Hjem
Srdjan Djurovics bilde

Srdjan Djurovic

Professor
  • E-postSrdjan.Djurovic@uib.no
  • Besøksadresse
    Haukeland universitetssykehus, Laboratoriebygget
  • Postadresse
    Postboks 7804
    5020 Bergen
Vitenskapelig artikkel
  • Vis forfatter(e) 2020. The genetic architecture of human brainstem structures and their involvement in common brain disorders. Nature Communications. 14 sider.
  • Vis forfatter(e) 2020. Shared genetic loci between body mass index and major psychiatric disorders: A genome-wide association study. JAMA psychiatry. 503-512.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2019. Identification of genetic overlap and novel risk loci for attention-deficit/hyperactivity disorder and bipolar disorder. Molecular Psychiatry. 1-11.
  • Vis forfatter(e) 2019. Identification of genetic loci shared between ADHD, intelligence and educational attainment . Biological Psychiatry. 1052-1062.
  • Vis forfatter(e) 2019. Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics. 431-444.
  • Vis forfatter(e) 2019. Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk. Nature Genetics. 404-413.
  • Vis forfatter(e) 2019. Exploring lithium's transcriptional mechanisms of action in bipolar disorder: a multi-step study. Neuropsychopharmacology. 1-9.
  • Vis forfatter(e) 2019. Examining the association between genetic liability for schizophrenia and psychotic symptoms in Alzheimer's disease. Translational Psychiatry. 1-10.
  • Vis forfatter(e) 2019. Brain heterogeneity in schizophrenia and its association with polygenic risk. JAMA psychiatry. 739-748.
  • Vis forfatter(e) 2019. Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder. Translational Psychiatry. 1-9.
  • Vis forfatter(e) 2019. Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA psychiatry. 11 sider.
  • Vis forfatter(e) 2018. Vitamin D levels, brain volume, and genetic architecture in patients with psychosis. PLOS ONE. 17 sider.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2018. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications. 1-16.
  • Vis forfatter(e) 2018. Stability of the Brain Functional Connectome Fingerprint in Individuals With Schizophrenia. JAMA psychiatry.
  • Vis forfatter(e) 2018. Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci. Scientific Reports. 8 sider.
  • Vis forfatter(e) 2018. In Vivo Two-Photon Voltage Imaging with Sulfonated Rhodamine Dyes. ACS Central Science. 1371-1378.
  • Vis forfatter(e) 2018. Improving genetic prediction by leveraging genetic correlations among human diseases and traits. Nature Communications. 1-17.
  • Vis forfatter(e) 2018. Immunomodulatory capacity of the serotonin receptor 5-HT2B in a subset of human dendritic cells. Scientific Reports. 1-12.
  • Vis forfatter(e) 2018. Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. Nature Genetics. 912-919.
  • Vis forfatter(e) 2018. Expression of TCN1 in Blood is Negatively Associated with Verbal Declarative Memory Performance. Scientific Reports. 1-11.
  • Vis forfatter(e) 2018. Exploring the Wnt signaling pathway in schizophrenia and bipolar disorder. Translational Psychiatry. 1-10.
  • Vis forfatter(e) 2018. Enrichment of genetic markers of recent human evolution in educational and cognitive traits. Scientific Reports. 1-9.
  • Vis forfatter(e) 2018. Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia. Molecular Psychiatry. 1-16.
  • Vis forfatter(e) 2018. Deep 2-photon imaging and artifact-free optogenetics through transparent graphene microelectrode arrays. Nature Communications. 1-12.
  • Vis forfatter(e) 2018. Cross-tissue eQTL enrichment of associations in schizophrenia. PLOS ONE.
  • Vis forfatter(e) 2018. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics. 381-389.
  • Vis forfatter(e) 2018. Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder. Neuropsychopharmacology. 620-628.
  • Vis forfatter(e) 2018. Attenuated Notch signaling in schizophrenia and bipolar disorder. Scientific Reports. 1-8.
