The differential associations of positive and negative symptoms with suicidality by Grover, Laura E., Jones, Rebecca, Bass, Nicholas J., McQuillin, Andrew

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Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD by Patel, Kejal H. S., Walters, G. Bragi, Stefánsson, Hreinn, Stefánsson, Kári, Degenhardt, Franziska, Nothen, Markus, Van Der Veen, Tracey, Demontis, Ditte, Borglum, Anders, Kristiansen, Mark, Bass, Nicholas J., McQuillin, Andrew

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Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease by Jones, Lesley, Holmans, Peter A, Hamshere, Marian L, Harold, Denise, Moskvina, Valentina, Ivanov, Dobril, Pocklington, Andrew, Abraham, Richard, Hollingworth, Paul, Sims, Rebecca, Gerrish, Amy, Pahwa, Jaspreet Singh, Jones, Nicola, Stretton, Alexandra, Morgan, Angharad R, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K, Brayne, Carol, Rubinsztein, David C, Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S, Passmore, Peter A, Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A David, Love, Seth, Kehoe, Patrick G, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Schürmann, Britta, Heun, Reinhard, Kölsch, Heike, van den Bussche, Hendrik, Heuser, Isabella, Peters, Oliver, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M, Kauwe, John S K, Cruchaga, Carlos, Nowotny, Petra, Morris, John C, Mayo, Kevin, Livingston, Gill, Bass, Nicholas J, Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panos, Al-Chalabi, Ammar, Shaw, Christopher E, Singleton, Andrew B, Guerreiro, Rita, Mühleisen, Thomas W, Nöthen, Markus M, Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H-Erich, Rüther, Eckhard, Carrasquillo, Minerva M, Pankratz, V Shane, Younkin, Steven G, Hardy, John, O'Donovan, Michael C, Owen, Michael J, Williams, Julie

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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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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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Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia by Al Eissa, Mariam M., Fiorentino, Alessia, Sharp, Sally I., O'Brien, Niamh L., Wolfe, Kate, Giaroli, Giovanni, Curtis, David, Bass, Nicholas J., McQuillin, Andrew

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Genetic association and functional characterization of MCPH1 gene variation in bipolar disorder and schizophrenia by Al Eissa, Mariam M., Sharp, Sally I., O'Brien, Niamh L., Fiorentino, Alessia, Bass, Nicholas J., Curtis, David, McQuillin, Andrew

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Polygenic risk and hazard scores for Alzheimer's disease prediction by Leonenko, Ganna, Sims, Rebecca, Shoai, Maryam, Frizzati, Aura, Bossù, Paola, Spalletta, Gianfranco, Fox, Nick C., Williams, Julie, Hardy, John, Escott‐Price, Valentina

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Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia by Leonenko, Ganna, Richards, Alexander L., Walters, James T., Pocklington, Andrew, Chambert, Kimberly, Al Eissa, Mariam M., Sharp, Sally I., O'Brien, Niamh L., Curtis, David, Bass, Nicholas J., McQuillin, Andrew, Hultman, Christina, Moran, Jennifer L., McCarroll, Steven A., Sklar, Pamela, Neale, Benjamin M., Holmans, Peter A., Owen, Michael J., Sullivan, Patrick F., O'Donovan, Michael C.

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Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample by MCQUILLIN, Andrew, BASS, Nicholas, ANJORIN, Adebayo, LAWRENCE, Jacob, KANDASWAMY, Radhika, LYDALL, Greg, MORAN, Jennifer, SKLAR, Pamela, PURCELL, Shaun, GURLING, Hugh

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Evidence for the association of the DAOA (G72) gene with schizophrenia and bipolar disorder but not for the association of the DAO gene with schizophrenia by Bass, Nicholas J, Datta, Susmita R, McQuillin, Andrew, Puri, Vinay, Choudhury, Khalid, Thirumalai, Srinivasa, Lawrence, Jacob, Quested, Digby, Pimm, Jonathan, Curtis, David, Gurling, Hugh Md

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A Genetic Association Study of Chromosome 11q22-24 in Two Different Samples Implicates the FXYD6 Gene, Encoding Phosphohippolin, in Susceptibility to Schizophrenia by Choudhury, Khalid, McQuillin, Andrew, Puri, Vinay, Pimm, Jonathan, Datta, Susmita, Thirumalai, Srinivasa, Krasucki, Robert, Lawrence, Jacob, Bass, Nicholas J., Quested, Digby, Crombie, Caroline, Fraser, Gillian, Walker, Nicholas, Nadeem, Haitham, Johnson, Sophie, Curtis, David, St. Clair, David, Gurling, Hugh M.D.

