Gene‐based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: Association with HMG2L1 and TOM1

No abstract is available for this paper.

• Publication year

  2008

• Venue

  American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

• Publication date

  2008-01-05

• Fields of study

  Biology, Medicine, Psychology

• Identifiers
  DOI 10.1002/ajmg.b.30574PMID 17671966
• 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.

• Haploview: analysis and visualization of LD and haplotype maps

  2005cited by this paper
• The genetics of schizophrenia and bipolar disorder: dissecting psychosis

  2005cited by this paper
• A single nucleotide polymorphism in glycogen synthase kinase 3-beta promoter gene influences onset of illness in patients affected by bipolar disorder.

  2004cited by this paper
• Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin

  2004cited by this paper
• Convergent evidence for impaired AKT1-GSK3β signaling in schizophrenia

  2004cited by this paper
• A case-control study provides evidence of association for a functional polymorphism -197C/G in XBP1 to schizophrenia and suggests a sex-dependent effect.

  2004influential reference
• Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

  2004cited by this paper
• Tom1 (target of Myb 1) is a novel negative regulator of interleukin-1- and tumor necrosis factor-induced signaling pathways.

  2004cited by this paper
• COMT: A common susceptibility gene in bipolar disorder and schizophrenia

  2004cited by this paper
• Lithium antagonizes dopamine-dependent behaviors mediated by an AKT/glycogen synthase kinase 3 signaling cascade.

  2004cited by this paper
• Genome-wide scan in Portuguese Island families identifies 5q31–5q35 as a susceptibility locus for schizophrenia and psychosis

  2004cited by this paper
• Decoding randomly ordered DNA arrays.

  2004cited by this paper
• The effects of clozapine on the GSK‐3‐mediated signaling pathway

  2004cited by this paper
• Mutation screening and association study of the beta-adrenergic receptor kinase 2 gene in schizophrenia families.

  2004influential reference
• Clinical features of psychotic disorders and polymorphisms in HT2A, DRD2, DRD4, SLC6A3 (DAT1), and BDNF: A family based association study

  2004cited by this paper
• Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

  2003influential reference
• Evidence that a single nucleotide polymorphism in the promoter of the G protein receptor kinase 3 gene is associated with bipolar disorder

  2003influential reference
• Family, twin, and adoption studies of bipolar disorder

  2003cited by this paper
• Familial aggregation of delusional proneness in schizophrenia and bipolar pedigrees.

  2003cited by this paper
• Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder

  2003influential reference
• Analysis of a cluster of polymorphisms in AKT1 gene in bipolar pedigrees: a family-based association study.

  2003cited by this paper
• Negative regulation of Wnt signalling by HMG2L1, a novel NLK‐binding protein

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

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

  2003cited by this paper
• Suggestive linkage to chromosomal regions 13q31 and 22q12 in families with psychotic bipolar disorder.

  2003cited by this paper
• Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia

  2003cited by this paper
• Familial aggregation of psychotic symptoms in a replication set of 69 bipolar disorder pedigrees

  2003cited by this paper
• Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies.

  2003cited by this paper
• Sibling pairs with affective disorders: resemblance of demographic and clinical features

  2002cited by this paper
• A highly significant association between a COMT haplotype and schizophrenia.

  2002cited by this paper
• A first-generation linkage disequilibrium map of human chromosome 22

  2002influential reference
• Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

  2002cited by this paper
• Gene expression analysis in schizophrenia: Reproducible up-regulation of several members of the apolipoprotein L family located in a high-susceptibility locus for schizophrenia on chromosome 22

  2002cited by this paper
• A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes.

  2002cited by this paper
• Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

  2002cited by this paper
• Power calculations for a general class of family-based association tests: dichotomous traits.

  2002cited by this paper
• Serial analysis of gene expression in the frontal cortex of patients with bipolar disorder

  2001cited by this paper
• The familial aggregation of psychotic symptoms in bipolar disorder pedigrees.

  2001cited by this paper
• A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22.

  2001cited by this paper
• A search for specific and common susceptibility loci for schizophrenia and bipolar disorder: a linkage study in 13 target chromosomes

  2001cited by this paper
• Cytokine serum levels, autologous mixed lymphocyte reaction and surface marker analysis in never medicated and chronically medicated schizophrenic patients.

