Starnawska, A., Tan, Q., Lenart, A., McGue, M., Mors, O., Børglum, A. D., Christensen, K., Nyegaard, M. & Christiansen, L. (2017). Blood DNA methylation age is not associated with cognitive functioning in middle-aged monozygotic twins. Neurobiology of Aging, 50, 60-63. https://doi.org/10.1016/j.neurobiolaging.2016.10.025

Amidi , A., Agerbæk, M., Wu, L. M., Pedersen, A. D., Mehlsen, M. Y., Clausen, C. R., Demontis, D., Børglum, A., Harbøll, A. & Zachariae, R. (2017). Changes in cognitive functions and cerebral grey matter and their associations with inflammatory markers, endocrine markers, and APOE genotypes in testicular cancer patients undergoing treatment. Brain Imaging and Behavior, 11(3), 769-783. https://doi.org/10.1007/s11682-016-9552-3

Debost, J.-C., Debost, M., Grove, J., Mors, O., Hougaard, D. M., Børglum, A. D., Mortensen, P. B. & Petersen, L. (2017). COMT Val158Met and MTHFR C677T moderate risk of schizophrenia in response to childhood adversity. Acta Psychiatrica Scandinavica, 136(1), 85-95. https://doi.org/10.1111/acps.12761

Johannesen, M. D., Qvist, P., Lichota, J., Larsen, K. E., Nyegaard, M., Børglum, A. D. & Christensen, J. H. (2017). DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele. P L o S One, 12(1), Article e0170121. https://doi.org/10.1371/journal.pone.0170121

Rajkumar, A. P., Horsdal, H. T., Wimberley, T., Cohen, D., Mors, O., Børglum, A. D. & Gasse, C. (2017). Endogenous and Antipsychotic-Related Risks for Diabetes Mellitus in Young People With Schizophrenia: A Danish Population-Based Cohort Study. American Journal of Psychiatry, 174(7), 686-694. https://doi.org/10.1176/appi.ajp.2016.16040442

Starnawska, A., Tan, Q., McGue, M., Mors, O., Borglum, A. D., Christensen, K., Nyegaard, M. & Christiansen, L. (2017). Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins. Frontiers in Aging Neuroscience, 9(DEC), Article 413. https://doi.org/10.3389/fnagi.2017.00413

Project MinE GWAS Consortium & Schizophrenia Working Group of the Psychiatric Genomics Consortium (2017). Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Nature Communications, 8, 14774. Article 14774. https://doi.org/10.1038/ncomms14774

Power, R. A., Tansey, K. E., Buttenschøn, H. N., Cohen-Woods, S., Bigdeli, T., Hall, L. S., Kutalik, Z., Lee, S. H., Ripke, S., Steinberg, S., Teumer, A., Viktorin, A., Wray, N. R., Arolt, V., Baune, B. T., Boomsma, D. I., Børglum, A. D., Castelao, E., Craddock, N. ... CONVERGE Consortium, CARDIoGRAM Consortium, GERAD1 Consortium (2017). Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. Biological Psychiatry, 81(4), 325–335. https://doi.org/10.1016/j.biopsych.2016.05.010

Witt, S. H., Streit, F., Jungkunz, M., Frank, J., Awasthi, S., Reinbold, C. S., Treutlein, J., Degenhardt, F., Forstner, A. J., Heilmann-Heimbach, S., Dietl, L., Schwarze, C. E., Schendel, D., Strohmaier, J., Abdellaoui, A., Adolfsson, R., Air, T. M., Akil, H., Alda, M. ... Bipolar Disorders Working Group of the Psychiatric Genomics Consortium (2017). Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. Translational Psychiatry, 7(6), e1155. https://doi.org/10.1038/tp.2017.115

Joshi, P. K., Pirastu, N., Kentistou, K. A., Fischer, K., Hofer, E., Schraut, K. E., Clark, D. W., Nutile, T., Barnes, C. L. K., Timmers, P. R. H. J., Shen, X., Gandin, I., McDaid, A. F., Hansen, T. F., Gordon, S. D., Giulianini, F., Boutin, T. S., Abdellaoui, A., Zhao, W. ... Wilson, J. F. (2017). Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nature Communications, 8(1), Article 910. https://doi.org/10.1038/s41467-017-00934-5