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The Epsin 4 Gene on Chromosome 5q, Which Encodes the Clathrin-Associated Protein Enthoprotin, Is Involved in the Genetic Susceptibility to Schizophrenia by Pimm, Jonathan, McQuillin, Andrew, Thirumalai, Srinivasa, Lawrence, Jacob, Quested, Digby, Bass, Nicholas, Lamb, Graham, Moorey, Helen, Datta, Susmita R., Kalsi, Gursharan, Badacsonyi, Allison, Kelly, Katie, Morgan, Jenny, Punukollu, Bhaskar, Curtis, David, Gurling, Hugh

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No evidence that extended tracts of homozygosity are associated with Alzheimer's disease by Sims, Rebecca, Dwyer, Sarah, Harold, Denise, Gerrish, Amy, Hollingworth, Paul, Chapman, Jade, Jones, Nicola, Abraham, Richard, Ivanov, Dobril, Pahwa, Jaspreet Singh, Moskvina, Valentina, Dowzell, Kimberley, Thomas, Charlene, Stretton, Alexandra, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuiness, Bernadette, Todd, Stephen, Johnston, Janet A., Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Jones, Lesley, Holmans, Peter A., O'Donovan, Michael, Owen, Michael J., Williams, Julie

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Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors by Andreassen, Ole A., Djurovic, Srdjan, Thompson, Wesley K., Schork, Andrew J., Kendler, Kenneth S., O’Donovan, Michael C., Rujescu, Dan, Werge, Thomas, van de Bunt, Martijn, Morris, Andrew P., McCarthy, Mark I., Roddey, J. Cooper, McEvoy, Linda K., Desikan, Rahul S., Dale, Anders M.

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F27. NORTH THAMES GENOMIC MEDICINE SERVICE ALLIANCE LOCAL TRANSFORMATION PROJECT: EMBEDDING GENOMIC MEDICINE IN MENTAL HEALTH SERVICES - A PILOT PROJECT IN INTELLECTUAL DISABILITY... by Bass, Nicholas, Ryves, Paul, Trim, Corinne, Faravelli, Francesca, Raheem, Ali, Ambreen, Asma, Gaynair, Niah, Mikova, Jana, Nelson, Sanjay, Eady, Nicole

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Does rare matter? Copy number variants at 16p11.2 and the risk of psychosis: A systematic review of literature and meta-analysis by Giaroli, Giovanni, Bass, Nicholas, Strydom, Andre, Rantell, Khadijia, McQuillin, Andrew

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Common polygenic variation enhances risk prediction for Alzheimer's disease by Escott-Price, Valentina, Sims, Rebecca, Bannister, Christian, Harold, Denise, Vronskaya, Maria, Majounie, Elisa, Badarinarayan, Nandini, Morgan, Kevin, Passmore, Peter, Holmes, Clive, Powell, John, Brayne, Carol, Gill, Michael, Mead, Simon, Goate, Alison, Cruchaga, Carlos, Lambert, Jean-Charles, van Duijn, Cornelia, Maier, Wolfgang, Ramirez, Alfredo, Holmans, Peter, Jones, Lesley, Hardy, John, Seshadri, Sudha, Schellenberg, Gerard D, Amouyel, Philippe, Williams, Julie

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Identification of the Slynar Gene (AY070435) and Related Brain Expressed Sequences as a Candidate Gene for Susceptibility to Affective Disorders Through Allelic and Haplotypic Asso... by Kalsi, Gursharan, McQuillin, Andrew, Degn, Birte, Lundorf, Mikkel D., Bass, Nicholas J., Lawrence, Jacob, Choudhury, Khalid, Puri, Vinay, Nyegaard, Mette, Curtis, David, Mors, Ole, Kruse, Torben, Kerwin, Simon, Gurling, Hugh

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A novel Alzheimer disease locus located near the gene encoding tau protein by Jun, G, Ibrahim-Verbaas, C A, Lambert, J-C, Chung, J, Naj, A C, Kunkle, B W, Wang, L-S, Bis, J C, Bellenguez, C, Harold, D, Lunetta, K L, Grenier-Boley, B, Sims, R, Chouraki, V, Hamilton-Nelson, K L, Denning, N, Martin, E R, Schmidt, H, Valladares, O, Laza, A R, Zelenika, D, Ramirez, A, Foroud, T M, Choi, S-H, Boland, A, Becker, T, Kukull, W A, van der Lee, S J, Pasquier, F, Cruchaga, C, Beekly, D, Fitzpatrick, A L, Hanon, O, Gill, M, Barber, R, Gudnason, V, Campion, D, Love, S, Bennett, D A, Amin, N, Berr, C, Tsolaki, Magda, Buxbaum, J D, Lopez, O L, Deramecourt, V, Fox, N C, Cantwell, L B, Dufouil, C, Hardy, J, Crane, P K, Eiriksdottir, G, Hannequin, D, Clarke, R, Evans, D, Mosley, Jr, T H, Letenneur, L, Brayne, C, Maier, W, De Jager, P, Hampel, H, Kamboh, M I, de Bruijn, R F A G, Tzourio, C, Pastor, P, Larson, E B, O'Donovan, M C, Montine, T J, Nalls, M A, Mead, S, Reiman, E M, Jonsson, P V, Holmes, C, St George-Hyslop, P H, Boada, M, Wendland, J R, Schmidt, R, Morgan, K, Winslow, A R, Carasquillo, M, Younkin, S G, Jakobsdóttir, J, Wilhelmsen, K C, Rujescu, D, Nöthen, M M, Hofman, A, Jones, L, Psaty, B M, Van Broeckhoven, C, Launer, L J, Mayeux, R, Lathrop, M, Goate, A M, Escott-Price, V, Seshadri, S, Pericak-Vance, M A, Amouyel, P, Williams, J, van Duijn, C M, Schellenberg, G D, Farrer, L A

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