recent publications

• academic article

  • 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
  • Andreou, D., Saetre, P., Werge, T., Andreassen, O. A., Agartz, I., Sedvall, G. C., Hall, H., Terenius, L., Jonsson, E. G. D-amino acid oxidase activator gene (daoa) variation affects cerebrospinal fluid homovanillic acid concentrations in healthy caucasians European Archives of Psychiatry and Clinical Neuroscience  2012 262:549-556  DOI:10.1007/s00406-012-0313-z  PMID:22454242  PMCID:PMC3464385
  • Holtze, M., Saetre, P., Engberg, G., Schwieler, L., Werge, T., Andreassen, O. A., Hall, H., Terenius, L., Agartz, I., Jonsson, E. G., Schalling, M., Erhardt, S. Kynurenine 3-monooxygenase polymorphisms: Relevance for kynurenic acid synthesis in patients with schizophrenia and healthy controls Journal of Psychiatry and Neuroscience  2012 37:53-57  DOI:10.1503/jpn.100175  PMID:21693093  PMCID:PMC3244499
  • Saetre, P., Grove, J., Borglum, A. D., Mors, O., Werge, T., Andreassen, O. A., Vares, M., Agartz, I., Terenius, L., Jonsson, E. G. Methylenetetrahydrofolate reductase (mthfr) c677t polymorphism and age at onset of schizophrenia: No consistent evidence for an association in the nordic population American Journal of Medical Genetics Part B-Neuropsychiatric Genetics  2012 159B:981-986  DOI:10.1002/ajmg.b.32104  PMID:23076983  PMCID:PMC3739001
  • 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
  • Andreou, D., Saetre, P., Kahler, A. K., Werge, T., Andreassen, O. A., Agartz, I., Sedvall, G. C., Hall, H., Terenius, L., Jonsson, E. G. Dystrobrevin-binding protein 1 gene (dtnbp1) variants associated with cerebrospinal fluid homovanillic acid and 5-hydroxyindoleacetic acid concentrations in healthy volunteers European Neuropsychopharmacology  2011 21:700-704  DOI:10.1016/j.euroneuro.2010.12.008  PMID:21295953
  • 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
  • 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
  • Saetre, P., Vares, M., Werge, T., Andreassen, O. A., Arinami, T., Ishiguro, H., Nanko, S., Tan, E. C., Han, D. H., Roffman, J. L., Muntjewerff, J. W., Jagodzinski, P. P., et al. Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and age of onset in schizophrenia: a combined analysis of independent samples American Journal of Medical Genetics Part B-Neuropsychiatric Genetics  2011 156B:215-224  DOI:10.1002/ajmg.b.31160  PMID:21302350
  • 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
  • Andreou, D., Saetre, P., Werge, T., Andreassen, O. A., Agartz, I., Sedvall, G. C., Hall, H., Terenius, L., Jonsson, E. G. Tryptophan hydroxylase gene 1 (tph1) variants associated with cerebrospinal fluid 5-hydroxyindole acetic acid and homovanillic acid concentrations in healthy volunteers Psychiatry Research  2010 180:63-67  DOI:10.1016/j.psychres.2009.11.018  PMID:20580984
  • Adolfsson, R., Carroll, L., Cichon, S., Collaboration, Molecular Genetics of Schizophrenia, Corvin, A. P., Craddock, N., Darvasi, A., Duan, J., Dwyer, S., Feng, G., Gejman, P. V., Georgieva, L., et al. Analysis of 10 independent samples provides evidence for association between schizophrenia and a snp flanking fibroblast growth factor receptor 2 Molecular Psychiatry  2009 14:30-36  DOI:10.1038/mp.2008.108  PMID:18813210  PMCID:PMC3016613
  • 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
  • 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
  • Saetre, P., Agartz, I., De Franciscis, A., Lundmark, P., Djurovic, S., Kahler, A., Andreassen, O. A., Jakobsen, K. D., Rasmussen, H. B., Werge, T., Hall, H., Terenius, L., et al. Association between a disrupted-in-schizophrenia 1 (disc1) single nucleotide polymorphism and schizophrenia in a combined scandinavian case-control sample Schizophrenia Research  2008 106:237-241  DOI:10.1016/j.schres.2008.08.024  PMID:18818052
