- E-postSrdjan.Djurovic@uib.no
- BesøksadresseHaukeland universitetssykehus, Laboratoriebygget5009 Bergen
- PostadressePostboks 78045020 Bergen
Vitenskapelig artikkel
- (2024). Divergent epigenetic responses to perinatal asphyxia in severe mental disorders. Translational Psychiatry. 12 sider.
- (2024). Bipolar patients display stoichiometric imbalance of gene expression in post-mortem brain samples. Molecular Psychiatry.
- (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.
- (2022). Shared genetic loci between depression and cardiometabolic traits. PLoS Genetics. 25 sider.
- (2022). Multimodal monitoring of human cortical organoids implanted in mice reveal functional connection with visual cortex. Nature Communications. 15 sider.
- (2022). Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. 502-508.
- (2022). Inflammation and cognition in severe mental illness: patterns of covariation and subgroups. Molecular Psychiatry. 1284-1292.
- (2022). Genetic overlap between mood instability and alcohol-related phenotypes suggests shared biological underpinnings. Neuropsychopharmacology. 1883-1891.
- (2022). Elevated Systemic Levels of Markers Reflecting Intestinal Barrier Dysfunction and Inflammasome Activation Are Correlated in Severe Mental Illness. Schizophrenia Bulletin. 635-645.
- (2022). Composite immune marker scores associated with severe mental disorders and illness course. Brain, Behavior, and Immunity - Health (BBI - Health).
- (2022). Charting the Landscape of Genetic Overlap Between Mental Disorders and Related Traits Beyond Genetic Correlation. American Journal of Psychiatry. 833-843.
- (2022). Boosting Schizophrenia Genetics by Utilizing Genetic Overlap With Brain Morphology. Biological Psychiatry. 291-298.
- (2021). Telomeres are shorter and associated with number of suicide attempts in affective disorders. Journal of Affective Disorders. 1032-1039.
- (2021). Lower circulating neuron-specific enolase concentrations in adults and adolescents with severe mental illness. Psychological Medicine. 1-10.
- (2021). Increased circulating IL-18 levels in severe mental disorders indicate systemic inflammasome activation. Brain, Behavior, and Immunity. 299-306.
- (2021). Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature Genetics. 817-829.
- (2021). Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium. Journal of Psychiatric Research. 215-224.
- (2021). Genetic Association Between Schizophrenia and Cortical Brain Surface Area and Thickness. JAMA psychiatry. 1020-1030.
- (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.
- (2021). Characterisation of age and polarity at onset in bipolar disorder. British Journal of Psychiatry. 659-669.
- (2021). 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Translational Psychiatry. 16 sider.
- (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.
- (2020). Genetic control of variability in subcortical and intracranial volumes. Molecular Psychiatry. 1-8.
- (2019). The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia. Schizophrenia Bulletin. 9 sider.
- (2019). Telomere length is associated with childhood trauma in patients with severe mental disorders. Translational Psychiatry. 7 sider.
- (2019). Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk. Nature Genetics. 404-413.
- (2019). Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics. 793-803.
- (2019). GWASinlps: Non-local prior based iterative SNP selection tool for genome-wide association studies. Bioinformatics. 1-11.
- (2019). GWAS of suicide attempt in psychiatric disorders and association with major depression polygenic risk scores. American Journal of Psychiatry. 651-660.
- (2019). GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study. Scientific Reports.
- (2019). Common brain disorders are associated with heritable patterns of apparent aging of the brain. Nature Neuroscience. 1617-1623.
- (2019). Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder. Translational Psychiatry. 1-9.
- (2019). Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA psychiatry. 11 sider.
- (2019). Alterations in schizophrenia-associated genes can lead to increased power in delta oscillations. Cerebral Cortex. 875-891.
- (2018). Vitamin D levels, brain volume, and genetic architecture in patients with psychosis. PLOS ONE. 17 sider.
- (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 sider.
- (2018). Stability of the Brain Functional Connectome Fingerprint in Individuals With Schizophrenia. JAMA psychiatry.
- (2018). Improving genetic prediction by leveraging genetic correlations among human diseases and traits. Nature Communications. 1-17.
