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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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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A microarray gene expression study of the molecular pharmacology of lithium carbonate on mouse brain mRNA to understand the neurobiology of mood stabilization and treatment of bipo... von McQuillin, Andrew, Rizig, Mie, Gurling, Hugh M.D

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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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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 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 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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Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder von Pereira, Ana C. Parente, McQuillin, Andrew, Puri, Vinay, Anjorin, Adebayo, Bass, Nicholas, Kandaswamy, Radhika, Lawrence, Jacob, Curtis, David, Sklar, Pamela, Purcell, Shaun M., Gurling, Hugh M.D.

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Three-dimensional textural analysis of brain images reveals distributed grey-matter abnormalities in schizophrenia von Ganeshan, Balaji, Miles, Kenneth A., Young, Rupert C. D., Chatwin, Christopher R., Gurling, Hugh M. D., Critchley, Hugo 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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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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The importance of alcohol misuse, malnutrition and genetic susceptibility on brain growth and plasticity von Guerrini, Irene, Thomson, Allan D., Gurling, Hugh D.

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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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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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Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes von Curtis, David, Vine, Anna E, McQuillin, Andrew, Bass, Nicholas James, Pereira, Ana, Kandaswamy, Radhika, Lawrence, Jacob, Anjorin, Adebayo, Choudhury, Khalid, Datta, Susmita R, Puri, Vinay, Krasucki, Robert, Pimm, Jonathan, Thirumalai, Srinivasa, Quested, Digby, Gurling, Hugh M D

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A nonconservative amino acid change in the UPF3B gene in a patient with schizophrenia von Szyszka, Paulina, Sharp, Sally I, Dedman, Alexandra, Gurling, Hugh M D, McQuillin, Andrew

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No evidence for excess runs of homozygosity in bipolar disorder von Vine, Anna E, McQuillin, Andrew, Bass, Nicholas J, Pereira, Ana, Kandaswamy, Radhika, Robinson, Michele, Lawrence, Jacob, Anjorin, Adebayo, Sklar, Pamela, Gurling, Hugh M D, Curtis, David

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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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Evidence for genetic susceptibility to the alcohol dependence syndrome from the thiamine transporter 2 gene solute carrier SLC19A3 von Quadri, Giorgia, McQuillin, Andrew, Guerrini, Irene, Thomson, Allan D, Cherian, Raquin, Saini, Jit, Ruparelia, Kush, Lydall, Greg J, Ball, David, Smith, Iain, Way, Michael, Kasiakogia-Worlley, Katherine, Patel, Shamir, Kottalgi, Girija, Gunawardena, Priyanthi, Rao, Harish, Hillman, Audrey, Douglas, Ewen, Qureshi, Sherzhad Y, Reynolds, Gerry, Jauhar, Sameer, O’Kane, Aideen, Sharp, Sally, Kandaswamy, Radhika, Dar, Karim, Curtis, David, Morgan, Marsha Y, Gurling, Hugh M.D

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