recent publications
-
academic article
- Chen, C. H., Schork, A. J., Lo, M. T., Fan, C. C., Wang, Y., Desikan, R. S., Bettella, F., Hagler, D. J., Pediatric Imaging, Neurocognition, Alzheimer's Disease Neuroimaging Initiative, Westlye, L. T., Kremen, W. S. Large-scale genomics unveil polygenic architecture of human cortical surface area Nature Communications 2015 6:7549 DOI:10.1038/ncomms8549 PMID:26189703 PMCID:PMC4518289
- Boraska, V., Franklin, C. S., Floyd, J. A. B., Thornton, L. M., Huckins, L. M., Southam, L., Rayner, N. W., Tachmazidou, I., Klump, K. L., Treasure, J., Lewis, C. M., Schmidt, U., et al. A genome-wide association study of anorexia nervosa Molecular Psychiatry 2014 19:1085-1094 DOI:10.1038/mp.2013.187 PMID:24514567 PMCID:PMC4325090
- 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
- Schork, A. J., Thompson, W. K., Pham, P., Torkamani, A., Roddey, J. C., Sullivan, P. F., Kelsoe, J. R., O'Donovan, M. C., Furberg, H., The Tobacco & Genetics Consortium, The Bipolar Disorder Psychiatric Genomics Consortium, Schizophrenia Psychiatric Genomics Consortium, et al. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs PLoS Genetics 2013 9:e1003449 DOI:10.1371/journal.pgen.1003449 PMID:23637621 PMCID:PMC3636284
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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., 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