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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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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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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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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Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes by Ruderfer, Douglas M., Boocock, James, Stahl, Eli A., Charney, Alexander W., Ori, Anil P.S., Alliey-Rodriguez, Ney, Anjorin, Adebayo, Badner, Judith A., Band, Gavin, Bruggeman, Richard, Buccola, Nancy G., Bumpstead, Suzannah J., Casas, Juan P., Chan, Raymond C.K., Chen, Ronald Y.L., Collier, David A., Cormican, Paul, Craddock, Nicholas, Crowley, James J., Curtis, David, Dannlowski, Udo, Davidson, Michael, Demontis, Ditte, Dronov, Serge, Elvsashagen, Torbjorn, Etain, Bruno, Fan, Chun Chieh, Forty, Liz, Fraser, Christine, Garnham, Julie, Gill, Michael, Gillman, Matthew, Gratten, Jacob, Gwilliam, Rhian, Hammer, Christian, Hansen, Thomas, Henskens, Frans A., Jamain, Stephane, Jankowski, Janusz, Joa, Inge, Julia, Antonio, Kandaswamy, Radhika, Kavanagh, David, Keller, Matthew C., Khrunin, Andrey, Lee, Phil H., Legge, Sophie E., Lencz, Todd, Levinson, Douglas F., Levy, Shawn E., Li, Tao, Lin, Kuang, Macek, Milan, McCarley, Robert W., McGuffin, Peter, McInnis, Melvin G., Meijer, Carin J., Melegh, Bela, Mesholam-Gately, Raquelle I., Myin-Germeys, Inez, Nicodemus, Kristin K., Nimgaonkar, Vishwajit, Nordin, Annelie, Nöthen, Markus M., Van Os, Jim, Owen, Michael J., Palmer, Colin N.A., Palotie, Aarno, Papadimitriou, George N., Pato, Michele T., Perlis, Roy H., Petryshen, Tracey L., Plomin, Robert, Potash, James B., Powell, John, Ramos-Quiroga, Josep Antoni, Rautanen, Anna, Reichenberg, Abraham, Ribases, Marta, Rice, John P., Richards, Alexander L., Ricketts, Michelle, Sanchez-Mora, Cristina, Sanders, Alan R., Schall, Ulrich, Serretti, Alessandro, Sham, Pak C., Straub, Richard E., Strauss, John S., Szatkiewicz, Jin P., Thompson, Robert C., Thorgeirsson, Thorgeir E., Treutlein, Jens, Vedder, Helmut, Wang, Qiang, Wu, Jing Qin, Sullivan, Patrick F., Wray, Naomi R., Sklar, Pamela, Kendler, Kenneth S.

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New insights into the genetic etiology of Alzheimer's disease and related dementias by Amin, Najaf, Naj, Adam C, Grenier-Boley, Benjamin, Boland, Anne, van der Lee, Sven J, Yang, Qiong, de Rojas, Itziar, Yaqub, Amber, Chapuis, Julien, Alarcón-Martín, Emilio, Tsolaki, Anthoula, Antúnez, Carmen, Bailly, Henri, Barral, Sandra, Pastor, Ana Belén, Below, Jennifer E, Benussi, Luisa, Binetti, Giuliano, Boada, Mercè, Bråthen, Geir, Bresner, Catherine, Brodaty, Henry, Brusco, Luis Ignacio, Burholt, Vanessa, Cuccaro, Michael L, Clark, Christopher, Custodero, Carlo, Dalmasso, Maria Carolina, Daniele, Antonio, Debette, Stéphanie, Dichgans, Martin, Escott-Price, Valentina, Ferreira, Catarina B, Fladby, Tormod, Fließbach, Klaus, García-Alberca, Jose Maria, Garcia-Madrona, Sebastian, Garcia-Ribas, Guillermo, Giegling, Ina, Grande, Giulia, Gudnason, Vilmundur, Haapasalo, Annakaisa, Hampel, Harald, Hanon, Olivier, Hardy, John, Harwood, Janet, Hoffmann, Per, Hulsman, Marc, Kilander, Lena, Kornhuber, Johannes, Lage, Carmen, Love, Seth, Löwemark, Malin, Marquié, Marta, Mead, Simon, Medina, Miguel, Mir, Pablo, Mol, Merel, Ngandu, Tiia, Ortega, Gemma, Paolo, Caffarra, Pasquier, Florence, Pastor, Pau, Polak, Thomas, Priller, Josef, Thomassen, Jesper Qvist, Rainero, Innocenzo, Rajabli, Farid, Reinders, Marcel J T, Reitz, Christiane, Rongve, Arvid, Rosende-Roca, Maitée, Rujescu, Dan, Sakka, Paraskevi, Sánchez-Arjona, María Bernal, Sánchez-Valle, Raquel, Scamosci, Michela, Scheltens, Philip, Scherbaum, Norbert, Snijders, Gijsje J L, Spalletta, Gianfranco, Tartan, Juan Pablo, Tárraga, Lluís, Tesí, Niccolo, Traykov, Latchezar, Ulstein, Ingun, van Rooij, Jeroen, van Swieten, John, Vandenberghe, Rik, Wagner, Michael, Wiltfang, Jens, Yannakoulia, Mary, Zulaica, Miren, Sachdev, Perminder, Ikram, M Arfan, de Mendonça, Alexandre, Hort, Jakub, Ingelsson, Martin, Sims, Rebecca, Ruiz, Agustín

