Nudel, R., Wang, Y., Appadurai, V., Schork, A. J., Buil, A., Agerbo, E. ... Benros, M. E. (2019). A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population. Translational Psychiatry, 9, [283]. https://doi.org/10.1038/s41398-019-0622-3

Horsdal, H. T., Agerbo, E., McGrath, J. J., Vilhjálmsson, B. J., Antonsen, S., Closter, A. M. ... Pedersen, C. B. (2019). Association of Childhood Exposure to Nitrogen Dioxide and Polygenic Risk Score for Schizophrenia With the Risk of Developing Schizophrenia. JAMA network open, 2(11), [e1914401]. https://doi.org/10.1001/jamanetworkopen.2019.14401

Barbu, M. C., Zeng, Y., Shen, X., Cox, S. R., Clarke, T-K., Gibson, J. ... Whalley, H. C. (2019). Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank. Biological psychiatry. Cognitive neuroscience and neuroimaging, 4(1), 91-100. https://doi.org/10.1016/j.bpsc.2018.07.006

Paternoster, V., Svanborg, M., Edhager, A. V., Rajkumar, A. P., Eickhardt, E. A., Pallesen, J. ... Christensen, J. H. (2019). Brain proteome changes in female Brd1+/- mice unmask dendritic spine pathology and show enrichment for schizophrenia risk. Neurobiology of Disease, 124, 479-488. https://doi.org/10.1016/j.nbd.2018.12.011

Demontis, D., Walters, R. K., Martin, J., Mattheisen, M., Als, T. D., Agerbo, E. ... Børglum, A. D. (2019). Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nature Genetics, 51, 63–75. https://doi.org/10.1038/s41588-018-0269-7

Starnawska, A., Tan, Q., Soerensen, M., McGue, M., Mors, O., Børglum, A. D. ... Christiansen, L. (2019). Epigenome-wide association study of depression symptomatology in elderly monozygotic twins. Translational Psychiatry, 9(1), [214]. https://doi.org/10.1038/s41398-019-0548-9

Pineda-Cirera, L., Shivalikanjli, A., Cabana-Domínguez, J., Demontis, D., Rajagopal, V. M., Børglum, A. D. ... Fernàndez-Castillo, N. (2019). Exploring genetic variation that influences brain methylation in attention-deficit/hyperactivity disorder. Translational Psychiatry, 9(1), [242]. https://doi.org/10.1038/s41398-019-0574-7

Meier, S. M., Trontti, K., Purves, K. L., Als, T. D., Grove, J., Laine, M. ... Mors, O. (2019). Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. J A M A Psychiatry, 76(9), 924-932. https://doi.org/10.1001/jamapsychiatry.2019.1119

Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Attention Deficit/Hyperactivity Disorder Working Group of the iPSYCH-Broad-PGC Consortium, Autism Spectrum Disorder Working Group of the iPSYCH-Broad-PGC Consortium, Bipolar Disorder Working Group of the PGC, Eating Disorder Working Group of the PGC, Major Depressive Disorder Working Group of the PGC, Obsessive Compulsive Disorders and Tourette Syndrome Working Group of the PGC, Schizophrenia CLOZUK, Substance Use Disorder Working Group of the PGC , Agrawal, A. ... Polderman, T. J. C. (2019). 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. Psychological Medicine, 49(7), 1166-1173. https://doi.org/10.1017/S0033291718002039

Klein, M., Walters, R. K., Demontis, D., Stein, J. L., Hibar, D. P., Adams, H. H. ... Franke, B. (2019). Genetic markers of ADHD-related variations in intracranial volume. American Journal of Psychiatry, 176(3), 228-238. https://doi.org/10.1176/appi.ajp.2018.18020149

Stahl, E. A., Breen, G., Forstner, A. J., McQuillin, A., Ripke, S., Trubetskoy, V. ... eQTLGen Consortium (2019). Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics, 51(5), 793-803. https://doi.org/10.1038/s41588-019-0397-8

Demontis, D., Rajagopal, V. M., Thorgeirsson, T. E., Als, T. D., Grove, J., Leppälä, K. ... Børglum, A. D. (2019). Genome-wide association study implicates CHRNA2 in cannabis use disorder. Nature Neuroscience, 22, 1066-1074. https://doi.org/10.1038/s41593-019-0416-1

Grove, J., Ripke, S., Als, T. D., Mattheisen, M., Walters, R. K., Won, H. ... Børglum, A. D. (2019). Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics, 51(3), 431-444. https://doi.org/10.1038/s41588-019-0344-8

Nudel, R., Benros, M. E., Krebs, M. D., Allesøe, R. L., Lemvigh, C. K., Bybjerg-Grauholm, J. ... Thompson, W. K. (2019). Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders. European Journal of Human Genetics, 27(9), 1445-1455. https://doi.org/10.1038/s41431-019-0402-9

Czamara, D., Eraslan, G., Page, C. M., Lahti, J., Lahti-Pulkkinen, M., Hämäläinen, E. ... Binder, E. B. (2019). Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nature Communications, 10, [2548]. https://doi.org/10.1038/s41467-019-10461-0

