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

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

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How Mutations in the nAChRs Can Cause ADNFLE Epilepsy by 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 by 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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Nationwide Genomic Study in Denmark Reveals Remarkable Population Homogeneity by Athanasiadis, Georgios, Cheng, Jade Y, Vilhjálmsson, Bjarni J, Jørgensen, Frank G, Als, Thomas D, Le Hellard, Stephanie, Espeseth, Thomas, Sullivan, Patrick F, Hultman, Christina M, Kjærgaard, Peter C, Schierup, Mikkel H, Mailund, Thomas

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Psychotic patients who used cannabis frequently before illness onset have higher genetic predisposition to schizophrenia than those who did not by 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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A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE) by 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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Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes by Stokowy, Tomasz, Polushina, Tatiana, Sønderby, Ida E., Karlsson, Robert, Giddaluru, Sudheer, Le Hellard, Stephanie, Bergen, Sarah E., Sullivan, Patrick F., Andreassen, Ole A., Djurovic, Srdjan, Hultman, Christina M., Steen, Vidar M.

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Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder by 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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A possible genetic association with chronic fatigue in primary Sjögren’s syndrome: a candidate gene study by Norheim, Katrine Brække, Le Hellard, Stephanie, Nordmark, Gunnel, Harboe, Erna, Gøransson, Lasse, Brun, Johan G., Wahren-Herlenius, Marie, Jonsson, Roland, Omdal, Roald

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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 by 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 by 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 by 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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Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE) by Djurovic, Srdjan, Le Hellard, Stephanie, Kähler, Anna K, Jönsson, Erik G, Agartz, Ingrid, Steen, Vidar M, Hall, Håkan, Wang, August G, Rasmussen, Henrik B, Melle, Ingrid, Werge, Thomas, Andreassen, Ole A

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GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium by 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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A genetic association study of CSMD1 and CSMD2 with cognitive function by Athanasiu, Lavinia, Giddaluru, Sudheer, Fernandes, Carla, Christoforou, Andrea, Reinvang, Ivar, Lundervold, Astri J, Nilsson, Lars-Göran, Kauppi, Karolina, Adolfsson, Rolf, Eriksson, Elias, Sundet, Kjetil, Djurovic, Srdjan, Espeseth, Thomas, Nyberg, Lars, Steen, Vidar M, Andreassen, Ole A, Le Hellard, Stephanie

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Divergent epigenetic responses to perinatal asphyxia in severe mental disorders by Wortinger, Laura A., Stavrum, Anne-Kristin, Shadrin, Alexey A., Szabo, Attila, Rukke, Sondre Høeg, Nerland, Stener, Smelror, Runar Elle, Jørgensen, Kjetil Nordbø, Barth, Claudia, Andreou, Dimitrios, Weibell, Melissa A., Djurovic, Srdjan, Andreassen, Ole A., Thoresen, Marianne, Ursini, Gianluca, Agartz, Ingrid, Le Hellard, Stephanie

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Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs by Meer, Dennis, Agartz, Ingrid, Arango, Celso, Ayesa‐Arriola, Rosa, Bakker, Geor, Boomsma, Dorret I., Bülow, Robin, Butcher, Nancy J., Caspers, Svenja, Crespo‐Facorro, Benedicto, Dale, Anders M., Dazzan, Paola, Zubicaray, Greig I., Donohoe, Gary, Espeseth, Thomas, Fisher, Simon E., Ge, Tian, Glahn, David C., Grabe, Hans J., Gur, Raquel E., Håberg, Asta K., Hashimoto, Ryota, Hibar, Derrek P., Holmes, Avram J., Hulshoff Pol, Hilleke E., Kushan, Leila, Liu, Jingyu, Martin‐Brevet, Sandra, Martínez, Kenia, Mather, Karen A., Mathias, Samuel R., Medland, Sarah E., Modenato, Claudia, Mühleisen, Thomas W., Prieto, Carlos, Ragothaman, Anjanibhargavi, Reinbold, Céline S., Reis Marques, Tiago, Repetto, Gabriela M., Reymond, Alexandre, Sachdev, Perminder S., Schmitt, James E., Schofield, Peter R., Silva, Ana I., Stefansson, Hreinn, Stein, Dan J., Tamnes, Christian K., Ulfarsson, Magnus O., Vajdi, Ariana, Ent, Dennis, Bree, Marianne B. M., Vassos, Evangelos, Vázquez‐Bourgon, Javier, Vila‐Rodriguez, Fidel, Walters, G. Bragi, Wen, Wei, Zackai, Elaine H., Thompson, Paul M., Bearden, Carrie E., Blackburn, Nicholas B., Bøen, Rune, Zwarte, Sonja M. C., Forti, Marta Di, Frei, Oleksandr, Fukunaga, Masaki, Hehir‐Kwa, Jayne Y., Hoffmann, Per, Homuth, Georg, Jahanshad, Neda, Koops, Sanne, Kumar, Kuldeep, Kikuchi, Masataka, Le Hellard, Stephanie, Leu, Costin, Murray, Robin M, Nyberg, Lars, Shumskaya, Elena, Sisodiya, Sanjay M., Steen, Vidar M., Teumer, Alexander, Uhlmann, Anne, Wright, Margaret J., Campbell, Linda E., Crossley, Nicolas A., Crowley, T. Blaine, Daly, Eileen, Fiksinski, Ania M., Fremont, Wanda, Goodrich‐Hunsaker, Naomi J., Gudbrandsen, Maria, Jonas, Rachel K., Kates, Wendy R., Lin, Amy, Moss, Hayley, Murphy, Declan G., Murphy, Kieran C., Owen, Michael J., Simon, Tony. J., Amelsvoort, Therese, Vorstman, Jacob A. S.