- (2018). Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes. Cell. 1705-1715.
- (2018). Expression of TCN1 in Blood is Negatively Associated with Verbal Declarative Memory Performance. Scientific Reports. 1-11.
- (2018). Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics. 381-389.
- (2018). Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder. Neuropsychopharmacology. 620-628.
- (2018). Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Communications Biology. 10 sider.
- (2018). An association between YKL-40 and type 2 diabetes in psychotic disorders. Acta Psychiatrica Scandinavica. 37-45.
- (2018). Age at first birth in women is genetically associated with increased risk of schizophrenia. Scientific Reports. 14 sider.
- (2017). Task modulations and clinical manifestations in the brain functional connectome in 1615 fMRI datasets. NeuroImage. 243-252.
- (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.
- (2017). Probing the association between early evolutionary markers and schizophrenia. PLOS ONE. 1-15.
- (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.
- (2017). Parents’ Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder—Data from a Norwegian Sample. International Journal of Molecular Sciences. 1-14.
- (2017). Novel genetic loci associated with hippocampal volume. Nature Communications. 1-12.
- (2017). Leveraging genome characteristics to improve gene discovery for putamen subcortical brain structure. Scientific Reports. 1-9.
- (2017). Large-scale cognitive GWAS meta-analysis reveals tissue-specific neural expression and potential nootropic drug targets. Cell reports. 2597-2613.
- (2017). Identification of genetic loci shared between schizophrenia and the Big Five personality traits. Scientific Reports. 1-9.
- (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.
- (2017). Identification of gene loci that overlap between schizophrenia and educational attainment. Schizophrenia Bulletin. 654-664.
- (2017). Genome-wide pleiotropy between Parkinson disease and autoimmune diseases. JAMA Neurology. 780-792.
- (2017). Genetic overlap between schizophrenia and volumes of hippocampus, putamen, and intracranial volume indicates shared molecular genetic mechanisms. Schizophrenia Bulletin. 854-864.
- (2017). Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Nature Communications. 1-12.
- (2017). Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis. Biological Psychiatry. 634-641.
- (2017). GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report form the COGENT consortium. Molecular Psychiatry. 336-345.
- (2017). Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations. NPJ GENOMIC MEDICINE. 12 sider.
- (2017). Distinct multivariate brain morphological patterns and their added predictive value with cognitive and polygenic risk scores in mental disorders. NeuroImage: Clinical. 719-731.
- (2017). Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nature Genetics. 27-35.
- (2017). Combinations of genetic variants associated with bipolar disorder. PLOS ONE.
- (2017). Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data. Translational Psychiatry.
- (2017). A study of TNF pathway activation in schizophrenia and bipolar disorder in plasma and brain tissue. Schizophrenia Bulletin. 881-890.
- (2017). A genetic association study of CSMD1 and CSMD2 with cognitive function. Brain, Behavior, and Immunity. 209-216.
- (2016). VRK2 gene expression in schizophrenia, bipolar disorder and healthy controls. British Journal of Psychiatry. 114-120.
- (2016). The roadmap for estimation of cell-typespecific neuronal activity from noninvasive measurements. Philosophical Transactions of the Royal Society of London. Biological Sciences. 16 sider.
- (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.
- (2016). Parents' attitudes toward genetic research in autism spectrum disorder. Psychiatric Genetics. 74-80.
- (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience. 1569-1582.
- (2016). Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS. PLoS Genetics. 22 sider.
- (2016). Inflammatory evidence for the psychosis continuum model. Psychoneuroendocrinology. 189-197.
- (2016). Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disorders. Nordic Journal of Psychiatry. 276-279.
- (2016). Genome-wide autozygosity is associated with lower general cognitive ability. Molecular Psychiatry. 837-843.
- (2016). Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple Sclerosis. 1783-1793.
- (2016). Functional effects of schizophrenia-linked genetic variants on intrinsic single-neuron excitability: a modeling study. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. 49-59.
- (2016). Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women. JAMA psychiatry. 497-505.
- (2016). Contribution of oxytocin receptor polymorphisms to amygdala activation in schizophrenia spectrum disorders. BJPsych Open. 353-358.
