Publications

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Johannesen, M. D., Qvist, P., Lichota, J., et al., 1.2017, "DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele", P L o S One. Journal article
Power, R. A., Tansey, K. E., Buttenschøn, H. N., et al., 2017, "Genome-wide Association for Major Depression Through Age at Onset Stratification", Biological psychiatry. Journal article
Starnawska, A., Tan, Q., Lenart, A., et al., 4.11.2016, "Blood DNA methylation age is not associated with cognitive functioning in middle-aged monozygotic twins", Neurobiology of Aging. Journal article
Qvist, P., Christensen, J. H., Vardya, I., et al., 15.9.2016, "The Schizophrenia-Associated BRD1 Gene Regulates Behavior, Neurotransmission, and Expression of Schizophrenia Risk Enriched Gene Sets in Mice", Biological psychiatry. Journal article
Hauberg, M. E., Holm-Nielsen, M. H., Mattheisen, M., et al., 9.2016, "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. Journal article
Rohde, P. D., Demontis, D., Castro Dias Cuyabano, B., Børglum, A., Sørensen, P., 25.8.2016, "Covariance Association Test (CVAT) Identifies Genetic Markers Associated with Schizophrenia in Functionally Associated Biological Processes". Poster
Rohde, P. D., Demontis, D., Castro Dias Cuyabano, B., Børglum, A., Sørensen, P., 1.8.2016, "Covariance Association Test (CVAT) Identifies Genetic Markers Associated with Schizophrenia in Functionally Associated Biological Processes", Genetics (Print). Journal article
Staunstrup, N. H., Starnawska, A., Nyegaard, M., et al., 26.7.2016, "Genome-wide DNA methylation profiling with MeDIP-seq using archived dried blood spots", Clinical Epigenetics (Print). Journal article
Viuff, A. F., Pedersen, L. H., Kyng, K. J., Staunstrup, N. H., Børglum, A., Henriksen, T. B., 22.6.2016, "Epigenetic changes in newborns exposed to antidepressant medication during pregnancy - a planned genome wide study". Poster
Rohde, P. D., Demontis, D., Castro Dias Cuyabano, B., Børglum, A., Sørensen, P., 12.6.2016, "Covariance Association Test (CVAT) Identifies Genetic Markers Associated with Schizophrenia in Functionally Associated Biological Processes". Poster
Starnawska, A., Demontis, D., Pen, A., et al., 7.6.2016, "CACNA1C hypermethylation is associated with bipolar disorder", Translational Psychiatry. Journal article
Demontis, D., Lescai, F., Børglum, A., et al., 6.2016, "Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder", American Academy of Child and Adolescent Psychiatry. Journal. Journal article
Starnawska, A., Demontis, D., McQuillin, A., et al., 11.5.2016, "Hypomethylation of FAM63B in bipolar disorder patients", Clinical Epigenetics (Print). Journal article
Fryland, T., Christensen, J. H., Pallesen, J., et al., 3.5.2016, "Identification of the BRD1 interaction network and its impact on mental disorder risk", Genome Medicine. Journal article
Benros, M. E., Trabjerg, B. B., Meier, S., et al., 19.4.2016, "Influence of Polygenic Risk Scores on the Association Between Infections and Schizophrenia", Biological psychiatry. Journal article
Paternoster, V., Edhager, A. V., Sibbersen, C., et al., 15.4.2016, "Quantitative assessment of methyl-esterification and other side reactions in a standard propionylation protocol for detection of histone modifications", Proteomics. Journal article
Hauberg, M. E., Roussos, P., Grove, J., Børglum, A. D., Mattheisen, M., , , 9.3.2016, "Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants", JAMA Psychiatry. Journal article
Poulsen, J. B., Lescai, F., Grove, J., et al., 2016, "High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA", PloS one. Journal article
Robinson, E. B., St Pourcain, B., Anttila, V., et al., 2016, "Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population", Nature genetics. Journal article
Nissen, J. B., Søholm Hansen, C., Starnawska, A., et al., 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. Journal article
Viuff, A. 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", Clinical Epigenetics (Print). Journal article
Liu, S., Huang, S., Rao, J., et al., 1.12.2015, "Discovery, genotyping and characterization of structural variation and novel sequence at single nucleotide resolution from de novo genome assemblies on a population scale", GigaScience. Journal article
Bak, S. T., Staunstrup, N. H., Starnawska, A., et al., 5.11.2015, "Evaluating the Usability of Long-Term Stored Human Brain Bank Tissue for the Analysis of Epigenetic Markers". Poster
