(Q33625398)

28 July 2017

title

Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls (English)

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28 July 2017

2

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28 July 2017

15

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28 July 2017

4

Henrik Anckarsäter

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28 July 2017

Stéphane Jamain

6

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Marion Leboyer

object named as

Marion Leboyer

13

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Richard Delorme

object named as

Richard Delorme

1

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Christopher Gillberg

14

object named as

Christopher Gillberg

1 reference

28 July 2017

Isabelle Scheid

3

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28 July 2017

Pauline Chaste

5

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28 July 2017

Franck Schuroff

7

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28 July 2017

Gudrun Nygren

8

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28 July 2017

Evelyn Herbrecht

9

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28 July 2017

Anne Dumaine

10

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28 July 2017

Marie Christine Mouren

11

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28 July 2017

Maria Råstam

12

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28 July 2017

publication date

5 July 2010

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28 July 2017

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28 July 2017

volume

11

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28 July 2017

page(s)

108

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Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

NMDA receptor-nitric oxide transmission mediates neuronal iron homeostasis via the GTPase Dexras1.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

MPZL1/PZR, a novel candidate predisposing schizophrenia in Han Chinese

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Does the CAPON gene confer susceptibility to schizophrenia?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Obsessions and compulsions in Asperger syndrome and high-functioning autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Genome-wide scan for loci of Asperger syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Confirming RGS4 as a susceptibility gene for schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Defining the broader phenotype of autism: genetic, brain, and behavioral perspectives.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

The structure of haplotype blocks in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Association and linkage analyses of RGS4 polymorphisms in schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Chromosome 1 loci in Finnish schizophrenia families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2919462

Linkage of schizophrenia with chromosome 1q loci in Taiwanese families.

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-108

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-108

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/10.1186%2F1471-2350-11-108

Support for RGS4 as a susceptibility gene for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-108

Putative association of the carboxy-terminal PDZ ligand of neuronal nitric oxide synthase gene (CAPON) with schizophrenia in a Colombian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-108

Contact in the genetics of autism and schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-108

[Linkage analysis of susceptibility genes for familial schizophrenia on chromosome 1 in Chinese population]

21 January 2018

1 reference

12 December 2020

Retrospective assessment of prepubertal major depression with the Kiddie-SADS-e

1 reference

12 December 2020

Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q and 6q

1 reference

12 December 2020

Family-based association studies of CAPON and schizophrenia in the Chinese Han population

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-11-108

1 reference

Dimensions Publication ID

28 July 2017

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28 July 2017

1 reference