Genome-wide association study reveals two new risk loci for bipolar disorder by Mühleisen, Thomas W., Leber, Markus, Schulze, Thomas G., Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Forstner, Andreas J., Schumacher, Johannes, Breuer, René, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, André, Witt, Stephanie H., Reif, Andreas, Müller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne, Priebe, Lutz, Czerski, Piotr M., Hauser, Joanna, Lissowska, Jolanta, Szeszenia-Dabrowska, Neonila, Brennan, Paul, McKay, James D., Wright, Adam, Mitchell, Philip B., Fullerton, Janice M., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Krasnow, Valery, Chuchalin, Alexander, Babadjanova, Gulja, Pantelejeva, Galina, Abramova, Lilia I., Tiganov, Alexander S., Polonikov, Alexey, Khusnutdinova, Elza, Alda, Martin, Grof, Paul, Rouleau, Guy A., Turecki, Gustavo, Laprise, Catherine, Rivas, Fabio, Mayoral, Fermin, Kogevinas, Manolis, Grigoroiu-Serbanescu, Maria, Propping, Peter, Becker, Tim, Rietschel, Marcella, Nöthen, Markus M., Cichon, Sven

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Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study by Campa, Daniele, Pardini, Barbara, Naccarati, Alessio, Vodickova, Ludmila, Novotny, Jan, Steinke, Verena, Rahner, Nils, Holinski-Feder, Elke, Morak, Monika, Schackert, Hans K, Görgens, Heike, Kötting, Judith, Betz, Beate, Kloor, Matthias, Engel, Christoph, Büttner, Reinhard, Propping, Peter, Försti, Asta, Hemminki, Kari, Barale, Roberto, Vodicka, Pavel, Canzian, Federico

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Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder by Hou, Liping, Bergen, Sarah E, Akula, Nirmala, Song, Jie, Hultman, Christina M, Landén, Mikael, Adli, Mazda, Alda, Martin, Ardau, Raffaella, Arias, Bárbara, Aubry, Jean-Michel, Backlund, Lena, Badner, Judith A, Barrett, Thomas B, Bauer, Michael, Baune, Bernhard T, Bellivier, Frank, Benabarre, Antonio, Bengesser, Susanne, Berrettini, Wade H, Bhattacharjee, Abesh Kumar, Biernacka, Joanna M, Birner, Armin, Bloss, Cinnamon S, Brichant-Petitjean, Clara, Bui, Elise T, Byerley, William, Cervantes, Pablo, Chillotti, Caterina, Cichon, Sven, Colom, Francesc, Coryell, William, Craig, David W, Cruceanu, Cristiana, Czerski, Piotr M, Davis, Tony, Dayer, Alexandre, Degenhardt, Franziska, Del Zompo, Maria, DePaulo, J Raymond, Edenberg, Howard J, Étain, Bruno, Falkai, Peter, Foroud, Tatiana, Forstner, Andreas J, Frisén, Louise, Frye, Mark A, Fullerton, Janice M, Gard, Sébastien, Garnham, Julie S, Gershon, Elliot S, Goes, Fernando S, Greenwood, Tiffany A, Grigoroiu-Serbanescu, Maria, Hauser, Joanna, Heilbronner, Urs, Heilmann-Heimbach, Stefanie, Herms, Stefan, Hipolito, Maria, Hitturlingappa, Shashi, Hoffmann, Per, Hofmann, Andrea, Jamain, Stephane, Jiménez, Esther, Kahn, Jean-Pierre, Kassem, Layla, Kelsoe, John R, Kittel-Schneider, Sarah, Kliwicki, Sebastian, Koller, Daniel L, König, Barbara, Lackner, Nina, Laje, Gonzalo, Lang, Maren, Lavebratt, Catharina, Lawson, William B, Leboyer, Marion, Leckband, Susan G, Liu, Chunyu, Maaser, Anna, Mahon, Pamela B, Maier, Wolfgang, Maj, Mario, Manchia, Mirko, Martinsson, Lina, McCarthy, Michael J, McElroy, Susan L, McInnis, Melvin G, McKinney, Rebecca, Mitchell, Philip B, Mitjans, Marina, Mondimore, Francis M, Monteleone, Palmiero, Mühleisen, Thomas W, Nievergelt, Caroline M, Nöthen, Markus M, Novák, Tomas, Nurnberger, Jr, John I, Nwulia, Evaristus A, Ösby, Urban

