Srdjan Djurovic

Professor

Department of Clinical Science

E-mailSrdjan.Djurovic@uib.no
Visitor Address
Haukeland universitetssykehus, Laboratoriebygget

5009 Bergen
Postal Address
Postboks 7804

5020 Bergen

Publications

Academic article

Show author(s) (2024). Divergent epigenetic responses to perinatal asphyxia in severe mental disorders. Translational Psychiatry. 12 pages.
Show author(s) (2024). Bipolar patients display stoichiometric imbalance of gene expression in post-mortem brain samples. Molecular Psychiatry.

Show author(s) (2022). The shared genetic basis of mood instability and psychiatric disorders: A cross-trait genome-wide association analysis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 207-218.
Show author(s) (2022). Shared genetic loci between depression and cardiometabolic traits. PLoS Genetics. 25 pages.
Show author(s) (2022). Multimodal monitoring of human cortical organoids implanted in mice reveal functional connection with visual cortex. Nature Communications. 15 pages.
Show author(s) (2022). Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. 502-508.
Show author(s) (2022). Inflammation and cognition in severe mental illness: patterns of covariation and subgroups. Molecular Psychiatry. 1284-1292.
Show author(s) (2022). Genetic overlap between mood instability and alcohol-related phenotypes suggests shared biological underpinnings. Neuropsychopharmacology. 1883-1891.
Show author(s) (2022). Elevated Systemic Levels of Markers Reflecting Intestinal Barrier Dysfunction and Inflammasome Activation Are Correlated in Severe Mental Illness. Schizophrenia Bulletin. 635-645.
Show author(s) (2022). Composite immune marker scores associated with severe mental disorders and illness course. Brain, Behavior, and Immunity - Health (BBI - Health).
Show author(s) (2022). Charting the Landscape of Genetic Overlap Between Mental Disorders and Related Traits Beyond Genetic Correlation. American Journal of Psychiatry. 833-843.
Show author(s) (2022). Boosting Schizophrenia Genetics by Utilizing Genetic Overlap With Brain Morphology. Biological Psychiatry. 291-298.

Show author(s) (2021). Telomeres are shorter and associated with number of suicide attempts in affective disorders. Journal of Affective Disorders. 1032-1039.
Show author(s) (2021). Lower circulating neuron-specific enolase concentrations in adults and adolescents with severe mental illness. Psychological Medicine. 1-10.
Show author(s) (2021). Increased circulating IL-18 levels in severe mental disorders indicate systemic inflammasome activation. Brain, Behavior, and Immunity. 299-306.
Show author(s) (2021). Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature Genetics. 817-829.
Show author(s) (2021). Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium. Journal of Psychiatric Research. 215-224.
Show author(s) (2021). Genetic Association Between Schizophrenia and Cortical Brain Surface Area and Thickness. JAMA psychiatry. 1020-1030.
Show author(s) (2021). Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs. Human Brain Mapping. 470-499.
Show author(s) (2021). Characterisation of age and polarity at onset in bipolar disorder. British Journal of Psychiatry. 659-669.
Show author(s) (2021). 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Translational Psychiatry. 16 pages.

Show author(s) (2020). Identification of a novel polymorphism associated with reduced clozapine concentration in schizophrenia patients—a genome-wide association study adjusting for smoking habits. Translational Psychiatry. 1-10.
Show author(s) (2020). Genetic control of variability in subcortical and intracranial volumes. Molecular Psychiatry. 1-8.

Show author(s) (2019). The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia. Schizophrenia Bulletin. 9 pages.
Show author(s) (2019). Telomere length is associated with childhood trauma in patients with severe mental disorders. Translational Psychiatry. 7 pages.
Show author(s) (2019). Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk. Nature Genetics. 404-413.
Show author(s) (2019). Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics. 793-803.
Show author(s) (2019). GWASinlps: Non-local prior based iterative SNP selection tool for genome-wide association studies. Bioinformatics. 1-11.
Show author(s) (2019). GWAS of suicide attempt in psychiatric disorders and association with major depression polygenic risk scores. American Journal of Psychiatry. 651-660.
Show author(s) (2019). GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study. Scientific Reports.
Show author(s) (2019). Common brain disorders are associated with heritable patterns of apparent aging of the brain. Nature Neuroscience. 1617-1623.
Show author(s) (2019). Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder. Translational Psychiatry. 1-9.
Show author(s) (2019). Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA psychiatry. 11 pages.
Show author(s) (2019). Alterations in schizophrenia-associated genes can lead to increased power in delta oscillations. Cerebral Cortex. 875-891.

