(Q50305785)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22865819%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

title

Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility (English)

1 reference

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10 February 2020

0 references

10

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10 February 2020

author name string

Cheng Bi

1

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10 February 2020

Jinyu Wu

2

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10 February 2020

Tao Jiang

3

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10 February 2020

Qi Liu

4

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10 February 2020

Wanshi Cai

5

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10 February 2020

Ping Yu

6

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10 February 2020

Tao Cai

7

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10 February 2020

Mei Zhao

8

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10 February 2020

Yong-hui Jiang

9

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10 February 2020

publication date

24 August 2012

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10 February 2020

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10 February 2020

volume

33

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10 February 2020

issue

12

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10 February 2020

page(s)

1635-1638

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Physiological roles of axonal ankyrins in survival of premyelinated axons and localization of voltage-gated sodium channels

10 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Genetics of austim: complex aetiology for a heterogeneous disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

De Novo Gene Disruptions in Children on the Autistic Spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Genetics of Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Ubiquitination in postsynaptic function and plasticity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Patterns and rates of exonic de novo mutations in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Ank3-dependent SVZ niche assembly is required for the continued production of new neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Allelic variants in HTR3C show association with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Genome-wide association study identifies five new schizophrenia loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

Identification of a novel Cys146X mutation of SOD1 in familial amyotrophic lateral sclerosis by whole-exome sequencing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22174

21 January 2018

Identifiers

DOI

10.1002/HUMU.22174

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22865819%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

1 reference