Nievergelt, C. M., Maihofer, A. X., Klengel, T., Atkinson, E. G., Chen, C. Y., Choi, K. W. ... Koenen, K. C. (2019). International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nature Communications, 10(1), [4558]. https://doi.org/10.1038/s41467-019-12576-w

Speed, M. S., Jefsen, O. H., Børglum, A. D., Speed, D. & Østergaard, S. D. (2019). Investigating the association between body fat and depression via Mendelian randomization. Translational Psychiatry, 9, [184]. https://doi.org/10.1038/s41398-019-0516-4

Speed, D., Hemani, G., Speed, M. S., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium & Børglum, A. D. (2019). Investigating the causal relationship between neuroticism and depression via Mendelian Randomization. Acta Psychiatrica Scandinavica, 139(4), 395-397. https://doi.org/10.1111/acps.13009

Skogstrand, K., Hagen, C. M., Borbye-Lorenzen, N., Christiansen, M., Bybjerg-Grauholm, J., Bækvad-Hansen, M. ... Hougaard, D. M. (2019). Reduced neonatal brain-derived neurotrophic factor is associated with autism spectrum disorders. Translational Psychiatry, 9(1), [252]. https://doi.org/10.1038/s41398-019-0587-2

Gasse, C., Wimberley, T., Wang, Y., Mors, O., Børglum, A., Als, T. D. ... Horsdal, H. T. (2019). Schizophrenia polygenic risk scores, urbanicity and treatment-resistant schizophrenia. Schizophrenia Research, 212, 79-85. https://doi.org/10.1016/j.schres.2019.08.008

Warrier, V., Toro, R., Won, H., Leblond, C. S., Cliquet, F., Delorme, R. ... Baron-Cohen, S. (2019). Social and non-social autism symptoms and trait domains are genetically dissociable. Communications Biology, 2(1), [328]. https://doi.org/10.1038/s42003-019-0558-4

Leduc-Galindo, D., Qvist, P., Tóth, A. E., Fryland, T., Nielsen, M. S., Børglum, A. D. & Christensen, J. H. (2019). The effect of hypoxia on ZEB1 expression in a mimetic system of the blood-brain barrier. Microvascular Research, 122, 131-135. https://doi.org/10.1016/j.mvr.2018.08.004

Hannon, E., Schendel, D., Ladd-Acosta, C., Grove, J., Hansen, C. S., Hougaard, D. M. ... Mill, J. (2019). Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight. Philosophical Transactions of the Royal Society B: Biological Sciences, 374(1770), [20180120]. https://doi.org/10.1098/rstb.2018.0120

Liu, X., Helenius, D., Skotte, L., Beaumont, R. N., Wielscher, M., Geller, F. ... Jacobsson, B. (2019). Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. Nature Communications, 10(1), 1-13. [3927]. https://doi.org/10.1038/s41467-019-11881-8

23andMe Research Team, Psychiatric Genomics Consortium: ADHD Subgroup & iPSYCH–Broad ADHD Workgroup (2018). A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. Biological Psychiatry, 83(12), 1044-1053. https://doi.org/10.1016/j.biopsych.2017.11.026

Brainstorm Consortium (2018). Analysis of shared heritability in common disorders of the brain. Science, 360(6395), eaap8757. [8757]. https://doi.org/10.1126/science.aap8757

Qvist, P., Eskildsen, S. F., Hansen, B., Baragji, M., Ringgaard, S., Roovers, J. ... Christensen, J. H. (2018). Brain volumetric alterations accompanied with loss of striatal medium-sized spiny neurons and cortical parvalbumin expressing interneurons in Brd1+/- mice. Scientific Reports, 8(1), 16486. https://doi.org/10.1038/s41598-018-34729-5

GERAD1 Consortium: (2018). Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics, 50(3), 381-389. https://doi.org/10.1038/s41588-018-0059-2

Bybjerg-Grauholm, J., Hagen, C. M., Gonçalves, V. F., Bækvad-Hansen, M., Hansen, C. S., Hedley, P. L. ... Christiansen, M. (2018). Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes. PLOS ONE, 13(12), [e0208829]. https://doi.org/10.1371/journal.pone.0208829

Peyrot, W. J., Van der Auwera, S., Milaneschi, Y., Dolan, C. V., Madden, P. A. F., Sullivan, P. F. ... Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2018). Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium. Biological Psychiatry, 84(2), 138-147. https://doi.org/10.1016/j.biopsych.2017.09.009

Hannon, E., Schendel, D., Ladd-Acosta, C., Grove, J., Hansen, C. S., Andrews, S. V. ... iPSYCH-Broad ASD Group (Mette Nyegaard, Per Qvist, Jane Hvarregaard Christensen - members of -) (2018). Elevated polygenic burden for autism is associated with differential DNA methylation at birth. Genome Medicine, 10(1). https://doi.org/10.1186/s13073-018-0527-4