  • Jonsson, E. G., Saetre, P., Edman-Ahlbom, B., Sillen, A., Gunnar, A., Andreou, D., Agartz, I., Sedvall, G., Hall, H., Terenius, L. Brain-derived neurotrophic factor gene variation influences cerebrospinal fluid 3-methoxy-4-hydroxyphenylglycol concentrations in healthy volunteers Journal of Neural Transmission  2008 115:1695-1699  DOI:10.1007/s00702-008-0113-9  PMID:18781277
  • Varnas, K., Lawyer, G., Jonsson, E. G., Kulle, B., Nesvag, R., Hall, H., Terenius, L., Agartz, I. Brain-derived neurotrophic factor polymorphisms and frontal cortex morphology in schizophrenia Psychiatric Genetics  2008 18:177-183  DOI:10.1097/YPG.0b013e3283050a94  PMID:18628679
  • Jonsson, E. G., Larsson, K., Vares, M., Hansen, T., Wang, A. G., DjuroviC, S., Ronningen, K. S., Andreassen, O. A., Agartz, I., Werge, T., Terenius, L., Hall, H. Two methylenetetrahydrofolate reductase gene (mthfr) polymorphisms, schizophrenia and bipolar disorder: An association study American Journal of Medical Genetics Part B-Neuropsychiatric Genetics  2008 147B:976-982  DOI:10.1002/ajmg.b.30671  PMID:18165967
  • Hall, H., Lawyer, G., Sillen, A., Jonsson, E. G., Agartz, I., Terenius, L., Arnborg, S. Potential genetic variants in schizophrenia: A bayesian analysis World Journal of Biological Psychiatry  2007 8:12-22  DOI:10.1080/15622970600892004  PMID:17366345
  • Agartz, I., Sedvall, G. C., Terenius, L., Kulle, B., Frigessi, A., Hall, H., Jonsson, E. G. Bdnf gene variants and brain morphology in schizophrenia American Journal of Medical Genetics Part B-Neuropsychiatric Genetics  2006 141B:513-523  DOI:10.1002/ajmg.b.30338  PMID:16741916
  • Jonsson, E. G., Edman-Ahlbom, B., Sillen, A., Gunnar, A., Kulle, B., Frigessi, A., Vares, M., Ekholm, B., Wode-Helgodt, B., Schumacher, J., Cichon, S., Agartz, I., et al. Brain-derived neurotrophic factor gene (bdnf) variants and schizophrenia: An association study Progress in Neuro-Psychopharmacology & Biological Psychiatry  2006 30:924-933  DOI:10.1016/j.pnpbp.2006.02.008  PMID:16581172
  • Jonsson, E. G., Sillen, A., Vares, M., Ekholm, B., Terenius, L., Sedvall, G. C. Dopamine D2 receptor gene Ser311Cys variant and schizophrenia: association study and meta-analysis American Journal of Medical Genetics Part B-Neuropsychiatric Genetics  2003 119B:28-34  DOI:10.1002/ajmg.b.20004  PMID:12707934
  • Persson, M. L., Wasserman, D., Jonsson, E. G., Bergman, H., Terenius, L., Gyllander, A., Neiman, J., Geijer, T. Search for the influence of the tyrosine hydroxylase (tcat)(n) repeat polymorphism on personality traits Psychiatry Research  2000 95:1-8  DOI:10.1016/s0165-1781(00)00160-8  PMID:10904118
  • Jonsson, E. G., Nimgaonkar, V. L., Zhang, X. R., Shaw, S. H., Burgert, E., Crocq, M. A., Chakravarti, A., Sedvall, G. C. Trend for an association between schizophrenia and d3s1310, a marker in proximity to the dopamine d3 receptor gene American Journal of Medical Genetics  1999 88:352-357  DOI:10.1002/(sici)1096-8628(19990820)88:4<352::aid-ajmg12>3.3.co;2-s  PMID:10402502
  • Jonsson, E. G., Geijer, T., Gyllander, A., Terenius, L., Sedvall, G. C. Failure to replicate an association between a rare allele of a tyrosine hydroxylase gene microsatellite and schizophrenia European Archives of Psychiatry and Clinical Neuroscience  1998 248:61-63  DOI:10.1007/s004060050018  PMID:9684913
  • Persson, M. L., Wasserman, D., Geijer, T., Jonsson, E. G., Terenius, L. Tyrosine hydroxylase allelic distribution in suicide attempters Psychiatry Research  1997 72:73-80  DOI:10.1016/s0165-1781(97)00068-1  PMID:9335198