Vidar M. Steen norsk forsker
Steen, Vidar M.
VIAF ID: 294148997624859870003 ( Personal )
Permalink: http://viaf.org/viaf/294148997624859870003
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100 0 _ ‡a Vidar M. Steen ‡c norsk forsker
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Works
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Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence |
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Genome-wide association studies establish that human intelligence is highly heritable and polygenic |
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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. |
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Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations |
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Genome-wide autozygosity is associated with lower general cognitive ability |
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Genomic structure and sequence analysis of a human inositol polyphosphate 1-phosphatase gene (INPP1) |
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Global gene expression profiling of human osteosarcomas reveals metastasis-associated chemokine pattern |
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GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. |
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GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. |
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Homologous unequal cross-over involving a 2.8 kb direct repeat as a mechanism for the generation of allelic variants of human cytochrome P450 CYP2D6 gene. |
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Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins. |
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Human platelet signal transduction and responses : a study with special reference to the platelet-stimulating effect of adrenaline (epinephrine) |
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Hyperoxia retards growth and induces apoptosis and loss of glands and blood vessels in DMBA-induced rat mammary tumors |
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Identification of common variants associated with human hippocampal and intracranial volumes |
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Identification of Gene Loci That Overlap Between Schizophrenia and Educational Attainment. |
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Identification of genes co-upregulated with Arc during BDNF-induced long-term potentiation in adult rat dentate gyrus in vivo. |
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Imaging and cognitive genetics: the Norwegian Cognitive NeuroGenetics sample. |
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Incident users of antipsychotic agents and future use of cholesterol-lowering drugs: an observational, pharmacoepidemiologic study |
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Increase in serum HDL level is associated with less negative symptoms after one year of antipsychotic treatment in first-episode psychosis. |
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Increased expression of lipid biosynthesis genes in peripheral blood cells of olanzapine-treated patients. |
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Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment |
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Inhibition of ADP-induced responses in human platelets by agents elevating the cyclic AMP level: comparison of aggregation and shape change |
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Is pharmacogenetic CYP2D6 testing useful? |
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Lack of association of the rs1344706 ZNF804A variant with cognitive functions and DTI indices of white matter microstructure in two independent healthy populations. |
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Lack of Ovarian Secretions Reverts the Anabolic Action of Olanzapine in Female Rats. |
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Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. |
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Large-scale genomics unveil polygenic architecture of human cortical surface area |
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Linkage-disequilibrium-based binning affects the interpretation of GWASs |
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Lipid-lowering effects of tetradecylthioacetic acid in antipsychotic-exposed, female rats: challenges with long-term treatment |
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Lipogenic effects of psychotropic drugs: focus on the SREBP system |
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Lithium differentially affects clock gene expression in serum-shocked NIH-3T3 cells. |
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LOC689986, a unique gene showing specific expression in restricted areas of the rodent neocortex |
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MicroRNAs enrichment in GWAS of complex human phenotypes. |
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Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018) |
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Mutations in ABHD12 cause the neurodegenerative disease PHARC: An inborn error of endocannabinoid metabolism |
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Neomycin inhibits platelet functions and inositol phospholipid metabolism upon stimulation with thrombin, but not with ionomycin or 12-O-tetradecanoyl-phorbol 13-acetate |
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Neurogenetic effects on cognition in aging brains: a window of opportunity for intervention? |
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Neuropsychological deficits in mice depleted of the schizophrenia susceptibility gene CSMD1. |
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Nomenclature for human CYP2D6 alleles. |
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Non-functional CYP2D6 alleles and risk for neuroleptic-induced movement disorders in schizophrenic patients |
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Novel genetic loci underlying human intracranial volume identified through genome-wide association |
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Obesity, dyslipidemia, and diabetes with selective serotonin reuptake inhibitors: the Hordaland Health Study. |
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Olanzapine, but not aripiprazole, weight-independently elevates serum triglycerides and activates lipogenic gene expression in female rats. |
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Olanzapine depot exposure in male rats: Dose-dependent lipogenic effects without concomitant weight gain. |
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Olanzapine depot formulation in rat: a step forward in modelling antipsychotic-induced metabolic adverse effects. |
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Olanzapine-induced hyperphagia and weight gain associate with orexigenic hypothalamic neuropeptide signaling without concomitant AMPK phosphorylation |
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The phospholipase C-gamma1 gene (PLCG1) and lithium-responsive bipolar disorder: re-examination of an intronic dinucleotide repeat polymorphism |
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The platelet-stimulating effect of adrenaline through alpha 2-adrenergic receptors requires simultaneous activation by a true stimulatory platelet agonist. Evidence that adrenaline per se does not induce human platelet activation in vitro |
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Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways |
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The polymorphic inositol polyphosphate 1-phosphatase gene as a candidate for pharmacogenetic prediction of lithium-responsive manic-depressive illness |
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Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism? |
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Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples. |
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Psychotropic drugs up-regulate the expression of cholesterol transport proteins including ApoE in cultured human CNS- and liver cells |
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Publisher Correction: Common brain disorders are associated with heritable patterns of apparent aging of the brain |
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RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data |
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Recently evolved human-specific methylated regions are enriched in schizophrenia signals. |
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A retroviral element in the human CYP2D gene cluster. |
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Role of the Neutral Amino Acid Transporter Slc7a10 in Adipocyte Lipid Storage, Obesity and Insulin Resistance |
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Runaway multi-allelic copy number variation at the α-defensin locus in African and Asian populations |
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[Schizophrenia and molecular genetics] |
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Ser9Gly dopamine D3 receptor polymorphism and spontaneous dyskinesia in never-medicated schizophrenic patients. |
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Serum concentrations of tamoxifen and its metabolites increase with age during steady-state treatment |
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The serum level of C-reactive protein (CRP) is associated with cognitive performance in acute phase psychosis |
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SREBP activation by antipsychotic- and antidepressant-drugs in cultured human liver cells: relevance for metabolic side-effects? |
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Stimulation of human platelets with low concentrations of thrombin: evidence for equimolar accumulation of inositol trisphosphates and phosphatidic acid |
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Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function |
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SU117. Peripheral Cytokines After 3 Weeks of Antipsychotic Treatment. |
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Subchronic olanzapine exposure leads to increased expression of myelination-related genes in rat fronto-medial cortex. |
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Switch from stress response to homeobox transcription factors in adipose tissue after profound fat loss |
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Synaptic activity-induced global gene expression patterns in the dentate gyrus of adult behaving rats: induction of immunity-linked genes. |
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Syndromic X-linked intellectual disability segregating with a missense variant in RLIM. |
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Synergism between thrombin and epinephrine in human platelets: different dose-response relationships for aggregation and dense granule secretion. |
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Transcriptional, post-transcriptional and chromatin-associated regulation of pri-miRNAs, pre-miRNAs and moRNAs |
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Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene |
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Upregulation of immunoglobulin-related genes in cortical sections from multiple sclerosis patients. |
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Usefulness of factor V Leiden mutation testing in clinical practice |
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Variants in doublecortin- and calmodulin kinase like 1, a gene up-regulated by BDNF, are associated with memory and general cognitive abilities |
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Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes. |
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