Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia (Q35956878)

11 August 2017

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia. (English)

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11 August 2017

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Mary-Claire King

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Vladimir Vacic

Vladimir Vacic

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Lilia M. Iakoucheva

Lilia M Iakoucheva

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Jonathan Sebat

Jonathan Sebat

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Derek W. Morris

Derek W Morris

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Aiden Corvin

Aiden Corvin

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Fiona Murray

Fiona Murray

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Deborah M Levy

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Deborah L Levy

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John R Kelsoe

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Elliot S Gershon

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Dheeraj Malhotra

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Shane McCarthy

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Jon McClellan

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Olga Krastoshevsky

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Verena Krause

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Hsun-Hua Chou

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Roser Corominas

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Verónica Larach-Walters

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Verónica Larach-Walters

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Marie Dell Aquila

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Aine Peoples

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Vladimir Makarov

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Seungtai Yoon

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Abhishek Bhandari

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David K Welsh

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David Craig

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Suzanne M Leal

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Paul A Insel

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Maria Karayiorgou

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Lynn E DeLisi

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11 August 2017

language of work or name

English

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publication date

23 February 2011

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471

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7339

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499-503

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https://scigraph.springernature.com/pub.10.1038/nature09884

11 August 2017

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cites work

Microdeletions of 3q29 confer high risk for schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Emergence of orphan drugs in the United States: a quantitative assessment of the first 25 years

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Microduplications of 16p11.2 are associated with schizophrenia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Common variants on chromosome 6p22.1 are associated with schizophrenia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Vasoactive intestinal peptide acts via multiple signal pathways to regulate hippocampal NMDA receptors and synaptic transmission

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Singleton deletions throughout the genome increase risk of bipolar disorder

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

An odor-specific threshold deficit implicates abnormal intracellular cyclic AMP signaling in schizophrenia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Disruption of the neurexin 1 gene is associated with schizophrenia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Large recurrent microdeletions associated with schizophrenia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Rare chromosomal deletions and duplications increase risk of schizophrenia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Select cognitive deficits in vasoactive intestinal peptide deficient mice

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Disrupted neuronal activity rhythms in the suprachiasmatic nuclei of vasoactive intestinal polypeptide-deficient mice

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Human telomeric position effect is determined by chromosomal context and telomeric chromatin integrity

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

The VPAC(2) receptor is essential for circadian function in the mouse suprachiasmatic nuclei

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Y chromosome sequence variation and the history of human populations

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Transmitter role of vasoactive intestinal peptide

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Vasoactive intestinal peptide: an important trophic factor and developmental regulator?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Position effect at S. cerevisiae telomeres: reversible repression of Pol II transcription

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Identification and characterization of a small molecule antagonist of human VPAC(2) receptor

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

The neurotransmitter VIP expands the pool of symmetrically dividing postnatal dentate gyrus precursors via VPAC2 receptors or directs them toward a neuronal fate via VPAC1 receptors.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3351382

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH

24 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNATURE09884

Small inherited terminal duplication of 7q with hydrocephalus, cleft palate, joint contractures, and severe hypotonia

21 January 2018

2 references

Crossref

https://api.crossref.org/works/10.1038%2FNATURE09884

21 January 2018

12 December 2020

Development of selective agonists and antagonists for the human vasoactive intestinal polypeptide VPAC(2) receptor

1 reference

PubMed

12 December 2020

The distribution of vasoactive intestinal peptide2 receptor messenger RNA in the rat brain and pituitary gland as assessed by in situ hybridization

1 reference

PubMed

12 December 2020

Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis

1 reference

PubMed

12 December 2020

Identifiers

DOI

10.1038/NATURE09884

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Dimensions Publication ID

11 August 2017

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11 August 2017

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