Show author(s) (2018). Vitamin D levels, brain volume, and genetic architecture in patients with psychosis. PLOS ONE. 17 pages.
Show author(s) (2018). The relationship between physical activity, clinical and cognitive characteristics and BDNF mRNA levels in patients with severe mental disorders. World Journal of Biological Psychiatry. 24 pages.
Show author(s) (2018). Stability of the Brain Functional Connectome Fingerprint in Individuals With Schizophrenia. JAMA psychiatry.
Show author(s) (2018). Improving genetic prediction by leveraging genetic correlations among human diseases and traits. Nature Communications. 1-17.
Show author(s) (2018). Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes. Cell. 1705-1715.
Show author(s) (2018). Expression of TCN1 in Blood is Negatively Associated with Verbal Declarative Memory Performance. Scientific Reports. 1-11.
Show author(s) (2018). Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics. 381-389.
Show author(s) (2018). Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder. Neuropsychopharmacology. 620-628.
Show author(s) (2018). Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Communications Biology. 10 pages.
Show author(s) (2018). An association between YKL-40 and type 2 diabetes in psychotic disorders. Acta Psychiatrica Scandinavica. 37-45.
Show author(s) (2018). Age at first birth in women is genetically associated with increased risk of schizophrenia. Scientific Reports. 14 pages.

Show author(s) (2017). Task modulations and clinical manifestations in the brain functional connectome in 1615 fMRI datasets. NeuroImage. 243-252.
Show author(s) (2017). Psychotic patients who used cannabis frequently before illness onset have higher genetic predisposition to schizophrenia than those who did not. Psychological Medicine. 43-49.
Show author(s) (2017). Probing the association between early evolutionary markers and schizophrenia. PLOS ONE. 1-15.
Show author(s) (2017). Persistent increase in TNF and IL-1 markers in severe mental disorders suggests trait-related inflammation: a one year follow-up study. Acta Psychiatrica Scandinavica. 400-408.
Show author(s) (2017). Parents’ Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder—Data from a Norwegian Sample. International Journal of Molecular Sciences. 1-14.
Show author(s) (2017). Novel genetic loci associated with hippocampal volume. Nature Communications. 1-12.
Show author(s) (2017). Leveraging genome characteristics to improve gene discovery for putamen subcortical brain structure. Scientific Reports. 1-9.
Show author(s) (2017). Large-scale cognitive GWAS meta-analysis reveals tissue-specific neural expression and potential nootropic drug targets. Cell reports. 2597-2613.
Show author(s) (2017). Identification of genetic loci shared between schizophrenia and the Big Five personality traits. Scientific Reports. 1-9.
Show author(s) (2017). Identification of genetic loci jointly influencing schizophrenia risk and the cognitive traits of verbal-numerical reasoning, reaction time, and general cognitive function. JAMA psychiatry. 1065-1075.
Show author(s) (2017). Identification of gene loci that overlap between schizophrenia and educational attainment. Schizophrenia Bulletin. 654-664.
Show author(s) (2017). Genome-wide pleiotropy between Parkinson disease and autoimmune diseases. JAMA Neurology. 780-792.
Show author(s) (2017). Genetic overlap between schizophrenia and volumes of hippocampus, putamen, and intracranial volume indicates shared molecular genetic mechanisms. Schizophrenia Bulletin. 854-864.
Show author(s) (2017). Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Nature Communications. 1-12.
Show author(s) (2017). Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis. Biological Psychiatry. 634-641.
Show author(s) (2017). GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report form the COGENT consortium. Molecular Psychiatry. 336-345.
Show author(s) (2017). Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations. NPJ GENOMIC MEDICINE. 12 pages.
Show author(s) (2017). Distinct multivariate brain morphological patterns and their added predictive value with cognitive and polygenic risk scores in mental disorders. NeuroImage: Clinical. 719-731.
Show author(s) (2017). Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nature Genetics. 27-35.
Show author(s) (2017). Combinations of genetic variants associated with bipolar disorder. PLOS ONE.
Show author(s) (2017). Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data. Translational Psychiatry.
Show author(s) (2017). A study of TNF pathway activation in schizophrenia and bipolar disorder in plasma and brain tissue. Schizophrenia Bulletin. 881-890.
Show author(s) (2017). A genetic association study of CSMD1 and CSMD2 with cognitive function. Brain, Behavior, and Immunity. 209-216.

