A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability. (Q54261485)

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English	A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability.	scientific article

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Europe PubMed Central

PubMed publication ID

23633123

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26 May 2018

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http://europepmc.org/abstract/MED/23633123

title

A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability. (English)

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Europe PubMed Central

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23633123

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26 May 2018

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http://europepmc.org/abstract/MED/23633123

author name string

Jurate Kasnauskiene

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1

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Europe PubMed Central

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23633123

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26 May 2018

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http://europepmc.org/abstract/MED/23633123

Zivile Ciuladaite

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2

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Europe PubMed Central

PubMed publication ID

23633123

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26 May 2018

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http://europepmc.org/abstract/MED/23633123

Egle Preiksaitiene

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3

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Europe PubMed Central

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23633123

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26 May 2018

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http://europepmc.org/abstract/MED/23633123

Algirdas Utkus

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4

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Europe PubMed Central

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23633123

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26 May 2018

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http://europepmc.org/abstract/MED/23633123

Agnė Peciulyte

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5

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23633123

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26 May 2018

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http://europepmc.org/abstract/MED/23633123

Vaidutis Kučinskas

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6

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Europe PubMed Central

PubMed publication ID

23633123

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26 May 2018

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http://europepmc.org/abstract/MED/23633123

language of work or name

English

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publication date

30 April 2013

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Europe PubMed Central

PubMed publication ID

23633123

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26 May 2018

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http://europepmc.org/abstract/MED/23633123

published in

American Journal of Medical Genetics

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Europe PubMed Central

PubMed publication ID

23633123

retrieved

26 May 2018

reference URL

http://europepmc.org/abstract/MED/23633123

volume

161A

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Europe PubMed Central

PubMed publication ID

23633123

retrieved

26 May 2018

reference URL

http://europepmc.org/abstract/MED/23633123

issue

6

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Europe PubMed Central

PubMed publication ID

23633123

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26 May 2018

reference URL

http://europepmc.org/abstract/MED/23633123

page(s)

1487-1490

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PubMed publication ID

23633123

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26 May 2018

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http://europepmc.org/abstract/MED/23633123

cites work

Early myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Neuregulin 1-erbB4 pathway in schizophrenia: From genes to an interactome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Aberrant neural and cardiac development in mice lacking the ErbB4 neuregulin receptor

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Heregulin, but not ErbB2 or ErbB3, heterozygous mutant mice exhibit hyperactivity in multiple behavioral tasks

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Behavioral characteristics of a nervous system-specific erbB4 knock-out mouse

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Disease-associated intronic variants in the ErbB4 gene are related to altered ErbB4 splice-variant expression in the brain in schizophrenia

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Conserved interneuron-specific ErbB4 expression in frontal cortex of rodents, monkeys, and humans: implications for schizophrenia

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Neuregulin 1 and susceptibility to schizophrenia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Neuregulin 1 represses limbic epileptogenesis through ErbB4 in parvalbumin-expressing interneurons

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.35911

retrieved

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.35911

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23633123

retrieved

26 May 2018

reference URL

http://europepmc.org/abstract/MED/23633123

PubMed publication ID

23633123

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23633123

retrieved

26 May 2018

reference URL

http://europepmc.org/abstract/MED/23633123

 

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