Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia von Ruderfer, D M, Fanous, A H, Ripke, S, McQuillin, A, Amdur, R L, Gejman, P V, O'Donovan, M C, Andreassen, O A, Djurovic, S, Hultman, C M, Kelsoe, J R, Jamain, S, Landén, M, Leboyer, M, Nimgaonkar, V, Nurnberger, J, Smoller, J W, Craddock, N, Corvin, A, Sullivan, P F, Holmans, P, Sklar, P, Kendler, K S

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Whole-genome association study of bipolar disorder von Sklar, P, Smoller, J W, Fan, J, Ferreira, M A R, Perlis, R H, Chambert, K, Nimgaonkar, V L, McQueen, M B, Faraone, S V, Kirby, A, de Bakker, P I W, Ogdie, M N, Thase, M E, Sachs, G S, Todd-Brown, K, Gabriel, S B, Sougnez, C, Gates, C, Blumenstiel, B, Defelice, M, Ardlie, K G, Franklin, J, Muir, W J, McGhee, K A, MacIntyre, D J, McLean, A, VanBeck, M, McQuillin, A, Bass, N J, Robinson, M, Lawrence, J, Anjorin, A, Curtis, D, Scolnick, E M, Daly, M J, Blackwood, D H, Gurling, H M, Purcell, S M

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Prevalence of attention deficit hyperactivity disorder symptoms in patients with schizophrenia von Arican, I., Bass, N., Neelam, K., Wolfe, K., McQuillin, A., Giaroli, G.

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Rare chromosomal deletions and duplications increase risk of schizophrenia von 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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DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder von Hennah, W, Thomson, P, McQuillin, A, Bass, N, Loukola, A, Anjorin, A, Blackwood, D, Curtis, D, Deary, I J, Harris, S E, Isometsä, E T, Lawrence, J, Lönnqvist, J, Muir, W, Palotie, A, Partonen, T, Paunio, T, Pylkkö, E, Robinson, M, Soronen, P, Suominen, K, Suvisaari, J, Thirumalai, S, Clair, D St, Gurling, H, Peltonen, L, Porteous, D

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Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder von Jia, Xiaoming, Goes, Fernando S., Locke, Adam E., Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U., Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M., Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Gonçalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Chapman, Sinéad, DelaBastide, Melissa, Juréus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z., Levy, Shawn E., Monson, Eric T., Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zöllner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick, DiFlorio, Arianna, Hultman, Christina M., Landen, Mikael, Lewis, Cathryn, McCarroll, Steven A., Richard McCombie, W., McGuffin, Peter, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, Myers, Richard M., O’Donovan, Michael, Ophoff, Roel, Boks, Marco, Kahn, Rene, Ouwehand, Willem, Owen, Michael, Pato, Carlos, Pato, Michele, Posthuma, Danielle, Potash, James B., Reif, Andreas, Sklar, Pamela, Smoller, Jordan, Sullivan, Patrick F., Vincent, John, Walters, James, Neale, Benjamin, Purcell, Shaun, Risch, Neil, Schaefer, Catherine, Stahl, Eli A., Zandi, Peter P., Scott, Laura J.

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Drinking behaviour and rs738409:G in PNPLA3 are associated with slower recovery of liver function following severe alcoholic hepatitis von Atkinson, S.R, Way, M.J, McQuillin, A, Morgan, M.Y, Thursz, M.R

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Genome-wide association study of Alzheimer's disease with psychotic symptoms von Hollingworth, P, Sweet, R, Sims, R, Harold, D, Russo, G, Abraham, R, Stretton, A, Jones, N, Gerrish, A, Chapman, J, Ivanov, D, Moskvina, V, Lovestone, S, Priotsi, P, Lupton, M, Brayne, C, Gill, M, Lawlor, B, Lynch, A, Craig, D, McGuinness, B, Johnston, J, Holmes, C, Livingston, G, Bass, N J, Gurling, H, McQuillin, A, Holmans, P, Jones, L, Devlin, B, Klei, L, Barmada, M M, Demirci, F Y, DeKosky, S T, Lopez, O L, Passmore, P, Owen, M J, O'Donovan, M C, Mayeux, R, Kamboh, M I, Williams, J

