Schizophrenia genetics: uncovering positional candidate genes (Q36403410)

14 August 2017

Schizophrenia genetics: uncovering positional candidate genes (English)

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14 August 2017

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Joseph A Gogos

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14 August 2017

Maria Karayiorgou

1

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14 August 2017

1 May 2006

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European Journal of Human Genetics

14 August 2017

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14 August 2017

14

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14 August 2017

5

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14 August 2017

512-519

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201587

14 August 2017

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cites work

The early stages of schizophrenia: speculations on pathogenesis, pathophysiology, and therapeutic approaches

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Relationship between duration of untreated psychosis and outcome in first-episode schizophrenia: a critical review and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

A turning point in schizophrenia genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Demonstrating stratification in a European American population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

The use of single nucleotide polymorphisms in the isolation of common disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Neuregulin 1 and susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

The molecular genetics of the 22q11-associated schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Association between PRODH and schizophrenia is not confirmed

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Functional consequences of PRODH missense mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Untranslated region haplotype in dysbindin gene: analysis in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Human dysbindin (DTNBP1) gene expression in normal brain and in schizophrenic prefrontal cortex and midbrain

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Confirmation and refinement of an 'at-risk' haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

A case control and family based association study of the neuregulin1 gene and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Association study of neuregulin 1 gene with schizophrenia.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Neuregulin 1 (NRG1 ) and schizophrenia: analysis of a US family sample and the evidence in the balance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Neuregulin 1-erbB signaling and the molecular/cellular basis of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Neuregulin-1 immunoglobulin-like domain mutant mice: clozapine sensitivity and impaired latent inhibition

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

A cysteine-rich isoform of neuregulin controls the level of expression of neuronal nicotinic receptor channels during synaptogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Association of G72/G30 with schizophrenia in the Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Is the G72/G30 locus associated with schizophrenia? single nucleotide polymorphisms, haplotypes, and gene expression analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

A family-based study of the association between the G72/G30 genes and schizophrenia in the Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

D-serine is an endogenous ligand for the glycine site of the N-methyl-D-aspartate receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

A genetic mechanism implicates chromosome 11 in schizophrenia and bipolar diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Chromosome 1 loci in Finnish schizophrenia families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Replication of 1q42 linkage in Finnish schizophrenia pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Increased expression in dorsolateral prefrontal cortex of CAPON in schizophrenia and bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Association of the carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase gene with schizophrenia in the Chinese Han population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Failure to confirm allelic association between markers at the CAPON gene locus and schizophrenia in a British sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

CAPON: a protein associated with neuronal nitric oxide synthase that regulates its interactions with PSD95

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Protein palmitoylation: a regulator of neuronal development and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Failure to find association between TRAR4 and schizophrenia in the Chinese Han population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

No association of haplotype-tagging SNPs in TRAR4 with schizophrenia in Japanese patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Trace amines: identification of a family of mammalian G protein-coupled receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Genome-wide scan in Portuguese Island families identifies 5q31-5q35 as a susceptibility locus for schizophrenia and psychosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Cortical inhibitory neurons and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

A highly significant association between a COMT haplotype and schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Catechol-O-methyltransferase gene Val/Met functional polymorphism and risk of schizophrenia: a large-scale association study plus meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Lack of association of the COMT (Val158/108 Met) gene and schizophrenia: a meta-analysis of case-control studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

No association between schizophrenia and polymorphisms in COMT in two large samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flow.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

A haplotype map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

A family-based and case–control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

Support for involvement of neuregulin 1 in schizophrenia pathophysiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

The mammalian brain high-affinity L-proline transporter is enriched preferentially in synaptic vesicles in a subpopulation of excitatory nerve terminals in rat forebrain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

7 January 2021

Family-based association study of DTNBP1 in 6p22.3 and schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

7 January 2021

The contribution of three strong candidate schizophrenia susceptibility genes in demographically distinct populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

7 January 2021

No association with the neuregulin 1 haplotype to Japanese schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

7 January 2021

Polymorphisms within 5' end of the Neuregulin 1 gene are genetically associated with schizophrenia in the Chinese population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

7 January 2021

No evidence for association to the G72/G30 locus in an independent sample of schizophrenia families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

7 January 2021

Genetics. Two genes link two distinct psychoses

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

7 January 2021

Lack of association of catechol-O-methyltransferase gene Val108/158Met polymorphism with schizophrenia: a family-based association study in a Chinese population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

7 January 2021

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201587

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201587

1 reference

PubMed ID

16493444

Dimensions Publication ID

14 August 2017

0 references

1 reference

PubMed ID

16493444