Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder von Schumacher, J, Abon Jamra, R, Freudenberg, J, Becker, T, Ohlraun, S, Otte, A C J, Tullius, M, Kovalenko, S, Van Den Bogaert, A, Maier, W, Rietschel, M, Propping, P, Nöthen, M M, Cichon, S

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Thalidomide causes sinus bradycardia in ALS von Meyer, T., Maier, A., Borisow, N., Dullinger, J. S., Splettstößer, G., Ohlraun, S., Münch, C., Linke, P.

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A family-based and case-control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder von Abou Jamra, R, Sircar, I, Becker, T, Freudenberg-Hua, Y, Ohlraun, S, Freudenberg, J, Brockschmidt, F, Schulze, T G, Gross, M, Spira, F, Deschner, M, Schmäl, C, Maier, W, Propping, P, Rietschel, M, Cichon, S, Nöthen, M M, Schumacher, J

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Investigation of the DAOA G30 locus in panic disorder von Schumacher, J, Abou Jamra, R, Becker, T, Klopp, N, Franke, P, Jacob, C, Sand, P, Fritze, J, Ohlraun, S, Schulze, T G, Rietschel, M, Illig, T, Propping, P, Cichon, S, Deckert, J, Nöthen, M M

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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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Moclobemide Response in Depressed Patients: Association Study with a Functional Polymorphism in the Monoamine Oxidase A Promoter von Müller, D. J., Schulze, T. G., Macciardi, F., Ohlraun, S., Gross, M. M., Scherk, H., Neidt, H., Syagailo, Y. V., Grässle, M., Nöthen, M. M., Maier, W., Lesch, K.-P., Rietschel, M.

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The power of sample size and homogenous sampling: Association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder von Hoefgen, Barbara, Schulze, Thomas G., Ohlraun, Stephanie, von Widdern, Olrik, Höfels, Susanne, Gross, Magdalena, Heidmann, Vivien, Kovalenko, Svetlana, Eckermann, Anita, Kölsch, Heike, Metten, Martin, Zobel, Astrid, Becker, Tim, Nöthen, Markus M., Propping, Peter, Heun, Reinhard, Maier, Wolfgang, Rietschel, Marcella

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Genotype-Phenotype Studies in Bipolar Disorder Showing Association Between the DAOA G30 Locus and Persecutory Delusions: A First Step Toward a Molecular Genetic Classification of P... von Schulze, Thomas G., Ohlraun, Stephanie, Czerski, Piotr M., Schumacher, Johannes, Kassem, Layla, Deschner, Monika, Gross, Magdalena, Tullius, Monja, Heidmann, Vivien, Kovalenko, Svetlana, Jamra, Rami Abou, Becker, Tim, Leszczynska-Rodziewicz, Anna, Hauser, Joanna, Illig, Thomas, Klopp, Norman, Wellek, Stefan, Cichon, Sven, Henn, Fritz A., McMahon, Francis J., Maier, Wolfgang, Propping, Peter, Nöthen, Markus M., Rietschel, Marcella

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The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease von Van Den Bogaert, Ann, Schumacher, Johannes, Schulze, Thomas G., Otte, Andreas C., Ohlraun, Stephanie, Kovalenko, Svetlana, Becker, Tim, Freudenberg, Jan, Jönsson, Erik G., Mattila-Evenden, Marja, Sedvall, Göran C., Czerski, Piotr M., Kapelski, Pawel, Hauser, Joanna, Maier, Wolfgang, Rietschel, Marcella, Propping, Peter, Nöthen, Markus M., Cichon, Sven

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Pharmacogenetics of Tardive Dyskinesia: Combined Analysis of 780 Patients Supports Association with Dopamine D3 Receptor Gene Ser9Gly Polymorphism von Lerer, Bernard, Segman, Ronnen H., Fangerau, Heiner, Daly, Ann K., Basile, Vincenzo S., Cavallaro, Roberto, Aschauer, Harald N., McCreadie, Robin G., Ohlraun, Stephanie, Ferrier, Nicol, Masellis, Mario, Verga, Massimiliano, Scharfetter, Joachim, Rietschel, Marcella, Lovlie, Roger, Levy, Uriel Heresco, Meltzer, Herbert Y., Kennedy, James L., Steen, Vidar M., Macciardi, Fabio

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Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage... von Etain, B, Mathieu, F, Rietschel, M, Maier, W, Albus, M, McKeon, P, Roche, S, Kealey, C, Blackwood, D, Muir, W, Bellivier, F, Henry, C, Dina, C, Gallina, S, Gurling, H, Malafosse, A, Preisig, M, Ferrero, F, Cichon, S, Schumacher, J, Ohlraun, S, Borrmann-Hassenbach, M, Propping, P, Abou Jamra, R, Schulze, T G, Marusic, A, Dernovsek, Z M, Giros, B, Bourgeron, T, Lemainque, A, Bacq, D, Betard, C, Charon, C, Nöthen, M M, Lathrop, M, Leboyer, M

