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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Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers von Jönsson, E G, Nöthen, M M, Grünhage, F, Farde, L, Nakashima, Y, Propping, P, Sedvall, G C

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Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles von Herrera-Rivero, Marisol, Hochfeld, Lara M, Sivalingam, Sugirthan, Nöthen, Markus M, Heilmann-Heimbach, Stefanie

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Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study von Beaty, T. H., Taub, M. A., Scott, A. F., Murray, J. C., Marazita, M. L., Schwender, H., Parker, M. M., Hetmanski, J. B., Balakrishnan, P., Mansilla, M. A., Mangold, E., Ludwig, K. U., Noethen, M. M., Rubini, M., Elcioglu, N., Ruczinski, I.

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Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement von Baum, A E, Hamshere, M, Green, E, Cichon, S, Rietschel, M, Noethen, M M, Craddock, N, McMahon, F J

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Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder von Walker, Rosie M., Christoforou, Andrea, Thomson, Pippa A., McGhee, Kevin A., Maclean, Alan, Mühleisen, Thomas W., Strohmaier, Jana, Nieratschker, Vanessa, Nöthen, Markus M., Rietschel, Marcella, Cichon, Sven, Morris, Stewart W., Jilani, Omer, StClair, David, Blackwood, Douglas H., Muir, Walter J., Porteous, David J., Evans, Kathryn L.

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Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task von Walter, H, Schnell, K, Erk, S, Arnold, C, Kirsch, P, Esslinger, C, Mier, D, Schmitgen, M M, Rietschel, M, Witt, S H, Nöthen, M M, Cichon, S, Meyer-Lindenberg, A

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Breakthrough in understanding the molecular causes of psychiatric disorders von Nöthen, Markus M, Degenhardt, Franziska, Forstner, Andreas J

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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder von Baum, A E, Akula, N, Cabanero, M, Cardona, I, Corona, W, Klemens, B, Schulze, T G, Cichon, S, Rietschel, M, Nöthen, M M, Georgi, A, Schumacher, J, Schwarz, M, Abou Jamra, R, Höfels, S, Propping, P, Satagopan, J, Detera-Wadleigh, S D, Hardy, J, McMahon, F J

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G72 and Its Association With Major Depression and Neuroticism in Large Population-Based Groups From Germany von Rietschel, Marcella, Beckmann, Lars, Strohmaier, Jana, Georgi, Alexander, Karpushova, Anna, Schirmbeck, Frederike, Boesshenz, Katja V., Schmäl, Christine, Bürger, Christin, Jamra, Rami Abou, Schumacher, Johannes, Höfels, Susanne, Kumsta, Robert, Entringer, Sonja, Krug, Axel, Markov, Valentin, Maier, Wolfgang, Propping, Peter, Wüst, Stefan, Kircher, Tilo, Nöthen, Markus M., Cichon, Sven, Schulze, Thomas G.

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Heterodyne laser Doppler distance sensor with phase coding measuring stationary as well as laterally and axially moving objects von Pfister, T, Günther, P, Nöthen, M, Czarske, J

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First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children von Roeske, D, Ludwig, K U, Neuhoff, N, Becker, J, Bartling, J, Bruder, J, Brockschmidt, F F, Warnke, A, Remschmidt, H, Hoffmann, P, Müller-Myhsok, B, Nöthen, M M, Schulte-Körne, G

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Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogen... von Le Hellard, S, Theisen, F M, Haberhausen, M, Raeder, M B, Fernø, J, Gebhardt, S, Hinney, A, Remschmidt, H, Krieg, J C, Mehler-Wex, C, Nöthen, M M, Hebebrand, J, Steen, V M

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Genetic factors influencing the risk of multiple myeloma bone disease von Johnson, D C, Weinhold, N, Mitchell, J, Chen, B, Stephens, O W, Försti, A, Nickel, J, Kaiser, M, Gregory, W A, Cairns, D, Jackson, G H, Hoffmann, P, Noethen, M M, Hillengass, J, Bertsch, U, Barlogie, B, Davis, F E, Hemminki, K, Goldschmidt, H, Houlston, R S, Morgan, G J

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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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Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III von Björkqvist, Jenny, de Maat, Steven, Lewandrowski, Urs, Di Gennaro, Antonio, Oschatz, Chris, Schönig, Kai, Nöthen, Markus M, Drouet, Christian, Braley, Hal, Nolte, Marc W, Sickmann, Albert, Panousis, Con, Maas, Coen, Renné, Thomas

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Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding von Schott, B H, Assmann, A, Schmierer, P, Soch, J, Erk, S, Garbusow, M, Mohnke, S, Pöhland, L, Romanczuk-Seiferth, N, Barman, A, Wüstenberg, T, Haddad, L, Grimm, O, Witt, S, Richter, S, Klein, M, Schütze, H, Mühleisen, T W, Cichon, S, Rietschel, M, Noethen, M M, Tost, H, Gundelfinger, E D, Düzel, E, Heinz, A, Meyer-Lindenberg, A, Seidenbecher, C I, Walter, H

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Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian... von Le Hellard, S, Mühleisen, T W, Djurovic, S, Fernø, J, Ouriaghi, Z, Mattheisen, M, Vasilescu, C, Raeder, M B, Hansen, T, Strohmaier, J, Georgi, A, Brockschmidt, F F, Melle, I, Nenadic, I, Sauer, H, Rietschel, M, Nöthen, M M, Werge, T, Andreassen, O A, Cichon, S, Steen, V M

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Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature von JAMRA, Rami Abou, PHILIPPE, Orianne, MUNNICH, Arnold, STROM, Tim M, REIS, Andre, COLLEAUX, Laurence, RAAS-ROTHSCHILD, Annick, ECK, Sebastian H, GRAF, Elisabeth, BUCHERT, Rebecca, BORCK, Guntram, EKICI, Arif, BROCKSCHMIDT, Felix F, NÖTHEN, Markus M

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Systemic mast cell activation disease: the role of molecular genetic alterations in pathogenesis, heritability and diagnostics von Haenisch, Britta, Nöthen, Markus M., Molderings, Gerhard J.

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