Home
Srdjan Djurovic's picture

Srdjan Djurovic

Professor
  • E-mailSrdjan.Djurovic@uib.no
  • Visitor Address
    Haukeland universitetssykehus, Laboratoriebygget
    5009 Bergen
  • Postal Address
    Postboks 7804
    5020 Bergen
Academic article
  • Show author(s) (2021). Using iPSC Models to Understand the Role of Estrogen in Neuron–Glia Interactions in Schizophrenia and Bipolar Disorder. Cells. 33 pages.
  • Show author(s) (2021). Transcriptome analysis reveals disparate expression of inflammation-related miRNAs and their gene targets in iPSC-astrocytes from people with schizophrenia. Brain, Behavior, and Immunity.
  • Show author(s) (2021). Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Translational Psychiatry. 1-13.
  • Show author(s) (2021). Polygenic overlap and shared genetic loci between loneliness, severe mental disorders, and cardiovascular disease risk factors suggest shared molecular mechanisms. Translational Psychiatry. 11 pages.
  • Show author(s) (2021). Lithium increases mitochondrial respiration in iPSC-derived neural precursor cells from lithium responders. Molecular Psychiatry.
  • Show author(s) (2021). Identifying nootropic drug targets via large-scale cognitive GWAS and transcriptomics. Neuropsychopharmacology. 1788-1801.
  • Show author(s) (2021). Identification of pleiotropy at the gene level between psychiatric disorders and related traits. Translational Psychiatry. 8 pages.
  • Show author(s) (2021). Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease. Molecular Psychiatry. 5797-5811.
  • Show author(s) (2021). Genome-wide analysis reveals genetic overlap between alcohol use behaviours, schizophrenia and bipolar disorder and identifies novel shared risk loci. Addiction.
  • Show author(s) (2021). Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. The Pharmacogenomics Journal. 574-585 .
  • Show author(s) (2021). Genetic loci shared between major depression and intelligence with mixed directions of effect. Nature Human Behaviour. 1-9.
  • Show author(s) (2021). Extensive bidirectional genetic overlap between bipolar disorder and cardiovascular disease phenotypes. Translational Psychiatry. 9 pages.
  • Show author(s) (2021). Dose-dependent transcriptional effects of lithium and adverse effect burden in a psychiatric cohort. Progress in Neuro-psychopharmacology and Biological Psychiatry. 11 pages.
  • Show author(s) (2021). Derivation and Molecular Characterization of a Morphological Subpopulation of Human iPSC Astrocytes Reveal a Potential Role in Schizophrenia and Clozapine Response. Schizophrenia Bulletin.
  • Show author(s) (2021). Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores. Nature Communications. 1-16.
  • Show author(s) (2021). Characterizing the Genetic Overlap Between Psychiatric Disorders and Sleep-Related Phenotypes. Biological Psychiatry. 1-11.
  • Show author(s) (2021). Characterising the shared genetic determinants of bipolar disorder, schizophrenia and risk-taking. Translational Psychiatry. 1-10.
  • Show author(s) (2021). Cardiometabolic risk factors associated with brain age and accelerate brain ageing. Human Brain Mapping. 1-21.
  • Show author(s) (2021). Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. Molecular Psychiatry. 1286-1298.
  • Show author(s) (2021). Attitudes among parents of persons with autism spectrum disorder towards information about genetic risk and future health. European Journal of Human Genetics. 1-9.
  • Show author(s) (2021). Association between complement component 4A expression, cognitive performance and brain imaging measures in UK Biobank. Psychological Medicine. 1-11.
  • Show author(s) (2021). All-Optical Electrophysiology in hiPSC-Derived Neurons With Synthetic Voltage Sensors. Frontiers in Cellular Neuroscience. 11 pages.
  • Show author(s) (2021). A human iPSC-astroglia neurodevelopmental model reveals divergent transcriptomic patterns in schizophrenia. Translational Psychiatry. 13 pages.
  • Show author(s) (2021). A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease. Nature Genetics. 1276-1282.
  • Show author(s) (2020). The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls. Biological Psychiatry.
  • Show author(s) (2020). Shared genetic loci between body mass index and major psychiatric disorders: A genome-wide association study. JAMA psychiatry. 503-512.
  • Show author(s) (2020). Runaway multi-allelic copy number variation at the α-defensin locus in African and Asian populations. Scientific Reports. 1-8.
  • Show author(s) (2020). Polygenic scores for schizophrenia and general cognitive ability: associations with six cognitive domains, premorbid intelligence, and cognitive composite score in individuals with a psychotic disorder and in healthy controls. Translational Psychiatry. 1-9.
  • Show author(s) (2020). Phenotype-specific differences in polygenicity and effect size distribution across functional annotation categories revealed by AI-MiXeR. Bioinformatics.
  • Show author(s) (2020). Genome-wide Association Analysis of Parkinson’s Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci. Biological Psychiatry. 227-235.
  • Show author(s) (2020). Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Nature Communications.