  2001cited by this paper
• Serum IL-1 b , sIL-2 R , IL-6 , IL-8 and TNF-a in schizophrenic patients , relation with symptomatology and responsiveness to risperidone treatment

  2001cited by this paper
• GRR: graphical representation of relationship errors

  2001cited by this paper
• Are schizophrenic and bipolar disorders related? A review of family and molecular studies.

  2000cited by this paper
• Implementing a unified approach to family‐based tests of association

  2000influential reference
• Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes

  2000cited by this paper
• A Robust Identity-by-Descent Procedure Using Affected Sib Pairs: Multipoint Mapping for Complex Diseases

  2000influential reference
• The Mood‐Stabilizing Agent Valproate Inhibits the Activity of Glycogen Synthase Kinase‐3

  2000cited by this paper
• Genetic associations with clinical characteristics in bipolar affective disorder and recurrent unipolar depressive disorder.

  2000cited by this paper
• High rates of schizophrenia in adults with velo-cardio-facial syndrome.

  1999cited by this paper
• A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

  1999cited by this paper
• Genomic Survey of Bipolar Illness in the NIMH Genetics Initiative Pedigrees: A Preliminary Report

  1997cited by this paper
• Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.

  1997cited by this paper
• Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22.

  1997cited by this paper
• A molecular mechanism for the effect of lithium on development.

  1996cited by this paper
• Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: a preliminary report.

  1996cited by this paper
• A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

  1996cited by this paper
• Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative.

  1994cited by this paper
• Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1.

  1994cited by this paper
• The Diagnostic Interview for Genetic Studies

  1994influential reference
• Assessment of lineality in bipolar I linkage studies.

  1992cited by this paper
• A Bipolar Pedigree Series for Genomic Mapping of Disease Genes: Diagnostic and Analytic Considerations

  1991cited by this paper
• Affective disorders in five United States communities

  1988cited by this paper
• A diagnostic interview: the schedule for affective disorders and schizophrenia.

  1978cited by this paper
• Reliability of a Procedure for Measuring and Classifying “Present Psychiatric State”

  1967cited by this paper

• Excess Wnt in neurological disease

  2025cites this paper
• Acknowledging the use of botanicals to treat diabetic foot ulcer during the 21st century: A systematic review

  2023cites this paper
• Neurodevelopmental Perspectives on Wnt Signaling in Psychiatry

  2017cites this paper
• Electroconvulsive therapy for depression : optimising treatment and exploring molecular mechanisms

  2016cites this paper
• Expression and neural correlates of schizophrenia risk gene ZNF804A

  2013influential citation
• Hypothesis review: are clathrin-mediated endocytosis and clathrin-dependent membrane and protein trafficking core pathophysiological processes in schizophrenia and bipolar disorder?

  2012cites this paper
• [Mapping genes related to early onset major depressive disorder in Dagestan genetic isolates].

  2012cites this paper
• Genome-wide linkage scan of major depressive disorder in two Dagestan genetic isolates

  2011cites this paper
• Synapsin III: role in neuronal plasticity and disease.

  2011cites this paper
• Roles of the Akt/GSK-3 and Wnt signaling pathways in schizophrenia and antipsychotic drug action.

  2010cites this paper
• Pathway-based approaches to imaging genetics association studies: Wnt signaling, GSK3beta substrates and major depression

  2010cites this paper
• Are working memory deficits in bipolar disorder markers for psychosis?

  2010cites this paper
• Coming to grips with complex disorders: Genetic risk prediction in bipolar disorder using panels of genes identified through convergent functional genomics

  2010cites this paper
• EFFECTS OF OMEGA-3 FATTY ACIDS ON RODENT MODELS OF BIPOLAR DISORDER AND ALCOHOLISM

  2010cites this paper
• Repression of Smooth Muscle Differentiation by a Novel High Mobility Group Box-containing Protein, HMG2L1*

  2010cites this paper
• Suggestive linkage at 9p22 in bipolar disorder weighted by alcohol abuse

  2009cites this paper
• Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population.

  2009cites this paper
• Tom1l2 hypomorphic mice exhibit increased incidence of infections and tumors and abnormal immunologic response

  2008cites this paper
• The genetics of psychotic bipolar disorder

  2008cites this paper
• Association study of Wnt signaling pathway genes in bipolar disorder.

  2008cites this paper
• The genetics of bipolar disorder: genome ‘hot regions,’ genes, new potential candidates and future directions

  2008cites this paper
• Genetics of bipolar disorder

  2007cites this paper