Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.

No abstract is available for this paper.

• Publication year

  2010

• Venue

  Journal of Psychiatric Research

• Publication date

  2010-09-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/j.jpsychires.2010.02.002PMID 20185149PMCID PMC3224994
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

  2010influential reference
• Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

  2009influential reference
• Common variants conferring risk of schizophrenia

  2009cited by this paper
• Common variants on chromosome 6p22.1 are associated with schizophrenia

  2009influential reference
• Schizophrenia genetics: advancing on two fronts.

  2009influential reference
• Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study.

  2009cited by this paper
• Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

  2008cited by this paper
• Genomewide Association for Major Depressive Disorder: A possible role for the presynaptic protein Piccolo

  2008cited by this paper
• Genomewide association for schizophrenia in the CATIE study: results of stage 1

  2008cited by this paper
• Genome-wide association studies in psychiatry: lessons from early studies of non-psychiatric and psychiatric phenotypes

  2008cited by this paper
• Identification of loci associated with schizophrenia by genome-wide association and follow-up

  2008cited by this paper
• Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder

  2008cited by this paper
• A HapMap harvest of insights into the genetics of common disease.

  2008influential reference
• A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

  2008cited by this paper
• PLINK: a tool set for whole-genome association and population-based linkage analyses.

  2007influential reference
• The level of cardiovascular risk factors in bipolar disorder equals that of schizophrenia: a comparative study.

  2007cited by this paper
• Genetic analysis of the calcineurin pathway identifies members of the EGR gene family, specifically EGR3, as potential susceptibility candidates in schizophrenia

  2007cited by this paper
• Generalizability studies of the Global Assessment of Functioning-Split version.

  2007cited by this paper
• The L513S polymorphism in medium-chain acyl-CoA synthetase 2 (MACS2) is associated with risk factors of the metabolic syndrome in a Caucasian study population.

  2006cited by this paper
• The genetics of schizophrenia and bipolar disorder: dissecting psychosis

  2005cited by this paper
• Two medium-chain acyl-coenzyme A synthetase genes, SAH and MACS1, are associated with plasma high-density lipoprotein cholesterol levels, but they are not associated with essential hypertension

  2004cited by this paper
• The gene encoding phosphodiesterase 4D confers risk of ischemic stroke

  2003cited by this paper
• Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.

  2003cited by this paper
• Molecular genetics of schizophrenia: past, present and future

  2002cited by this paper
• Twin studies of schizophrenia: from bow-and-arrow concordances to star wars Mx and functional genomics.

  2000influential reference
• Cloning of the human phospholipase A2 activating protein (hPLAP) gene on the chromosome 9p21 melanoma deleted region.

  1999cited by this paper
• Association of the Ban I dimorphic site at the human cytosolic phospholipase A2 gene with schizophrenia.

  1998cited by this paper
• Training and quality assurance with the Structured Clinical Interview for DSM-IV (SCID-I/P).

  1998cited by this paper
• AnkyrinG. A new ankyrin gene with neural-specific isoforms localized at the axonal initial segment and node of Ranvier.

  1995cited by this paper
• The Structured Clinical Interview for DSM-III-R (SCID). I: History, rationale, and description.

  1992influential reference
• Intraclass correlations: uses in assessing rater reliability.

  1979influential reference
• The global assessment scale. A procedure for measuring overall severity of psychiatric disturbance.

  1976influential reference

• Single Nucleotide Polymorphisms in ANK3 and Psychiatric Risk: A Meta-Analysis, Systematic Review, and Quantitative Trait Locus Insights

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• Reduced expression of Ankyrin-G and E-cadherin in duodenal mucosal biopsy of subjects with celiac disease.

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• Current understanding of the etiology and pathogenesis of schizophrenia

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• The Risk Genes for Neuropsychiatric Disorders negr1 and opcml Are Expressed throughout Zebrafish Brain Development

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• ANK3 rs10994336 and ZNF804A rs7597593 polymorphisms: genetic interaction for emotional and behavioral symptoms of alcohol withdrawal syndrome

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• TWAS-GKF: a novel method for causal gene identification in transcriptome-wide association studies with knockoff inference

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• Psychological, Psychiatric, and Organic Brain Manifestations of Celiac Disease

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• Genome-Wide Association Study: Analysis of Association of Polymorphic Loci in 4p15.2 and 20q13.31 Regions with Paranoid Schizophrenia

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• Ankyrin2 is essential for neuronal morphogenesis and long-term courtship memory in Drosophila

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• Genome‐wide analyses reveal novel opioid use disorder loci and genetic overlap with schizophrenia, bipolar disorder, and major depression

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• Classification for psychiatric disorders including schizophrenia, bipolar disorder, and major depressive disorder using machine learning

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• Neuregulins: subcellular localization, signaling pathways and their relationship with neuroplasticity and neurological diseases

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• Polymodal Control of TMEM16x Channels and Scramblases

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• Association of common genetic variants in GPCPD1 with scaling Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans of visual cortical surface area in humans this document benefits you.

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• Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

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• Roles and mechanisms of ankyrin-G in neuropsychiatric disorders

  2022cites this paper
• Influence of Anoctamin-4 and -9 on ADAM10 and ADAM17 Sheddase Function

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• ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants

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• Genetic association of DISC1 variant rs3738401 with susceptibility to Schizophrenia risk in North Indian population

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• Prediction of Functional Consequences of Missense Mutations in ANO4 Gene

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• Identification of pleiotropy at the gene level between psychiatric disorders and related traits

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• Length impairments of the axon initial segment in rodent models of attention-deficit hyperactivity disorder and autism spectrum disorder.