Show author(s) (2016). VRK2 gene expression in schizophrenia, bipolar disorder and healthy controls. British Journal of Psychiatry. 114-120.
Show author(s) (2016). The roadmap for estimation of cell-typespecific neuronal activity from noninvasive measurements. Philosophical Transactions of the Royal Society of London. Biological Sciences. 16 pages.
Show author(s) (2016). The endogenous hallucinogen and trace amine N,N-dimethyltryptamine (DMT) displays potent protective effects against hypoxia via sigma-1 receptor activation in human primary iPSC-derived cortical neurons and microglia-like immune cells. Frontiers in Neuroscience.
Show author(s) (2016). Parents' attitudes toward genetic research in autism spectrum disorder. Psychiatric Genetics. 74-80.
Show author(s) (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience. 1569-1582.
Show author(s) (2016). Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS. PLoS Genetics. 22 pages.
Show author(s) (2016). Inflammatory evidence for the psychosis continuum model. Psychoneuroendocrinology. 189-197.
Show author(s) (2016). Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disorders. Nordic Journal of Psychiatry. 276-279.
Show author(s) (2016). Genome-wide autozygosity is associated with lower general cognitive ability. Molecular Psychiatry. 837-843.
Show author(s) (2016). Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple Sclerosis. 1783-1793.
Show author(s) (2016). Functional effects of schizophrenia-linked genetic variants on intrinsic single-neuron excitability: a modeling study. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. 49-59.
Show author(s) (2016). Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women. JAMA psychiatry. 497-505.
Show author(s) (2016). Contribution of oxytocin receptor polymorphisms to amygdala activation in schizophrenia spectrum disorders. BJPsych Open. 353-358.
Show author(s) (2016). Conservation of Distinct Genetically-Mediated Human Cortical Pattern. PLoS Genetics. 18 pages.
Show author(s) (2016). Cell type specificity of neurovascular coupling in cerebral cortex. eLIFE.
Show author(s) (2016). A sequence variant associating with educational attainment also affects childhood cognition. Scientific Reports.

Show author(s) (2015). Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature Neuroscience.
Show author(s) (2015). Polygenic risk scores in bipolar disorders subgroups. Journal of Affective Disorders. 310-314.
Show author(s) (2015). Polygenic risk for schizophrenia associated with working memory-related prefrontal brain activation in patients with schizophrenia and healthy controls. Schizophrenia Bulletin. 736-743.
Show author(s) (2015). Polygenic overlap between C-reactive protein, plasma lipids, and Alzheimer disease. Circulation. 2061-2069.
Show author(s) (2015). New data and an old puzzle: The negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology. 1706-1721.
Show author(s) (2015). Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. American Journal of Human Genetics.
Show author(s) (2015). Microarray analysis of copy number variants on the human y chromosome reveals novel and frequent duplications overrepresented in specific haplogroups. PLOS ONE.
Show author(s) (2015). MicroRNAs enrichment in GWAS of complex human phenotypes. BMC Genomics.
Show author(s) (2015). Loss-of-function variants in ABCA7 confer risk of Alzheimer’s disease. Nature Genetics. 445-447.
Show author(s) (2015). Large-scale genomics unveil polygenic architecture of human cortical surface area. Nature Communications.
Show author(s) (2015). LD score regression distinguishes confounding from polygenicity in genome-wide association studies. Nature Genetics. 291-295.
Show author(s) (2015). Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. American Journal of Human Genetics. 283-294.
Show author(s) (2015). Investigation of the genetic interaction between BDNF and DRD3 genes in suicidical behaviour in psychiatric disorders. World Journal of Biological Psychiatry. 171-179.
Show author(s) (2015). Inflammatory markers are associated with general cognitive abilities in schizophrenia and bipolar disorder patients and healthy controls. Schizophrenia Research. 188-194.
Show author(s) (2015). Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 363-373.
Show author(s) (2015). Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes with Several Cardiovascular Risk Factors. Circulation Research. 83-94.
Show author(s) (2015). Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs. Journal of Psychopharmacology. 884-891.
Show author(s) (2015). Genome-wide analysis of attention deficit hyperactivity disorder in Norway. PLOS ONE. 17 pages.
Show author(s) (2015). Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci. PLOS ONE.
Show author(s) (2015). Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci. Molecular Psychiatry. 207-214.
Show author(s) (2015). Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus. Molecular Psychiatry. 1588-1595.
Show author(s) (2015). Genetic Markers of Human Evolution Are Enriched in Schizophrenia. Biological Psychiatry.
Show author(s) (2015). Common genetic variants influence human subcortical brain structures. Nature. 224-229.
Show author(s) (2015). Combinations of genetic data present in bipolar patients, but absent in control persons. PLOS ONE. 7 pages.
Show author(s) (2015). Association between genetic variation in the oxytocin receptor gene and emotional withdrawal, but not between oxytocin pathway genes and diagnosis in psychotic disorders. Frontiers in Human Neuroscience. 1-7.
Show author(s) (2015). Association between altered brain morphology and elevated peripheral endothelial markers — Implications for psychotic disorders . Schizophrenia Research. 222-228.
Show author(s) (2015). Altered brain activation during emotional face processing in relation to both diagnosis and polygenic risk of bipolar disorder. PLOS ONE.
Show author(s) (2015). Abundant genetic overlap between blood lipids and immune-mediated diseases indicates shared molecular genetic mechanisms. PLOS ONE.
Show author(s) (2015). A Loss-of-Function Variant in a Minor Isoform of ANK3 Protects Against Bipolar Disorder and Schizophrenia. Biological Psychiatry.