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Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci by Witoelar, Aree, Rongve, Arvid, Almdahl, Ina S., Ulstein, Ingun D., Engvig, Andreas, White, Linda R., Selbæk, Geir, Stordal, Eystein, Andersen, Fred, Brækhus, Anne, Saltvedt, Ingvild, Engedal, Knut, Hughes, Timothy, Bergh, Sverre, Bråthen, Geir, Bogdanovic, Nenad, Bettella, Francesco, Wang, Yunpeng, Athanasiu, Lavinia, Bahrami, Shahram, Le Hellard, Stephanie, Giddaluru, Sudheer, Dale, Anders M., Sando, Sigrid B., Steinberg, Stacy, Stefansson, Hreinn, Snaedal, Jon, Desikan, Rahul S., Stefansson, Kari, Aarsland, Dag, Djurovic, Srdjan, Fladby, Tormod, Andreassen, Ole A.

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1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans by Sønderby, Ida E., van der Meer, Dennis, Moreau, Clara, Abdellaoui, Abdel, Amunts, Katrin, Armstrong, Nicola J., Bernard, Manon, Blackburn, Nicholas B., Blangero, John, Brouwer, Rachel M., Bøen, Rune, Cahn, Wiepke, Calhoun, Vince D., Caspers, Svenja, Ching, Christopher R. K., Cichon, Sven, Ciufolini, Simone, Curran, Joanne E., Dale, Anders M., Dazzan, Paola, de Geus, Eco J. C., de Zubicaray, Greig I., de Zwarte, Sonja M. C., Doherty, Joanne L., Eising, Else, Fejgin, Kim, Fisher, Simon E., Fladby, Tormod, Frei, Oleksandr, Frouin, Vincent, Fukunaga, Masaki, Gareau, Thomas, Ge, Tian, Glahn, David C., Groenewold, Nynke A., Hashimoto, Ryota, Hehir-Kwa, Jayne Y., Hibar, Derrek P., Hoffmann, Per, Holleran, Laurena, Holmes, Avram J., Hottenga, Jouke-Jan, Hulshoff Pol, Hilleke E., Ikeda, Masashi, Jahanshad, Neda, Johansson, Stefan, Jørgensen, Niklas R., Kikuchi, Masataka, Kumar, Kuldeep, Le Hellard, Stephanie, Liu, Jingyu, Lundervold, Arvid, Lundervold, Astri Johansen, Maillard, Anne M., Martin, Nicholas G., Mather, Karen A., Mathias, Samuel R., McMahon, Katie L., McRae, Allan F., Meyer-Lindenberg, Andreas, Modenato, Claudia, Mühleisen, Thomas W., Murray, Robin M., Nielsen, Jacob, Nordvik, Jan E., Nyberg, Lars, Loohuis, Loes M. Olde, Owen, Michael J., Paus, Tomas, Pausova, Zdenka, Peralta, Juan M., Pike, G. Bruce, Prieto, Carlos, Quinlan, Erin B., Reinbold, Céline S., Sachdev, Perminder S., Sando, Sigrid B., Schofield, Peter R., Silva, Ana I., Sisodiya, Sanjay M., Steen, Vidar M., Stein, Dan J., Strike, Lachlan T., Suzuki, Ikuo K., Tamnes, Christian K., Thalamuthu, Anbupalam, Tordesillas-Gutiérrez, Diana, Uhlmann, Anne, Ulfarsson, Magnus O., van ‘t Ent, Dennis, van den Bree, Marianne B. M., Vanderhaeghen, Pierre, Vassos, Evangelos, Wen, Wei, Wittfeld, Katharina, Wright, Margaret J., Westlye, Lars T., Stefansson, Hreinn, Jacquemont, Sébastien, Andreassen, Ole A.

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