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Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder by Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miró, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Alexander, Michael, Vollmer, Jennifer, Breuer, René, Schmäl, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H.-Erich, Schreiber, Stefan, Müller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon, Hamshere, Marian, O'Donovan, Michael C., Owen, Michael J., Craddock, Nick, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Reif, Andreas, Sasse, Johanna, Bauer, Michael, Hautzinger, Martin, Wright, Adam, Mitchell, Philip B., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Gustafsson, Omar, Andreassen, Ole, Djurovic, Srdjan, Sigurdsson, Engilbert, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Kapur-Pojskic, Lejla, Oruc, Liliana, Rivas, Fabio, Mayoral, Fermín, Chuchalin, Alexander, Babadjanova, Gulja, Tiganov, Alexander S., Pantelejeva, Galina, Abramova, Lilia I., Grigoroiu-Serbanescu, Maria, Diaconu, Carmen C., Czerski, Piotr M., Hauser, Joanna, Zimmer, Andreas, Lathrop, Mark, Schulze, Thomas G., Wienker, Thomas F., Schumacher, Johannes, Maier, Wolfgang, Propping, Peter, Rietschel, Marcella, Nöthen, Markus M.

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From degeneration to genetic susceptibility, from eugenics to genethics, from Bezugsziffer to LOD score: the history of psychiatric genetics by Schulze, Thomas G., Fangerau, Heiner, Propping, Peter

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The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders by Chang, H, Hoshina, N, Zhang, C, Ma, Y, Cao, H, Wang, Y, Wu, D-d, Bergen, S E, Landén, M, Hultman, C M, Preisig, M, Kutalik, Z, Castelao, E, Grigoroiu-Serbanescu, M, Forstner, A J, Strohmaier, J, Hecker, J, Schulze, T G, Müller-Myhsok, B, Reif, A, Mitchell, P B, Martin, N G, Schofield, P R, Cichon, S, Nöthen, M M, Walter, H, Erk, S, Heinz, A, Amin, N, van Duijn, C M, Meyer-Lindenberg, A, Tost, H, Xiao, X, Yamamoto, T, Rietschel, M, Li, M

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MUTYH‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype by Aretz, Stefan, Uhlhaas, Siegfried, Goergens, Heike, Siberg, Kirsten, Vogel, Matthias, Pagenstecher, Constanze, Mangold, Elisabeth, Caspari, Reiner, Propping, Peter, Friedl, Waltraut

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Monoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteers by Jönsson, Erik G, Bah, Jessica, Melke, Jonas, Abou Jamra, Rami, Schumacher, Johannes, Westberg, Lars, Ivo, Roland, Cichon, Sven, Propping, Peter, Nöthen, Markus M, Eriksson, Elias, Sedvall, Göran C

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Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP) by Aretz, Stefan, Stienen, Dietlinde, Friedrichs, Nicolaus, Stemmler, Susanne, Uhlhaas, Siegfried, Rahner, Nils, Propping, Peter, Friedl, Waltraut

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The biography of psychiatric genetics: From early achievements to historical burden, from an anxious society to critical geneticists by Propping, Peter

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Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response by Fabbri, Chiara, Hosak, Ladislav, Mössner, Rainald, Giegling, Ina, Mandelli, Laura, Bellivier, Frank, Claes, Stephan, Collier, David A., Corrales, Alejo, Delisi, Lynn E., Gallo, Carla, Gill, Michael, Kennedy, James L., Leboyer, Marion, Lisoway, Amanda, Maier, Wolfgang, Marquez, Miguel, Massat, Isabelle, Mors, Ole, Muglia, Pierandrea, Nöthen, Markus M., O'Donovan, Michael C., Ospina-Duque, Jorge, Propping, Peter, Shi, Yongyong, St Clair, David, Thibaut, Florence, Cichon, Sven, Mendlewicz, Julien, Rujescu, Dan, Serretti, Alessandro

