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) (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.

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