W41. VERBAL MEMORY AS A PSYCHOSIS ENDOPHENOTYPE: A GENOME-WIDE ASSOCIATION STUDY IN AN ANCESTRALLY DIVERSE SAMPLE OF ADOLESCENTS by Wang, Baihan, Kuchenbäcker, Karoline, McQuillin, Andrew, Giannakopoulou, Olga, Austin-Zimmerman, Isabelle, Irizar, Haritz, Harju-Seppanen, Jasmine, Zartaloudi, Eirini, Bhat, Anjali, Lam, Chor Lai, Lumer, Estella, Bramon, Elvira

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W66. JOINT EFFECTS OF CYP2C19 OR CYP2D6 GENETIC VARIATION AND PSYCHOTROPIC DRUGS ON THE QT INTERVAL by Zartaloudi, Eirini, Lam, Chor Lai, Bhat, Anjali, Wang, Baihan, Austin-Zimmerman, Isabelle, Irizar, Haritz, Harju-Seppanen, Jasmine, McQuillin, Andrew, Wronska, Marta, Lumer, Estella, Kuchenbaecker, Karoline, Bramon, Elvira

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TH67. THE INFLUENCE OF CYP2D6 AND CYP2C19 GENETIC VARIATION ON DIABETES MELLITUS RISK IN PEOPLE TAKING ANTIDEPRESSANTS AND ANTIPSYCHOTICS by Austin-Zimmerman, Isabelle, Wronska, Marta, Wang, Baihan, Irizar, Haritz, Thygesen, Johan Hilge, Bhat, Anjali, Harju-Seppanen, Jasmine, Giannakopoulou, Olga, Kuchenbaecker, Karoline, Zartaloudi, Eirini, McQuillin, Andrew, Bramon, Elvira

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Genetic variation in the miR-708 gene and its binding targets in bipolar disorder by Fiorentino, Alessia, O'Brien, Niamh Louise, Sharp, Sally Isabel, Curtis, David, Bass, Nicholas James, McQuillin, Andrew

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Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders by Andlauer, Till F. M., Guzman-Parra, Jose, Streit, Fabian, Strohmaier, Jana, González, Maria José, Gil Flores, Susana, Cabaleiro Fabeiro, Francisco J., del Río Noriega, Francisco, Perez, Fermin Perez, Haro González, Jesus, Orozco Diaz, Guillermo, de Diego-Otero, Yolanda, Moreno-Küstner, Berta, Auburger, Georg, Degenhardt, Franziska, Heilmann-Heimbach, Stefanie, Herms, Stefan, Hoffmann, Per, Frank, Josef, Foo, Jerome C., Treutlein, Jens, Witt, Stephanie H., Cichon, Sven, Kogevinas, Manolis, Rivas, Fabio, Mayoral, Fermín, Müller-Myhsok, Bertram, Forstner, Andreas J., Nöthen, Markus M., Rietschel, Marcella

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67 - GENOME-WIDE ASSOCIATION STUDY OF SUICIDE ATTEMPT IN MAJOR PSYCHIATRIC DISORDERS by Mullins, Niamh, Bigdeli, Tim, Power, Robert, McQuillin, Andrew, Stahl, Eli, Mehta, Divya, Lewis, Cathryn

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F130EXOME SEQUENCE ANALYSIS IDENTIFY RARE GENETIC VARIANT IMPLICATED IN SUSCEPTIBILITY TO SCHIZOPHRENIA by Aleissa, Mariam, Bass, Nicholas, McQuillin, Andrew, Sharp, Sally, Fiorentino, Alessia, O'Brien, Niamh, Curtis, David

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M23 - GENETIC ASSOCIATION AND FUNCTIONAL CHARACTERIZATION OF A VARIANT IN THE MCPH1 GENE IN BIPOLAR DISORDER AND SCHIZOPHRENIA by Aleissa, Mariam, Sharp, Sally, Fiorentino, Alessia, O'Brien, Niamh, Bass, Nicholas, Curtis, David, McQuillin, Andrew

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GENOME-WIDE ASSOCIATION STUDY OF SUICIDE ATTEMPT IN MAJOR PSYCHIATRIC DISORDERS by Mullins, Niamh, Bigdeli, Tim, Power, Robert, McQuillin, Andrew, Stahl, Eli, Mehta, Divya, Lewis, Cathryn

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GENETIC ASSOCIATION AND FUNCTIONAL CHARACTERIZATION OF A VARIANT IN THE MCPH1 GENE IN BIPOLAR DISORDER AND SCHIZOPHRENIA by Aleissa, Mariam, Sharp, Sally, Fiorentino, Alessia, O'Brien, Niamh, Bass, Nicholas, Curtis, David, McQuillin, Andrew

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T103. LINKING PSYCHOSIS POLYGENIC RISK SCORES (PRS) AND CNV BURDEN WITH COGNITIVE FUNCTIONING ENDOPHENOTYPES by Cotic, Marius, Varney, Lauren, Lau, Robin, Wang, Baihan, Khani, Noushin Saadullah, Richards-Belle, Alvin, Zartaloudi, Eirini, Austin-Zimmerman, Isabelle, McQuillin, Andrew, PEIC (Psychosis Endophenotypes International Consortium), Thygesen, Johan, Irizar, Aritz, Bramon, Elvira

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STATE-OF-THE-ART OF GENETIC TESTING, COUNSELLING AND TRAINING IN PSYCHIATRY IN EUROPE: OPPORTUNITIES AND PITFALLS OF THE IMPLEMENTATION OF PSYCHIATRIC GENETICS IN MEDICAL PRACTICE by Koido, Kati, Ingvoldstad-Malmgren, Charlotta, Pojskic, Lejla, Soller, Maria Johansson, Van Assche, Evelien, Borg, Isabella, Jensen, Uffe Birk, Members of EnGagE, Coviello, Domenico, Rietschel, Marcella, Grigoroiu-Serbanescu, Maria, McQuillin, Andrew, Degenhardt, Franziska, Tammimies, Kristiina, Chaumette, Boris