  • Vis forfatter(e) 2018. Associations between persistent organic pollutants and metabolic syndrome in morbidly obese individuals. NMCD. Nutrition Metabolism and Cardiovascular Diseases. 1-8.
  • Vis forfatter(e) 2018. An association between YKL-40 and type 2 diabetes in psychotic disorders. Acta Psychiatrica Scandinavica. 37-45.
  • Vis forfatter(e) 2018. Age at first birth in women is genetically associated with increased risk of schizophrenia. Scientific Reports. 14 sider.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2017. Task modulations and clinical manifestations in the brain functional connectome in 1615 fMRI datasets. NeuroImage. 243-252.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2017. Probing the association between early evolutionary markers and schizophrenia. PLOS ONE. 1-15.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2017. Parents’ Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder—Data from a Norwegian Sample. International Journal of Molecular Sciences. 1-14.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2017. Novel genetic loci associated with hippocampal volume. Nature Communications. 1-12.
  • Vis forfatter(e) 2017. Leveraging genome characteristics to improve gene discovery for putamen subcortical brain structure. Scientific Reports. 1-9.
  • Vis forfatter(e) 2017. Large-scale cognitive GWAS meta-analysis reveals tissue-specific neural expression and potential nootropic drug targets. Cell reports. 2597-2613.
  • Vis forfatter(e) 2017. Identification of genetic loci shared between schizophrenia and the Big Five personality traits. Scientific Reports. 1-9.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2017. Identification of gene loci that overlap between schizophrenia and educational attainment. Schizophrenia Bulletin. 654-664.
  • Vis forfatter(e) 2017. Genome-wide pleiotropy between Parkinson disease and autoimmune diseases. JAMA Neurology. 780-792.
  • Vis forfatter(e) 2017. Genetic risk scores and family history as predictors of schizophrenia in Nordic registers. Psychological Medicine. 1201-1208.
  • Vis forfatter(e) 2017. Genetic overlap between schizophrenia and volumes of hippocampus, putamen, and intracranial volume indicates shared molecular genetic mechanisms. Schizophrenia Bulletin. 854-864.
  • Vis forfatter(e) 2017. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Nature Communications. 1-12.
  • Vis forfatter(e) 2017. GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report form the COGENT consortium. Molecular Psychiatry. 336-345.
  • Vis forfatter(e) 2017. Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations. NPJ GENOMIC MEDICINE. 12 sider.
  • Vis forfatter(e) 2017. Distinct multivariate brain morphological patterns and their added predictive value with cognitive and polygenic risk scores in mental disorders. NeuroImage: Clinical. 719-731.
  • Vis forfatter(e) 2017. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nature Genetics. 27-35.
  • Vis forfatter(e) 2017. Combinations of genetic variants associated with bipolar disorder. PLOS ONE.
  • Vis forfatter(e) 2017. Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data. Translational Psychiatry.
  • Vis forfatter(e) 2017. A study of TNF pathway activation in schizophrenia and bipolar disorder in plasma and brain tissue. Schizophrenia Bulletin. 881-890.
  • Vis forfatter(e) 2017. A genetic association study of CSMD1 and CSMD2 with cognitive function. Brain, behavior, and immunity. 209-216.
  • Vis forfatter(e) 2016. VRK2 gene expression in schizophrenia, bipolar disorder and healthy controls. British Journal of Psychiatry. 114-120.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2016. Parents' attitudes toward genetic research in autism spectrum disorder. Psychiatric Genetics. 74-80.
  • Vis forfatter(e) 2016. Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience. 1569-1582.
  • Vis forfatter(e) 2016. Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS. PLoS Genetics. 22 sider.
  • Vis forfatter(e) 2016. Inflammatory evidence for the psychosis continuum model. Psychoneuroendocrinology. 189-197.
  • Vis forfatter(e) 2016. Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disorders. Nordic Journal of Psychiatry. 276-279.