Luo, Y., Friis, J. B., Fernandes, A. M., et al., 11.2015, "EWS and FUS bind a subset of transcribed genes encoding proteins enriched in RNA regulatory functions", BMC Genomics. Journal article
Als, T. D., Lescai, F., Dahl, H., et al., 17.10.2015, "Identifying Rare Variation in Cases of Schizophrenia in the Isolated Population of the Faroe Islands using Whole-genome Sequencing". Poster
Vilhjálmsson, B. J., Yang, J., Finucane, H. K., et al., 1.10.2015, "Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores", American Journal of Human Genetics. Journal article
Meier, S. M., Agerbo, E., Maier, R., et al., 1.9.2015, "High loading of polygenic risk in cases with chronic schizophrenia", Molecular Psychiatry. Journal article
Agerbo, E., Sullivan, P. F., Vilhjálmsson, B. J., et al., 7.2015, "Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia", J A M A Psychiatry. Journal article
Nyegaard, M., Rendtorff, N. D., Nielsen, M. S., et al., 7.2015, "A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment", P L o S Genetics. Journal article
Debost, J., Petersen, L., Grove, J., et al., 11.6.2015, "Investigating interactions between early life stress and two single nucleotide polymorphisms in HSD11B2 on the risk of schizophrenia", Psychoneuroendocrinology. Journal article
Starnawska, A., McQuillin, A., Demontis, D., et al., 5.6.2015, "DNA methylation of CACNA1C in bipolar disorder". Poster
Rohde, P. D., Demontis, D., Arvidson, S. M. N., et al., 19.5.2015, "Functional Insight From Fruit Flies on Human ADHD Candidate Genes", Genes, Brain, and Behavior 2015. Article in proceedings
Luo, X., Mattheisen, M., Li, M., et al., 10.3.2015, "Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function", Schizophrenia Bulletin. Journal article
Bolund, L., Brunak, S., Brünner, N., et al., 20.1.2015, "Paradigmeskifte i dansk sundhedsvidenskab: Nye muligheder i diagnostik og behandling", Videnskab.dk. Comment/debate
Björkman, A., Qvist, P., Du, L., et al., 7.1.2015, "Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells", PNAS (Proceedings of the National Academy of Sciences of the United States of America). Journal article
Rajkumar, A., Christensen, J. H., Mattheisen, M., et al., 1.1.2015, "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). Journal article
Besenbacher, S., Liu, S., Izarzugaza, J. M. G., et al., 2015, "Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios", Nature Communications. Journal article
Rajkumar, A. P., Qvist, P., Lazarus, R., et al., 2015, "Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq", B M C Genomics. Journal article
Buttenschøn, H. N., Demontis, D., Ollendorff, M. K., et al., 2015, "Increased serum levels of sortilin are associated with depression and correlated with BDNF and VEGF", Translational Psychiatry. Journal article
Eickhardt, E. A., Als, T. D., Mattheisen, M., et al., 2015, "Genome-Wide Landscape of Genetic Variation with a Functional Impact on Predicted Binding Activity of Transcription Factor Binding Sites". Poster
Loh, P., Bhatia, G., Gusev, A., et al., 2015, "Contrasting regional architectures of schizophrenia and other complex diseases using fast variance components analysis", Nature Genetics. Journal article
Grove, J., Børglum, A., Pearce, B. D., 12.2014, "GWAS, Cytomegalovirus Infection, and Schizophrenia", Current Behavioral Neuroscience Reports. Journal article
Mors, O., Børglum, A. D., 10.11.2014, "Genomet og psykiatrien", Ugeskrift for laeger. Journal article
, , Mattheisen, M., Børglum, A., et al., 24.7.2014, "Biological insights from 108 schizophrenia-associated genetic loci", Nature. Journal article
Marcheco-Teruel, B., Parra, E. J., Fuentes-Smith, E., et al., 7.2014, "Cuba", P L o S Genetics. Journal article
Juraeva, D., Haenisch, B., Zapatka, M., et al., 6.2014, "Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia", P L o S Genetics. Journal article
Elfving, B., Buttenschøn, H. N., Foldager, L., et al., 17.3.2014, "Depression and BMI influences the serum vascular endothelial growth factor level", International Journal of Neuropsychopharmacology. Journal article
Gregersen, N. O., Buttenschøn, H. N., Hedemand, A., et al., 2.2014, "Are TMEM genes potential candidate genes for panic disorder?", Psychiatric Genetics. Journal article
Steinberg, S., de Jong, S., Mattheisen, M., et al., 2014, "Common variant at 16p11.2 conferring risk of psychosis", Molecular Psychiatry. Journal article
Børglum, A. D., Demontis, D., Grove, J., et al., 2014, "Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci", Molecular Psychiatry. Journal article

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Susanne Schousboe Sjøgaard

Revised 18.01.2017