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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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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder by Purcell, Shaun M, Wray, Naomi R, Stone, Jennifer L, Visscher, Peter M, O'Donovan, Michael C, Sullivan, Patrick F, Sklar, Pamela

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The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls by de Leeuw, Christiaan A., McQuillin, Andrew, Ripke, Stephan, Trzaskowski, Maciej, Agerbo, Esben, Alliey-Rodriguez, Ney, Andlauer, Till F.M., Awasthi, Swapnil, Badner, Judith A., Bækvad-Hansen, Marie, Bøen, Erlend, Castelao, Enrique, Cerrato, Felecia, Cervantes, Pablo, Colodro-Conde, Lucía, Davies, Gail, Del-Favero, Jurgen, Dumont, Ashley, Fischer, Sascha B., Foo, Jerome C., Forty, Liz, Gordon, Scott D., Green, Melissa J., Grove, Jakob, Hansen, Christine Søholm, Hansen, Thomas F., Heilbronner, Urs, van Hemert, Albert M., Hipolito, Maria, Hoffmann, Per, Holland, Dominic, Jamain, Stéphane, Jansen, Rick, Johnson, Jessica S., de Jong, Simone, Hassan Kiadeh, Farnush Farhadi, Kraft, Julia, Krogh, Jesper, Lawson, William B., Li, Yihan, Maaser, Anna, MacKinnon, Dean F., Mahon, Pamela B., Maier, Robert M., Medland, Sarah E., Mehta, Divya, Mihailov, Evelin, Montgomery, Grant W., Mullins, Niamh, Nyholt, Dale R., Ösby, Urban, Peterson, Roseann E., Pistis, Giorgio, Reinbold, Céline S., Ryu, Euijung, Schoevers, Robert, Schork, Nicholas J., Schulte, Eva C., Shehktman, Tatyana, Streit, Fabian, Thompson, Robert C., Traylor, Matthew, Vedder, Helmut, Viktorin, Alexander, Visscher, Peter M., Watson, Stanley J., Weinsheimer, Shantel Marie, Wu, Yang, Zhang, Peng, Agartz, Ingrid, Backlund, Lena, Bellivier, Frank, Blackwood, Douglas H.R., Domenici, Enrico, Fullerton, Janice M., Goes, Fernando, Hayward, Caroline, Hultman, Christina M., Jones, Ian, Kahn, René S., Kloiber, Stefan, Leboyer, Marion, Li, Qingqin S., Lucae, Susanne, Madden, Pamela A.F., Magnusson, Patrik K., Martin, Nicholas G., Mortensen, Preben Bo, Neale, Benjamin M., Nordentoft, Merete, O'Donovan, Michael C., Pato, Carlos, Pato, Michele T., Penninx, Brenda W.J. H., Posthuma, Danielle, Stefansson, Kari, Vieta, Eduard, Di Florio, Arianna, Ophoff, Roel A., Wray, Naomi R.

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Rare chromosomal deletions and duplications increase risk of schizophrenia by Stone, Jennifer L., O'Donovan, Michael C., Gurling, Hugh, Kirov, George K., Blackwood, Douglas H. R., Corvin, Aiden, Craddock, Nick J., Gill, Michael, Hultman, Christina M., Lichtenstein, Paul, McQuillin, Andrew, Pato, Carlos N., Ruderfer, Douglas M., Owen, Michael J., St Clair, David, Sullivan, Patrick F., Sklar, Pamela, Purcell, Shaun M.

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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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