  • Vis forfatter(e) 2016. Genome-wide autozygosity is associated with lower general cognitive ability. Molecular Psychiatry. 837-843.
  • Vis forfatter(e) 2016. Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple Sclerosis. 1783-1793.
  • Vis forfatter(e) 2016. Functional effects of schizophrenia-linked genetic variants on intrinsic single-neuron excitability: a modeling study. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. 49-59.
  • Vis forfatter(e) 2016. Contribution of oxytocin receptor polymorphisms to amygdala activation in schizophrenia spectrum disorders. BJPsych Open. 353-358.
  • Vis forfatter(e) 2016. Conservation of Distinct Genetically-Mediated Human Cortical Pattern. PLoS Genetics. 18 sider.
  • Vis forfatter(e) 2016. Cell type specificity of neurovascular coupling in cerebral cortex. eLIFE.
  • Vis forfatter(e) 2016. A sequence variant associating with educational attainment also affects childhood cognition. Scientific Reports.
  • Vis forfatter(e) 2015. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature Neuroscience.
  • Vis forfatter(e) 2015. Polygenic risk scores in bipolar disorders subgroups. Journal of Affective Disorders. 310-314.
  • Vis forfatter(e) 2015. Polygenic risk for schizophrenia associated with working memory-related prefrontal brain activation in patients with schizophrenia and healthy controls. Schizophrenia Bulletin. 736-743.
  • Vis forfatter(e) 2015. Polygenic overlap between C-reactive protein, plasma lipids, and Alzheimer disease. Circulation. 2061-2069.
  • Vis forfatter(e) 2015. New data and an old puzzle: The negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology. 1706-1721.
  • Vis forfatter(e) 2015. Microarray analysis of copy number variants on the human y chromosome reveals novel and frequent duplications overrepresented in specific haplogroups. PLOS ONE.
  • Vis forfatter(e) 2015. MicroRNAs enrichment in GWAS of complex human phenotypes. BMC Genomics.
  • Vis forfatter(e) 2015. Loss-of-function variants in ABCA7 confer risk of Alzheimer’s disease. Nature Genetics. 445-447.
  • Vis forfatter(e) 2015. Large-scale genomics unveil polygenic architecture of human cortical surface area. Nature Communications.
  • Vis forfatter(e) 2015. LD score regression distinguishes confounding from polygenicity in genome-wide association studies. Nature Genetics. 291-295.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2015. Investigation of the genetic interaction between BDNF and DRD3 genes in suicidical behaviour in psychiatric disorders. World Journal of Biological Psychiatry. 171-179.
  • Vis forfatter(e) 2015. Inflammatory markers are associated with general cognitive abilities in schizophrenia and bipolar disorder patients and healthy controls. Schizophrenia Research. 188-194.
  • Vis forfatter(e) 2015. Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes with Several Cardiovascular Risk Factors. Circulation Research. 83-94.
  • Vis forfatter(e) 2015. Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs. Journal of Psychopharmacology. 884-891.
  • Vis forfatter(e) 2015. Genome-wide analysis of attention deficit hyperactivity disorder in Norway. PLOS ONE. 17 sider.
  • Vis forfatter(e) 2015. Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci. PLOS ONE.
  • Vis forfatter(e) 2015. Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus. Molecular Psychiatry. 1588-1595.
  • Vis forfatter(e) 2015. Genetic Markers of Human Evolution Are Enriched in Schizophrenia. Biological Psychiatry.
  • Vis forfatter(e) 2015. Common genetic variants influence human subcortical brain structures. Nature. 224-229.
  • Vis forfatter(e) 2015. Combinations of genetic data present in bipolar patients, but absent in control persons. PLOS ONE. 7 sider.
  • Vis forfatter(e) 2015. Association between altered brain morphology and elevated peripheral endothelial markers — Implications for psychotic disorders . Schizophrenia Research. 222-228.
  • Vis forfatter(e) 2015. Abundant genetic overlap between blood lipids and immune-mediated diseases indicates shared molecular genetic mechanisms. PLOS ONE.
