Items where Author is "Nöthen, Markus M."

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.

2015

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.

Debette, Stéphanie and Ibrahim Verbaas, Carla A. and Bressler, Jan and Schuur, Maaike and Smith, Albert and Bis, Joshua C. and Davies, Gail and Wolf, Christiane and Gudnason, Vilmundur and Chibnik, Lori B. and Yang, Qiong and deStefano, Anita L. and de Quervain, Dominique J. F. and Srikanth, Velandai and Lahti, Jari and Grabe, Hans J. and Smith, Jennifer A. and Priebe, Lutz and Yu, Lei and Karbalai, Nazanin and Hayward, Caroline and Wilson, James F. and Campbell, Harry and Petrovic, Katja and Fornage, Myriam and Chauhan, Ganesh and Yeo, Robin and Boxall, Ruth and Becker, James and Stegle, Oliver and Mather, Karen A. and Chouraki, Vincent and Sun, Qi and Rose, Lynda M. and Resnick, Susan and Oldmeadow, Christopher and Kirin, Mirna and Wright, Alan F. and Jonsdottir, Maria K. and Au, Rhoda and Becker, Albert and Amin, Najaf and Nalls, Mike A. and Turner, Stephen T. and Kardia, Sharon L. R. and Oostra, Ben and Windham, Gwen and Coker, Laura H. and Zhao, Wei and Knopman, David S. and Heiss, Gerardo and Griswold, Michael E. and Gottesman, Rebecca F. and Vitart, Veronique and Hastie, Nicholas D. and Zgaga, Lina and Rudan, Igor and Polasek, Ozren and Holliday, Elizabeth G. and Schofield, Peter and Choi, Seung Hoan and Tanaka, Toshiko and An, Yang and Perry, Rodney T. and Kennedy, Richard E. and Sale, Michèle M. and Wang, Jing and Wadley, Virginia G. and Liewald, David C. and Ridker, Paul M. and Gow, Alan J. and Pattie, Alison and Starr, John M. and Porteous, David and Liu, Xuan and Thomson, Russell and Armstrong, Nicola J. and Eiriksdottir, Gudny and Assareh, Arezoo A. and Kochan, Nicole A. and Widen, Elisabeth and Palotie, Aarno and Hsieh, Yi-Chen and Eriksson, Johan G. and Vogler, Christian and van Swieten, John C. and Shulman, Joshua M. and Beiser, Alexa and Rotter, Jerome and Schmidt, Carsten O. and Hoffmann, Wolfgang and Nöthen, Markus M. and Ferrucci, Luigi and Attia, John and Uitterlinden, Andre G. and Amouyel, Philippe and Dartigues, Jean-François and Amieva, Hélène and Räikkönen, Katri and Garcia, Melissa and Wolf, Philip A. and Hofman, Albert and Longstreth, W. T. and Psaty, Bruce M. and Boerwinkle, Eric and DeJager, Philip L. and Sachdev, Perminder S. and Schmidt, Reinhold and Breteler, Monique M. B. and Teumer, Alexander and Lopez, Oscar L. and Cichon, Sven and Chasman, Daniel I. and Grodstein, Francine and Müller-Myhsok, Bertram and Tzourio, Christophe and Papassotiropoulos, Andreas and Bennett, David A. and Ikram, M. Arfan and Deary, Ian J. and van Duijn, Cornelia M. and Launer, Lenore and Fitzpatrick, Annette L. and Seshadri, Sudha and Mosley, Thomas H. and Cohorts for Heart, and Aging Research in Genomic Epidemiology Consortium, . (2015) Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium. Biological psychiatry, 77 (8). pp. 749-763.

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.

Marenholz, Ingo and Esparza-Gordillo, Jorge and Rüschendorf, Franz and Bauerfeind, Anja and Strachan, David P. and Spycher, Ben D. and Baurecht, Hansjörg and Margaritte-Jeannin, Patricia and Sääf, Annika and Kerkhof, Marjan and Ege, Markus and Baltic, Svetlana and Matheson, Melanie C. and Li, Jin and Michel, Sven and Ang, Wei Q. and McArdle, Wendy and Arnold, Andreas and Homuth, Georg and Demenais, Florence and Bouzigon, Emmanuelle and Söderhäll, Cilla and Pershagen, Göran and de Jongste, Johan C. and Postma, Dirkje S. and Braun-Fahrländer, Charlotte and Horak, Elisabeth and Ogorodova, Ludmila M. and Puzyrev, Valery P. and Bragina, Elena Yu and Hudson, Thomas J. and Morin, Charles and Duffy, David L. and Marks, Guy B. and Robertson, Colin F. and Montgomery, Grant W. and Musk, Bill and Thompson, Philip J. and Martin, Nicholas G. and James, Alan and Sleiman, Patrick and Toskala, Elina and Rodriguez, Elke and Fölster-Holst, Regina and Franke, Andre and Lieb, Wolfgang and Gieger, Christian and Heinzmann, Andrea and Rietschel, Ernst and Keil, Thomas and Cichon, Sven and Nöthen, Markus M. and Pennell, Craig E. and Sly, Peter D. and Schmidt, Carsten O. and Matanovic, Anja and Schneider, Valentin and Heinig, Matthias and Hübner, Norbert and Holt, Patrick G. and Lau, Susanne and Kabesch, Michael and Weidinger, Stefan and Hakonarson, Hakon and Ferreira, Manuel A. R. and Laprise, Catherine and Freidin, Maxim B. and Genuneit, Jon and Koppelman, Gerard H. and Melén, Erik and Dizier, Marie-Hélène and Henderson, A. John and Lee, Young Ae. (2015) Meta-analysis identifies seven susceptibility loci involved in the atopic march. Nature communications, 6. p. 8804.

