(Q37161534)

18 August 2017

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title

Genomic structural variation and schizophrenia (English)

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18 August 2017

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Jennifer Gladys Mulle

series ordinal

1

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PubMed ID

18474211

18 August 2017

language of work or name

English

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publication date

1 April 2008

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18 August 2017

7

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Current Psychiatry Reports

inferred from page(s)

published in

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18 August 2017

10

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18 August 2017

2

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18 August 2017

171-177

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https://scigraph.springernature.com/pub.10.1007/s11920-008-0029-y

18 August 2017

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cites work

Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15

1 reference

https://api.crossref.org/works/10.1007%2FS11920-008-0029-Y

Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G-protein signaling 4 protein (RGS4).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11920-008-0029-Y

Failure to confirm association between RGS4 haplotypes and schizophrenia in Caucasians

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11920-008-0029-Y

Clinical features of 78 adults with 22q11 Deletion Syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11920-008-0029-Y

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

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Evidence for a susceptibility locus for schizophrenia on chromosome 6pter-p22

1 reference

12 December 2020

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

12 December 2020

Genetic Restriction of HIV-1 Infection and Progression to AIDS by a Deletion Allele of the CKR5 Structural Gene

1 reference

12 December 2020

Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

1 reference

12 December 2020

A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.

1 reference

12 December 2020

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

1 reference

12 December 2020

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

1 reference

12 December 2020

Increase inGSK3β gene copy number variation in bipolar disorder

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Association and linkage analyses of RGS4 polymorphisms in schizophrenia

1 reference

12 December 2020

Support for RGS4 as a susceptibility gene for schizophrenia

1 reference

12 December 2020

Path Analysis of Qualitative Data on Pairs of Relatives: Application to Schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci

1 reference

12 December 2020

Gene copy number variation in schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

1 reference

12 December 2020

Preferential transmission of the high activity allele of COMT in schizophrenia

1 reference

12 December 2020

Confirming RGS4 as a susceptibility gene for schizophrenia

1 reference

12 December 2020

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

1 reference

12 December 2020

No association with the neuregulin 1 haplotype to Japanese schizophrenia

1 reference

12 December 2020

Fine-scale structural variation of the human genome

1 reference

12 December 2020

A high-resolution survey of deletion polymorphism in the human genome

1 reference

12 December 2020

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

1 reference

12 December 2020

Large-scale copy number polymorphism in the human genome

1 reference

12 December 2020

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

1 reference

12 December 2020

Association analysis of the RGS4 gene in Han Chinese and Scottish populations with schizophrenia.

1 reference

12 December 2020

22q11 deletion syndrome in childhood onset schizophrenia: an update

1 reference

12 December 2020

The geographic spread of the CCR5 Delta32 HIV-resistance allele

1 reference

12 December 2020

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

1 reference

12 December 2020

Segmental duplications and copy-number variation in the human genome

1 reference

12 December 2020

Global variation in copy number in the human genome

1 reference

12 December 2020

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

1 reference

12 December 2020

Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22

1 reference

12 December 2020

Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q

1 reference

12 December 2020

A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6

1 reference

12 December 2020

Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia

1 reference

12 December 2020

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

1 reference

12 December 2020

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

1 reference

12 December 2020

Detection of large-scale variation in the human genome

1 reference

12 December 2020

Linkage of familial schizophrenia to chromosome 13q32

1 reference

12 December 2020

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

1 reference

12 December 2020

Genomic scan for genes predisposing to schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

Common deletion polymorphisms in the human genome.

1 reference

12 December 2020

Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population

1 reference

12 December 2020

DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Neuregulin 1 and susceptibility to schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Schizophrenia and 22q11.2 deletion syndrome

1 reference

12 December 2020

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

1 reference

12 December 2020

Failure to find association between PRODH deletion and schizophrenia

1 reference

12 December 2020

A genome-wide search for schizophrenia susceptibility genes

1 reference

12 December 2020

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

1 reference

12 December 2020

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

12 December 2020

Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection

1 reference

12 December 2020

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

1 reference

12 December 2020

No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder

1 reference

12 December 2020

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

1 reference

12 December 2020

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

1 reference

12 December 2020

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

1 reference

12 December 2020

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Case-control and family-based association studies between the neuregulin 1 (Arg38Gln) polymorphism and schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

1 reference

12 December 2020

10.1007/S11920-008-0029-Y

Identifiers

DOI

1 reference

18 August 2017

1 reference

PubMed ID

18474211