  • Show author(s) (2020). Decreased IL-1β-induced CCL20 response in human iPSC-astrocytes in schizophrenia: Potential attenuating effects on recruitment of regulatory T cells. Brain, Behavior, and Immunity. 634-644.
  • Show author(s) (2020). Computationally efficient familywise error rate control in genome‐wide association studies using score tests for generalized linear models. Scandinavian Journal of Statistics.
  • Show author(s) (2020). Cannabis Use Is Associated With Increased Levels of Soluble gp130 in Schizophrenia but Not in Bipolar Disorder. Frontiers in Psychiatry. 1-10.
  • Show author(s) (2020). Atherogenic lipid ratios related to myeloperoxidase and C-reactive protein levels in psychotic disorders. Frontiers in Psychiatry. 10 pages.
  • Show author(s) (2019). Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. American Journal of Medical Genetics.
  • Show author(s) (2019). Pleiotropic meta-analysis of cognition, education, and schizophrenia differentiates roles of early neurodevelopmental and adult synaptic pathways. American Journal of Human Genetics. 334-350.
  • Show author(s) (2019). Identification of genetic overlap and novel risk loci for attention-deficit/hyperactivity disorder and bipolar disorder. Molecular Psychiatry. 1-11.
  • Show author(s) (2019). Identification of genetic loci shared between ADHD, intelligence and educational attainment . Biological Psychiatry. 1052-1062.
  • Show author(s) (2019). Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics. 431-444.
  • 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). Exploring lithium's transcriptional mechanisms of action in bipolar disorder: a multi-step study. Neuropsychopharmacology. 1-9.
  • Show author(s) (2019). Examining the association between genetic liability for schizophrenia and psychotic symptoms in Alzheimer's disease. Translational Psychiatry. 1-10.
  • Show author(s) (2019). Brain heterogeneity in schizophrenia and its association with polygenic risk. JAMA psychiatry. 739-748.
  • Show author(s) (2019). Bivariate causal mixture model quantifies polygenic overlap between complex traits beyond genetic correlation. Nature Communications.
  • Show author(s) (2019). A polygenic resilience score moderates the genetic risk for schizophrenia. Molecular Psychiatry.
  • Show author(s) (2018). Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications. 1-16.
  • Show author(s) (2018). Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci. Scientific Reports. 8 pages.
  • Show author(s) (2018). In Vivo Two-Photon Voltage Imaging with Sulfonated Rhodamine Dyes. ACS Central Science. 1371-1378.
  • Show author(s) (2018). Improving genetic prediction by leveraging genetic correlations among human diseases and traits. Nature Communications. 1-17.
  • Show author(s) (2018). Immunomodulatory capacity of the serotonin receptor 5-HT2B in a subset of human dendritic cells. Scientific Reports. 1-12.
  • Show author(s) (2018). Identification of shared genetic variants between schizophrenia and lung cancer. Scientific Reports. 1-8.
  • Show author(s) (2018). Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. Nature Genetics. 912-919.
  • Show author(s) (2018). Genetic factors influencing prostate cancer risk in Norwegian men. The Prostate. 186-192.
  • 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). Exploring the Wnt signaling pathway in schizophrenia and bipolar disorder. Translational Psychiatry. 1-10.
  • Show author(s) (2018). Enrichment of genetic markers of recent human evolution in educational and cognitive traits. Scientific Reports. 1-9.
  • Show author(s) (2018). Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia. Molecular Psychiatry. 1-16.
  • Show author(s) (2018). Deep 2-photon imaging and artifact-free optogenetics through transparent graphene microelectrode arrays. Nature Communications. 1-12.
  • Show author(s) (2018). Attenuated Notch signaling in schizophrenia and bipolar disorder. Scientific Reports. 1-8.
  • Show author(s) (2018). A molecule-based genetic association approach implicates a range of voltage-gated calcium channels associated with schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 454-467.
  • 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). Probing the association between early evolutionary markers and schizophrenia. PLOS ONE. 1-15.
  • 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 loci associated with attention-deficit/hyperactivity disorder are revealed by leveraging polygenic overlap with educational attainment. Journal of the American Academy of Child and Adolescent Psychiatry. 86-95.
  • 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). Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. Translational Psychiatry. e1155.
  • Show author(s) (2017). Genetic risk scores and family history as predictors of schizophrenia in Nordic registers. Psychological Medicine. 1201-1208.
  • 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). 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). 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). 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). Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS. PLoS Genetics. 22 pages.
  • 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). 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). Polygenic risk scores in bipolar disorders subgroups. Journal of Affective Disorders. 310-314.
  • Show author(s) (2015). Polygenic overlap between C-reactive protein, plasma lipids, and Alzheimer disease. Circulation. 2061-2069.
  • 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). LD score regression distinguishes confounding from polygenicity in genome-wide association studies. Nature Genetics. 291-295.
  • 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). 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). 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). 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). 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). 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). An attempt to identify single nucleotide polymorphisms contributing to possible relationships between personality traits and oxytocin-related genes. Neuropsychobiology. 25-30.
