Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls von Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Agrawal, A., Børglum, A. D., Bulik, C. M., Daly, M. J., Davis, L. K., Demontis, D., Edenberg, H. J., Grove, J., Gelernter, J., Neale, B. M., Pardiñas, A. F., Stahl, E., Walters, J. T. R., Walters, R., Sullivan, P. F., Posthuma, D., Polderman, T. J. C.

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Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci von Børglum, A D, Demontis, D, Grove, J, Pallesen, J, Hollegaard, M V, Pedersen, C B, Hedemand, A, Mattheisen, M, Uitterlinden, A, Nyegaard, M, Ørntoft, T, Wiuf, C, Didriksen, M, Nordentoft, M, Nöthen, M M, Rietschel, M, Ophoff, R A, Cichon, S, Yolken, R H, Hougaard, D M, Mortensen, P B, Mors, O

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Association analysis identifies TLR7 and TLR8 as novel risk genes in asthma and related disorders von Møller-Larsen, S, Nyegaard, M, Haagerup, A, Vestbo, J, Kruse, T A, Børglum, A D

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Epigenome-wide association study of depression symptomatology in elderly monozygotic twins von Starnawska, A., Tan, Q., Soerensen, M., McGue, M., Mors, O., Børglum, A. D., Christensen, K., Nyegaard, M., Christiansen, L.

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ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties von St Pourcain, B, Robinson, E B, Anttila, V, Sullivan, B B, Maller, J, Golding, J, Skuse, D, Ring, S, Evans, D M, Zammit, S, Fisher, S E, Neale, B M, Anney, R J L, Ripke, S, Hollegaard, M V, Werge, T, Ronald, A, Grove, J, Hougaard, D M, Børglum, A D, Mortensen, P B, Daly, M J, Davey Smith, G

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Blood DNA methylation age is not associated with cognitive functioning in middle-aged monozygotic twins von Starnawska, A, Tan, Q, Lenart, A, McGue, M, Mors, O, Børglum, A.D, Christensen, K, Nyegaard, M, Christiansen, L

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Investigating the causal relationship between neuroticism and depression via Mendelian randomization von Speed, D., Hemani, G., Speed, M. S., Børglum, A. D., Østergaard, S. D.

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High loading of polygenic risk in cases with chronic schizophrenia von Meier, S M, Agerbo, E, Maier, R, Pedersen, C B, Lang, M, Grove, J, Hollegaard, M V, Demontis, D, Trabjerg, B B, Hjorthøj, C, Ripke, S, Degenhardt, F, Nöthen, M M, Rujescu, D, Maier, W, Werge, T, Mors, O, Hougaard, D M, Børglum, A D, Wray, N R, Rietschel, M, Nordentoft, M, Mortensen, P B, Mattheisen, M

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Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM von Pettersson, E, Lichtenstein, P, Larsson, H, Song, J, Agrawal, A, Børglum, A D, Bulik, C M, Daly, M J, Davis, L K, Demontis, D, Edenberg, H J, Grove, J, Gelernter, J, Neale, B M, Pardiñas, A F, Stahl, E, Walters, J T R, Walters, R, Sullivan, P F, Posthuma, D, Polderman, T J C

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COMT Val158Met and MTHFR C677T moderate risk of schizophrenia in response to childhood adversity von Debost, J.‐C., Debost, M., Grove, J., Mors, O., Hougaard, D. M., Børglum, A. D., Mortensen, P. B., Petersen, L.

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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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The iPSYCH2012 case–cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders von Pedersen, C B, Bybjerg-Grauholm, J, Pedersen, M G, Grove, J, Agerbo, E, Bækvad-Hansen, M, Poulsen, J B, Hansen, C S, McGrath, J J, Als, T D, Goldstein, J I, Neale, B M, Daly, M J, Hougaard, D M, Mors, O, Nordentoft, M, Børglum, A D, Werge, T, Mortensen, P B

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Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes von Ribasés, M., Mitjans, M., Hartman, CA, Soler Artigas, M., Demontis, D., Larsson, H., Ramos-Quiroga, JA, Kuntsi, J., Faraone, SV, Børglum, AD, Reif, A., Franke, B., Cormand, B.