Show author(s) (2014). The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior. 153-182.
Show author(s) (2014). Shared common variants in prostate cancer and blood lipids. International Journal of Epidemiology. 1205-1214.
Show author(s) (2014). Polygenic risk score and the psychosis continuum model. Acta Psychiatrica Scandinavica. 311-317.
Show author(s) (2014). Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Molecular Psychiatry. 1017-1024.
Show author(s) (2014). Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: A report from the Cognitive Genomics consorTium (COGENT). Molecular Psychiatry. 168-174.
Show author(s) (2014). Interplay between childhood trauma and BDNF val66met variants on blood BDNF mRNA levels and on hippocampus subfields volumes in schizophrenia spectrum and bipolar disorders. Journal of Psychiatric Research. 14-21.
Show author(s) (2014). Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes. Hypertension. 819-826.
Show author(s) (2014). GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. Genes, Brain and Behavior.
Show author(s) (2014). Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry. 108-114.
Show author(s) (2014). Biological insights from 108 schizophrenia-associated genetic loci. Nature. 421-427.
Show author(s) (2014). Association analysis between suicidal behaviour and candidate genes of bipolar disorder and schizophrenia. Journal of Affective Disorders. 110-114.
Show author(s) (2014). An attempt to identify single nucleotide polymorphisms contributing to possible relationships between personality traits and oxytocin-related genes. Neuropsychobiology. 25-30.
Show author(s) (2014). ANK3 gene expression in bipolar disorder and schizophrenia. British Journal of Psychiatry. 244-245.

Show author(s) (2013). ZNF804A and cortical thickness in schizophrenia and bipolar disorder. Psychiatry Research : Neuroimaging. 154-157.
Show author(s) (2013). Pathway analysis of genetic markers associated with a functional MRI faces paradigm implicates polymorphisms in calcium responsive pathways. NeuroImage. 143-149.
Show author(s) (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 984-994.
Show author(s) (2013). CACNA1C Risk Variant and Amygdala Activity in Bipolar Disorder, Schizophrenia and Healthy Controls. PLOS ONE. 6 pages.
Show author(s) (2013). BDNF val66met modulates the association between childhood trauma, cognitive and brain abnormalities in psychoses. Progress in Neuro-psychopharmacology and Biological Psychiatry. 181-188.
Show author(s) (2013). A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder. PLOS ONE. 9 pages.

Show author(s) (2012). Up-Regulation of NOTCH4 Gene Expression in Bipolar Disorder. American Journal of Psychiatry. 1292-1300.
Show author(s) (2012). TCF4 sequence variants and mRNA levels are associated with neurodevelopmental characteristics in psychotic disorders. Translational Psychiatry.
Show author(s) (2012). Serotonin Transporter Gene Polymorphism, Childhood Trauma, and Cognition in Patients With Psychotic Disorders. Schizophrenia Bulletin. 15-22.
Show author(s) (2012). Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics. 552-561.
Show author(s) (2012). Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function. Journal of Psychiatric Research. 271-278.
Show author(s) (2012). Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment - a cross-sectional naturalistic study. Psychiatry Research. 327-336.
Show author(s) (2012). 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. 3985-3990.
Show author(s) (2012). Association between a genetic variant in the serotonin transporter gene (SLC6A4) and suicidal behavior in patients with schizophrenia. Behavioral and Brain Functions. 8 pages.