- (2016). Conservation of Distinct Genetically-Mediated Human Cortical Pattern. PLoS Genetics. 18 sider.
- (2016). Cell type specificity of neurovascular coupling in cerebral cortex. eLIFE.
- (2016). A sequence variant associating with educational attainment also affects childhood cognition. Scientific Reports.
- (2015). Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature Neuroscience.
- (2015). Polygenic risk scores in bipolar disorders subgroups. Journal of Affective Disorders. 310-314.
- (2015). Polygenic risk for schizophrenia associated with working memory-related prefrontal brain activation in patients with schizophrenia and healthy controls. Schizophrenia Bulletin. 736-743.
- (2015). Polygenic overlap between C-reactive protein, plasma lipids, and Alzheimer disease. Circulation. 2061-2069.
- (2015). New data and an old puzzle: The negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology. 1706-1721.
- (2015). Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. American Journal of Human Genetics.
- (2015). Microarray analysis of copy number variants on the human y chromosome reveals novel and frequent duplications overrepresented in specific haplogroups. PLOS ONE.
- (2015). MicroRNAs enrichment in GWAS of complex human phenotypes. BMC Genomics.
- (2015). Loss-of-function variants in ABCA7 confer risk of Alzheimer’s disease. Nature Genetics. 445-447.
- (2015). Large-scale genomics unveil polygenic architecture of human cortical surface area. Nature Communications.
- (2015). LD score regression distinguishes confounding from polygenicity in genome-wide association studies. Nature Genetics. 291-295.
- (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.
- (2015). Investigation of the genetic interaction between BDNF and DRD3 genes in suicidical behaviour in psychiatric disorders. World Journal of Biological Psychiatry. 171-179.
- (2015). Inflammatory markers are associated with general cognitive abilities in schizophrenia and bipolar disorder patients and healthy controls. Schizophrenia Research. 188-194.
- (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.
- (2015). Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes with Several Cardiovascular Risk Factors. Circulation Research. 83-94.
- (2015). Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs. Journal of Psychopharmacology. 884-891.
- (2015). Genome-wide analysis of attention deficit hyperactivity disorder in Norway. PLOS ONE. 17 sider.
- (2015). Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci. PLOS ONE.
- (2015). Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci. Molecular Psychiatry. 207-214.
- (2015). Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus. Molecular Psychiatry. 1588-1595.
- (2015). Genetic Markers of Human Evolution Are Enriched in Schizophrenia. Biological Psychiatry.
- (2015). Common genetic variants influence human subcortical brain structures. Nature. 224-229.
- (2015). Combinations of genetic data present in bipolar patients, but absent in control persons. PLOS ONE. 7 sider.
- (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.
- (2015). Association between altered brain morphology and elevated peripheral endothelial markers — Implications for psychotic disorders . Schizophrenia Research. 222-228.
- (2015). Altered brain activation during emotional face processing in relation to both diagnosis and polygenic risk of bipolar disorder. PLOS ONE.
- (2015). Abundant genetic overlap between blood lipids and immune-mediated diseases indicates shared molecular genetic mechanisms. PLOS ONE.
- (2015). A Loss-of-Function Variant in a Minor Isoform of ANK3 Protects Against Bipolar Disorder and Schizophrenia. Biological Psychiatry.
- (2014). The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior. 153-182.
- (2014). Shared common variants in prostate cancer and blood lipids. International Journal of Epidemiology. 1205-1214.
- (2014). Polygenic risk score and the psychosis continuum model. Acta Psychiatrica Scandinavica. 311-317.
- (2014). Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Molecular Psychiatry. 1017-1024.
- (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.
- (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.
- (2014). Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes. Hypertension. 819-826.
- (2014). GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. Genes, Brain and Behavior.
- (2014). Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry. 108-114.
- (2014). Biological insights from 108 schizophrenia-associated genetic loci. Nature. 421-427.
- (2014). Association analysis between suicidal behaviour and candidate genes of bipolar disorder and schizophrenia. Journal of Affective Disorders. 110-114.