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Risk of schizophrenia in relation to parental origin and genome-wide divergence von Pedersen, C. B., Demontis, D., Pedersen, M. S., Agerbo, E., Mortensen, P. B., Børglum, A. D., Hougaard, D. M., Hollegaard, M. V., Mors, O., Cantor-Graae, E.

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The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group von Kamm, C., Healy, D. G., Quinn, N. P., Wüllner, U., Moller, J. C., Schols, L., Geser, F., Burk, K., Børglum, A. D., Pellecchia, M. T., Tolosa, E., del Sorbo, F., Nilsson, C., Bandmann, O., Sharma, M., Mayer, P., Gasteiger, M., Haworth, A., Ozawa, T., Lees, A. J., Short, J., Giunti, P., Holinski-Feder, E., Illig, T., Wichmann, H. E., Wenning, G. K., Wood, N. W., Gasser, T.

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The norepinephrine transporter gene is a candidate gene for panic disorder von Buttenschøn, H. N., Kristensen, A. S., Buch, H. N., Andersen, J. H., Bonde, J. P., Grynderup, M., Hansen, A. M., Kolstad, H., Kaergaard, A., Kaerlev, L., Mikkelsen, S., Thomsen, J. F., Koefoed, P., Erhardt, A., Woldbye, D. P. D., Børglum, A. D., Mors, O.

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Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci von Fadista, João, Skotte, Line, Karjalainen, Juha, Abner, Erik, Sørensen, Erik, Ullum, Henrik, Werge, Thomas, Esko, Tõnu, Milani, Lili, Palotie, Aarno, Daly, Mark, Melbye, Mads, Feenstra, Bjarke, Geller, Frank

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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism von Fu, Jack M., Satterstrom, F. Kyle, Peng, Minshi, Brand, Harrison, Collins, Ryan L., Dong, Shan, Wamsley, Brie, Klei, Lambertus, Wang, Lily, Hao, Stephanie P., Stevens, Christine R., Cusick, Caroline, Babadi, Mehrtash, Banks, Eric, Collins, Brett, Dodge, Sheila, Gabriel, Stacey B., Gauthier, Laura, Lee, Samuel K., Liang, Lindsay, Ljungdahl, Alicia, Mahjani, Behrang, Sloofman, Laura, Smirnov, Andrey N., Barbosa, Mafalda, Betancur, Catalina, Brusco, Alfredo, Chung, Brian H. Y., Cook, Edwin H., Cuccaro, Michael L., Domenici, Enrico, Ferrero, Giovanni Battista, Gargus, J. Jay, Herman, Gail E., Hertz-Picciotto, Irva, Maciel, Patricia, Manoach, Dara S., Passos-Bueno, Maria Rita, Persico, Antonio M., Renieri, Alessandra, Sutcliffe, James S., Tassone, Flora, Trabetti, Elisabetta, Campos, Gabriele, Cardaropoli, Simona, Carli, Diana, Chan, Marcus C. Y., Fallerini, Chiara, Giorgio, Elisa, Girardi, Ana Cristina, Hansen-Kiss, Emily, Lee, So Lun, Lintas, Carla, Ludena, Yunin, Nguyen, Rachel, Pavinato, Lisa, Pericak-Vance, Margaret, Pessah, Isaac N., Schmidt, Rebecca J., Smith, Moyra, Costa, Claudia I. S., Trajkova, Slavica, Wang, Jaqueline Y. T., Yu, Mullin H. C., Cutler, David J., De Rubeis, Silvia, Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J., Talkowski, Michael E.

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The role of genetic liability in the association of urbanicity at birth and during upbringing with schizophrenia in Denmark von Paksarian, D., Trabjerg, B. B., Merikangas, K. R., Mors, O., Børglum, A. D., Hougaard, D. M., McGrath, J. J., Pedersen, C. B., Mortensen, P. B., Agerbo, E.

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A genome-wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba von Marcheco-Teruel, B., Flint, T.J., Wikman, F.P., Torralbas, M., González, L., Blanco, L., Tan, Q., Ewald, H., Orntoft, T., Kruse, T.A., Børglum, A.D., Mors, O.

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