Items where Author is "Cichon, Sven"
Number of items: 39. 2022Rickenbacher, Marc and Reinbold, Céline S. and Herms, Stefan and Hoffmann, Per and Cichon, Sven and Wueest, Alexandra S. and Monsch, Andreas U. and Steiner, Luzius A. and Goettel, Nicolai. (2022) Genome-wide Association Study of Postoperative Cognitive Dysfunction in Older Surgical Patients. Journal of neurosurgical anesthesiology, 34 (2). pp. 248-250. 2020Imahorn, Elias and Aushev, Magomet and Herms, Stefan and Hoffmann, Per and Cichon, Sven and Reichelt, Julia and Itin, Peter H. and Burger, Bettina. (2020) Gene expression is stable in a complete CIB1 knockout keratinocyte model. Scientific reports, 10 (1). p. 14952. 2016Degenhardt, 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. 2015Heilbronner, 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. 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. 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. Paternoster, Lavinia and Standl, Marie and Waage, Johannes and Baurecht, Hansjörg and Hotze, Melanie and Strachan, David P. and Curtin, John A. and Bønnelykke, Klaus and Tian, Chao and Takahashi, Atsushi and Esparza-Gordillo, Jorge and Alves, Alexessander Couto and Thyssen, Jacob P. and den Dekker, Herman T. and Ferreira, Manuel A. and Altmaier, Elisabeth and Sleiman, Patrick M. and Xiao, Feng Li and Gonzalez, Juan R. and Marenholz, Ingo and Kalb, Birgit and Pino-Yanes, Maria and Xu, Cheng Jian and Carstensen, Lisbeth and Groen-Blokhuis, Maria M. and Venturini, Cristina and Pennell, Craig E. and Barton, Sheila J. and Levin, Arbet M. and Curjuric, Ivan and Bustamante, Mariona and Kreiner-Møller, Eskil and Lockett, Gabrielle A. and Bacelis, Jonas and Bunyavanich, Supinda and Myers, Rachel A. and Matanovic, Anja and Kumar, Ashish and Tung, Joyce Y and Hirota, Tomomitsu and Kubo, Michiaki and McArdle, Wendy L. and Henderson, A. John and Kemp, John P. and Zheng, Jie and Smith, George Davey and Rüschendorf, Franz and Bauerfeind, Anja and Lee-Kirsch, Min Ae and Arnold, Andreas and Homuth, Georg and Schmidt, Carsten O. and Mangold, Elisabeth and Cichon, Sven and Keil, Thomas and Rodríguez, Elke and Peters, Annette and Franke, Andre and Lieb, Wolfgang and Novak, Natalija and Fölster-Holst, Regina and Horikoshi, Momoko and Pekkanen, Juha and Sebert, Sylvain and Husemoen, Lise L. and Grarup, Niels and de Jongste, Johan C. and Rivadeneira, Fernando and Hofman, Albert and Jaddoe, Vincent W. V. and Pasmans, Suzanne G. M. A. and Elbert, Niels J. and Uitterlinden, André G. and Marks, Guy B. and Thompson, Philip J. and Matheson, Melanie C. and Robertson, Colin F. and Australian Asthma Genetics, Consortium (AAGC) and Ried, Janina S. and Li, Jin and Zuo, Xian Bo and Zheng, Xiao Dong and Yin, Xian Yong Yin and Sun, Liang Dan and McAleer, Maeve A. and O'Regan, Grainne M. and Fahy, Caoimhe M. R. and Campbell, Linda E. and Macek, Milan and Kurek, Michael and Hu, Donglei and Eng, Celeste and Postma, Dirkje S. and Feenstra, Bjarke and Geller, Frank and Hottenga, Jouke Jan and Middeldorp, Christel M. and Hysi, Pirro and Bataille, Veronique and Spector, Tim and Tiesler, Carla M. T. and Thiering, Elisabeth and Pahukasahasram, Badri and Yang, James J. and Imboden, Madea and Huntsman, Scott and Vilor-Tejedor, Natàlia and Relton, Caroline L. and Myhre, Ronny and Nystad, Wenche and