Show author(s) (2011). The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia. Biological Psychiatry. 35-42.
Show author(s) (2011). Intron 12 in NTRK3 is associated with bipolar disorder. Psychiatry Research. 358-362.
Show author(s) (2011). Genome-wide association study identifies five new schizophrenia loci. Nature Genetics. 969-976.
Show author(s) (2011). Copy number variations in affective disorders and meta-analysis. Psychiatric Genetics. 319-322.
Show author(s) (2011). Common Sequence Variants in the Major Histocompatibility Complex Region Associate with Cerebral Ventricular Size in Schizophrenia. Biological Psychiatry. 696-698.
Show author(s) (2011). Candidate Gene Analysis of the Human Natural Killer-1 Carbohydrate Pathway and Perineuronal Nets in Schizophrenia: B3GAT2 Is Associated with Disease Risk and Cortical Surface Area. Biological Psychiatry. 90-96.
Show author(s) (2011). Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia. Archives of General Psychiatry. 781-790.
Show author(s) (2011). Association Analysis of ANK3 Gene Variants in Nordic Bipolar Disorder and Schizophrenia Case-Control Samples. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 969-974.

Show author(s) (2010). 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. 387-396.
Show author(s) (2010). 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. 384-388.
Show author(s) (2010). Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples. Molecular Psychiatry. 463-472.
Show author(s) (2010). Osteoprotegerin levels in patients with severe mental disorders. Journal of Psychiatry & Neuroscience. 304-310.
Show author(s) (2010). Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. Journal of Psychiatric Research. 748-753.
Show author(s) (2010). Catechol O-methyltransferase variants and cognitive performance in schizophrenia and bipolar disorder versus controls. Schizophrenia Research. 31-37.
Show author(s) (2010). Association Study of PDE48 gene variants in Scandinavian schizophrenia and bipolar disorder multicenter case-control samples. American Journal of Medical Genetics. 86-96.
Show author(s) (2010). Association Analysis of PALB2 and BRCA2 in Bipolar Disorder and Schizophrenia in a Scandinavian Case–Control Sample. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 1276-1280.
Show author(s) (2010). A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. Human Molecular Genetics. 1379-1386.
Show author(s) (2010). A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample. Journal of Affective Disorders. 312-316.

Show author(s) (2009). Tyrosine hydroxylase Val81Met polymorphism: lack of association with schizophrenia. Psychiatric Genetics. 273-274.
Show author(s) (2009). Three-cohort targeted gene screening reveals a non-synonymous TRKA polymorphism associated with schizophrenia. Journal of Psychiatric Research. 1195-1199.
Show author(s) (2009). No association between DGKH and bipolar disorder in a Scandinavian case-control sample. Psychiatric Genetics. 269-272.
Show author(s) (2009). Disruption of the neurexin 1 gene is associated with schizophrenia. Human Molecular Genetics. 988-996.
Show author(s) (2009). DTNBP1, NRG1, DAOA, DAO and GRM3 Polymorphisms and Schizophrenia: An Association Study. Neuropsychobiology. 142-150.
Show author(s) (2009). Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Molecular Psychiatry. 1-9.
Show author(s) (2009). Common variants conferring risk of schizophrenia. Nature. 744-747.
Show author(s) (2009). Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE). Psychiatry Research. 256-258.
Show author(s) (2009). A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE). Schizophrenia Research. 242-248.
Show author(s) (2009). 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. 15483-15488.

Show author(s) (2008). Two methylenetetrahydrofolate reductase gene (MTHFR) polymorphisms, schizophrenia and bipolar disorder: An association study. American Journal of Medical Genetics. 976-982.
Show author(s) (2008). Large recurrent microdeletions associated with schizophrenia. Nature. 232-U61.
Show author(s) (2008). Association between a disrupted-in-schizophrenia 1 (DISC1) single nucleotide polymorphism and schizophrenia in a combined Scandinavian case-control sample. Schizophrenia Research. 237-241.
Show author(s) (2008). Association Analysis of Schizophrenia on 18 Genes Involved in Neuronal Migration: MDGA1 as a New Susceptibility Gene. American Journal of Medical Genetics. 1089-1100.
Show author(s) (2008). A novel myogenic cell line with phenotypic properties of muscle progenitors. Journal of Molecular Medicine. 105-115.

Show author(s) (2007). The effect of red wine on plasma leptin levels and vasoactive factors from adipose tissue: A randomized crossover trial. Alcohol and Alcoholism. 525-528.