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Meta-analysis of 32 genome-wide linkage studies of schizophrenia von Ng, M Y M, Levinson, D F, Faraone, S V, Suarez, B K, DeLisi, L E, Arinami, T, Riley, B, Paunio, T, Pulver, A E, Irmansyah, Holmans, P A, Escamilla, M, Wildenauer, D B, Williams, N M, Laurent, C, Mowry, B J, Brzustowicz, L M, Maziade, M, Sklar, P, Garver, D L, Abecasis, G R, Lerer, B, Fallin, M D, Gurling, H M D, Gejman, P V, Lindholm, E, Moises, H W, Byerley, W, Wijsman, E M, Forabosco, P, Tsuang, M T, Hwu, H-G, Okazaki, Y, Kendler, K S, Wormley, B, Fanous, A, Walsh, D, O'Neill, F A, Peltonen, L, Nestadt, G, Lasseter, V K, Liang, K Y, Papadimitriou, G M, Dikeos, D G, Schwab, S G, Owen, M J, O'Donovan, M C, Norton, N, Hare, E, Raventos, H, Nicolini, H, Albus, M, Maier, W, Nimgaonkar, V L, Terenius, L, Mallet, J, Jay, M, Godard, S, Nertney, D, Alexander, M, Crowe, R R, Silverman, J M, Bassett, A S, Roy, M-A, Mérette, C, Pato, C N, Pato, M T, Roos, J Louw, Kohn, Y, Amann-Zalcenstein, D, Kalsi, G, McQuillin, A, Curtis, D, Brynjolfson, J, Sigmundsson, T, Petursson, H, Sanders, A R, Duan, J, Jazin, E, Myles-Worsley, M, Karayiorgou, M, Lewis, C M

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Rare variant analysis in multiply affected families, association studies and functional analysis suggest a role for the ITGΒ4 gene in schizophrenia and bipolar disorder von O'Brien, N.L., Fiorentino, A., Curtis, D., Rayner, C., Petrosellini, C., Al Eissa, M., Bass, N.J., McQuillin, A., Sharp, S.I.

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Variations in the Promoter Region of the Glutaminase Gene and the Development of Hepatic Encephalopathy in Patients with Cirrhosis von Goh, E.T, Way, M.J, Atkinson, S.R, McQuillin, A, Morgan, M.Y

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A Genome-Wide Association Study Identifies PNPLA3 and SLC38A4 as Risk Loci for Alcoholic Hepatitis von Atkinson, S, Way, M, McQuillin, A, Morgan, M, Thursz, M

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Case-control studies show that a non-conservative amino-acid change from a glutamine to arginine in the P2RX7 purinergic receptor protein is associated with both bipolar- and unipo... von McQuillin, A, Bass, N J, Choudhury, K, Puri, V, Kosmin, M, Lawrence, J, Curtis, D, Gurling, H M D

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Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder von Lescai, F, Als, T D, Li, Q, Nyegaard, M, Andorsdottir, G, Biskopstø, M, Hedemand, A, Fiorentino, A, O'Brien, N, Jarram, A, Liang, J, Grove, J, Pallesen, J, Eickhardt, E, Mattheisen, M, Bolund, L, Demontis, D, Wang, A G, McQuillin, A, Mors, O, Wang, J, Børglum, A D

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P1123 : A functional variant in TM6SF2 associates with alcohol-related cirrhosis risk in a British and Irish population von Way, M.J, Atkinson, S, McQuillin, A, Thursz, M.R, Morgan, M.Y

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Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to S... von Gurling, Hugh M.D., Kalsi, Gursharan, Brynjolfson, Jon, Sigmundsson, Thordur, Sherrington, Robin, Mankoo, Baljinder S., Read, Timothy, Murphy, Patrice, Blaveri, Ekaterina, McQuillin, Andrew, Petursson, Hannes, Curtis, David

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CACNA1C hypermethylation is associated with bipolar disorder von Starnawska, A, Demontis, D, Pen, A, Hedemand, A, Nielsen, A L, Staunstrup, N H, Grove, J, Als, T D, Jarram, A, O'Brien, N L, Mors, O, McQuillin, A, Børglum, A D, Nyegaard, M

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1404 THE PNPA3 I148M MUTATION SIGNIFICANTLY INCREASES THE RISK OF DEVELOPING ALCOHOL-RELATED CIRRHOSIS IN ALCOHOL DEPENDENT INDIVIDUALS von Way, M.J, McQuillin, A, Gurling, H.M.D, Morgan, M.Y

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P1121 : Homozygosity for the Ile148Met variant in PNPLA3 is significantly associated with reduced survival following an episode of severe alcoholic hepatitis von Atkinson, S, Way, M, Mellor, J, McQuillin, A, Morgan, M, Thursz, M

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Fine mapping of a susceptibility locus for bipolar and genetically related unipolar affective disorders, to a region containing the C21ORF29 and TRPM2 genes on chromosome 21q22.3 von McQuillin, A, Bass, N J, Kalsi, G, Lawrence, J, Puri, V, Choudhury, K, Detera-Wadleigh, S D, Curtis, D, Gurling, H M D

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