Bak, S. T., Staunstrup, N. H., Starnawska, A., Daugaard, T. F., Nyengaard, J. R., Nyegaard, M. ... Nielsen, A. L. (2018). Evaluating the Feasibility of DNA Methylation Analyses Using Long-Term Archived Brain Formalin-Fixed Paraffin-Embedded Samples. Molecular Neurobiology, 55(1), 668-681. https://doi.org/10.1007/s12035-016-0345-x

the iPSYCH-Broad autism group & the 23andMe Research Team (2018). Genome-wide analyses of self-reported empathy: Correlations with autism, schizophrenia, and anorexia nervosa. Translational Psychiatry, 8(1), [35]. https://doi.org/10.1038/s41398-017-0082-6

Wray, N. R., Ripke, S., Mattheisen, M., Trzaskowski, M., Byrne, E. M., Abdellaoui, A. ... Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2018). Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics, 50(5), 668-681. https://doi.org/10.1038/s41588-018-0090-3

Generation Scotland & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2018). Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. PLOS ONE, 13(12), [e0209160]. https://doi.org/10.1371/journal.pone.0209160

Maier, R. M., Zhu, Z., Lee, S. H., Trzaskowski, M., Ruderfer, D. M., Stahl, E. A. ... Zammit, S. (2018). Improving genetic prediction by leveraging genetic correlations among human diseases and traits. Nature Communications, 9(1), [02769-6]. https://doi.org/10.1038/s41467-017-02769-6

Olsen, L., Sparsø, T., Weinsheimer, S. M., Dos Santos, M. B. Q., Mazin, W., Rosengren, A. ... Werge, T. (2018). Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study. The Lancet Psychiatry, 5(7), 573-580. https://doi.org/10.1016/S2215-0366(18)30168-8

Sullivan, P. F., Agrawal, A., Bulik, C. M., Andreassen, O. A., Børglum, A. D., Breen, G. ... Psychiatric Genomics Consortium (2018). Psychiatric Genomics: An Update and an Agenda. The American Journal of Psychiatry (Spanish Edition), 175(1), 15-27. https://doi.org/10.1176/appi.ajp.2017.17030283

GoT2D/T2D-GENES Consortium (2018). Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. American Journal of Human Genetics, 102(6), 1204-1211. https://doi.org/10.1016/j.ajhg.2018.05.002

Mors, O. & Børglum, A. D. (2018). Risikofaktorer og ætiologi for udvikling af skizofreni. Ugeskrift for Laeger, 180(3), 233-236.

Hagen, C. M., Gonçalves, V. F., Hedley, P. L., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Hansen, C. S. ... Christiansen, M. (2018). Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease. PLOS ONE, 13(12), [e0208828]. https://doi.org/10.1371/journal.pone.0208828

Eyles, D. W., Trzaskowski, M., Vinkhuyzen, A. A. E., Mattheisen, M., Meier, S., Gooch, H. ... McGrath, J. J. (2018). The association between neonatal vitamin D status and risk of schizophrenia. Scientific Reports, 8(1), [17692]. https://doi.org/10.1038/s41598-018-35418-z

Pedersen, C. B., Bybjerg-Grauholm, J., Pedersen, M. G., Grove, J., Agerbo, E., Bækvad-Hansen, M. ... Mortensen, P. B. (2018). The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders. Molecular Psychiatry, 23(1), 6–14. https://doi.org/10.1038/mp.2017.196

Paternoster, V., Rajkumar, A. P., Nyengaard, J. R., Børglum, A. D., Grove, J. & Christensen, J. H. (2018). The importance of data structure in statistical analysis of dendritic spine morphology. Journal of Neuroscience Methods, 296, 93-98. https://doi.org/10.1016/j.jneumeth.2017.12.022

Paksarian, D., Trabjerg, B. B., Merikangas, K. R., Mors, O., Børglum, A. D., Hougaard, D. M. ... Agerbo, E. (2018). The role of genetic liability in the association of urbanicity at birth and during upbringing with schizophrenia in Denmark. Psychological Medicine, 48(2), 305-314. https://doi.org/10.1017/S0033291717001696

St Pourcain, B., Robinson, E. B., Anttila, V., Sullivan, B. B., Maller, J., Golding, J. ... iPSYCH-SSI-Broad Autism Group (2017). ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties. Molecular Psychiatry, 23, 263-270. https://doi.org/10.1038/mp.2016.198

Direk, N., Williams, S., Smith, J. A., Ripke, S., Air, T., Amare, A. T. ... Sullivan, P. F. (2017). An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype. Biological Psychiatry, 82(5), 322-329. https://doi.org/10.1016/j.biopsych.2016.11.013

Jensen, J. M., Villesen, P., Friborg, R. M., Mailund, T., Besenbacher, S., Schierup, M. H. & Danish Pan-Genome Consortium (Jakob Grove, member of -) (2017). Assembly and analysis of 100 full MHC haplotypes from the Danish population. Genome Research, 1597-1607. https://doi.org/10.1101/gr.218891.116

Laursen, T. M., Trabjerg, B. B., Mors, O., Børglum, A. D., Hougaard, D. M., Mattheisen, M. ... Agerbo, E. (2017). Association of the polygenic risk score for schizophrenia with mortality and suicidal behavior - A Danish population-based study. Schizophrenia Research, 184, 122-127. https://doi.org/10.1016/j.schres.2016.12.001