Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia von Juraeva, Dilafruz, Haenisch, Britta, Zapatka, Marc, Frank, Josef, Witt, Stephanie H, Mühleisen, Thomas W, Treutlein, Jens, Strohmaier, Jana, Meier, Sandra, Degenhardt, Franziska, Giegling, Ina, Ripke, Stephan, Leber, Markus, Lange, Christoph, Schulze, Thomas G, Mössner, Rainald, Nenadic, Igor, Sauer, Heinrich, Rujescu, Dan, Maier, Wolfgang, Børglum, Anders, Ophoff, Roel, Cichon, Sven, Nöthen, Markus M, Rietschel, Marcella, Mattheisen, Manuel, Brors, Benedikt

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Striatal Response to Reward Anticipation: Evidence for a Systems-Level Intermediate Phenotype for Schizophrenia von Grimm, Oliver, Heinz, Andreas, Walter, Henrik, Kirsch, Peter, Erk, Susanne, Haddad, Leila, Plichta, Michael M, Romanczuk-Seiferth, Nina, Pöhland, Lydia, Mohnke, Sebastian, Mühleisen, Thomas W, Mattheisen, Manuel, Witt, Stephanie H, Schäfer, Axel, Cichon, Sven, Nöthen, Markus, Rietschel, Marcella, Tost, Heike, Meyer-Lindenberg, Andreas

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Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk von Chubb, Daniel, Weinhold, Niels, Broderick, Peter, Chen, Bowang, Johnson, David C, Försti, Asta, Vijayakrishnan, Jayaram, Migliorini, Gabriele, Dobbins, Sara E, Holroyd, Amy, Hose, Dirk, Walker, Brian A, Davies, Faith E, Gregory, Walter A, Jackson, Graham H, Irving, Julie A, Pratt, Guy, Fegan, Chris, Fenton, James A L, Neben, Kai, Hoffmann, Per, Nöthen, Markus M, Mühleisen, Thomas W, Eisele, Lewin, Ross, Fiona M, Straka, Christian, Einsele, Hermann, Langer, Christian, Dörner, Elisabeth, Allan, James M, Jauch, Anna, Morgan, Gareth J, Hemminki, Kari, Houlston, Richard S, Goldschmidt, Hartmut

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Corrigendum to “Effect of CACNA1C rs1006737 on neural correlates of verbal fluency in healthy individuals” [NeuroImage volume 49 (2010) 1831-1836] von Krug, Axel, Nieratschker, Vanessa, Markov, Valentin, Krach, Sören, Jansen, Andreas, Zerres, Klaus, Eggermann, Thomas, Stöcker, Tony, Jon Shah, N., Treutlein, Jens, Mühleisen, Thomas W., Kircher, Tilo

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Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia von Cao, Hengyi, Bertolino, Alessandro, Walter, Henrik, Schneider, Michael, Schäfer, Axel, Taurisano, Paolo, Blasi, Giuseppe, Haddad, Leila, Grimm, Oliver, Otto, Kristina, Dixson, Luanna, Erk, Susanne, Mohnke, Sebastian, Heinz, Andreas, Romanczuk-Seiferth, Nina, Mühleisen, Thomas W, Mattheisen, Manuel, Witt, Stephanie H, Cichon, Sven, Noethen, Markus, Rietschel, Marcella, Tost, Heike, Meyer-Lindenberg, Andreas

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The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia von Håvik, Bjarte, Le Hellard, Stephanie, Rietschel, Marcella, Lybæk, Helle, Djurovic, Srdjan, Mattheisen, Manuel, Mühleisen, Thomas W, Degenhardt, Franziska, Priebe, Lutz, Maier, Wolfgang, Breuer, Rene, Schulze, Thomas G, Agartz, Ingrid, Melle, Ingrid, Hansen, Thomas, Bramham, Clive R, Nöthen, Markus M, Stevens, Beth, Werge, Thomas, Andreassen, Ole A, Cichon, Sven, Steen, Vidar M

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A GWAS top hit for circulating leptin is associated with weight gain but not with leptin protein levels in lithium-augmented patients with major depression von Bopp, Sandra K, Heilbronner, Urs, Schlattmann, Peter, Buspavanich, Pichit J, Lang, Undine E, Heinz, Andreas, Schulze, Thomas G, Adli, Mazda, Mühleisen, Thomas W, Ricken, Roland

