Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder by Yousaf, Afsheen, Waltes, Regina, Haslinger, Denise, Klauck, Sabine M., Duketis, Eftichia, Sachse, Michael, Voran, Anette, Biscaldi, Monica, Schulte-Rüther, Martin, Cichon, Sven, Nöthen, Markus, Ackermann, Jörg, Koch, Ina, Freitag, Christine M., Chiocchetti, Andreas G.

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Sex differences in cognitive domains and their clinical correlates in higher-functioning autism spectrum disorders by Bölte, Sven, Duketis, Eftichia, Poustka, Fritz, Holtmann, Martin

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Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder by Moser, Gerhard, Agartz, Ingrid, Andreassen, Ole A., Anjorin, Adebayo, Bass, Nicholas, Bergen, Sarah E., Betancur, Catalina, Black, Donald W., Bloss, Cinnamon S., Buxbaum, Joseph D., Cantor, Rita M., Cormand, Bru, Coryell, William H., Craig, Ian W., Crosbie, Jennifer, Djurovic, Srdjan, Ebstein, Richard P., Etain, Bruno, Faraone, Stephen V., Farmer, Anne E., Ferrier, I. Nicol, Fombonne, Eric, Frank, Josef, Franke, Barbara, Freitag, Christine M., Friedl, Marion, Gershon, Elliot S., Gill, Michael, Gordon, Scott D., Green, Elaine K., De Haan, Lieuwe, Haines, Jonathan L., Hakonarson, Hakon, Hallmayer, Joachim, Hamilton, Steven P., Hamshere, Marian L., Hoogendijk, Witte J., Hottenga, Jouke-Jan, Hus, Vanessa, Jamain, Stéphane, Jones, Lisa, Kenny, Elaine, Krabbendam, Lydia, Kuntsi, Jonna, Landén, Mikael, Lesch, Klaus-Peter, Lichtenstein, Paul, Lieberman, Jeffrey A., Linszen, Don H., Loo, Sandra K., Lowe, Jennifer K., Lucae, Susanne, Magnusson, Patrik K.E., Mahon, Pamela B., Martin, Christa L., McGhee, Kevin A., McGuffin, Peter, McInnis, Melvin G., McIntosh, Andrew, McLean, Alan W., McMahon, William M., Meier, Sandra, Meng, Fan, Meyer, Jobst, Middeldorp, Christel M., Miranda, Ana, Montgomery, Grant W., Mühleisen, Thomas W., Neale, Benjamin M., Nyholt, Dale R., O’Donovan, Michael C., Olsen, Line, Penninx, Brenda W., Pergadia, Michele L., Pericak-Vance, Margaret A., Perlis, Roy H., Posthuma, Danielle, Rasmussen, Henrik B., Reif, Andreas, Ribasés, Marta, Rice, John P., Rossin, Lizzy, Sanders, Stephan J., Schachar, Russell, Schellenberg, Gerard D., Schumacher, Johannes, Scott, Laura J., Smalley, Susan L., Smit, Johannes H., Szelinger, Szabocls, Thapar, Anita, Thirumalai, Srinivasa, Treutlein, Jens, Visscher, Peter M., Willemsen, Gonneke, Young, Allan H., Zammit, Stanley, Zitman, Frans G., Potash, James B., Shi, Jianxin

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Genetics of autistic disorders: review and clinical implications by Freitag, Christine M., Staal, Wouter, Klauck, Sabine M., Duketis, Eftichia, Waltes, Regina

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Bipolar disorder in children and adolescents in Germany: national trends in the rates of inpatients, 2000-2007 by Holtmann, Martin, Duketis, Eftichia, Poustka, Luise, Zepf, Florian Daniel, Poustka, Fritz, Bölte, Sven

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Severe affective and behavioral dysregulation in youth is associated with increased serum TSH by Holtmann, Martin, Duketis, Eftichia, Goth, Kirstin, Poustka, Luise, Boelte, Sven

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Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders by Waltes, Regina, Duketis, Eftichia, Knapp, Michael, Anney, Richard J. L., Huguet, Guillaume, Schlitt, Sabine, Jarczok, Tomasz A., Sachse, Michael, Kämpfer, Laura M., Kleinböck, Tina, Poustka, Fritz, Bölte, Sven, Schmötzer, Gabriele, Voran, Anette, Huy, Ellen, Meyer, Jobst, Bourgeron, Thomas, Klauck, Sabine M., Freitag, Christine M., Chiocchetti, Andreas G.

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The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism by Hadley, Dexter, Wu, Zhi-liang, Kao, Charlly, Kini, Akshata, Mohamed-Hadley, Alisha, Thomas, Kelly, Vazquez, Lyam, Qiu, Haijun, Mentch, Frank, Pellegrino, Renata, Kim, Cecilia, Connolly, John, Glessner, Joseph, Hakonarson, Hakon

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Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder by Kranz, Thorsten M., Kopp, Marnie, Waltes, Regina, Sachse, Michael, Duketis, Eftichia, Jarczok, Tomasz A., Degenhardt, Franziska, Görgen, Katharina, Meyer, Jobst, Freitag, Christine M., Chiocchetti, Andreas G.