  • Vis forfatter(e) 2015. A Loss-of-Function Variant in a Minor Isoform of ANK3 Protects Against Bipolar Disorder and Schizophrenia. Biological Psychiatry.
  • Vis forfatter(e) 2014. The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior. 153-182.
  • Vis forfatter(e) 2014. Shared common variants in prostate cancer and blood lipids. International Journal of Epidemiology. 1205-1214.
  • Vis forfatter(e) 2014. Polygenic risk score and the psychosis continuum model. Acta Psychiatrica Scandinavica. 311-317.
  • Vis forfatter(e) 2014. Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Molecular Psychiatry. 1017-1024.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2014. Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes. Hypertension. 819-826.
  • Vis forfatter(e) 2014. GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. Genes, Brain and Behavior.
  • Vis forfatter(e) 2014. Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry. 108-114.
  • Vis forfatter(e) 2014. Biological insights from 108 schizophrenia-associated genetic loci. Nature. 421-427.
  • Vis forfatter(e) 2014. Association analysis between suicidal behaviour and candidate genes of bipolar disorder and schizophrenia. Journal of Affective Disorders. 110-114.
  • Vis forfatter(e) 2014. An attempt to identify single nucleotide polymorphisms contributing to possible relationships between personality traits and oxytocin-related genes. Neuropsychobiology. 25-30.
  • Vis forfatter(e) 2014. ANK3 gene expression in bipolar disorder and schizophrenia. British Journal of Psychiatry. 244-245.
  • Vis forfatter(e) 2013. ZNF804A and cortical thickness in schizophrenia and bipolar disorder. Psychiatry Research : Neuroimaging. 154-157.
  • Vis forfatter(e) 2013. Variant of TREM2 Associated with the Risk of Alzheimer's Disease. New England Journal of Medicine. 107-116.
  • Vis forfatter(e) 2013. Pathway analysis of genetic markers associated with a functional MRI faces paradigm implicates polymorphisms in calcium responsive pathways. NeuroImage. 143-149.
  • Vis forfatter(e) 2013. No evidence for association between bipolar disorder risk gene variants and brain structural phenotypes. Journal of Affective Disorders. 291-297.
  • Vis forfatter(e) 2013. Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors. American Journal of Human Genetics. 197-209.
  • Vis forfatter(e) 2013. Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate. PLoS Genetics. 16 sider.
  • Vis forfatter(e) 2013. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 984-994.
  • Vis forfatter(e) 2013. CACNA1C Risk Variant and Amygdala Activity in Bipolar Disorder, Schizophrenia and Healthy Controls. PLOS ONE. 6 sider.
  • Vis forfatter(e) 2013. BDNF val66met modulates the association between childhood trauma, cognitive and brain abnormalities in psychoses. Progress in Neuro-psychopharmacology and Biological Psychiatry. 181-188.
  • Vis forfatter(e) 2013. A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder. PLOS ONE. 9 sider.
  • Vis forfatter(e) 2013. A comprehensive family-based replication study of schizophrenia genes. JAMA psychiatry. 573-581.
  • Vis forfatter(e) 2012. Up-Regulation of NOTCH4 Gene Expression in Bipolar Disorder. American Journal of Psychiatry. 1292-1300.
  • Vis forfatter(e) 2012. TCF4 sequence variants and mRNA levels are associated with neurodevelopmental characteristics in psychotic disorders. Translational Psychiatry.
  • Vis forfatter(e) 2012. Serotonin Transporter Gene Polymorphism, Childhood Trauma, and Cognition in Patients With Psychotic Disorders. Schizophrenia Bulletin. 15-22.
  • Vis forfatter(e) 2012. Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder. Biological Psychiatry. 645-650.
  • Vis forfatter(e) 2012. Linkage-disequilibrium-based binning affects the interpretation of GWASs. American Journal of Human Genetics. 727-733.
