Combined analysis of cytoarchitectonic, molecular and transcriptomic patterns reveal differences in brain organization across human functional brain systems von Zachlod, Daniel, Bludau, Sebastian, Cichon, Sven, Palomero-Gallagher, Nicola, Amunts, Katrin

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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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Neural Mechanisms of a Genome-Wide Supported Psychosis Variant von Esslinger, Christine, Walter, Henrik, Kirsch, Peter, Erk, Susanne, Schnell, Knut, Arnold, Claudia, Haddad, Leila, Mier, Daniela, Opitz von Boberfeld, Carola, Raab, Kyeon, Witt, Stephanie H, Rietschel, Marcella, Cichon, Sven, Meyer-Lindenberg, Andreas

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Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus von Schulz, Herbert, Ruppert, Ann-Kathrin, Herms, Stefan, Wolf, Christiane, Mirza-Schreiber, Nazanin, Stegle, Oliver, Czamara, Darina, Forstner, Andreas J., Sivalingam, Sugirthan, Schoch, Susanne, Moebus, Susanne, Pütz, Benno, Hillmer, Axel, Fricker, Nadine, Vatter, Hartmut, Müller-Myhsok, Bertram, Nöthen, Markus M., Becker, Albert J., Hoffmann, Per, Sander, Thomas, Cichon, Sven

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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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Gene expression is stable in a complete CIB1 knockout keratinocyte model von Imahorn, Elias, Aushev, Magomet, Herms, Stefan, Hoffmann, Per, Cichon, Sven, Reichelt, Julia, Itin, Peter H., Burger, Bettina

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Functional Subclone Profiling for Prediction of Treatment-Induced Intratumor Population Shifts and Discovery of Rational Drug Combinations in Human Glioblastoma von Reinartz, Roman, Wang, Shanshan, Kebir, Sied, Silver, Daniel J, Wieland, Anja, Zheng, Tong, Küpper, Marius, Rauschenbach, Laurèl, Fimmers, Rolf, Shepherd, Timothy M, Trageser, Daniel, Till, Andreas, Schäfer, Niklas, Glas, Martin, Hillmer, Axel M, Cichon, Sven, Smith, Amy A, Pietsch, Torsten, Liu, Ying, Reynolds, Brent A, Yachnis, Anthony, Pincus, David W, Simon, Matthias, Brüstle, Oliver, Steindler, Dennis A, Scheffler, Björn

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Common variants on 8p12 and 1q24.2 confer risk of schizophrenia von Shi, Yongyong, Li, Zhiqiang, Xu, Qi, Wang, Ti, Li, Tao, Shen, Jiawei, Zhang, Fengyu, Chen, Jianhua, Zhou, Guoquan, Ji, Weidong, Li, Baojie, Xu, Yifeng, Liu, Dengtang, Wang, Peng, Yang, Ping, Liu, Benxiu, Sun, Wensheng, Wan, Chunling, Qin, Shengying, He, Guang, Steinberg, Stacy, Cichon, Sven, Werge, Thomas, Sigurdsson, Engilbert, Tosato, Sarah, Palotie, Aarno, Nöthen, Markus M, Rietschel, Marcella, Ophoff, Roel A, Collier, David A, Rujescu, Dan, Clair, David St, Stefansson, Hreinn, Stefansson, Kari, Ji, Jue, Wang, Qingzhong, Li, Wenjin, Zheng, Linqing, Zhang, Hairong, Feng, Guoyin, He, Lin

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Identification of pleiotropy at the gene level between psychiatric disorders and related traits von Polushina, Tatiana, Banerjee, Niladri, Giddaluru, Sudheer, Bettella, Francesco, Espeseth, Thomas, Lundervold, Astri J., Djurovic, Srdjan, Cichon, Sven, Hoffmann, Per, Nöthen, Markus M., Steen, Vidar M., Andreassen, Ole A., Le Hellard, Stéphanie

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Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III von Cichon, Sven, Martin, Ludovic, Hennies, Hans Christian, Müller, Felicitas, Van Driessche, Karen, Karpushova, Anna, Stevens, Wim, Colombo, Roberto, Renné, Thomas, Drouet, Christian, Bork, Konrad, Nöthen, Markus M.

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Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder von Lencz, Todd, Guha, Saurav, Liu, Chunyu, Rosenfeld, Jeffrey, Mukherjee, Semanti, DeRosse, Pamela, John, Majnu, Cheng, Lijun, Zhang, Chunling, Badner, Judith A., Ikeda, Masashi, Iwata, Nakao, Cichon, Sven, Rietschel, Marcella, Nöthen, Markus M., Cheng, A.T.A., Hodgkinson, Colin, Yuan, Qiaoping, Kane, John M., Lee, Annette T., Pisanté, Anne, Gregersen, Peter K., Pe’er, Itsik, Malhotra, Anil K., Goldman, David, Darvasi, Ariel

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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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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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AN AGENDA FOR EVALUATING THE CLINICAL RELEVANCE OF CNVS IN PSYCHIATRIC DISORDERS von Cichon, Sven

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Associations between antagonistic SNPs for neuropsychiatric disorders and human brain structure von Federmann, Lydia M., David, Friederike S., Jockwitz, Christiane, Mühleisen, Thomas W., Pelzer, Dominique I., Nöthen, Markus M., Caspers, Svenja, Amunts, Katrin, Goltermann, Janik, Andlauer, Till F. M., Stein, Frederike, Brosch, Katharina, Kircher, Tilo, Cichon, Sven, Dannlowski, Udo, Sindermann, Lisa, Forstner, Andreas J.

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Enzymatic assays for the diagnosis of bradykinin-dependent angioedema von Defendi, Federica, Charignon, Delphine, Ghannam, Arije, Baroso, Remi, Csopaki, Françoise, Allegret-Cadet, Marion, Ponard, Denise, Favier, Bertrand, Cichon, Sven, Nicolie, Brigitte, Fain, Olivier, Martin, Ludovic, Drouet, Christian

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SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE von Drouet, Christian, López-Lera, Alberto, Ghannam, Arije, López-Trascasa, Margarita, Cichon, Sven, Ponard, Denise, Parsopoulou, Faidra, Grombirikova, Hana, Freiberger, Tomáš, Rijavec, Matija, Veronez, Camila L., Pesquero, João Bosco, Germenis, Anastasios E.

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Identification of Phonology-Related Genes and Functional Characterization of Broca's and Wernicke's Regions in Language and Learning Disorders von Unger, Nina, Heim, Stefan, Hilger, Dominique I., Bludau, Sebastian, Pieperhoff, Peter, Cichon, Sven, Amunts, Katrin, Muehleisen, Thomas W.

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Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression von Schumacher, Johannes, Jamra, Rami Abou, Becker, Tim, Ohlraun, Stephanie, Klopp, Norman, Binder, Elisabeth B., Schulze, Thomas G., Deschner, Monika, Schmäl, Christine, Höfels, Susanne, Zobel, Astrid, Illig, Thomas, Propping, Peter, Holsboer, Florian, Rietschel, Marcella, Nöthen, Markus M., Cichon, Sven

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Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder von Yousaf, Afsheen, Waltes, Regina, Haslinger, Denise, Klauck, Sabine M., Duketis, Eftichia, Sachse, Michael, Voran, Anette, Biscaldi, Monica, Schulte-Rüther, Martin, Cichon, Sven, Nöthen, Markus, Ackermann, Jörg, Koch, Ina, Freitag, Christine M., Chiocchetti, Andreas G.

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