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Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder von Schulze, Thomas G., Müller, Daniel J., Krauss, Harald, Scherk, Harald, Ohlraun, Stephanie, Syagailo, Yana V., Windemuth, Christine, Neidt, Helge, Grässle, Markus, Papassotiropoulos, Andreas, Heun, Reinhard, Nöthen, Markus M., Maier, Wolfgang, Lesch, Klaus-Peter, Rietschel, Marcella

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Genomewide Scan and Fine-Mapping Linkage Studies in Four European Samples with Bipolar Affective Disorder Suggest a New Susceptibility Locus on Chromosome 1p35-p36 and Provides Fur... von Schumacher, Johannes, Kaneva, Radka, Jamra, Rami Abou, Diaz, Guillermo Orozco, Ohlraun, Stephanie, Milanova, Vihra, Lee, Young-Ae, Rivas, Fabio, Mayoral, Fermin, Fuerst, Robert, Flaquer, Antonia, Windemuth, Christine, Gay, Eudoxia, Sanz, Sebastian, González, Maria José, Gil, Susana, Cabaleiro, Francisco, del Rio, Francisco, Perez, Fermin, Haro, Jesus, Kostov, Christian, Chorbov, Vesselin, Nikolova-Hill, Amelia, Stoyanova, Vessela, Onchev, George, Kremensky, Ivo, Strauch, Konstantin, Schulze, Thomas G., Nürnberg, Peter, Gaebel, Wolfgang, Klimke, Ansgar, Auburger, Georg, Wienker, Thomas F., Kalaydjieva, Luba, Propping, Peter, Cichon, Sven, Jablensky, Assen, Rietschel, Marcella, Nöthen, Markus M.

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Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin von Cichon, Sven, Buervenich, Silvia, Kirov, George, Akula, Nirmala, Dimitrova, Albena, Green, Elaine, Schumacher, Johannes, Klopp, Norman, Becker, Tim, Ohlraun, Stephanie, Schulze, Thomas G, Tullius, Monja, Gross, Magdalena M, Jones, Lisa, Krastev, Stefan, Nikolov, Ivan, Hamshere, Marian, Jones, Ian, Czerski, Piotr M, Leszczynska-Rodziewicz, Anna, Kapelski, Pawel, Bogaert, Ann Van Den, Illig, Thomas, Hauser, Joanna, Maier, Wolfgang, Berrettini, Wade, Byerley, William, Coryell, William, Gershon, Elliot S, Kelsoe, John R, McInnis, Melvin G, Murphy, Dennis L, Nurnberger, John I, Reich, Theodore, Scheftner, William, O'Donovan, Michael C, Propping, Peter, Owen, Michael J, Rietschel, Marcella, Nöthen, Markus M, McMahon, Francis J, Craddock, Nick

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Haplotype-based systematic association studies of ATP1A2 in migraine with aura von Netzer, Christian, Todt, Unda, Heinze, Axel, Freudenberg, Jan, Zumbroich, Vera, Becker, Tim, Goebel, Ingrid, Ohlraun, Stephanie, Goebel, Hartmut, Kubisch, Christian

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No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples von Glaser, Beate, Schumacher, Johannes, Williams, Hywel J., Jamra, Rami Abou, Ianakiev, Nikolai, Milev, Radoi, Ohlraun, Stephanie, Schulze, Thomas G., Czerski, Piotr M., Hauser, Joanna, Jönsson, Erick G., Sedvall, Göran C., Klopp, Norman, Illig, Thomas, Becker, Tim, Propping, Peter, Williams, Nigel M., Cichon, Sven, Kirov, George, Rietschel, Marcella, Murphy, Kieran C., O’Donovan, Michael C., Nöthen, Markus M., Owen, Michael J.

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Computer-Assisted Phenotype Characterization for Genetic Research in Psychiatry von Fangerau, Heiner, Ohlraun, Stephanie, Granath, Ralf O., Nöthen, Markus M., Rietschel, Marcella, Schulze, Thomas G.

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Further evidence for age of onset being an indicator for severity in bipolar disorder von Schulze, Thomas G., Müller, Daniel J., Krauss, Harald, Gross, Magdalena, Fangerau-Lefèvre, Heiner, Ill≐s, Franciska, Ohlraun, Stephanie, Cichon, Sven, Held, Tilo, Propping, Peter, Nöthen, Markus M., Maier, Wolfgang, Rietschel, Marcella

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Family history influences age of onset in bipolar I disorder in females but not in males von Grigoroiu-Serbanescu, Maria, Nöthen, Markus M., Ohlraun, Stephanie, Propping, Peter, Maier, Wolfgang, Wickramaratne, Priya, Georgescu, Marie-Jana, Prelipceanu, Dan, Grimberg, Mihaela, Sima, Dorina, Rietschel, Marcella

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DRD4 exon 3 variants are not associated with symptomatology of major psychoses in a German population von Serretti, Alessandro, Lorenzi, Cristina, Mandelli, Laura, Cichon, Sven, Schumacher, Johannes, Nöthen, Markus M., Rietschel, Marcella, Tullius, Monja, Ohlraun, Stephanie

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