  • Vis forfatter(e) 2012. Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics. 552-561.
  • Vis forfatter(e) 2012. Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function. Journal of Psychiatric Research. 271-278.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2012. Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach. Translational Psychiatry.
  • Vis forfatter(e) 2012. Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders. PLOS ONE. 14 sider.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2012. DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLOS ONE. 12 sider.
  • Vis forfatter(e) 2012. Connection between Genetic and Clinical Data in Bipolar Disorder. PLOS ONE. 9 sider.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2011. The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia. Biological Psychiatry. 35-42.
  • Vis forfatter(e) 2011. Syndecan-4 is essential for development of concentric myocardial hypertrophy via stretch-induced activation of the calcineurin-NFAT pathway. PLOS ONE.
  • Vis forfatter(e) 2011. Meta-Analysis of Heterogeneous Data Sources for Genome-Scale Identification of Risk Genes in Complex Phenotypes. Genetic Epidemiology. 318-332.
  • Vis forfatter(e) 2011. Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness. American Journal of Psychiatry. 408-417.
  • Vis forfatter(e) 2011. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nature Genetics. 977-983.
  • Vis forfatter(e) 2011. Intron 12 in NTRK3 is associated with bipolar disorder. Psychiatry Research. 358-362.
  • Vis forfatter(e) 2011. Genome-wide association study identifies five new schizophrenia loci. Nature Genetics. 969-976.
  • Vis forfatter(e) 2011. Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder. American Journal of Human Genetics. 372-381.
  • Vis forfatter(e) 2011. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Molecular Psychiatry. 1117-1129.
  • Vis forfatter(e) 2011. Expanding the range of ZNF804A variants conferring risk of psychosis. Molecular Psychiatry. 59-66.
  • Vis forfatter(e) 2011. Dual association of a TRKA polymorphism with schizophrenia. Psychiatric Genetics. 125-131.
  • Vis forfatter(e) 2011. Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Molecular Psychiatry. 17-25.
  • Vis forfatter(e) 2011. Copy number variations in affective disorders and meta-analysis. Psychiatric Genetics. 319-322.
  • Vis forfatter(e) 2011. Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Human Molecular Genetics. 4076-4081.
  • Vis forfatter(e) 2011. Common Sequence Variants in the Major Histocompatibility Complex Region Associate with Cerebral Ventricular Size in Schizophrenia. Biological Psychiatry. 696-698.
  • Vis forfatter(e) 2011. Combinations of SNPs Related to Signal Transduction in Bipolar Disorder. PLOS ONE. 11 sider.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2011. At-Risk Variant in TCF7L2 for Type II Diabetes Increases Risk of Schizophrenia. Biological Psychiatry. 59-63.
  • Vis forfatter(e) 2011. Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia. Archives of General Psychiatry. 781-790.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2010. Osteoprotegerin levels in patients with severe mental disorders. Journal of Psychiatry & Neuroscience. 304-310.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2010. Catechol O-methyltransferase variants and cognitive performance in schizophrenia and bipolar disorder versus controls. Schizophrenia Research. 31-37.
  • Vis forfatter(e) 2010. Association Study of PDE48 gene variants in Scandinavian schizophrenia and bipolar disorder multicenter case-control samples. American Journal of Medical Genetics. 86-96.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2009. Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Molecular Psychiatry. 1-9.
  • Vis forfatter(e) 2009. Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2008. Disruption of the neurexin 1 gene is associated with schizophrenia. Human Molecular Genetics.
  • Vis forfatter(e) 2008. A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE). Schizophrenia Research.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2007. Brain expressed microRNAs implicated in schizophrenia etiology. PLOS ONE. e873.
  • Vis forfatter(e) 2005. Activity of peroxisomal enzymes, and levels of polyamines in LPA-transgenic mice on two different diets. Lipids in Health and Disease. 12 sider.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2004. Human apoB contributes to increased serum total apo(a) level in LPA transgenic mice. Lipids in Health and Disease. 8.