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Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1 von MCMAHON, Francis J, AKULA, Nirmala, MATTHEISEN, Manuel, MÜHLEISEN, Thomas W, MAIER, Wolfgang, NÖTHEN, Markus M, CICHON, Sven, FARMER, Anne, VINCENT, John B, HOLSBOER, Florian, PREISIG, Martin, RIETSCHEL, Marcella, SCHULZE, Thomas G, MUGLIA, Pierandrea, TOZZI, Federica, DETERA-WADLEIGH, Sevilla D, STEELE, C. J. M, BREUER, René, STROHMAIER, Jana, WENDLAND, Jens R

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Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus von Zhao, Ling, Mühleisen, Thomas W., Pelzer, Dominique I., Burger, Bettina, Beins, Eva C., Forstner, Andreas J., Herms, Stefan, Hoffmann, Per, Amunts, Katrin, Palomero-Gallagher, Nicola, Cichon, Sven

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Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder von ETAIN, Bruno, DUMAINE, Anne, MATHIEU, Flavie, HENRY, Chantal, KAHN, Jean-Pierre, LAUNAY, Jean-Marie, MÜHLEISEN, Thomas W, CICHON, Sven, BOURGERON, Thomas, LEBOYER, Marion, JAMAIN, Stéphane, BELLIVIER, Frank, PAGAN, Cécile, FRANCELLE, Laetitia, GOUBRAN-BOTROS, Hany, MORENO, Sarah, DESHOMMES, Jasmine, MOUSTAFA, Khaled, LE DUDAL, Katia

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Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults von Bittner, Nora, Jockwitz, Christiane, Mühleisen, Thomas W., Hoffstaedter, Felix, Eickhoff, Simon B., Moebus, Susanne, Bayen, Ute J., Cichon, Sven, Zilles, Karl, Amunts, Katrin, Caspers, Svenja

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Genetic Associations with Valvular Calcification and Aortic Stenosis von Thanassoulis, George, Campbell, Catherine Y, Owens, David S, Smith, J. Gustav, Smith, Albert V, Peloso, Gina M, Kerr, Kathleen F, Pechlivanis, Sonali, Budoff, Matthew J, Harris, Tamara B, Malhotra, Rajeev, O'Brien, Kevin D, Kamstrup, Pia R, Nordestgaard, Børge G, Tybjaerg-Hansen, Anne, Allison, Matthew A, Aspelund, Thor, Criqui, Michael H, Heckbert, Susan R, Hwang, Shih-Jen, Liu, Yongmei, Sjogren, Marketa, van der Pals, Jesper, Kälsch, Hagen, Mühleisen, Thomas W, Nöthen, Markus M, Cupples, L. Adrienne, Caslake, Muriel, Di Angelantonio, Emanuele, Danesh, John, Rotter, Jerome I, Sigurdsson, Sigurdur, Wong, Quenna, Erbel, Raimund, Kathiresan, Sekar, Melander, Olle, Gudnason, Vilmundur, O'Donnell, Christopher J, Post, Wendy S

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Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype von Migliorini, Gabriele, Fiege, Bettina, Hosking, Fay J., Ma, Yussanne, Kumar, Rajiv, Sherborne, Amy L., da Silva Filho, Miguel Inacio, Vijayakrishnan, Jayaram, Koehler, Rolf, Thomsen, Hauke, Irving, Julie A., Allan, James M., Lightfoot, Tracy, Roman, Eve, Kinsey, Sally E., Sheridan, Eamonn, Thompson, Pamela, Hoffmann, Per, Nöthen, Markus M., Mühleisen, Thomas W., Eisele, Lewin, Zimmermann, Martin, Bartram, Claus R., Schrappe, Martin, Greaves, Mel, Stanulla, Martin, Hemminki, Kari, Houlston, Richard S.