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A 15q13.3 microdeletion segregating with autism by Pagnamenta, Alistair T, Wing, Kirsty, Sadighi Akha, Elham, Knight, Samantha JL, Bölte, Sven, Schmötzer, Gabriele, Duketis, Eftichia, Poustka, Fritz, Klauck, Sabine M, Poustka, Annemarie, Ragoussis, Jiannis, Bailey, Anthony J, Monaco, Anthony P

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Lack of replication of previous autism spectrum disorder GWAS hits in European populations by Torrico, Bàrbara, Chiocchetti, Andreas G., Bacchelli, Elena, Trabetti, Elisabetta, Hervás, Amaia, Franke, Barbara, Buitelaar, Jan K., Rommelse, Nanda, Yousaf, Afsheen, Duketis, Eftichia, Freitag, Christine M., Caballero‐Andaluz, Rafaela, Martinez‐Mir, Amalia, Scholl, Francisco G., Ribasés, Marta, Battaglia, Agatino, Malerba, Giovanni, Delorme, Richard, Benabou, Marion, Maestrini, Elena, Bourgeron, Thomas, Cormand, Bru, Toma, Claudio

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Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities by Chiocchetti, Andreas G., Yousaf, Afsheen, Bour, Hannah S., Haslinger, Denise, Waltes, Regina, Duketis, Eftichia, Jarczok, Tomas, Sachse, Michael, Biscaldi, Monica, Degenhardt, Franziska, Herms, Stefan, Cichon, Sven, Ackermann, Jörg, Koch, Ina, Klauck, Sabine M., Freitag, Christine M.

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Pilot evaluation of the Frankfurt Social Skills Training for children and adolescents with autism spectrum disorder by Herbrecht, Evelyn, Poustka, Fritz, Birnkammer, Sabine, Duketis, Eftichia, Schlitt, Sabine, Schmötzer, Gabriele, Bölte, Sven

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A genome-wide linkage and association scan reveals novel loci for autism by Arking, Dan E, Weiss, Lauren A

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SPECIFIC ASD PHENOTYPES ARE MODULATED BY DISTINCT GENETIC VARIANTS CONVERGING AT NETWORK LEVEL by Chiocchetti, Andreas G., Waltes, Regina, Haslinger, Denise, Lindlar, Silvia, Klauck, Sabine, Duketis, Eftichia, Sachse, Michael, Voran, Anette, Biscaldi, Monica, Schulte-Rüther, Martin, Kupferschmid, Stephan, Cichon, Sven, Nöthen, Markus, Ackermann, Jörg, Koch, Ina, Freitag, Christine M.

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T8. GLUTAMATERGIC SIGNALLING AND AUTISM: A FAMILY BASED ASSOCIATION STUDY ON THE GLUTAMATERGIC NEUROTRANSMITTER SYSTEM by Freitag, Christine M., Yousaf, Afsheen, Bour, Hannah, Haslinger, Denise, Duketis, Eftichia, Jarczok, Tomasz, Sachse, Michael, Voran, Anette, Biscaldi-Schäfer, Monika, Kupferschmid, Stefan, Schulte-Rüther, Michael, Degenhard, Franziska, Herms, Stefan, Cichon, Sven, Koch, Ina, Anney, Ric, Chiocchetti, Andreas

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M14 - SPECIFIC ASD PHENOTYPES ARE MODULATED BY DISTINCT GENETIC VARIANTS CONVERGING AT NETWORK LEVEL by Chiocchetti, Andreas G., Waltes, Regina, Haslinger, Denise, Lindlar, Silvia, Klauck, Sabine, Duketis, Eftichia, Sachse, Michael, Voran, Anette, Biscaldi, Monica, Schulte-Rüther, Martin, Kupferschmid, Stephan, Cichon, Sven, Nöthen, Markus, Ackermann, Jörg, Koch, Ina, Freitag, Christine M.

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Validation of the Hypomania Checklist (HCL-32) in a nonclinical sample of German adolescents by Holtmann, Martin, Pörtner, Franca, Duketis, Eftichia, Flechtner, Hans-Henning, Angst, Jules, Lehmkuhl, Gerd

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Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders by Anney, Richard J L, Kenny, Elaine M, O'Dushlaine, Colm, Yaspan, Brian L, Parkhomenka, Elena, Buxbaum, Joseph D, Sutcliffe, James, Gill, Michael, Gallagher, Louise

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No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder by Curran, Sarah, Bolton, Patrick, Rozsnyai, Kinga, Chiocchetti, Andreas, Klauck, Sabine M., Duketis, Eftichia, Poustka, Fritz, Schlitt, Sabine, Freitag, Christine M., Lee, Irene, Muglia, Pierandrea, Poot, Martin, Staal, Wouter, de Jonge, Maretha V., Ophoff, Roel A., Lewis, Cathryn, Skuse, David, Mandy, Will, Vassos, Evangelos, Fossdal, Ragnheidur, Magnusson, Páll, Hreidarsson, Stefan, Saemundsen, Evald, Stefansson, Hreinn, Stefansson, Kari, Collier, David

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