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Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders by Thygesen, Johan H., Wolfe, Kate, McQuillin, Andrew, Viñas-Jornet, Marina, Baena, Neus, Brison, Nathalie, D'Haenens, Greet, Esteba-Castillo, Susanna, Gabau, Elisabeth, Ribas-Vidal, Núria, Ruiz, Anna, Vermeesch, Joris, Weyts, Eddy, Novell, Ramon, Buggenhout, Griet Van, Strydom, André, Bass, Nick, Guitart, Miriam, Vogels, Annick

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Predictive power of the ADHD GWAS 2019 polygenic risk scores in independent samples of bipolar patients with childhood ADHD by Grigoroiu-Serbanescu, Maria, Giaroli, Giovanni, Thygesen, Johan H., Shenyan, Oris, Bigdeli, Tim B., Bass, Nicholas J., Diaconu, Carmen C., Neagu, Ana Iulia, Forstner, Andreas J., Degenhardt, Franziska, Herms, Stefan, Nöthen, Markus M., McQuillin, Andrew

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Genetic linkage analysis supports the presence of two susceptibility loci for alcoholism and heavy drinking on chromosome 1p22.1-11.2 and 1q21.3-24.2 by Guerrini, Irene, Cook, Christopher C H, Kest, Wendy, Devitgh, Audrey, McQuillin, Andrew, Curtis, David, Gurling, Hugh M D

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Psychosis Endophenotypes: A Gene-Set-Specific Polygenic Risk Score Analysis by Wang, Baihan, Irizar, Haritz, Thygesen, Johan H, Zartaloudi, Eirini, Austin-Zimmerman, Isabelle, Bhat, Anjali, Harju-Seppänen, Jasmine, Pain, Oliver, Bass, Nick, Gkofa, Vasiliki, Alizadeh, Behrooz Z, van Amelsvoort, Therese, Arranz, Maria J, Bender, Stephan, Cahn, Wiepke, Stella Calafato, Maria, Crespo-Facorro, Benedicto, Di Forti, Marta, Giegling, Ina, de Haan, Lieuwe, Hall, Jeremy, Hall, Mei-Hua, van Haren, Neeltje, Iyegbe, Conrad, Kahn, René S, Kravariti, Eugenia, Lawrie, Stephen M, Lin, Kuang, Luykx, Jurjen J, Mata, Ignacio, McDonald, Colm, McIntosh, Andrew M, Murray, Robin M, Picchioni, Marco, Powell, John, Prata, Diana P, Rujescu, Dan, Rutten, Bart P F, Shaikh, Madiha, Simons, Claudia J P, Toulopoulou, Timothea, Weisbrod, Matthias, van Winkel, Ruud, Kuchenbaecker, Karoline, McQuillin, Andrew, Bramon, Elvira

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EXOME SEQUENCING IN BIPOLAR DISORDER REVEALS SHARED RISK GENE AKAP11 WITH SCHIZOPHRENIA by Palmer, Duncan, Howrigan, Daniel, Adolfsson, Rolf, Blackwood, Douglas, Corvin, Aiden, Florio, Arianna Di, Dickerson, Faith, Goes, Fernando, Landen, Mikael, McQuillin, Andrew, Ophoff, Roel, Reif, Andreas, Smoller, Jordan, Zandi, Peter, Neale, Benjamin

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Genetic Testing in Intellectual Disability Psychiatry: Opinions and Practices of UK Child and Intellectual Disability Psychiatrists by Wolfe, Kate, Stueber, Kerstin, McQuillin, Andrew, Jichi, Fatima, Patch, Christine, Flinter, Frances, Strydom, André, Bass, Nick

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SLC19A1 Genetic Variation Leads to Altered Thiamine Diphosphate Transport: Implications for the Risk of Developing Wernicke–Korsakoff’s Syndrome by O’Brien, Niamh L, Quadri, Giorgia, Lightley, Iain, Sharp, Sally I, Guerrini, Irene, Smith, Iain, Heydtmann, Mathis, Morgan, Marsha Y, Thomson, Allan D, Bass, Nicholas J, McHugh, Patrick C, McQuillin, Andrew

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Whole-genome sequence-based analysis of thyroid function by Taylor, Peter N., Porcu, Eleonora, Chew, Shelby, Campbell, Purdey J., Traglia, Michela, Brown, Suzanne J., Mullin, Benjamin H., Shihab, Hashem A., Min, Josine, Walter, Klaudia, Memari, Yasin, Huang, Jie, Barnes, Michael R., Beilby, John P., Charoen, Pimphen, Danecek, Petr, Dudbridge, Frank, Forgetta, Vincenzo, Greenwood, Celia, Grundberg, Elin, Johnson, Andrew D., Hui, Jennie, Lim, Ee M., McCarthy, Shane, Muddyman, Dawn, Panicker, Vijay, Perry, John R.B., Bell, Jordana T., Yuan, Wei, Relton, Caroline, Gaunt, Tom, Schlessinger, David, Abecasis, Goncalo, Cucca, Francesco, Surdulescu, Gabriela L., Woltersdorf, Wolfram, Zeggini, Eleftheria, Zheng, Hou-Feng, Toniolo, Daniela, Dayan, Colin M., Naitza, Silvia, Walsh, John P., Spector, Tim, Davey Smith, George, Durbin, Richard, Brent Richards, J., Sanna, Serena, Soranzo, Nicole, Timpson, Nicholas J., Wilson, Scott G.

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