Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 von Sklar, Pamela, Ripke, Stephan, Scott, Laura J, Andreassen, Ole A, Cichon, Sven, Craddock, Nick, Edenberg, Howard J, Nurnberger, John I, Rietschel, Marcella, Blackwood, Douglas, Corvin, Aiden, Flickinger, Matthew, Guan, Weihua, Mattingsdal, Morten, McQuillin, Andrew, Kwan, Phoenix, Wienker, Thomas F, Daly, Mark, Dudbridge, Frank, Holmans, Peter A, Lin, Danyu, Burmeister, Margit, Greenwood, Tiffany A, Hamshere, Marian L, Muglia, Pierandrea, Smith, Erin N, Zandi, Peter P, Nievergelt, Caroline M, McKinney, Rebecca, Shilling, Paul D, Schork, Nicholas J, Bloss, Cinnamon S, Foroud, Tatiana, Koller, Daniel L, Gershon, Elliot S, Liu, Chunyu, Badner, Judith A, Scheftner, William A, Lawson, William B, Nwulia, Evaristus A, Hipolito, Maria, Coryell, William, Rice, John, Byerley, William, McMahon, Francis J, Schulze, Thomas G, Berrettini, Wade, Lohoff, Falk W, Potash, James B, Mahon, Pamela B, McInnis, Melvin G, Zöllner, Sebastian, Zhang, Peng, Craig, David W, Szelinger, Szabocls, Barrett, Thomas B, Breuer, René, Meier, Sandra, Strohmaier, Jana, Witt, Stephanie H, Tozzi, Federica, Farmer, Anne, McGuffin, Peter, Strauss, John, Xu, Wei, Kennedy, James L, Vincent, John B, Matthews, Keith, Day, Richard, Ferreira, Manuel A, O'Dushlaine, Colm, Perlis, Roy, Raychaudhuri, Soumya, Ruderfer, Douglas, Lee, Phil H, Smoller, Jordan W, Li, Jun, Absher, Devin, Bunney, William E, Barchas, Jack D, Schatzberg, Alan F, Jones, Edward G, Meng, Fan, Thompson, Robert C, Watson, Stanley J, Myers, Richard M, Akil, Huda, Boehnke, Michael, Chambert, Kim, Moran, Jennifer, Scolnick, Ed, Djurovic, Srdjan, Melle, Ingrid, Morken, Gunnar, Gill, Michael, Morris, Derek, Quinn, Emma, Mühleisen, Thomas W, Degenhardt, Franziska A, Mattheisen, Manuel

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Expanded Extracolonic Tumor Spectrum in MUTYH -Associated Polyposis von Vogt, Stefanie, Jones, Natalie, Christian, Daria, Engel, Christoph, Nielsen, Maartje, Kaufmann, Astrid, Steinke, Verena, Vasen, Hans F, Propping, Peter, Sampson, Julian R, Hes, Frederik J, Aretz, Stefan

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Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome von ENGEL, Christoph, LOEFFLER, Markus, SCHMIEGEL, Wolff, BUETTNER, Reinhard, MOESLEIN, Gabriela, LETTEBOER, Tom G. W, GOMEZ GARCIA, Encarna, HES, Frederik J, HOOGERBRUGGE, Nicoline, MENKO, Fred H, VAN OS, Theo A. M, SIJMONS, Rolf H, STEINKE, Verena, WAGNER, Anja, KLUIJT, Irma, PROPPING, Peter, VASEN, Hans F. A, RAHNER, Nils, HOLINSKI-FEDER, Elke, DIETMAIER, Wolfgang, SCHACKERT, Hans K, GOERGENS, Heike, VON KNEBEL DOEBERITZ, Magnus, GOECKE, Timm O

