Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIalpha gene (PIP5K2A) with schizophrenia (Q34542095)

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English	Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIalpha gene (PIP5K2A) with schizophrenia	scientific article

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Europe PubMed Central

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2 August 2017

Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIalpha gene (PIP5K2A) with schizophrenia (English)

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2 August 2017

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Maier W

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2 August 2017

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Schwab SG

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2 August 2017

Knapp M

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2 August 2017

Sklar P

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2 August 2017

Eckstein GN

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2 August 2017

Sewekow C

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2 August 2017

Borrmann-Hassenbach M

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2 August 2017

Albus M

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2 August 2017

Becker T

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2 August 2017

Hallmayer JF

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Lerer B

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Wildenauer DB

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27 June 2006

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2 August 2017

Molecular Psychiatry

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11

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9

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2 August 2017

837-846

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2 August 2017

Searching for genetic determinants in the new millennium

1 reference

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Linkage and associated studies of schizophrenia

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Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

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Neuregulin 1 and susceptibility to schizophrenia

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Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

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A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

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Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

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The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease

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Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families

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Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria

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Association of the DTNBP1 locus with schizophrenia in a U.S. population

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Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia

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Association and linkage analyses of RGS4 polymorphisms in schizophrenia

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Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22.

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Disruption of two novel genes by a translocation co-segregating with schizophrenia

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Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

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Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia

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The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia

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Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III

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Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12.

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A schizophrenia locus may be located in region 10p15-p11.

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A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder

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The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data

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A genomic screen of autism: evidence for a multilocus etiology

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Phosphatidylinositol Phosphate Kinases Put PI4,5P 2 in Its Place

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Phosphatidylinositol phosphate kinases, a multifaceted family of signaling enzymes.

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A new pathway for synthesis of phosphatidylinositol-4,5-bisphosphate

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A polydiagnostic application of operational criteria in studies of psychotic illness. Development and reliability of the OPCRIT system

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Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

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Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Brain-derived neutrophic factor

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Maximum-likelihood estimation of haplotype frequencies in nuclear families

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Transmission/disequilibrium tests using multiple tightly linked markers

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A powerful strategy to account for multiple testing in the context of haplotype analysis

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A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

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Construction and characterization of a human bacterial artificial chromosome library

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The sequence of phosphatidylinositol-4-phosphate 5-kinase defines a novel family of lipid kinases

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Whole-genome patterns of common DNA variation in three human populations

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Lithium and bipolar mood disorder: the inositol-depletion hypothesis revisited

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A novel interaction between the juxtamembrane region of the p55 tumor necrosis factor receptor and phosphatidylinositol-4-phosphate 5-kinase

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Association of tumor necrosis factor alpha gene -G308A polymorphism with schizophrenia

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Association between −G308A tumor necrosis factor alpha gene polymorphism and schizophrenia

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A phospholipase C-dependent inositol polyphosphate kinase pathway required for efficient messenger RNA export

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Phosphoinositide signaling pathways in nuclei are associated with nuclear speckles containing pre-mRNA processing factors

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The phosphatidylinositol (PI)-5-phosphate 4-kinase type II enzyme controls insulin signaling by regulating PI-3,4,5-trisphosphate degradation

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Convergent evidence for impaired AKT1-GSK3beta signaling in schizophrenia

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Structure of Type IIβ Phosphatidylinositol Phosphate Kinase

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Polymorphism Screening of PIP5K2A: A Candidate Gene for Chromosome 10p‐Linked Psychiatric Disorders

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10.1038/SJ.MP.4001864

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Europe PubMed Central

PubMed publication ID

2 August 2017

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PubMed publication ID

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Europe PubMed Central

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2 August 2017

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