CORtisolNETwork (CORNET) Consortium, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (PGC) & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (PGC) (2017). Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes. Scientific Reports, 7(1), Article 15351. https://doi.org/10.1038/s41598-017-11852-3

Bolund, A. C. S., Starnawska, A., Miller, M. R., Schlünssen, V., Backer, V., Børglum, A. D., Christensen, K., Tan, Q., Christiansen, L. & Sigsgaard, T. (2017). Lung function discordance in monozygotic twins and associated differences in blood DNA methylation. Clinical Epigenetics (Print), 9(1), 132. Article 132. https://doi.org/10.1186/s13148-017-0427-2

The Autism Spectrum Disorders Working Group of the Psychiatric Genomics Consortium (2017). Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Autism, 8(21), Article 21. https://doi.org/10.1186/s13229-017-0137-9

Qvist, P., Rajkumar, A. P., Redrobe, J. P., Nyegaard, M., Christensen, J. H., Mors, O., Wegener, G., Didriksen, M. & Børglum, A. D. (2017). Mice heterozygous for an inactivated allele of the schizophrenia associated Brd1 gene display selective cognitive deficits with translational relevance to schizophrenia. Neurobiology of Learning and Memory, 141, 44-52. https://doi.org/10.1016/j.nlm.2017.03.009

Weiner, D. J., Wigdor, E. M., Ripke, S., Walters, R. K., Kosmicki, J. A., Grove, J., Samocha, K. E., Goldstein, J. I., Okbay, A., Bybjerg-Grauholm, J., Werge, T., Hougaard, D. M., Taylor, J., Skuse, D., Devlin, B., Anney, R., Sanders, S. J., Bishop, S., Mortensen, P. B. ... iPSYCH-Broad Autism Group (2017). Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nature Genetics, 49(7), 978-985. https://doi.org/10.1038/ng.3863

Maretty, L., Jensen, J. M., Petersen, B., Sibbesen, J. A., Liu, S., Villesen, P., Skov, L., Belling, K. C., Theil Have, C., Izarzugaza, J. M. G., Grosjean, M., Bork-Jensen, J., Grove, J., Als, T. D., Huang, S., Chang, Y., Xu, R., Ye, W., Rao, J. ... Schierup, M. H. (2017). Sequencing and de novo assembly of 150 genomes from Denmark as a population reference. Nature, 548(7665), 87-91. https://doi.org/10.1038/nature23264

Staunstrup, N. H., Starnawska, A., Nyegaard, M., Nielsen, A. L., Borglum, A. D. & Mors, O. (2017). The Genome-Wide DNA Methylation Profile of Peripheral Blood Is Not Systematically Changed by Short-Time Storage at Room Temperature. Epigenomes, 1(3), Article 23. https://doi.org/10.3390/epigenomes1030023

Qvist, P., Christensen, J. H., Vardya, I., Rajkumar, A. P., Mørk, A., Paternoster, V., Füchtbauer, E.-M., Pallesen, J., Fryland, T., Dyrvig, M., Hauberg, M. E., Lundsberg, B., Fejgin, K., Nyegaard, M., Jensen, K., Nyengaard, J. R., Mors, O., Didriksen, M. & Børglum, A. D. (2017). The Schizophrenia-Associated BRD1 Gene Regulates Behavior, Neurotransmission, and Expression of Schizophrenia Risk Enriched Gene Sets in Mice. Biological Psychiatry, 82(1), 62-76. https://doi.org/10.1016/j.biopsych.2016.08.037

Lescai, F., Als, T. D., Li, Q., Nyegaard, M., Andorsdottir, G., Biskopstø, M., Hedemand, A., Fiorentino, A., O'Brien, N. L., Jarram, A., Liang, T. J., Grove, J., Pallesen, J., Eickhardt, E., Mattheisen, M., Bolund, L., Demontis, D., Wang, A. G., McQuillin, A. ... Børglum, A. D. (2017). Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder. Translational Psychiatry, 7(2), e1034. Article 3. https://doi.org/10.1038/tp.2017.3

Hauberg, M. E., Roussos, P., Grove, J., Børglum, A. D., Mattheisen, M. & Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016). Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants. JAMA Psychiatry, 73(4), 369-377. https://doi.org/10.1001/jamapsychiatry.2015.3018

Viuff, A.-C. F., Pedersen, L. H., Kyng, K., Staunstrup, N. H., Børglum, A. & Henriksen, T. B. (2016). Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review. Clinical Epigenetics (Print), 8(1), Article 94. https://doi.org/10.1186/s13148-016-0262-x

