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, , Pardiñas, A. F., Holmans, P., et al., 3.2018, "Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection", Nature genetics. Journal article
Paternoster, V., Rajkumar, A. P., Nyengaard, J. R., Børglum, A. D., Grove, J., Christensen, J. H., 15.2.2018, "The importance of data structure in statistical analysis of dendritic spine morphology", Journal of Neuroscience Methods. Journal article
Sullivan, P. F., Agrawal, A., Bulik, C. M., et al., 1.1.2018, "Psychiatric Genomics", The American Journal of Psychiatry (Spanish Edition). Journal article
Bak, S. T., Staunstrup, N. H., Starnawska, A., et al., 1.2018, "Evaluating the Feasibility of DNA Methylation Analyses Using Long-Term Archived Brain Formalin-Fixed Paraffin-Embedded Samples", Molecular Neurobiology. Journal article
Paksarian, D., Trabjerg, B. B., Merikangas, K. R., et al., 2018, "The role of genetic liability in the association of urbanicity at birth and during upbringing with schizophrenia in Denmark", Psychological Medicine. Journal article
Pedersen, C. B., Bybjerg-Grauholm, J., Pedersen, M. G., et al., 2018, "The iPSYCH2012 case-cohort sample", Molecular Psychiatry. Journal article
, , , , Warrier, V., et al., 2018, "Genome-wide analyses of self-reported empathy", Translational Psychiatry. Journal article
, , Hannon, E., Schendel, D., et al., 2018, "Elevated polygenic burden for autism is associated with differential DNA methylation at birth", Genome Medicine. Journal article
Starnawska, A., Tan, Q., McGue, M., et al., 12.12.2017, "Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins", Frontiers in Aging Neuroscience. Journal article
Rietschel, L., Streit, F., Zhu, G., et al., 10.11.2017, "Hair Cortisol in Twins", Scientific Reports. Journal article
Joshi, P. K., Pirastu, N., Kentistou, K. A., et al., 13.10.2017, "Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity", Nature Communications. Journal article
Direk, N., Williams, S., Smith, J. A., et al., 1.9.2017, "An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype", Biological psychiatry. Journal article
Jensen, J. M., Villesen, P., Friborg, R. M., et al., 9.2017, "Assembly and analysis of 100 full MHC haplotypes from the Danish population", Genome Research. Journal article
Maretty, L., Jensen, J. M., Petersen, B., et al., 3.8.2017, "Sequencing and de novo assembly of 150 genomes from Denmark as a population reference", Nature. Journal article
Witt, S. H., Streit, F., Jungkunz, M., et al., 20.6.2017, "Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia", Translational Psychiatry. Journal article
Debost, J., Debost, M., Grove, J., et al., 29.5.2017, "COMT Val158Met and MTHFR C677T moderate risk of schizophrenia in response to childhood adversity", Acta Psychiatrica Scandinavica. Journal article
Rohde, P. D., Demontis, D., Børglum, A., , , Sørensen, P., 27.5.2017, "Improved prediction of genetic predisposition to psychiatric disorders using genomic feature best linear unbiased prediction models". Poster
Weiner, D. J., Wigdor, E. M., Ripke, S., et al., 15.5.2017, "Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders", Nature genetics. Journal article
Qvist, P., Rajkumar, A. P., Redrobe, J. P., et al., 1.5.2017, "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. Journal article
McLaughlin, R. L., Schijven, D., van Rheenen, W., et al., 21.3.2017, "Genetic correlation between amyotrophic lateral sclerosis and schizophrenia", Nature Communications. Journal article
Lescai, F., Als, T. D., Li, Q., et al., 14.2.2017, "Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder", Translational Psychiatry. Journal article
Rajagopal, V. M., Agerbo, E., Timmermann, A., Børglum, A., Demontis, D., 27.1.2017, "Genome-wide association study of dyslexia in the Danish population". Poster
St Pourcain, B., Robinson, E. B., Anttila, V., et al., 3.1.2017, "ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties", Molecular Psychiatry. Journal article
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
Amidi , A., Agerbæk, M., Wu, L. M., et al., 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. 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
Laursen, T. M., Trabjerg, B. B., Mors, O., et al., 2017, "Association of the polygenic risk score for schizophrenia with mortality and suicidal behavior - A Danish population-based study", Schizophrenia Research. Journal article
Rajkumar, A. P., Horsdal, H. T., Wimberley, T., et al., 2017, "Endogenous and Antipsychotic-Related Risks for Diabetes Mellitus in Young People With Schizophrenia", American Journal of Psychiatry. Journal article
, , Grove, J., Børglum, A., 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. Journal article
Bolund, A. C. S., Starnawska, A., Miller, M. R., et al., 2017, "Lung function discordance in monozygotic twins and associated differences in blood DNA methylation", Clinical Epigenetics (Print). Journal article
Gregersen, N., Lescai, F., Liang, J., et al., 12.2016, "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. 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
Johnson, E. C., Bjelland, D. W., Howrigan, D. P., et al., 10.2016, "No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study", P L o S Genetics. 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

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Susanne Schousboe Sjøgaard

Revised 18.01.2017