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.

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.

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.

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.

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.

Caspers, Svenja and Moebus, Susanne and Lux, Silke and Pundt, Noreen and Schutz, Holger and Muhleisen, Thomas W. and Gras, Vincent and Eickhoff, Simon B. and Romanzetti, Sandro and Stocker, Tony and Stirnberg, Rüdiger and Kirlangic, Mehmet E. and Minnerop, Martina and Pieperhoff, Peter and Modder, Ulrich and Das, Samir and Evans, Alan C. and Jöckel, Karl-Heinz and Erbel, Raimund and Cichon, Sven and Nöthen, Markus M. and Sturma, Dieter and Bauer, Andreas and Shah, N. Jon and Zilles, Karl and Amunts, Katrin. (2014) Studying variability in human brain aging in a population-based German cohort-rationale and design of 1000BRAINS. Frontiers in Aging Neuroscience, 6. p. 149.

2013

Randall, Joshua C. and Winkler, Thomas W. and Kutalik, Zoltán and Berndt, Sonja I. and Jackson, Anne U. and Monda, Keri L. and Kilpeläinen, Tuomas O. and Esko, Tõnu and Mägi, Reedik and Li, Shengxu and Workalemahu, Tsegaselassie and Feitosa, Mary F. and Croteau-Chonka, Damien C. and Day, Felix R. and Fall, Tove and Ferreira, Teresa and Gustafsson, Stefan and Locke, Adam E. and Mathieson, Iain and Scherag, Andre and Vedantam, Sailaja and Wood, Andrew R. and Liang, Liming and Steinthorsdottir, Valgerdur and Thorleifsson, Gudmar and Dermitzakis, Emmanouil T. and Dimas, Antigone S. and Karpe, Fredrik and Min, Josine L. and Nicholson, George and Clegg, Deborah J. and Person, Thomas and Krohn, Jon P. and Bauer, Sabrina and Buechler, Christa and Eisinger, Kristina and Diagram Consortium, and Bonnefond, Amélie and Froguel, Philippe and Magic Investigators, and Hottenga, Jouke-Jan and Prokopenko, Inga and Waite, Lindsay L. and Harris, Tamara B. and Smith, Albert Vernon and Shuldiner, Alan R. and McArdle, Wendy L. and Caulfield, Mark J. and Munroe, Patricia B. and Grönberg, Henrik and Chen, Yii-Der Ida and Li, Guo and Beckmann, Jacques S. and Johnson, Toby and Thorsteinsdottir, Unnur and Teder-Laving, Maris and Khaw, Kay-Tee and Wareham, Nicholas J. and Zhao, Jing Hua and Amin, Najaf and Oostra, Ben A. and Kraja, Aldi T. and Province, Michael A. and Cupples, L. Adrienne and Heard-Costa, Nancy L. and Kaprio, Jaakko and Ripatti, Samuli and Surakka, Ida and Collins, Francis S. and Saramies, Jouko and Tuomilehto, Jaakko and Jula, Antti and Salomaa, Veikko and Erdmann, Jeanette and Hengstenberg, Christian and Loley, Christina and Schunkert, Heribert and Lamina, Claudia and Wichmann, H. Erich and Albrecht, Eva and Gieger, Christian and Hicks, Andrew A. and Johansson, Asa and Pramstaller, Peter P. and Kathiresan, Sekar and Speliotes, Elizabeth K. and Penninx, Brenda and Hartikainen, Anna-Liisa and Jarvelin, Marjo-Riitta and Gyllensten, Ulf and Boomsma, Dorret I. and Campbell, Harry and Wilson, James F. and Chanock, Stephen J. and Farrall, Martin and Goel, Anuj and Medina-Gomez, Carolina and Rivadeneira, Fernando and Estrada, Karol and Uitterlinden, André G. and Hofman, Albert and Zillikens, M. Carola and den Heijer, Martin and Kiemeney, Lambertus A. and Maschio, Andrea and Hall, Per and Tyrer, Jonathan and Teumer, Alexander and Völzke, Henry and Kovacs, Peter and Tönjes, Anke and Mangino, Massimo and Spector, Tim