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• Celiac disease poses significant risk in developing depression, anxiety, headache, epilepsy, panic disorder, dysthymia: A meta-analysis

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• Genetic Diversity of North Eurasia Populations by Genetic Markers Associated with Diseases Impairing Human Cognitive Functions

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• Interactions between maternal fluoxetine exposure, the maternal gut microbiome and fetal neurodevelopment in mice.

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• Pathophysiological Roles of Abnormal Axon Initial Segments in Neurodevelopmental Disorders

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• Human ankyrins and their contribution to disease biology: An update

  2020cites this paper
• Approaches to studying the genomic architecture of complex birth defects

  2020cites this paper
• [A new look at the genetics of neurocognitive deficits in schizophrenia].

  2020cites this paper
• and in

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• Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disorders

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• Genomic Basis of Psychiatric Illnesses and Response to Psychiatric Drug Treatment Modalities

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• Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disorders

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• Unravelling the genetic basis of schizophrenia and bipolar disorder with GWAS: A systematic review.

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• The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia

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• Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia

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• Approaches for unveiling the kinetic mechanisms of voltage gated ion channels in neurons

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• The Schizophrenia Susceptibility Gene OPCML Regulates Spine Maturation and Cognitive Behaviors through Eph-Cofilin Signaling.

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• Genome-Wide Causation Studies of Complex Diseases

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• GWAS of Behavioral Traits.

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• Positive and general psychopathology associated with specific gray matter reductions in inferior temporal regions in patients with schizophrenia.

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• Gene polymorphisms of DISC1 is associated with schizophrenia: Evidence from a meta‐analysis

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• Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes

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• Type 2 Diabetes Leads to Axon Initial Segment Shortening in db/db Mice

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• Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci

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• Association of psychosis, affective disorders and diseases affecting the immune system

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• High genetic predisposition to schizophrenia is associated with an increased frequency of use of cannabis before illness onset

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• Axon initial segments: structure, function, and disease

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• Psychotic patients who used cannabis frequently before illness onset have higher genetic predisposition to schizophrenia than those who did not

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• Mining the topography and dynamics of the 4D Nucleome to identify novel CNS drug pathways.

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• Genetic risk scores and family history as predictors of schizophrenia in Nordic registers

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• Defining a Registry of Candidate Regulatory Elements to Interpret Disease Associated Genetic Variation

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• The joint effect of air pollution exposure and copy number variation on risk for autism

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• A genetic association study of CSMD1 and CSMD2 with cognitive function.

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• Using whole genome sequencing to identify risk alleles for susceptibility to schizophrenia

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• Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data

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• Schizophrenia and neurogenesis: A stem cell approach.

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• Behavioural characterization of AnkyrinG deficient mice, a model for ANK3 related disorders

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• Genome-Wide Association Study of Dietary Pattern Scores

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• A Loss-of-Function Variant in a Minor Isoform of ANK3 Protects Against Bipolar Disorder and Schizophrenia.

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• Polymorphisms of the TCF4 gene are associated with the risk of schizophrenia in the Han Chinese

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• OBSESSIVE–COMPULSIVE PERSONALITY DISORDER: EVIDENCE FOR TWO DIMENSIONS

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• Mouse Models of Schizophrenia: Risk Genes

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• Association analysis of ANK3 gene variants with schizophrenia in a northern Chinese Han population

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• Xenobiotic/medium chain fatty acid: CoA ligase – a critical review on its role in fatty acid metabolism and the detoxification of benzoic acid and aspirin

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• Computationally efficient familywise error rate control in genome‐wide association studies using score tests for generalized linear models

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• VRK2 gene expression in schizophrenia, bipolar disorder and healthy controls.

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• Assembly of Lipoic Acid on Its Cognate Enzymes: an Extraordinary and Essential Biosynthetic Pathway

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• TMEM16 Membrane Proteins in Health and Disease

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• Contribution of oxytocin receptor polymorphisms to amygdala activation in schizophrenia spectrum disorders

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• Effects of ankyrin 3 gene risk variants on brain structures in patients with bipolar disorder and healthy subjects

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• From Linkage Studies to Epigenetics: What We Know and What We Need to Know in the Neurobiology of Schizophrenia

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• Shared and unique common genetic determinants between pediatric and adult celiac disease

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• Currently recognized genes for schizophrenia: High‐resolution chromosome ideogram representation

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• Microarray Analysis of Copy Number Variants on the Human Y Chromosome Reveals Novel and Frequent Duplications Overrepresented in Specific Haplogroups

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• Polygenic risk scores in imaging genetics: Usefulness and applications

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• Preliminary study integrating CACNA1C rs1006737, hippocampal and amygdala volumes, and peripheral endothelial function in youth with bipolar disorder

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• What is the impact of genome-wide supported risk variants for schizophrenia and bipolar disorder on brain structure and function? A systematic review

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• Identification and Functional Studies of Regulatory Variants Responsible for the Association of NRG3 with a Delusion Phenotype in Schizophrenia

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• Glia‐related genes and their contribution to schizophrenia

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• Polygenic risk scores in bipolar disorder subgroups.

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• Schizophrenia and Depression Co-Morbidity: What We have Learned from Animal Models

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• Genetic association of ACSM1 variation with schizophrenia and major depressive disorder in the Han Chinese population

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• Genetic analysis of SNPs in CACNA1C and ANK3 gene with schizophrenia: A comprehensive meta‐analysis

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• The Genomic Load of Deleterious Mutations: Relevance to Death in Infancy and Childhood

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• CACNA1C rs1006737 genotype and bipolar disorder: Focus on intermediate phenotypes and cardiovascular comorbidity.

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