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Activating ERBB2/HER2 mutations indicate susceptibility to pan-HER inhibitors in Lynch and Lynch-like colorectal cancer von Kloth, Michael, Ruesseler, Vanessa, Engel, Christoph, Koenig, Katharina, Peifer, Martin, Mariotti, Erika, Kuenstlinger, Helen, Florin, Alexandra, Rommerscheidt-Fuss, Ursula, Koitzsch, Ulrike, Wodtke, Claudia, Ueckeroth, Frank, Holzapfel, Stefanie, Aretz, Stefan, Propping, Peter, Loeffler, Markus, Merkelbach-Bruse, Sabine, Odenthal, Margarete, Friedrichs, Nicolaus, Heukamp, Lukas Carl, Zander, Thomas, Buettner, Reinhard

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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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Genetic Contribution to Variation in Cognitive Function: An fMRI Study in Twins von Koten, Jan Willem Jr, Wood, Guilherme, Hagoort, Peter, Goebel, Rainer, Propping, Peter, Willmes, Klaus, Boomsma, Dorret I

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High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome von Aretz, Stefan, Stienen, Dietlinde, Uhlhaas, Siegfried, Loff, Steffan, Back, Walter, Pagenstecher, Constanze, McLeod, D. Ross, Graham, Gail E., Mangold, Elisabeth, Santer, René, Propping, Peter, Friedl, Waltraut

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Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin von Carrai, Maura, Steinke, Verena, Vodicka, Pavel, Pardini, Barbara, Rahner, Nils, Holinski-Feder, Elke, Morak, Monika, Schackert, Hans K, Görgens, Heike, Stemmler, Susanne, Betz, Beate, Kloor, Matthias, Engel, Christoph, Büttner, Reinhard, Naccarati, Alessio, Vodickova, Ludmila, Novotny, Jan, Stein, Angelika, Hemminki, Kari, Propping, Peter, Försti, Asta, Canzian, Federico, Barale, Roberto, Campa, Daniele

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Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia von Schumacher, Johannes, Anthoni, Heidi, Dahdouh, Faten, König, Inke R., Hillmer, Axel M., Kluck, Nadine, Manthey, Malou, Plume, Ellen, Warnke, Andreas, Remschmidt, Helmut, Hülsmann, Jutta, Cichon, Sven, Lindgren, Cecilia M., Propping, Peter, Zucchelli, Marco, Ziegler, Andreas, Peyrard-Janvid, Myriam, Schulte-Körne, Gerd, Nöthen, Markus M., Kere, Juha

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Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder von Segurado, Ricardo, Detera-Wadleigh, Sevilla D., Levinson, Douglas F., Lewis, Cathryn M., Gill, Michael, Nurnberger, John I., Craddock, Nick, DePaulo, J. Raymond, Baron, Miron, Gershon, Elliot S., Ekholm, Jenny, Cichon, Sven, Turecki, Gustavo, Claes, Stephan, Kelsoe, John R., Schofield, Peter R., Badenhop, Renee F., Morissette, J., Coon, Hilary, Blackwood, Douglas, McInnes, L. Alison, Foroud, Tatiana, Edenberg, Howard J., Reich, Theodore, Rice, John P., Goate, Alison, McInnis, Melvin G., McMahon, Francis J., Badner, Judith A., Goldin, Lynn R., Bennett, Phil, Willour, Virginia L., Zandi, Peter P., Liu, Jianjun, Gilliam, Conrad, Juo, Suh-Hang, Berrettini, Wade H., Yoshikawa, Takeo, Peltonen, Leena, Lönnqvist, Jouko, Nöthen, Markus M., Schumacher, Johannes, Windemuth, Christine, Rietschel, Marcella, Propping, Peter, Maier, Wolfgang, Alda, Martin, Grof, Paul, Rouleau, Guy A., Del-Favero, Jurgen, Van Broeckhoven, Christine, Mendlewicz, Julien, Adolfsson, Rolf, Spence, M. Anne, Luebbert, Hermann, Adams, Linda J., Donald, Jennifer A., Mitchell, Philip B., Barden, Nicholas, Shink, Eric, Byerley, William, Muir, Walter, Visscher, Peter M., Macgregor, Stuart, Gurling, Hugh, Kalsi, Gursharan, McQuillin, Andrew, Escamilla, Michael A., Reus, Victor I., Leon, Pedro, Freimer, Nelson B., Ewald, Henrik, Kruse, Torben A., Mors, Ole, Radhakrishna, Uppala, Blouin, Jean-Louis, Antonarakis, Stylianos E., Akarsu, Nurten

