Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1 von Xu, Wei, Cohen-Woods, Sarah, Chen, Qian, Noor, Abdul, Knight, Jo, Hosang, Georgina, Parikh, Sagar V, De Luca, Vincenzo, Tozzi, Federica, Muglia, Pierandrea, Forte, Julia, McQuillin, Andrew, Hu, Pingzhao, Gurling, Hugh M D, Kennedy, James L, McGuffin, Peter, Farmer, Anne, Strauss, John, Vincent, John B

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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 von 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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Genetics of attention-deficit hyperactivity disorder (ADHD) von Sharp, Sally I., McQuillin, Andrew, Gurling, Hugh M.D.

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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 von Guerrini, Irene, Cook, Christopher C H, Kest, Wendy, Devitgh, Audrey, McQuillin, Andrew, Curtis, David, Gurling, Hugh M D

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Genetic association of the tachykinin receptor 1 TACR1 gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndrome von Sharp, Sally I., McQuillin, Andrew, Marks, Michael, Hunt, Stephen P., Stanford, S. Clare, Lydall, Greg J., Morgan, Marsha Y., Asherson, Philip, Curtis, David, Gurling, Hugh M. D.

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Genetic Association, Mutation Screening, and Functional Analysis of a Kozak Sequence Variant in the Metabotropic Glutamate Receptor 3 Gene in Bipolar Disorder von Kandaswamy, Radhika, McQuillin, Andrew, Sharp, Sally I, Fiorentino, Alessia, Anjorin, Adebayo, Blizard, Robert A, Curtis, David, Gurling, Hugh M. D

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Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia von Datta, Susmita R, McQuillin, Andrew, Puri, Vinay, Choudhury, Khalid, Thirumalai, Srinivasa, Lawrence, Jacob, Pimm, Jonathan, Bass, Nicholas, Lamb, Graham, Moorey, Helen, Morgan, Jenny, Punukollu, Bhaskar, Kandasami, Gomathinayagam, Kirwin, Simon, Sule, Akeem, Quested, Digby, Curtis, David, Gurling, Hugh Md

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Mutations in the Gabrb1 gene promote alcohol consumption through increased tonic inhibition von Anstee, Quentin M., Knapp, Susanne, Maguire, Edward P., Hosie, Alastair M., Thomas, Philip, Mortensen, Martin, Bhome, Rohan, Martinez, Alonso, Walker, Sophie E., Dixon, Claire I., Ruparelia, Kush, Montagnese, Sara, Kuo, Yu-Ting, Herlihy, Amy, Bell, Jimmy D., Robinson, Iain, Guerrini, Irene, McQuillin, Andrew, Fisher, Elizabeth M.C., Ungless, Mark A., Gurling, Hugh M.D., Morgan, Marsha Y., Brown, Steve D.M., Stephens, David N., Belelli, Delia, Lambert, Jeremy J., Smart, Trevor G., Thomas, Howard C.

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Genetic variants in or near ADH1B and ADH1C affect susceptibility to alcohol dependence in a British and Irish population von Way, Michael, McQuillin, Andrew, Saini, Jit, Ruparelia, Kush, Lydall, Gregory J., Guerrini, Irene, Ball, David, Smith, Iain, Quadri, Giorgia, Thomson, Allan D., Kasiakogia-Worlley, Katherine, Cherian, Raquin, Gunwardena, Priyanthi, Rao, Harish, Kottalgi, Girija, Patel, Shamir, Hillman, Audrey, Douglas, Ewen, Qureshi, Sherhzad Y., Reynolds, Gerry, Jauhar, Sameer, O'Kane, Aideen, Dedman, Alex, Sharp, Sally, Kandaswamy, Radhika, Dar, Karim, Curtis, David, Morgan, Marsha Y., Gurling, Hugh M. D.

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Support of association between BRD1 and both schizophrenia and bipolar affective disorder von Nyegaard, Mette, Severinsen, Jacob E., Als, Thomas D., Hedemand, Anne, Straarup, Steen, Nordentoft, Merete, McQuillin, Andrew, Bass, Nicholas, Lawrence, Jacob, Thirumalai, Srinivasa, Pereira, Ana C.P., Kandaswamy, Radhika, Lydall, Gregory J., Sklar, Pamela, Scolnick, Edward, Purcell, Shaun, Curtis, David, Gurling, Hugh M.D., Mortensen, Preben B., Mors, Ole, Børglum, Anders D.

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Genetic variant analysis of the putative regulatory regions of the LRRC7 gene in bipolar disorder von Fiorentino, Alessia, Sharp, Sally I, Kandaswamy, Radhika, Gurling, Hugh M D, Bass, Nicholas J, McQuillin, Andrew

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Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder von Lydall, Gregory John, Bass, Nicholas J, McQuillin, Andrew, Lawrence, Jacob, Anjorin, Adebayo, Kandaswamy, Radhika, Pereira, Ana, Guerrini, Irene, Curtis, David, Vine, Anna E, Sklar, Pamela, Purcell, Shaun M, Gurling, Hugh Malcolm Douglas

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The effect of clozapine on mRNA expression for genes encoding G protein-coupled receptors and the protein components of clathrin-mediated endocytosis von Sharp, Sally I, Hu, Ying, Weymer, Jon F, Rizig, Mie, McQuillin, Andrew, Hunt, Stephen P, Gurling, Hugh M.D

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Mutation screening of X-chromosomal neuroligin genes: No mutations in 196 autism probands von Vincent, John B., Kolozsvari, Debbie, Roberts, Wendy S., Bolton, Patrick F., Gurling, Hugh M.D., Scherer, Stephen W.

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Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome von Petek, Erwin, Schwarzbraun, Thomas, Noor, Abdul, Patel, Megha, Nakabayashi, Kazuhiko, Choufani, Sanaa, Windpassinger, Christian, Stamenkovic, Mara, Robertson, Mary M, Aschauer, Harald N, Gurling, Hugh M. D, Kroisel, Peter M, Wagner, Klaus, Scherer, Stephen W, Vincent, John B

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Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-... von Blaveri, E, Kalsi, G, Lawrence, J, Quested, D, Moorey, H, Lamb, G, Kohen, D, Shiwach, R, Chowdhury, U, Curtis, D, McQuillin, A, Gramoustianou, E S, Gurling, H M

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Genetic association of the tachykinin receptor 1 TACR1 gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndrome von Sharp, Sally I, McQuillin, Andrew, Marks, Michael, Hunt, Stephen P, Stanford, S Clare, Lydall, Greg J, Morgan, Marsha Y, Asherson, Philip, 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 von 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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Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS) von Guerrini, Irene, Thomson, Allan D., Cook, Cristopher C.H., McQuillin, Andrew, Sharma, Vishal, Kopelman, Michael, Reynolds, Gerald, Jauhar, Pramod, Harper, Clive, Gurling, Hugh M.D.

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Two microsatellite polymorphisms at the D5S39 locus von MANKOO, B. S, SHERRINGTON, R, DE LA CONCHA, A, KALSI, G, CURTIS, D, MELMER, G, GURLING, H. M. D

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