D. and Hayward, Caroline and Rudan, Igor and Hall, Alistair S. and Samani, Nilesh J. and Attwood, Antony Paul and Sambrook, Jennifer G. and Hung, Joseph and Palmer, Lyle J. and Lokki, Marja-Liisa and Sinisalo, Juha and Boucher, Gabrielle and Huikuri, Heikki and Lorentzon, Mattias and Ohlsson, Claes and Eklund, Niina and Eriksson, Johan G. and Barlassina, Cristina and Rivolta, Carlo and Nolte, Ilja M. and Snieder, Harold and Van der Klauw, Melanie M. and Van Vliet-Ostaptchouk, Jana V. and Gejman, Pablo V. and Shi, Jianxin and Jacobs, Kevin B. and Wang, Zhaoming and Bakker, Stephan J. L. and Mateo Leach, Irene and Navis, Gerjan and van der Harst, Pim and Martin, Nicholas G. and Medland, Sarah E. and Montgomery, Grant W. and Yang, Jian and Chasman, Daniel I. and Ridker, Paul M. and Rose, Lynda M. and Lehtimäki, Terho and Raitakari, Olli and Absher, Devin and Iribarren, Carlos and Basart, Hanneke and Hovingh, Kees G. and Hyppönen, Elina and Power, Chris and Anderson, Denise and Beilby, John P. and Hui, Jennie and Jolley, Jennifer and Sager, Hendrik and Bornstein, Stefan R. and Schwarz, Peter E. H. and Kristiansson, Kati and Perola, Markus and Lindström, Jaana and Swift, Amy J. and Uusitupa, Matti and Atalay, Mustafa and Lakka, Timo A. and Rauramaa, Rainer and Bolton, Jennifer L. and Fowkes, Gerry and Fraser, Ross M. and Price, Jackie F. and Fischer, Krista and Krjutå Kov, Kaarel and Metspalu, Andres and Mihailov, Evelin and Langenberg, Claudia and Luan, Jian'an and Ong, Ken K. and Chines, Peter S. and Keinanen-Kiukaanniemi, Sirkka M. and Saaristo, Timo E. and Edkins, Sarah and Franks, Paul W. and Hallmans, Göran and Shungin, Dmitry and Morris, Andrew David and Palmer, Colin N. A. and Erbel, Raimund and Moebus, Susanne and Nöthen, Markus M. and Pechlivanis, Sonali and Hveem, Kristian and Narisu, Narisu and Hamsten, Anders and Humphries, Steve E. and Strawbridge, Rona J. and Tremoli, Elena and Grallert, Harald and Thorand, Barbara and Illig, Thomas and Koenig, Wolfgang and Müller-Nurasyid, Martina and Peters, Annette and Boehm, Bernhard O. and Kleber, Marcus E. and März, Winfried and Winkelmann, Bernhard R. and Kuusisto, Johanna and Laakso, Markku and Arveiler, Dominique and Cesana, Giancarlo and Kuulasmaa, Kari and Virtamo, Jarmo and Yarnell, John W. G. and Kuh, Diana and Wong, Andrew and Lind, Lars and de Faire, Ulf and Gigante, Bruna and Magnusson, Patrik K. E. and Pedersen, Nancy L. and Dedoussis, George and Dimitriou, Maria and Kolovou, Genovefa and Kanoni, Stavroula and Stirrups, Kathleen and Bonnycastle, Lori L. and Njølstad, Inger and Wilsgaard, Tom and Ganna, Andrea and Rehnberg, Emil and Hingorani, Aroon and Kivimaki, Mika and Kumari, Meena and Assimes, Themistocles L. and Barroso, Inês and Boehnke, Michael and Borecki, Ingrid B. and Deloukas, Panos and Fox, Caroline S. and Frayling, Timothy and Groop, Leif C. and Haritunians, Talin and Hunter, David and Ingelsson, Erik and Kaplan, Robert and Mohlke, Karen L. and O'Connell, Jeffrey R. and Schlessinger, David and Strachan, David P. and Stefansson, Kari and van Duijn, Cornelia M. and Abecasis, Gonçalo R. and McCarthy, Mark I. and Hirschhorn, Joel N. and Qi, Lu and Loos, Ruth J. F. and Lindgren, Cecilia M. and North, Kari E. and Heid, Iris M.. (2013) Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. PLoS Genetics, 9 (6). e1003500.

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.