Starnawska, A., Demontis, D., Pen, A., Hedemand, A., Nielsen, A. L., Staunstrup, N. H., Grove, J., Als, T. D., Jarram, A., O'Brien, N. L., Mors, O., McQuillin, A., Børglum, A. D. & Nyegaard, M. (2016). CACNA1C hypermethylation is associated with bipolar disorder. Translational Psychiatry, 6(6), e831. Article e831. https://doi.org/10.1038/tp.2016.99

Rohde, P. D., Demontis, D., Castro Dias Cuyabano, B., Børglum, A. & Sørensen, P. (2016). Covariance Association Test (CVAT) Identifies Genetic Markers Associated with Schizophrenia in Functionally Associated Biological Processes. Genetics (Print), 203(4), 1901-1913. https://doi.org/10.1534/genetics.116.189498

Nissen, J. B., Søholm Hansen, C., Starnawska, A., Mattheisen, M., Børglum, A., Buttenschøn, H. N. & Hollegård, M. (2016). DNA Methylation at the Neonatal State and at the Time of Diagnosis: Preliminary Support for an Association with the Estrogen Receptor 1, Gamma-Aminobutyric Acid B Receptor 1, and Myelin Oligodendrocyte Glycoprotein in Female Adolescent Patients with OCD. Frontiers in Psychiatry, 7(35), Article 35. https://doi.org/10.3389/fpsyt.2016.00035

Robinson, E. B., St Pourcain, B., Anttila, V., Kosmicki, J. A., Bulik-Sullivan, B., Grove, J., Maller, J., Samocha, K. E., Sanders, S. J., Ripke, S., Martin, J., Hollegaard, M. V., Werge, T., Hougaard, D. M., Neale, B. M., Evans, D. M., Skuse, D., Mortensen, P. B., Børglum, A. D. ... Als, T. D. (2016). Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population. Nature Genetics, 48(5), 552–555. https://doi.org/10.1038/ng.3529

Staunstrup, N. H., Starnawska, A., Nyegaard, M., Christiansen, L., Nielsen, A. L., Børglum, A. & Mors, O. (2016). Genome-wide DNA methylation profiling with MeDIP-seq using archived dried blood spots. Clinical Epigenetics (Print), 8(81), Article 81. https://doi.org/10.1186/s13148-016-0242-1

Poulsen, J. B., Lescai, F., Grove, J., Bækvad-Hansen, M., Christiansen, M., Hagen, C. M., Maller, J., Stevens, C., Li, S., Li, Q., Sun, J., Wang, J., Nordentoft, M., Werge, T. M., Mortensen, P. B., Børglum, A. D., Daly, M., Hougaard, D. M., Bybjerg-Grauholm, J. & Hollegaard, M. V. (2016). High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA. PLOS ONE, 11(4), e0153253. Article e0153253. https://doi.org/10.1371/journal.pone.0153253

Starnawska, A., Demontis, D., McQuillin, A., O'Brien, N. L., Staunstrup, N. H., Mors, O., Nielsen, A. L., Børglum, A. D. & Nyegaard, M. (2016). Hypomethylation of FAM63B in bipolar disorder patients. Clinical Epigenetics (Print), 8(52), 1-6. Article 52. https://doi.org/10.1186/s13148-016-0221-6

Fryland, T., Christensen, J. H., Pallesen, J., Mattheisen, M., Palmfeldt, J., Bak, M., Grove, J., Demontis, D., Blechingberg, J., Ooi, H. S., Nyegaard, M., Hauberg, M. E., Tommerup, N., Gregersen, N., Mors, O., Corydon, T. J., Nielsen, A. L. & Børglum, A. D. (2016). Identification of the BRD1 interaction network and its impact on mental disorder risk. Genome Medicine, 8(1), 53. https://doi.org/10.1186/s13073-016-0308-x

Benros, M. E., Trabjerg, B. B., Meier, S., Mattheisen, M., Mortensen, P. B., Mors, O., Børglum, A. D., Hougaard, D. M., Nørgaard-Pedersen, B., Nordentoft, M. & Agerbo, E. (2016). Influence of Polygenic Risk Scores on the Association Between Infections and Schizophrenia. Biological Psychiatry, 80(8), 609–616. https://doi.org/10.1016/j.biopsych.2016.04.008

