Items where Author is "Mattheisen, Manuel"

2019

Demontis, Ditte and Walters, Raymond K. and Martin, Joanna and Mattheisen, Manuel and Als, Thomas D. and Agerbo, Esben and Baldursson, Gísli and Belliveau, Rich and Bybjerg-Grauholm, Jonas and Bækvad-Hansen, Marie and Cerrato, Felecia and Chambert, Kimberly and Churchhouse, Claire and Dumont, Ashley and Eriksson, Nicholas and Gandal, Michael and Goldstein, Jacqueline I. and Grasby, Katrina L. and Grove, Jakob and Gudmundsson, Olafur O. and Hansen, Christine S. and Hauberg, Mads Engel and Hollegaard, Mads V. and Howrigan, Daniel P. and Huang, Hailiang and Maller, Julian B. and Martin, Alicia R. and Martin, Nicholas G. and Moran, Jennifer and Pallesen, Jonatan and Palmer, Duncan S. and Pedersen, Carsten Bøcker and Pedersen, Marianne Giørtz and Poterba, Timothy and Poulsen, Jesper Buchhave and Ripke, Stephan and Robinson, Elise B. and Satterstrom, F. Kyle and Stefansson, Hreinn and Stevens, Christine and Turley, Patrick and Walters, G. Bragi and Won, Hyejung and Wright, Margaret J. and Adhd Working Group of the Psychiatric Genomics Consortium, and Early Lifecourse, and Genetic Epidemiology Consortium, and Andreassen, Ole A. and Asherson, Philip and Burton, Christie L. and Boomsma, Dorret I. and Cormand, Bru and Dalsgaard, Søren and Franke, Barbara and Gelernter, Joel and Geschwind, Daniel and Hakonarson, Hakon and Haavik, Jan and Kranzler, Henry R. and Kuntsi, Jonna and Langley, Kate and Lesch, Klaus-Peter and Middeldorp, Christel and Reif, Andreas and Rohde, Luis Augusto and Roussos, Panos and Schachar, Russell and Sklar, Pamela and Sonuga-Barke, Edmund J. S. and Sullivan, Patrick F. and Thapar, Anita and Tung, Joyce Y. and Waldman, Irwin D. and Medland, Sarah E. and Stefansson, Kari and Nordentoft, Merete and Hougaard, David M. and Werge, Thomas and Mors, Ole and Mortensen, Preben Bo and Daly, Mark J. and Faraone, Stephen V. and Børglum, Anders D. and Neale, Benjamin M.. (2019) Discovery of the First Genome-Wide Significant Risk Loci for Attention Deficit/Hyperactivity Disorder. Nature Genetics, 51 (1). pp. 63-75.

2018

Martin, Joanna and Walters, Raymond K. and Demontis, Ditte and Mattheisen, Manuel and Lee, S. Hong and Robinson, Elise and Brikell, Isabell and Ghirardi, Laura and Larsson, Henrik and Lichtenstein, Paul and Eriksson, Nicholas and Mountain View, California. and Psychiatric Genomics Consortium: Adhd Subgroup, and iPsych–Broad Adhd Workgroup, and Werge, Thomas and Mortensen, Preben Bo and Pedersen, Marianne Giørtz and Mors, Ole and Nordentoft, Merete and Hougaard, David M. and Bybjerg-Grauholm, Jonas and Wray, Naomi R. and Franke, Barbara and Faraone, Stephen V. and O'Donovan, Michael C. and Thapar, Anita and Børglum, Anders D. and Neale, Benjamin M.. (2018) A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. Biological Psychiatry, 83 (12). pp. 1044-1053.

2015

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.

Hommers, Leif and Raab, Annette and Bohl, Alexandra and Weber, Heike and Scholz, Claus-Jürgen and Erhardt, Angelika and Binder, Elisabeth and Arolt, Volker and Gerlach, Alexander and Gloster, Andrew and Kalisch, Raffael and Kircher, Tilo and Lonsdorf, Tina and Ströhle, Andreas and Zwanzger, Peter and Mattheisen, Manuel and Cichon, Sven and Lesch, Klaus-Peter and Domschke, Katharina and Reif, Andreas and Lohse, Martin J. and Deckert, Jürgen. (2015) MicroRNA hsa-miR-4717-5p Regulates RGS2 and May Be a Risk Factor for Anxiety-Related Traits. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics , 168B (4). pp. 296-306.

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.

Johnson, Michael R. and Behmoaras, Jacques and Bottolo, Leonardo and Krishnan, Michelle L. and Pernhorst, Katharina and Meza Santoscoy, Paola L. and Rossetti, Tiziana and Speed, Doug and Srivastava, Prashant K. and Chadeau-Hyam, Marc and Hajji, Nabil and Dabrowska, Dabrowska and Rotival, Maxime and Razzaghi, Banafsheh and Kovac, Stjepana and Wanisch, Klaus and Grillo, Federico W. and Slaviero, Anna and Langley, Sarah R. and Shkura, Kirill and Roncon, Paolo and De, Tisham and Mattheisen, Manuel and Niehusmann, Pitt and O'Brien, Terence J. and Petrovski, Slave and von Lehe, Marec and Hoffmann, Per and Eriksson, Johan and Coffey, Alison J. and Cichon, Sven and Walker, Matthew and Simonato, Michele and Danis, Bénédicte and Mazzuferi, Manuela and Foerch, Patrik and Schoch, Susanne and De Paola, Vincenzo and Kaminski, Rafal M. and Cunliffe, Vincent T. and Becker, Albert J. and Petretto, Enrico. (2015) Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus. Nature Communications, 6. p. 6031.

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

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.

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.

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.

Christoforou, Andrea and Espeseth, Thomas and Davies, Gail and Fernandes, Carla P. D. and Giddaluru, Sudheer and Mattheisen, Manuel and Tenesa, Albert and Harris, Sarah E. and McLachlan Liewald, David Cherry and Payton, Antony and Ollier, William and Horan, Michael A. and Pendleton, Neil and Haggarty, Paul and Djurovic, Srdjan and Herms, Stefan and Hoffmann, Per and Cichon, Sven and Starr, John M. and Lundervold, Astri J. and Reinvang, Ivar and Steen, Vidar M. and Deary, Ian J. and Le Hellard, Stephanie. (2014) GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. Genes, Brain and Behavior, 13 (7). pp. 663-674.

Quast, Carina and Reif, Andreas and Brückl, Tanja and Pfister, Hildegard and Weber, Heike and Mattheisen, Manuel and Cichon, Sven and Lang, Thomas and Hamm, Alfons and Fehm, Lydia and Ströhle, Andreas and Arolt, Volker and Domschke, Katharina and Kircher, Tilo and Wittchen, Hans-Ulrich and Pauli, Paul and Gerlach, Alexander L. and Alpers, Georg W. and Deckert, Jürgen and Rupprecht, Rainer and Binder, Elisabeth B. and Erhardt, Angelika. (2014) Gender-specific association of variants in the AKR1C1 gene with dimensional anxiety in patients with panic disorder: additional evidence for the importance of neurosteroids in anxiety? Depression and Anxiety, 31 (10). pp. 843-850.

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.

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.

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.

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. 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