Molecular genetic studies of schizophrenia (Q28242041)

European Journal of Human Genetics

Europe PubMed Central

title

Molecular genetic studies of schizophrenia (English)

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2

Kenneth S Kendler

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author name string

Brien Riley

series ordinal

1

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language of work or name

English

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publication date

June 2006

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published in

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volume

14

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issue

6

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page(s)

669-80

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cites work

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

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

Neuregulin 1 and susceptibility to schizophrenia

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunit

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

Conditional calcineurin knockout mice exhibit multiple abnormal behaviors related to schizophrenia

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

A genome-wide search for schizophrenia susceptibility genes

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

Disrupted-In-Schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

Disrupted-in-Schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

Confirming RGS4 as a susceptibility gene for schizophrenia

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

Genes for schizophrenia? Recent findings and their pathophysiological implications

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201571

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

The genetics of schizophrenia: a current, genetic-epidemiologic perspective

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Genotype-environment interaction in schizophrenia-spectrum disorder. Long-term follow-up study of Finnish adoptees.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Mental illness in the biological and adoptive relatives of schizophrenic adoptees. Replication of the Copenhagen Study in the rest of Denmark

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Resolving genetic models for the transmission of schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

The Roscommon Family Study. II. The risk of nonschizophrenic nonaffective psychoses in relatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

A highly significant association between a COMT haplotype and schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

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.5201571

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.5201571

A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

No association with the calcineurin A gamma subunit gene (PPP3CC) haplotype to Japanese schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

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.5201571

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.5201571

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.5201571

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.5201571

Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

Convergent evidence for impaired AKT1-GSK3beta signaling in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

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.5201571

Association of G72/G30 with schizophrenia in the Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

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.5201571

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.5201571

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.5201571

No major schizophrenia locus detected on chromosome 1q in a large multicenter sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar affective disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Association study of polymorphisms in the 5' upstream region of human DISC1 gene with schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Association study of the DISC1/TRAX locus with schizophrenia in a Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Analysis of complex brain disorders with gene expression microarrays: schizophrenia as a disease of the synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Association and linkage analyses of RGS4 polymorphisms in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Regulator of G-protein signaling 4 (RGS4) gene is associated with schizophrenia in Irish high density families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Association and linkage analysis of RGS4 polymorphisms with schizophrenia and bipolar disorder in Brazil.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Failure to confirm association between RGS4 haplotypes and schizophrenia in Caucasians

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Support for RGS4 as a susceptibility gene for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

Bringing order to the glutamate chaos in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

Interaction between genetic vulnerability and family environment: the Finnish adoptive family study of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

7 January 2021

Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

7 January 2021

Association of AKT1 with schizophrenia confirmed in a Japanese population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

7 January 2021

Failure to confirm association between AKT1 haplotype and schizophrenia in a Japanese case-control population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

7 January 2021

Further evidence for association of variants in the AKT1 gene with schizophrenia in a sample of European sib-pair families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

7 January 2021

Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

7 January 2021

Transmission disequilibrium and haplotype analyses of the G72/G30 locus: Suggestive linkage to schizophrenia in Palestinian Arabs living in the North of Israel

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201571

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.5201571

7 January 2021