Show author(s) (2005). Activity of peroxisomal enzymes, and levels of polyamines in LPA-transgenic mice on two different diets. Lipids in Health and Disease. 12 pages.

Academic lecture

Show author(s) (2018). Affective lability and polygenic risk in bipolar disorder.

Show author(s) (2017). Layer V pyramidal cells as mediators of delta oscillations: Insights from biophysically detailed modeling and connections with schizophrenia genetics.
Show author(s) (2017). Delta oscillations in schizophrenia: Insights from biophysically detailed modeling of networks of layer V pyramidal cells.
Show author(s) (2017). Conditional false discovery rate analysis of genome-wide association studies uncovers genetic loci shared between schizophrenia and volumes of hippocampus, putamen and intracranial volume.

Show author(s) (2016). Genetic overlap between schizophrenia and brain structural volumes indicates shared molecular genetic mechanisms with potential relevance for antipsychotics .

Show author(s) (2006). Syndecan-4 is an essential signal transducer for activation of the calcineurin-NFAT pathway and cardiac hypertrophy in mice.

Show author(s) (2005). Why syndecan-4 might be important in heart failure following myocardial infarction.
Show author(s) (2005). A role for syndecan-4 during development of heart failure following myocaridal infarction.
Show author(s) (2005). A role for syndecan-4 as a signal transducer during development of heart failure following myocardial infarction.

Abstract

Show author(s) (2019). Genome wide Association study: identifying Genetic markers in apathy in People with Alzheimer's disease. Alzheimer's & Dementia. P286-P286.

Show author(s) (2013). Is Met Variant of the BDNF VAL66MET-Combined with Childhood Trauma - A Risk Factor of Brain Abnormalities in Psychoses? Biological Psychiatry. 287S-287S.

Show author(s) (2012). Interactions between BDNF Val66Met gene polymorphism, childhood adverse events and brain volume changes in schizophrenia and bipolar disorder. Early Intervention in Psychiatry. 30-30.
Show author(s) (2012). Interaction between (BDNF) VAL66Met, childhood adverse events and impaired cognition in patients with schizophrenia spectrum and bipolar disorder. Early Intervention in Psychiatry. 45-45.

Show author(s) (2011). SEROTONIN TRANSPORTER GENE POLYMORPHISMS, CHILDHOOD TRAUMA AND COGNITION IN PATIENTS WITH PSYCHOTIC DISORDERS. Schizophrenia Bulletin. 80-80.

Show author(s) (2009). DYSBINDIN AND D-AMINO-ACID-OXIDASE GENE POLYMORPHISMS ASSOCIATED WITH POSITIVE AND NEGATIVE SYMPTOMS IN SCHIZOPHRENIA. Schizophrenia Bulletin. 105-105.
Show author(s) (2009). ASSOCIATION BETWEEN THE TRYPTOPHAN HYDROXYLASE 1 (TPH1) GENE, SCHIZOPHRENIA SUSCEPTIBILITY, AND SUICIDAL BEHAVIOR. Schizophrenia Bulletin. 121-121.

Show author(s) (2008). Interaction between health behaviour, mental distress and the polymorphism of the serotonin transporter gene among adolescents in Oslo, Norway. European psychiatry. S174-S174.

Show author(s) (2003). Effect of cholesterol feeding on apo(a), CYP7A1 and LXR alpha expression in LPA transgenic mice. Atherosclerosis Supplements. 296-296.

Academic literature review

Show author(s) (2024). How real-world data can facilitate the development of precision medicine treatment in psychiatry. Biological Psychiatry.

Show author(s) (2020). Copy number variants (CNVs): A powerful tool for iPSC-based modelling of ASD. Molecular Autism. 1-18.

Show author(s) (2019). Discovery of shared genomic loci using the conditional false discovery rate approach. Human Genetics. 1-10.
Show author(s) (2019). Biophysical Psychiatry—How Computational Neuroscience Can Help to Understand the Complex Mechanisms of Mental Disorders. Frontiers in Psychiatry. 14 pages.

Show author(s) (2017). Genetic evidence for role of integration of fast and slow neurotransmission in schizophrenia. Molecular Psychiatry. 792-801.

Show author(s) (2016). Modeling psychiatric disorders: From genomic findings to cellular phenotypes. Molecular Psychiatry. 1167-1179.

Show author(s) (2010). SRD5A2 is associated with increased cortisol metabolism in schizophrenia spectrum disorders. Progress in Neuro-psychopharmacology and Biological Psychiatry. 1500-1506.

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