Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression by 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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Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics by Giegling, Ina, Hosak, Ladislav, Mössner, Rainald, Serretti, Alessandro, Bellivier, Frank, Claes, Stephan, Collier, David A., Corrales, Alejo, DeLisi, Lynn E., Gallo, Carla, Gill, Michael, Kennedy, James L., Leboyer, Marion, Maier, Wolfgang, Marquez, Miguel, Massat, Isabelle, Mors, Ole, Muglia, Pierandrea, Nöthen, Markus M., Ospina-Duque, Jorge, Owen, Michael J., Propping, Peter, Shi, YongYong, St Clair, David, Thibaut, Florence, Cichon, Sven, Mendlewicz, Julien, O'Donovan, Michael C., Rujescu, Dan

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Genetic Contribution to Variation in Cognitive Function: An fMRI Study in Twins by 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 by 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 by 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 by 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 by 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 by 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 by Biervert, Christian, Schroeder, Björn C., Kubisch, Christian, Berkovic, Samuel F., Propping, Peter, Jentsch, Thomas J., Steinlein, Ortrud K.

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The power of sample size and homogenous sampling: Association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder by 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... by 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 by 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 by 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 by 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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Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in MSH2 and MLH1 genes by Wang, Yaping, Friedl, Waltraut, Lamberti, Christof, Jungck, Matthias, Mathiak, Micaela, Pagenstecher, Constanze, Propping, Peter, Mangold, Elisabeth

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Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers by FRIEDL, Waltraut, UHLHAAS, Siegfried, WEBER, Ruthild G, PISTORIUS, Steffen, BURGER, Bettina, PROPPING, Peter, SCHULMANN, Karsten, STOLTE, Manfred, LOFF, Steffan, BACK, Walter, MANGOLD, Elisabeth, STERN, Martin, KNAEBEL, Hanns-Peter, SUTTER, Christian

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Update German view of genetic testing by Propping, Peter, Schott, Heinz

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Embryo screening: update German view of genetic testing by Propping, Peter, Schott, Heinz

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An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics by Weiland, Sigrid, Witzemann, Veit, Villarroel, Alfredo, Propping, Peter, Steinlein, Ortrud

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European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset by Mathieu, Flavie, Dizier, Marie-Hélène, Etain, Bruno, Jamain, Stéphane, Rietschel, Marcella, Maier, Wolfgang, Albus, Margot, McKeon, Patrick, Roche, Siobhan, Blackwood, Douglas, Muir, Walter J., Henry, Chantal, Malafosse, Alain, Preisig, Martin, Ferrero, François, Cichon, Sven, Schumacher, Johannes, Ohlraun, Stephanie, Propping, Peter, Abou Jamra, Rami, Schulze, Thomas G., Zelenica, Diana, Charon, Céline, Marusic, Andrej, Dernovsek, Mojca C., Gurling, Hugh, Nöthen, Markus, Lathrop, Mark, Leboyer, Marion, Bellivier, Frank

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