  • Show author(s) (2013). Variant of TREM2 Associated with the Risk of Alzheimer's Disease. New England Journal of Medicine. 107-116.
  • Show author(s) (2013). Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors. American Journal of Human Genetics. 197-209.
  • Show author(s) (2013). Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate. PLoS Genetics. 16 pages.
  • Show author(s) (2013). A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder. PLOS ONE. 9 pages.
  • Show author(s) (2013). A comprehensive family-based replication study of schizophrenia genes. JAMA psychiatry. 573-581.
  • Show author(s) (2012). Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder. Biological Psychiatry. 645-650.
  • Show author(s) (2012). Linkage-disequilibrium-based binning affects the interpretation of GWASs. American Journal of Human Genetics. 727-733.
  • Show author(s) (2012). Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach. Translational Psychiatry.
  • Show author(s) (2012). Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders. PLOS ONE. 14 pages.
  • Show author(s) (2012). Effect of DISC1 SNPs on Brain Structure in Healthy Controls and Patients With a History of Psychosis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 722-730.
  • Show author(s) (2012). DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLOS ONE. 12 pages.
  • Show author(s) (2012). Connection between Genetic and Clinical Data in Bipolar Disorder. PLOS ONE. 9 pages.
  • Show author(s) (2012). Associations Between Variants Near a Monoaminergic Pathways Gene (PHOX2B) and Amygdala Reactivity: A Genome-Wide Functional Imaging Study. Twin Research and Human Genetics. 273-285.
  • Show author(s) (2011). Syndecan-4 is essential for development of concentric myocardial hypertrophy via stretch-induced activation of the calcineurin-NFAT pathway. PLOS ONE.
  • Show author(s) (2011). Meta-Analysis of Heterogeneous Data Sources for Genome-Scale Identification of Risk Genes in Complex Phenotypes. Genetic Epidemiology. 318-332.
  • Show author(s) (2011). Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness. American Journal of Psychiatry. 408-417.
  • Show author(s) (2011). Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nature Genetics. 977-983.
  • Show author(s) (2011). Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder. American Journal of Human Genetics. 372-381.
  • Show author(s) (2011). GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Molecular Psychiatry. 1117-1129.
  • Show author(s) (2011). Expanding the range of ZNF804A variants conferring risk of psychosis. Molecular Psychiatry. 59-66.
  • Show author(s) (2011). Dual association of a TRKA polymorphism with schizophrenia. Psychiatric Genetics. 125-131.
  • Show author(s) (2011). Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Molecular Psychiatry. 17-25.
  • Show author(s) (2011). Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Human Molecular Genetics. 4076-4081.
  • Show author(s) (2011). Combinations of SNPs Related to Signal Transduction in Bipolar Disorder. PLOS ONE. 11 pages.
  • Show author(s) (2011). At-Risk Variant in TCF7L2 for Type II Diabetes Increases Risk of Schizophrenia. Biological Psychiatry. 59-63.
  • 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). Association Between Methylenetetrahydrofolate Reductase (MTHFR) C677T Polymorphism and Age of Onset in Schizophrenia. American Journal of Medical Genetics. 610-618.
  • 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) (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). 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 Part B: Neuropsychiatric Genetics.
  • 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). Evidence for a possible association of neurotrophin receptor (NTRK-3) gene polymorphisms with hippocampal function and schizophrenia. Neurobiology of Disease. 518-524.
  • Show author(s) (2009). Dysbindin and D-Amino-Acid-Oxidase Gene Polymorphisms Associated with Positive and Negative Symptoms in Schizophrenia. Neuropsychobiology. 31-36.
  • 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 between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
  • 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). The estrogen hypothesis of schizophrenia implicates glucose metabolism: association study in three independent samples. BMC Medical Genetics. 39.
  • Show author(s) (2008). Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples. Molecular Psychiatry.
  • Show author(s) (2008). Large recurrent microdeletions associated with schizophrenia. Nature. 232-U61.
  • Show author(s) (2008). Disruption of the neurexin 1 gene is associated with schizophrenia. Human Molecular Genetics.
  • 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 possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE). Schizophrenia Research.
  • 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) (2007). Brief Research CommunicationTwo methylenetetrahydrofolate reductase gene (MTHFR) polymorphisms, schizophrenia and bipolar disorder: An association study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
  • Show author(s) (2007). Brain expressed microRNAs implicated in schizophrenia etiology. PLOS ONE. e873.
  • 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.
  • Show author(s) (2004). Variations in transfection efficiency of VEGF(165) and VEGF(121)-cDNA - Its effects on proliferation and migration of human endothelial cells. Molecular Biotechnology. 7-16.
  • Show author(s) (2004). Human apoB contributes to increased serum total apo(a) level in LPA transgenic mice. Lipids in Health and Disease. 8.
  • Show author(s) (2004). Comparison of nonviral transfection and adeno-associated viral transduction on cardiomyocytes. Molecular Biotechnology. 21-31.
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) (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.

More information in national current research information system (CRIStin)