  • Vis forfatter(e) 2004. Comparison of nonviral transfection and adeno-associated viral transduction on cardiomyocytes. Molecular Biotechnology. 21-31.
Vitenskapelig foredrag
  • Vis forfatter(e) 2018. Affective lability and polygenic risk in bipolar disorder.
  • Vis forfatter(e) 2017. Layer V pyramidal cells as mediators of delta oscillations: Insights from biophysically detailed modeling and connections with schizophrenia genetics.
  • Vis forfatter(e) 2017. Delta oscillations in schizophrenia: Insights from biophysically detailed modeling of networks of layer V pyramidal cells.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2016. Genetic overlap between schizophrenia and brain structural volumes indicates shared molecular genetic mechanisms with potential relevance for antipsychotics .
  • Vis forfatter(e) 2006. Syndecan-4 is an essential signal transducer for activation of the calcineurin-NFAT pathway and cardiac hypertrophy in mice.
  • Vis forfatter(e) 2005. Why syndecan-4 might be important in heart failure following myocardial infarction.
  • Vis forfatter(e) 2005. A role for syndecan-4 during development of heart failure following myocaridal infarction.
  • Vis forfatter(e) 2005. A role for syndecan-4 as a signal transducer during development of heart failure following myocardial infarction.
Sammendrag/abstract
  • Vis forfatter(e) 2019. Genome wide Association study: identifying Genetic markers in apathy in People with Alzheimer's disease. Alzheimer's & Dementia. P286-P286.
  • Vis forfatter(e) 2013. Is Met Variant of the BDNF VAL66MET-Combined with Childhood Trauma - A Risk Factor of Brain Abnormalities in Psychoses? Biological Psychiatry. 287S-287S.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2011. SEROTONIN TRANSPORTER GENE POLYMORPHISMS, CHILDHOOD TRAUMA AND COGNITION IN PATIENTS WITH PSYCHOTIC DISORDERS. Schizophrenia Bulletin. 80-80.
  • Vis forfatter(e) 2009. DYSBINDIN AND D-AMINO-ACID-OXIDASE GENE POLYMORPHISMS ASSOCIATED WITH POSITIVE AND NEGATIVE SYMPTOMS IN SCHIZOPHRENIA. Schizophrenia Bulletin. 105-105.
  • Vis forfatter(e) 2009. ASSOCIATION BETWEEN THE TRYPTOPHAN HYDROXYLASE 1 (TPH1) GENE, SCHIZOPHRENIA SUSCEPTIBILITY, AND SUICIDAL BEHAVIOR. Schizophrenia Bulletin. 121-121.
  • Vis forfatter(e) 2008. Interaction between health behaviour, mental distress and the polymorphism of the serotonin transporter gene among adolescents in Oslo, Norway. European psychiatry. S174-S174.
  • Vis forfatter(e) 2003. Effect of cholesterol feeding on apo(a), CYP7A1 and LXR alpha expression in LPA transgenic mice. Atherosclerosis Supplements. 296-296.
Vitenskapelig oversiktsartikkel/review
  • Vis forfatter(e) 2020. Copy number variants (CNVs): A powerful tool for iPSC-based modelling of ASD. Molecular Autism. 1-18.
  • Vis forfatter(e) 2019. Discovery of shared genomic loci using the conditional false discovery rate approach. Human Genetics. 1-10.
  • Vis forfatter(e) 2019. Biophysical Psychiatry—How Computational Neuroscience Can Help to Understand the Complex Mechanisms of Mental Disorders. Frontiers in Psychiatry. 14 sider.
  • Vis forfatter(e) 2017. Genetic evidence for role of integration of fast and slow neurotransmission in schizophrenia. Molecular Psychiatry. 792-801.
  • Vis forfatter(e) 2016. Modeling psychiatric disorders: From genomic findings to cellular phenotypes. Molecular Psychiatry. 1167-1179.
  • Vis forfatter(e) 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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