Custovic, Adnan and Weiss, Scott T. and Meyers, Deborah A. and Soderhall, Cilla and Melén, Erik and Ober, Carole and Raby, Benjamin A. and Simpson, Angela and Jacobsson, Bo and Holloway, John W. and Bisgaard, Hans and Sunyer, Jordi and Probst-Hensch, Nicole M. and Williams, L. Keoki and Godfrey, Keith M. and Wang, Carol A. and Boomsma, Dorret I. and Melbye, Mads and Koppelman, Gerard H. and Jarvis, Deborah and McLean, W. H. Irwin and Irvine, Alan D. and Zhang, Xue Jun and Hakonarson, Hakon and Gieger, Christian and Burchard, Esteban G. and Martin, Nicholas G. and Duijts, Liesbeth and Linneberg, Allan and Jarvelin, Marjo-Riitta and Noethen, Markus M. and Lau, Susanne and Hübner, Norbert and Lee, Young-Ae and Tamari, Mayum and Hinds, David A. and Glass, Daniel and Brown, Sara J. and Heinrich, Joachim and Evans, David M. and Weidinger, Stephan and EArly Genetics, and Lifecourse Epidemiology (EAGLE) Eczema Consortium, . (2015) Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nature Genetics, 47 (12). pp. 1449-1456. 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. 2014Hammer, 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. Boraska, Vesna and Franklin, Christopher S. and Floyd, James A.B. and Thornton, Laura M. and Huckins, Laura M. and Southam, Lorraine and Rayner, N. William and Tachmazidou, Ioanna and Klumpp, Kelly and Treasure, Janet and Lewis, Cathryn M. and Schmidt, Ulrike and Tozzi, Federica and Kiezebrink, Kirsty and Hebebrand, Johannes and Gorwood, Philip and Adan, Roger A. H. and Kas, Martin J. H. and Favaro, Angela and Santonastaso, Paolo and Fernández-Aranda, Fernando and Gratacòs, Mònica and Rybakowski, Filip and Dmitrzak-Weglarz, Monika and Kaprio, Jaakko and Keski-Rahkonen, Anna and Raevuori, Anu and Van Furth, Eric F. and Slof-Op 't Landt, Margarita and Hudson, James I. and Reichborn-Kjennerud, Ted and Knudsen, Gun Peggy S. and Monteleone, Palmiero and Kaplan, Allan S. and Karwautz, Andreas and Hakonarson, Hakon and Berrettini, Wade H. and Guo, Yiran and Li, Dong and Schork, Nicholas and Komaki, Gen and Ando, Tetsuya and Inoko, Hidetoshi and Esko, Tõnu and Fischer, Krista and Männik, Katrin and Metspalu, Andres and Baker, Jessica H. and Cone, Roger D. and Dackor, Jennifer and DeSocio, Janiece E. and Hilliard, Christopher E. and O'Toole, Julie K. and Pantel, Jacques and Szatkiewicz, Jin P. and Taico, Chrysecolla and Zerwas, Stephanie and Trace, Sara E. and Davis, Oliver S. P. and Helder, Sietske and Buhren, Katherina and Burghardt, Roland and de Zwaan, Martina and Egberts, Karin and Ehrlich, Stefan and Herpertz-Dahlmann, Beate and Herzog, Wolfgang and Imgart, Hartmut and Scherag, André and Scherag, Susann and Zipfel, Stephan and Boni, Claudette and Ramoz, Nicolas and Versini, Audrey and Brandys, Marek K. and Danner, Unna N. and de Kovel, Carolien and Hendriks, Judith and Koeleman, Bobby P. C. and Ophoff, Roel A. and Strengman, Eric and van Elburg, Annemarie A. and Bruson, Alice and Clementi, Maurizio and Degortes, Daniela and Forzan, Monica and Tenconi, Elena and Docampo, Elisa and Escaramis, Georgia and Jiménez-Murcia, Susana and Lissowska, Jolanta and Rajewski, Andrzej and Szeszenia-Dabrowska, Neonila and Slopien, Agnieszka and Hauser, Joanna and Karhunen, Leila and Meulenbelt, Ingrid and Slagboom, P. 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