Dopamine D2 receptor molecular variant and schizophrenia von Nöthen, MarkusM, Wildenauer, Dieter, Cichon, Sven, Albus, Margot, Maier, Wolfgang, Minges, Jürgen, Lichtermann, Dirk, Bondy, Brigitta, Rietschel, Marcella, Körner, Judith, Fimmers, Rolf, Propping, Peter

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Tourette's syndrome and homozygosity for the dopamine D3 receptor gene von Hebebrand, Johannes, Nöthen, MarkusM, Lehmkuhl, Gerd, Poustka, Fritz, Schmidt, Martin, Propping, Peter, Remschmidt, Helmut, Comings, DavidE, Muhleman, Donn, Dietz, George, Dino, Micaela, Legro, Rick, Gade, Radhika

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5HT 2a receptor T102C polymorphism and schizophrenia von Piers Clifford, C, Nunez, DerekJ.R, Malhotra, AnilK, Goldman, David, Buchanan, Robert, Breier, Alan, Pickar, David, Jönsson, Erik, Nöthen, MarkusM, Bunzel, Roland, Propping, Peter, Sedvall, Göran, Arranz, MariaJ, Lin, Ming-Wei, Powell, John, Kerwin, Robert, Collier, David, Sasaki, Tsukasa, Hattori, Mineko, Fukuda, Rimmei, Kunugi, Hiroshi, Nanko, Shinichiro, Crow, T.J

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5HT2a receptor T102C polymorphism and schizophrenia von Piers Clifford, C, Nunez, DerekJ.R, Malhotra, AnilK, Goldman, David, Buchanan, Robert, Breier, Alan, Pickar, David, Jönsson, Erik, Nöthen, MarkusM, Bunzel, Roland, Propping, Peter, Sedvall, Göran, Arranz, MariaJ, Lin, Ming-Wei, Powell, John, Kerwin, Robert, Collier, David, Sasaki, Tsukasa, Hattori, Mineko, Fukuda, Rimmei, Kunugi, Hiroshi, Nanko, Shinichiro, Crow, T.J

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Polygenic risk for schizophrenia affects working memory and its neural correlates in healthy subjects von Krug, Axel, Dietsche, Bruno, Zöllner, Rebecca, Yüksel, Dilara, Nöthen, Markus M., Forstner, Andreas J., Rietschel, Marcella, Dannlowski, Udo, Baune, Bernhard T., Maier, Robert, Witt, Stephanie H., Kircher, Tilo

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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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Common variation at 10p12.31 near MLLT10 influences meningioma risk von Dobbins, Sara E, Broderick, Peter, Melin, Beatrice, Feychting, Maria, Johansen, Christoffer, Andersson, Ulrika, Brännström, Thomas, Schramm, Johannes, Olver, Bianca, Lloyd, Amy, Ma, Yussanne P, Hosking, Fay J, Lönn, Stefan, Ahlbom, Anders, Henriksson, Roger, Schoemaker, Minouk J, Hepworth, Sarah J, Hoffmann, Per, Mühleisen, Thomas W, Nöthen, Markus M, Moebus, Susanne, Eisele, Lewin, Kosteljanetz, Michael, Muir, Kenneth, Swerdlow, Anthony, Simon, Matthias, Houlston, Richard S

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Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomes von VIERSBACH, R, SCHWANITZ, G, NÖTHEN, M. M

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