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Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmona... by Luo, Xiong-Jian, Mattheisen, Manuel, Li, Ming, Huang, Liang, Rietschel, Marcella, Børglum, Anders D, Als, Thomas D, van den Oord, Edwin J, Aberg, Karolina A, Mors, Ole, Mortensen, Preben Bo, Luo, Zhenwu, Degenhardt, Franziska, Cichon, Sven, Schulze, Thomas G, Nöthen, Markus M, Su, Bing, Zhao, Zhongming, Gan, Lin, Yao, Yong-Gang

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Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome by Steinke, Verena, Engel, Christoph, Büttner, Reinhard, Schackert, Hans Konrad, Schmiegel, Wolff H, Propping, Peter

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A Gene for Hypotrichosis Simplex of the Scalp Maps to Chromosome 6p21.3 by Betz, Regina C., Lee, Young-Ae, Bygum, Anette, Brandrup, Flemming, Bernal, Ana I., Toribio, Jaime, Alvarez, J. Ignacio, Kukuk, Guido M., Ibsen, Hans Henning W., Rasmussen, Hanne B., Wienker, Thomas F., Reis, André, Propping, Peter, Kruse, Roland, Cichon, Sven, Nöthen, Markus M.

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Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility by Li, Ming, Wang, Yi, Zheng, Xue-bin, Ikeda, Masashi, Iwata, Nakao, Luo, Xiong-jian, Chong, Siow-Ann, Lee, Jimmy, Rietschel, Marcella, Zhang, Fengyu, Müller-Myhsok, Bertram, Cichon, Sven, Weinberger, Daniel R, Mattheisen, Manuel, Schulze, Thomas G, Martin, Nicholas G, Mitchell, Philip B, Schofield, Peter R, Liu, Jian-jun, Su, Bing

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Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q by McQueen, Matthew B., Devlin, B., Faraone, Stephen V., Nimgaonkar, Vishwajit L., Sklar, Pamela, Smoller, Jordan W., Abou Jamra, Rami, Albus, Margot, Bacanu, Silviu-Alin, Baron, Miron, Barrett, Thomas B., Berrettini, Wade, Blacker, Deborah, Byerley, William, Cichon, Sven, Coryell, Willam, Craddock, Nick, Daly, Mark J., DePaulo, J. Raymond, Edenberg, Howard J., Foroud, Tatiana, Gill, Michael, Gilliam, T. Conrad, Hamshere, Marian, Jones, Ian, Jones, Lisa, Juo, Suh-Hang, Kelsoe, John R., Lambert, David, Lange, Christoph, Lerer, Bernard, Liu, Jianjun, Maier, Wolfgang, MacKinnon, James D., McInnis, Melvin G., McMahon, Francis J., Murphy, Dennis L., Nöthen, Markus M., Nurnberger, John I., Pato, Carlos N., Pato, Michele T., Potash, James B., Propping, Peter, Pulver, Ann E., Rice, John P., Rietschel, Marcella, Scheftner, William, Schumacher, Johannes, Segurado, Ricardo, Van Steen, Kristel, Xie, Weiting, Zandi, Peter P., Laird, Nan M.

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ISPG lifetime achievement award 2004 by Propping, Peter

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Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutation... by Aretz, Stefan, Koch, Arend, Uhlhaas, Siegfried, Friedl, Waltraut, Propping, Peter, Schweinitz, Dietrich von, Pietsch, Torsten

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Assisted reproduction: an important review of the literature on the risk of malformation after in vitro fertilization and intracytoplasmic sperm injection by Propping, Peter

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Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3 by Yang, Rongxi, Chen, Bowang, Pfütze, Katrin, Buch, Stephan, Steinke, Verena, Holinski-Feder, Elke, Stöcker, Sarah, von Schönfels, Witigo, Becker, Thomas, Schackert, Hans K, Royer-Pokora, Brigitte, Kloor, Matthias, Schmiegel, Wolff H, Büttner, Reinhard, Engel, Christoph, Lascorz Puertolas, Jesus, Försti, Asta, Kunkel, Nelli, Bugert, Peter, Schreiber, Stefan, Krawczak, Michael, Schafmayer, Clemens, Propping, Peter, Hampe, Jochen, Hemminki, Kari, Burwinkel, Barbara

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