Epigenetic association with environmental risk factors for mental disorders von Le Hellard, S.

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Genome-wide association studies in psychiatry: Current perspectives von Smajlagic, D., Zayats, T., Bekkehus, M., Le Hellard, S.

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Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population von Thomson, P A, Wray, N R, Millar, J K, Evans, K L, Hellard, S Le, Condie, A, Muir, W J, Blackwood, D H R, Porteous, D J

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Association between the insulin-induced gene 2 ( ) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis... von Le Hellard, S, Theisen, F M, Haberhausen, M, Raeder, M B, Fernø, J, Gebhardt, S, Hinney, A, Remschmidt, H, Krieg, J C, Mehler-Wex, C, Nöthen, M M, Hebebrand, J, Steen, V M

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Convergence of linkage, association and GWAS findings for a candidate region for bipolar disorder and schizophrenia on chromosome 4p von Christoforou, A, McGhee, K A, Morris, S W, Thomson, P A, Anderson, S, McLean, A, Torrance, H S, Le Hellard, S, Pickard, B S, StClair, D, Muir, W J, Blackwood, D H, Porteous, D J, Evans, K L

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Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian... von Le Hellard, S, Mühleisen, T W, Djurovic, S, Fernø, J, Ouriaghi, Z, Mattheisen, M, Vasilescu, C, Raeder, M B, Hansen, T, Strohmaier, J, Georgi, A, Brockschmidt, F F, Melle, I, Nenadic, I, Sauer, H, Rietschel, M, Nöthen, M M, Werge, T, Andreassen, O A, Cichon, S, Steen, V M

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How Mutations in the nAChRs Can Cause ADNFLE Epilepsy von Bertrand, D., Picard, F., Le Hellard, S., Weiland, S., Favre, I., Phillips, H., Bertrand, S., Berkovic, S. F., Malafosse, A., Mulley, J.

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GWAS‐based pathway analysis differentiates between fluid and crystallized intelligence von Christoforou, A., Espeseth, T., Davies, G., Fernandes, C. P. D., Giddaluru, S., Mattheisen, M., Tenesa, A., Harris, S. E., Liewald, D. C., Payton, A., Ollier, W., Horan, M., Pendleton, N., Haggarty, P., Djurovic, S., Herms, S., Hoffman, P., Cichon, S., Starr, J. M., Lundervold, A., Reinvang, I., Steen, V. M., Deary, I. J., Le Hellard, S.

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No association of primary Sjögren’s syndrome with Fcγ receptor gene variants von Haldorsen, K, Appel, S, Le Hellard, S, Bruland, O, Brun, J G, Omdal, R, Kristjansdottir, G, Theander, E, Fernandes, C P D, Kvarnström, M, Eriksson, P, Rönnblom, L, Herlenius, M W, Nordmark, G, Jonsson, R, Bolstad, A I

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Association analysis of the chromosome 4p15-p16 candidate region for bipolar disorder and schizophrenia von Christoforou, A, Le Hellard, S, Thomson, P A, Morris, S W, Tenesa, A, Pickard, B S, Wray, N R, Muir, W J, Blackwood, D H, Porteous, D J, Evans, K L

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Psychotic patients who used cannabis frequently before illness onset have higher genetic predisposition to schizophrenia than those who did not von Aas, M., Melle, I., Bettella, F., Djurovic, S., Le Hellard, S., Bjella, T., Ringen, P. A., Lagerberg, T. V., Smeland, O. B., Agartz, I., Andreassen, O. A., Tesli, M.

