang, Kristy S. and Jack, Clifford R. and Jenkinson, Mark and Johnston, Caroline and Jönsson, Erik G. and Kahn, René S. and Kasperaviciute, Dalia and Kelly, Sinead and Kim, Sungeun and Kochunov, Peter and Koenders, Laura and Kramer, Bernd and Kwok, John B. and Lagopoulos, Jim and Laje, Gonzalo and Landén, Mikael and Landman, Bennett A. and Lauriello, John and Lawrie, Stephen M. and Lee, Phil H. and Le Hellard, Stephanie and Lemaitre, Herve and Leonardo, Cassamdra C. and Li, Chiang-Shan and Liberg, Benny and Liewald, David C. and Liu, Xinmin and Lopez, Lorna M. and Loth, Eva and Lourdusamy, Anbarasu and Luciano, Michelle and Macciardi, Fabio and Machielsen, Marise W. J. and MacQueen, Glenda and Malt, Ulrik F. and Mandl, René and Manoach, Dara S. and Martinot, Jean-Luc and Matarin, Mar and Mather, Karen A. and Mattheisen, Manuel and Mattingsdal, Morten and Meyer-Lindenberg, Andreas and McDonald, Colm and McIntosh, Andrew M. and McMahon, Francis J. and McMahon, Katie L. and Meisenzahl, Eva and Melle, Ingrid and Milaneschi, Yuri and Mohnke, Sebastian and Montgomery, Grant W. and Morris, Derek W. and Moses, Eric K. and Mueller, Bryon A. and Munoz Maniega, Susana and Muhleisen, Thomas W. and Müller-Myhsok, Bertram and Mwangi, Benson and Nauck, Matthias and Nho, Kwangsik and Nichols, Thomas E. and Nilsson, Lars-Göran and Nugent, Allison C. and Nyberg, Lars and Olvera, Rene L. and Oosterlaan, Jaap and Ophoff, Roel A. and Pandolfo, Massimo and Papalampropoulou-Tsiridou, Melina and Papmeyer, Martina and Paus, Tomas and Pausova, Zdenka and Pearlson, Godfrey D. and Penninx, Brenda W. and Peterson, Charles P. and Pfennig, Andrea and Phillips, Mary and Pike, G. Bruce and Poline, Jean-Baptiste and Potkin, Steven G. and Pütz, Benno and Ramasamy, Adaikalavan and Rasmussen, Jerod and Rietschel, Marcella and Rijpkema, Mark and Risacher, Shannon L. and Roffman, Joshua L. and Roiz-Santiañez, Roberto and Romanczuk-Seiferth, Nina and Rose, Emma J. and Royle, Natalie A. and Rujescu, Dan and Ryten, Mina and Sachdev, Perminder S. and Salami, Alireza and Satterthwaite, Theodore D. and Savitz, Jonathan and Saykin, Andrew J. and Scanlon, Cathy and Schmaal, Lianne and Schnack, Hugo G. and Schork, Andrew J. and Schulz, S. Charles and Schur, Remmelt and Seidman, Larry J. and Shen, Li and Shoemaker, Jody M. and Simmons, Andrew and Sisodiya, Sanjay M. and Smith, Colin and Smoller, Jordan W. and Soares, Jair C. and Sponheim, Scott R. and Sprooten, Emma and Starr, John M. and Steen, Vidar M. and Strakowski, Stephen and Strike, Lachlan T. and Sussmann, Jessika E. and Sämann, Philipp G. and Teumer, Alexander and Toga, Arthur W. and Tordesillas-Gutierrez, Diana and Trabzuni, Daniah and Trost, Sarah and Turner, Jessica A. and Van den Heuvel, Martijn and van der Wee, Nic J. and van Eijk, Kristel R. and van Erp, Theo G. M. and van Haren, Neeltje E. M. and van 't Ent, Dennis and van Tol, Marie-Jose and Valdés Hernández, Maria C. and Veltman, Dick J. and Versace, Amelia and Völzke, Henry and Walker, Robert and Walter, Henrik and Wang, Lei and Wardlaw, Joanna M. and Weale, Michael E. and Weiner, Michael W. and Wen, Wei and Westlye, Lars T. and Whalley, Heather C. and Whelan, Christopher D. and White, Tonya and Winkler, Anderson M. and Wittfeld, Katharina and Woldehawariat, Girma and Wolf, Christiane and Zilles, David and Zwiers, Marcel P. and Thalamuthu, Anbupalam and Schofield, Peter R. and Freimer, Nelson B. and Lawrence, Natalia S. and Drevets, Wayne C. and the Alzheimer’s Disease Neuroimaging Initiative, EPIGEN Consorti, . (2014) The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior, 8 (2). pp. 153-182.

Schultz, Carl Christoph and Nenadic, Igor and Riley, Brien and Vladimirov, Vladimit I. and Wagner, Gerd and Koch, Kathrin and Schachtzabel, Claudia and Muhleisen, Thomas W. and Basmanav, Buket and Nothen, Markus M. and Deufel, Thomas and Kiehntopf, Michael and Rietschel, Marcella and Reichenbach, Jürgen R. and Cichon, Sven and Schlosser, Ralf G. M. and Sauer, Heinrich. (2014) ZNF804A and cortical structure in schizophrenia: in vivo and postmortem studies. Schizophrenia Bulletin, 40 (3). pp. 532-541.

2011

Kohli, Martin A. and Lucae, Susanne and Saemann, Philipp G. and Schmidt, Mathias V. and Demirkan, Ayse and Hek, Karin and Czamara, Darina and Alexander, Michael and Salyakina, Daria and Ripke, Stephan and Hoehn, David and Specht, Michael and Menke, Andreas and Hennings, Johannes and Heck, Angela and Wolf, Christiane and Ising, Marcus and Schreiber, Stefan and Czisch, Michael and Müller, Marianne B. and Uhr, Manfred and Bettecken, Thomas and Becker, Albert and Schramm, Johannes and Rietschel, Marcella and Maier, Wolfgang and Bradley, Bekh and Ressler, Kerry J. and Nöthen, Markus M. and Cichon, Sven and Craig, Ian W. and Breen, Gerome and Lewis, Cathryn M. and Hofman, Albert and Tiemeier, Henning and van Duijn, Cornelia M. and Holsboer, Florian and Müller-Myhsok, Bertram and Binder, Elisabeth B.. (2011) The neuronal transporter gene SLC6A15 confers risk to major depression. Neuron, 70 (2). pp. 252-265.