- (2014). An attempt to identify single nucleotide polymorphisms contributing to possible relationships between personality traits and oxytocin-related genes. Neuropsychobiology. 25-30.
- (2014). ANK3 gene expression in bipolar disorder and schizophrenia. British Journal of Psychiatry. 244-245.
- (2013). ZNF804A and cortical thickness in schizophrenia and bipolar disorder. Psychiatry Research : Neuroimaging. 154-157.
- (2013). Pathway analysis of genetic markers associated with a functional MRI faces paradigm implicates polymorphisms in calcium responsive pathways. NeuroImage. 143-149.
- (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 984-994.
- (2013). CACNA1C Risk Variant and Amygdala Activity in Bipolar Disorder, Schizophrenia and Healthy Controls. PLOS ONE. 6 sider.
- (2013). BDNF val66met modulates the association between childhood trauma, cognitive and brain abnormalities in psychoses. Progress in Neuro-psychopharmacology and Biological Psychiatry. 181-188.
- (2013). A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder. PLOS ONE. 9 sider.
- (2012). Up-Regulation of NOTCH4 Gene Expression in Bipolar Disorder. American Journal of Psychiatry. 1292-1300.
- (2012). TCF4 sequence variants and mRNA levels are associated with neurodevelopmental characteristics in psychotic disorders. Translational Psychiatry.
- (2012). Serotonin Transporter Gene Polymorphism, Childhood Trauma, and Cognition in Patients With Psychotic Disorders. Schizophrenia Bulletin. 15-22.
- (2012). Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics. 552-561.
- (2012). Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function. Journal of Psychiatric Research. 271-278.
- (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.
- (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.
- (2012). Association between a genetic variant in the serotonin transporter gene (SLC6A4) and suicidal behavior in patients with schizophrenia. Behavioral and Brain Functions. 8 sider.
- (2011). The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia. Biological Psychiatry. 35-42.
- (2011). Intron 12 in NTRK3 is associated with bipolar disorder. Psychiatry Research. 358-362.
- (2011). Genome-wide association study identifies five new schizophrenia loci. Nature Genetics. 969-976.
- (2011). Copy number variations in affective disorders and meta-analysis. Psychiatric Genetics. 319-322.
- (2011). Common Sequence Variants in the Major Histocompatibility Complex Region Associate with Cerebral Ventricular Size in Schizophrenia. Biological Psychiatry. 696-698.
- (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.
- (2011). Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia. Archives of General Psychiatry. 781-790.
- (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.
- (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.
- (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.
- (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.
- (2010). Osteoprotegerin levels in patients with severe mental disorders. Journal of Psychiatry & Neuroscience. 304-310.
- (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.
- (2010). Catechol O-methyltransferase variants and cognitive performance in schizophrenia and bipolar disorder versus controls. Schizophrenia Research. 31-37.
- (2010). Association Study of PDE48 gene variants in Scandinavian schizophrenia and bipolar disorder multicenter case-control samples. American Journal of Medical Genetics. 86-96.
- (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.
- (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.
- (2010). A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample. Journal of Affective Disorders. 312-316.
- (2009). Tyrosine hydroxylase Val81Met polymorphism: lack of association with schizophrenia. Psychiatric Genetics. 273-274.
- (2009). Three-cohort targeted gene screening reveals a non-synonymous TRKA polymorphism associated with schizophrenia. Journal of Psychiatric Research. 1195-1199.
- (2009). No association between DGKH and bipolar disorder in a Scandinavian case-control sample. Psychiatric Genetics. 269-272.
- (2009). Disruption of the neurexin 1 gene is associated with schizophrenia. Human Molecular Genetics. 988-996.
- (2009). DTNBP1, NRG1, DAOA, DAO and GRM3 Polymorphisms and Schizophrenia: An Association Study. Neuropsychobiology. 142-150.
- (2009). Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Molecular Psychiatry. 1-9.
- (2009). Common variants conferring risk of schizophrenia. Nature. 744-747.
- (2009). Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE). Psychiatry Research. 256-258.
- (2009). A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE). Schizophrenia Research. 242-248.
- (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.