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Association analysis of the chromosome 4p-located G protein-coupled receptor 78 (GPR78) gene in bipolar affective disorder and schizophrenia von Underwood, S L, Christoforou, A, Thomson, P A, Wray, N R, Tenesa, A, Whittaker, J, Adams, R A, Le Hellard, S, Morris, S W, Blackwood, D H R, Muir, W J, Porteous, D J, Evans, K L

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A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE) von Djurovic, S, Kähler, A.K, Kulle, B, Jönsson, E.G, Agartz, I, Le Hellard, S, Hall, H, Jakobsen, K.D, Hansen, T, Melle, I, Werge, T, Steen, V.M, Andreassen, O.A

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Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder von Hughes, Timothy, Sønderby, Ida E., Polushina, Tatiana, Hansson, Lars, Holmgren, Asbjørn, Athanasiu, Lavinia, Melbø-Jørgensen, Christian, Hassani, Sahar, Hoeffding, Louise K., Herms, Stefan, Bergen, Sarah E., Karlsson, Robert, Song, Jie, Rietschel, Marcella, Nöthen, Markus M., Forstner, Andreas J., Hoffmann, Per, Hultman, Christina M., Landén, Mikael, Cichon, Sven, Werge, Thomas, Andreassen, Ole A., Le Hellard, Stephanie, Djurovic, Srdjan

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Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population von Thomson, P A, Wray, N R, Millar, J K, Evans, K L, Le Hellard, S, Condie, A, Muir, W J, Blackwood, D H R, Porteous, D J

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Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins von Hill, W D, Davies, G, van de Lagemaat, L N, Christoforou, A, Marioni, R E, Fernandes, C P D, Liewald, D C, Croning, M D R, Payton, A, Craig, L C A, Whalley, L J, Horan, M, Ollier, W, Hansell, N K, Wright, M J, Martin, N G, Montgomery, G W, Steen, V M, Le Hellard, S, Espeseth, T, Lundervold, A J, Reinvang, I, Starr, J M, Pendleton, N, Grant, S G N, Bates, T C, Deary, I J

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SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis von Le Hellard, Stéphanie, Ballereau, Stéphane J., Visscher, Peter M., Torrance, Helen S., Pinson, Jeni, Morris, Stewart W., Thomson, Marian L., Semple, Colin A. M., Muir, Walter J., Blackwood, Douglas H. R., Porteous, David J., Evans, Kathryn L.

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Circadian clock gene variants and insomnia, sleepiness, and shift work disorder von Thun, Eirunn, Le Hellard, S., Osland, T. M., Bjorvatn, B., Moen, B. E., Magerøy, N., Steen, V. M., Giddaluru, S., Brattbakk, H.-R., Pallesen, S.

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Genome-wide association studies establish that human intelligence is highly heritable and polygenic von Davies, G, Tenesa, A, Payton, A, Yang, J, Harris, S E, Liewald, D, Ke, X, Le Hellard, S, Christoforou, A, Luciano, M, McGhee, K, Lopez, L, Gow, A J, Corley, J, Redmond, P, Fox, H C, Haggarty, P, Whalley, L J, McNeill, G, Goddard, M E, Espeseth, T, Lundervold, A J, Reinvang, I, Pickles, A, Steen, V M, Ollier, W, Porteous, D J, Horan, M, Starr, J M, Pendleton, N, Visscher, P M, Deary, I J

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GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium von Trampush, J W, Yang, M L Z, Yu, J, Knowles, E, Davies, G, Liewald, D C, Starr, J M, Djurovic, S, Melle, I, Sundet, K, Christoforou, A, Reinvang, I, DeRosse, P, Lundervold, A J, Steen, V M, Espeseth, T, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Giegling, I, Konte, B, Roussos, P, Giakoumaki, S, Burdick, K E, Payton, A, Ollier, W, Horan, M, Chiba-Falek, O, Attix, D K, Need, A C, Cirulli, E T, Voineskos, A N, Stefanis, N C, Avramopoulos, D, Hatzimanolis, A, Arking, D E, Smyrnis, N, Bilder, R M, Freimer, N A, Cannon, T D, London, E, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M A, Dickinson, D, Straub, R E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, D R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, M C, Andreassen, O A, Deary, I J, Glahn, D C, Malhotra, A K, Lencz, T

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