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Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups von Scherag, André, Dina, Christian, Hinney, Anke, Vatin, Vincent, Scherag, Susann, Vogel, Carla I G, Müller, Timo D, Grallert, Harald, Wichmann, H-Erich, Balkau, Beverley, Heude, Barbara, Jarvelin, Marjo-Riitta, Hartikainen, Anna-Liisa, Levy-Marchal, Claire, Weill, Jacques, Delplanque, Jérôme, Körner, Antje, Kiess, Wieland, Kovacs, Peter, Rayner, Nigel W, Prokopenko, Inga, McCarthy, Mark I, Schäfer, Helmut, Jarick, Ivonne, Boeing, Heiner, Fisher, Eva, Reinehr, Thomas, Heinrich, Joachim, Rzehak, Peter, Berdel, Dietrich, Borte, Michael, Biebermann, Heike, Krude, Heiko, Rosskopf, Dieter, Rimmbach, Christian, Rief, Winfried, Fromme, Tobias, Klingenspor, Martin, Schürmann, Annette, Schulz, Nadja, Nöthen, Markus M, Mühleisen, Thomas W, Erbel, Raimund, Jöckel, Karl-Heinz, Moebus, Susanne, Boes, Tanja, Illig, Thomas, Froguel, Philippe, Hebebrand, Johannes, Meyre, David

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

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Aging of blood can be tracked by DNA methylation changes at just three CpG sites von Weidner, Carola Ingrid, Lin, Qiong, Koch, Carmen Maike, Eisele, Lewin, Beier, Fabian, Ziegler, Patrick, Bauerschlag, Dirk Olaf, Jöckel, Karl-Heinz, Erbel, Raimund, Mühleisen, Thomas Walter, Zenke, Martin, Brümmendorf, Tim Henrik, Wagner, Wolfgang

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Effect of CACNA1C rs1006737 on neural correlates of verbal fluency in healthy individuals von Krug, Axel, Nieratschker, Vanessa, Markov, Valentin, Krach, Sören, Jansen, Andreas, Zerres, Klaus, Eggermann, Thomas, Stöcker, Tony, Shah, N. Jon, Treutlein, Jens, Mühleisen, Thomas W., Kircher, Tilo

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Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk von Broderick, Peter, Chubb, Daniel, Johnson, David C, Weinhold, Niels, Försti, Asta, Lloyd, Amy, Olver, Bianca, Ma, Yussanne P, Dobbins, Sara E, Walker, Brian A, Davies, Faith E, Gregory, Walter A, Child, J Anthony, Ross, Fiona M, Jackson, Graham H, Neben, Kai, Jauch, Anna, Hoffmann, Per, Mühleisen, Thomas W, Nöthen, Markus M, Moebus, Susanne, Tomlinson, Ian P, Goldschmidt, Hartmut, Hemminki, Kari, Morgan, Gareth J, Houlston, Richard S

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Hippocampal and Frontolimbic Function as Intermediate Phenotype for Psychosis: Evidence from Healthy Relatives and a Common Risk Variant in CACNA1C von Erk, Susanne, Meyer-Lindenberg, Andreas, Schmierer, Phöbe, Mohnke, Sebastian, Grimm, Oliver, Garbusow, Maria, Haddad, Leila, Poehland, Lydia, Mühleisen, Thomas W, Witt, Stephanie H, Tost, Heike, Kirsch, Peter, Romanczuk-Seiferth, Nina, Schott, Björn H, Cichon, Sven, Nöthen, Markus M, Rietschel, Marcella, Heinz, Andreas, Walter, Henrik

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Susceptibility variants for male-pattern baldness on chromosome 20p11 von Hillmer, Axel M, Brockschmidt, Felix F, Hanneken, Sandra, Eigelshoven, Sibylle, Steffens, Michael, Flaquer, Antonia, Herms, Stefan, Becker, Tim, Kortüm, Anne-Katrin, Nyholt, Dale R, Zhao, Zhen Zhen, Montgomery, Grant W, Martin, Nicholas G, Mühleisen, Thomas W, Alblas, Margrieta A, Moebus, Susanne, Jöckel, Karl-Heinz, Bröcker-Preuss, Martina, Erbel, Raimund, Reinartz, Roman, Betz, Regina C, Cichon, Sven, Propping, Peter, Baur, Max P, Wienker, Thomas F, Kruse, Roland, Nöthen, Markus M

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