- (2008). Two methylenetetrahydrofolate reductase gene (MTHFR) polymorphisms, schizophrenia and bipolar disorder: An association study. American Journal of Medical Genetics. 976-982.
- (2008). Large recurrent microdeletions associated with schizophrenia. Nature. 232-U61.
- (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.
- (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.
- (2008). A novel myogenic cell line with phenotypic properties of muscle progenitors. Journal of Molecular Medicine. 105-115.
- (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.
- (2005). Activity of peroxisomal enzymes, and levels of polyamines in LPA-transgenic mice on two different diets. Lipids in Health and Disease. 12 sider.
Vitenskapelig foredrag
- (2018). Affective lability and polygenic risk in bipolar disorder.
- (2017). Layer V pyramidal cells as mediators of delta oscillations: Insights from biophysically detailed modeling and connections with schizophrenia genetics.
- (2017). Delta oscillations in schizophrenia: Insights from biophysically detailed modeling of networks of layer V pyramidal cells.
- (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.
- (2016). Genetic overlap between schizophrenia and brain structural volumes indicates shared molecular genetic mechanisms with potential relevance for antipsychotics .
- (2006). Syndecan-4 is an essential signal transducer for activation of the calcineurin-NFAT pathway and cardiac hypertrophy in mice.
- (2005). Why syndecan-4 might be important in heart failure following myocardial infarction.
- (2005). A role for syndecan-4 during development of heart failure following myocaridal infarction.
- (2005). A role for syndecan-4 as a signal transducer during development of heart failure following myocardial infarction.
Sammendrag/abstract
- (2019). Genome wide Association study: identifying Genetic markers in apathy in People with Alzheimer's disease. Alzheimer's & Dementia. P286-P286.
- (2013). Is Met Variant of the BDNF VAL66MET-Combined with Childhood Trauma - A Risk Factor of Brain Abnormalities in Psychoses? Biological Psychiatry. 287S-287S.
- (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.
- (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.
- (2011). SEROTONIN TRANSPORTER GENE POLYMORPHISMS, CHILDHOOD TRAUMA AND COGNITION IN PATIENTS WITH PSYCHOTIC DISORDERS. Schizophrenia Bulletin. 80-80.
- (2009). DYSBINDIN AND D-AMINO-ACID-OXIDASE GENE POLYMORPHISMS ASSOCIATED WITH POSITIVE AND NEGATIVE SYMPTOMS IN SCHIZOPHRENIA. Schizophrenia Bulletin. 105-105.
- (2009). ASSOCIATION BETWEEN THE TRYPTOPHAN HYDROXYLASE 1 (TPH1) GENE, SCHIZOPHRENIA SUSCEPTIBILITY, AND SUICIDAL BEHAVIOR. Schizophrenia Bulletin. 121-121.
- (2008). Interaction between health behaviour, mental distress and the polymorphism of the serotonin transporter gene among adolescents in Oslo, Norway. European psychiatry. S174-S174.
- (2003). Effect of cholesterol feeding on apo(a), CYP7A1 and LXR alpha expression in LPA transgenic mice. Atherosclerosis Supplements. 296-296.
Vitenskapelig oversiktsartikkel/review
- (2024). How real-world data can facilitate the development of precision medicine treatment in psychiatry. Biological Psychiatry.
- (2020). Copy number variants (CNVs): A powerful tool for iPSC-based modelling of ASD. Molecular Autism. 1-18.
- (2019). Discovery of shared genomic loci using the conditional false discovery rate approach. Human Genetics. 1-10.
- (2019). Biophysical Psychiatry—How Computational Neuroscience Can Help to Understand the Complex Mechanisms of Mental Disorders. Frontiers in Psychiatry. 14 sider.
- (2017). Genetic evidence for role of integration of fast and slow neurotransmission in schizophrenia. Molecular Psychiatry. 792-801.
- (2016). Modeling psychiatric disorders: From genomic findings to cellular phenotypes. Molecular Psychiatry. 1167-1179.
- (2010). SRD5A2 is associated with increased cortisol metabolism in schizophrenia spectrum disorders. Progress in Neuro-psychopharmacology and Biological Psychiatry. 1500-1506.