recent publications

• academic article

  • Lee, S. H., Ripke, S., Neale, B. M., Faraone, S. V., Purcell, S. M., Perlis, R. H., Mowry, B. J., Thapar, A., Goddard, M. E., Witte, J. S., Absher, D., Agartz, I., et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Nature Genetics  2013 45:984-994  DOI:10.1038/ng.2711  PMID:23933821  PMCID:PMC3800159
  • Carlstrom, E. L., Saetre, P., Rosengren, A., Thygesen, J. H., Djurovic, S., Melle, I., Andreassen, O. A., Werge, T., Agartz, I., Hall, H., Terenius, L., Jonsson, E. G. Association between a genetic variant in the serotonin transporter gene (slc6a4) and suicidal behavior in patients with schizophrenia Behavioral and Brain Functions  2012 8:24  DOI:10.1186/1744-9081-8-24  PMID:22594806  PMCID:PMC3527134
  • Bakken, T. E., Roddey, J. C., Djurovic, S., Akshoomoff, N., Amaral, D. G., Bloss, C. S., Casey, B. J., Chang, L., Ernst, T. M., Gruen, J. R., Jernigan, T. L., Kaufmann, W. E., et al. Association of common genetic variants in gpcpd1 with scaling of visual cortical surface area in humans Proceedings of the National Academy of Sciences of the United States of America  2012 109:3985-3990  DOI:10.1073/pnas.1105829109  PMID:22343285  PMCID:PMC3309762
  • Steinberg, S., de Jong, S., Andreassen, O. A., Werge, T., Borglum, A. D., Mors, O., Mortensen, P. B., Gustafsson, O., Costas, J., Pietilainen, O. P. H., Demontis, D., Papiol, S., et al. Common variants at VRK(2) and TCF(4) conferring risk of schizophrenia Human Molecular Genetics  2011 20:4076-4081  DOI:10.1093/hmg/ddr325  PMID:21791550  PMCID:PMC3298077
  • Ripke, S., Sanders, A. R., Kendler, K. S., Levinson, D. F., Sklar, P., Holmans, P. A., Lin, D. Y., Duan, J., Ophoff, R. A., Andreassen, O. A., Scolnick, E., Cichon, S., et al. Genome-wide association study identifies five new schizophrenia loci Nature Genetics  2011 43:969-76  DOI:10.1038/ng.940  PMID:21926974  PMCID:PMC3303194
  • Sklar, P., Ripke, S., Scott, L. J., Andreassen, O. A., Cichon, S., Craddock, N., Edenberg, H. J., Nurnberger, J. I., Rietschel, M., Blackwood, D., Corvin, A., Flickinger, M., et al. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near odz4 Nature Genetics  2011 43:977-983  DOI:10.1038/ng.943  PMID:21926972  PMCID:PMC3637176
  • Bakken, T. E., Bloss, C. S., Roddey, J. C., Joyner, A. H., Rimol, L. M., Djurovic, S., Melle, I., Sundet, K., Agartz, I., Andreassen, O. A., Dale, A. M., Schork, N. J. Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia Archives of General Psychiatry  2011 68:781-790  DOI:10.1001/archgenpsychiatry.2011.81  PMID:21810643  PMCID:PMC3375053
  • Steinberg, S., Mors, O., Borglum, A. D., Gustafsson, O., Werge, T., Mortensen, P. B., Andreassen, O. A., Sigurdsson, E., Thorgeirsson, T. E., Bottcher, Y., Olason, P., Ophoff, R. A., et al. Expanding the range of ZNF804A variants conferring risk of psychosis Molecular Psychiatry  2011 16:59-66  DOI:10.1038/mp.2009.149  PMID:20048749  PMCID:PMC3242031
  • Vares, M., Saetre, P., Deng, H., Cai, G. Q., Liu, X. H., Hansen, T., Rasmussen, H. B., Werge, T., Melle, I., Djurovic, S., Andreassen, O. A., Agartz, I., et al. Association between methylenetetrahydrofolate reductase (mthfr) c677t polymorphism and age of onset in schizophrenia American Journal of Medical Genetics Part B-Neuropsychiatric Genetics  2010 153B:610-618  DOI:10.1002/ajmg.b.31030  PMID:19746410
  • Saetre, P., Lundmark, P., Wang, A., Hansen, T., Rasmussen, H. B., Djurovic, S., Melle, I., Andreassen, O. A., Werge, T., Agartz, I., Hall, H., Terenius, L., et al. The tryptophan hydroxylase 1 (tph1) gene, schizophrenia susceptibility, and suicidal behavior: A multi-centre case-control study and meta-analysis American Journal of Medical Genetics Part B-Neuropsychiatric Genetics  2010 153B:387-396  DOI:10.1002/ajmg.b.30991  PMID:19526457
  • Rimol, L. M., Agartz, I., Djurovic, S., Brown, A. A., Roddey, J. C., Kahler, A. K., Mattingsdal, M., Athanasiu, L., Joyner, A. H., Schork, N. J., Halgren, E., Sundet, K., et al. Sex-dependent association of common variants of microcephaly genes with brain structure Proceedings of the National Academy of Sciences of the United States of America  2010 107:384-388  DOI:10.1073/pnas.0908454107  PMID:20080800  PMCID:PMC2806758
  • Andreou, D., Saetre, P., Lundmark, P., Hansen, T., Timm, S., Melle, I., Djurovic, S., Andreassen, O. A., Werge, T., Hall, H., Agartz, I., Terenius, L., et al. Tyrosine hydroxylase val81met polymorphism: Lack of association with schizophrenia Psychiatric Genetics  2009 19:273-274  DOI:10.1097/YPG.0b013e32832a4fcd  PMID:19491717
  • Joyner, A. H., Roddey, J. C., Bloss, C. S., Bakken, T. E., Rimol, L. M., Melle, I., Agartz, I., Djurovic, S., Topol, E. J., Schork, N. J., Andreassen, O. A., Dale, A. M. A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations Proceedings of the National Academy of Sciences of the United States of America  2009 106:15483-15488  DOI:10.1073/pnas.0901866106  PMID:19717458  PMCID:PMC2741277
  • Stefansson, H., Ophoff, R. A., Steinberg, S., Andreassen, O. A., Cichon, S., Rujescu, D., Werge, T., Pietilainen, O. P. H., Mors, O., Mortensen, P. B., Sigurdsson, E., Gustafsson, O., et al. Common variants conferring risk of schizophrenia Nature  2009 460:744-7  DOI:10.1038/nature08186  PMID:19571808  PMCID:PMC3077530
  • Jonsson, E. G., Saetre, P., Vares, M., Andreou, D., Larsson, K., Timm, S., Rasmussen, H. B., Djurovic, S., Melle, I., Andreassen, O. A., Agartz, I., Werge, T., et al. Dtnbp1, nrg1, daoa, dao and grm3 polymorphisms and schizophrenia: An association study Neuropsychobiology  2009 59:142-150  DOI:10.1159/000218076  PMID:19439994