Johnson, E. C., Bjelland, D. W., Howrigan, D. P., Abdellaoui, A., Breen, G., Borglum, A., Cichon, S., Degenhardt, F., Forstner, A. J., Frank, J., Genovese, G., Heilmann-Heimbach, S., Herms, S., Hoffman, P., Maier, W., Mattheisen, M., Morris, D., Mowry, B., Müller-Mhysok, B. ... Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016). No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. P L o S Genetics, 12(10), e1006343. Article e1006343. https://doi.org/10.1371/journal.pgen.1006343

Hauberg, M. E., Holm-Nielsen, M. H., Mattheisen, M., Askou, A. L., Grove, J., Børglum, A. D. & Corydon, T. J. (2016). Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 26(9), 1522-6. https://doi.org/10.1016/j.euroneuro.2016.06.014

Gregersen, N., Lescai, F., Liang, J., Li, Q., Als, T. D., Buttenschøn, H. N., Hedemand, A., Biskopstø, M., Wang, J., Wang, A., Børglum, A., Mors, O. & Demontis, D. (2016). Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 171(8), 1013-1022. https://doi.org/10.1002/ajmg.b.32464

Demontis, D., Lescai, F., Børglum, A., Glerup, S., Østergaard, S. D., Mors, O., Li, Q., Liang, J., Jiang, H., Li, Y., Wang, J., Lesch, K.-P., Reif, A., Buitelaar, J. K. & Franke, B. (2016). Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 55(6), 521-3. https://doi.org/10.1016/j.jaac.2016.03.009

Björkman, A., Qvist, P., Du, L., Bartish, M., Zaravinos, A., Georgiou, K., Børglum, A., Gatti, R. A., Törngren, T. & Pan-Hammerström, Q. (2015). Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells. Proceedings of the National Academy of Sciences (PNAS), 112(7), 2157-2162. https://doi.org/10.1073/pnas.1418947112

Rajkumar, A. P., Christensen, J. H., Mattheisen, M., Jacobsen, I., Bache, I., Pallesen, J., Grove, J., Qvist, P., Mcquillin, A., Gurling, H. M., Tümer, Z., Mors, O. & Børglum, A. D. (2015). Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder. Bipolar Disorders (English Edition, Online), 17(2), 205-211. https://doi.org/10.1111/bdi.12239

Nyegaard, M., Rendtorff, N. D., Nielsen, M. S., Corydon, T. J., Demontis, D., Starnawska, A., Hedemand, A., Buniello, A., Niola, F., Overgaard, M. T., Leal, S. M., Ahmad, W., Wikman, F. P., Petersen, K. B., Crüger, D. G., Oostrik, J., Kremer, H., Tommerup, N., Frödin, M. ... Børglum, A. D. (2015). A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment. P L o S Genetics, 11(7), e1005386. https://doi.org/10.1371/journal.pgen.1005386

Loh, P.-R., Bhatia, G., Gusev, A., Finucane, H. K., Bulik-Sullivan, B. K., Pollack, S. J., Schizophrenia Working Group of the Psychiatric Genomics Consortium (Anders Børglum, Jakob Grove; members of -), O’Donovan, M. C., Neale, B. M., Patterson, N. & Price, A. L. (2015). Contrasting regional architectures of schizophrenia and other complex diseases using fast variance components analysis. Nature Genetics, 47, 1385–1392. https://doi.org/10.1038/ng.3431

Liu, S., Huang, S., Rao, J., Ye, W., Genome Denmark Consortium (Anders Børglum, member of -), Krogh, A. & Wang, J. (2015). Discovery, genotyping and characterization of structural variation and novel sequence at single nucleotide resolution from de novo genome assemblies on a population scale. GigaScience, 4, 64. https://doi.org/10.1186/s13742-015-0103-4

Rajkumar, A. P., Qvist, P., Lazarus, R., Lescai, F., Ju, J., Nyegaard, M., Mors, O., Børglum, A. D., Li, Q. & Christensen, J. H. (2015). Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq. B M C Genomics, 16, 548. https://doi.org/10.1186/s12864-015-1767-y

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. ... MooDS SCZ Consortium (2015). High loading of polygenic risk in cases with chronic schizophrenia. Molecular Psychiatry, 1-6. https://doi.org/10.1038/mp.2015.130