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Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia von Hillmer, Axel M., Hanneken, Sandra, Ritzmann, Sibylle, Becker, Tim, Freudenberg, Jan, Brockschmidt, Felix F., Flaquer, Antonia, Freudenberg-Hua, Yun, Jamra, Rami Abou, Metzen, Christine, Heyn, Uwe, Schweiger, Nadine, Betz, Regina C., Blaumeiser, Bettina, Hampe, Jochen, Schreiber, Stefan, Schulze, Thomas G., Hennies, Hans Christian, Schumacher, Johannes, Propping, Peter, Ruzicka, Thomas, Cichon, Sven, Wienker, Thomas F., Kruse, Roland, Nöthen, Markus M.

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A Potassium Channel Mutation in Neonatal Human Epilepsy von Biervert, Christian, Schroeder, Björn C., Kubisch, Christian, Berkovic, Samuel F., Propping, Peter, Jentsch, Thomas J., Steinlein, Ortrud K.

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Genotype-Phenotype Comparison of German MLH1 and MSH2 Mutation Carriers Clinically Affected With Lynch Syndrome: A Report by the German HNPCC Consortium von GOECKE, Timm, SCHULMANN, Karsten, DIETMAIER, Wolfgang, MANGOLD, Elisabeth, FRIEDRICHS, Nicolaus, PROPPING, Peter, KRÜGER, Stefan, GEBERT, Johannes, SCHMIEGEL, Wolff, RUESCHOFF, Josef, LOEFFLER, Markus, MOESLEIN, Gabriela, ENGEL, Christoph, HOLINSKI-FEDER, Eike, PAGENSTECHER, Constanze, SCHACKERT, Hans K, KLOOR, Matthias, KUNSTMANN, Erdmute, VOGELSANG, Holger, KELLER, Gisela

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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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Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies von Hardt, Karin, Heick, Sven Boris, Betz, Beate, Goecke, Timm, Yazdanparast, Haniyeh, Küppers, Robin, Servan, Kati, Steinke, Verena, Rahner, Nils, Morak, Monika, Holinski-Feder, Elke, Engel, Christoph, Möslein, Gabriela, Schackert, Hans-Konrad, von Knebel Doeberitz, Magnus, Pox, Christian, Hegemann, Johannes H., Royer-Pokora, Brigitte

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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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Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants von PAGENSTECHER, Constanze, WEHNER, Maria, MANGOLD, Elisabeth, FRIEDL, Waltraut, RAHNER, Nils, ARETZ, Stefan, FRIEDRICHS, Nicolaus, SENGTELLER, Marlies, HENN, Wolfram, BUETTNER, Reinhard, PROPPING, Peter

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CLCN2 variants in idiopathic generalized epilepsy von Propping, Peter, Fahlke, Christoph, Friedl, Waltraut, Schulz, Herbert, Alekov, Alexi, Lerche, Holger, Sander, Thomas, Kleefuß-Lie, Ailing, Maljevic, Snezana, Rebstock, Johannes, Ramirez, Alfredo, Cichon, Sven, Horvath, Steve, Rau, Birgit, Dullinger, Jörn S, Haverkamp, Fritz, Giese, Bernd, Elger, Christian E, Warnstedt, Maike, Beyenburg, Stefan, Hallmann, Kerstin, Hebeisen, Simon, Poser, Barbara, Kubisch, Christian, Haug, Karsten, Janz, Dieter, Müller-Newen, Gerhard

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Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in MSH2 and MLH1 genes von Wang, Yaping, Friedl, Waltraut, Lamberti, Christof, Jungck, Matthias, Mathiak, Micaela, Pagenstecher, Constanze, Propping, Peter, Mangold, Elisabeth

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