(Q36680149)

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Characterization of molecular and cellular phenotypes associated with a heterozygous CNTNAP2 deletion using patient-derived hiPSC neural cells.

scientific article published on June 2015

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scholarly article

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11 March 2020

Characterization of molecular and cellular phenotypes associated with a heterozygous CNTNAP2 deletion using patient-derived hiPSC neural cells (English)

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11 March 2020

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Panagiotis Douvaras

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11 March 2020

Kristen J. Brennand

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11 March 2020

James R. Lupski

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James R Lupski

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11 March 2020

Luciana Zuccherato

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Luciana W Zuccherato

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11 March 2020

Judith L. Rapoport

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Judith Rapoport

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11 March 2020

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Jonathan Sebat

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author name string

Inkyu S Lee

1

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11 March 2020

Claudia M B Carvalho

2

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11 March 2020

Seok-Man Ho

4

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11 March 2020

Brigham J Hartley

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11 March 2020

Ian G Ladran

7

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11 March 2020

Arthur J Siegel

8

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11 March 2020

Shane McCarthy

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11 March 2020

Dheeraj Malhotra

10

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11 March 2020

Valentina Fossati

13

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11 March 2020

Deborah L Levy

15

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11 March 2020

publication date

1 June 2015

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11 March 2020

NPJ schizophrenia

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11 March 2020

1

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11 March 2020

copyright license

Creative Commons Attribution 4.0 International

24 June 2015

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April 2022 Public Data File from Crossref

copyright status

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

Efficient generation of myelinating oligodendrocytes from primary progressive multiple sclerosis patients by induced pluripotent stem cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

Phenotypic differences in hiPSC NPCs derived from patients with schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

Rapid single-step induction of functional neurons from human pluripotent stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

Shining a light on CNTNAP2: complex functions to complex disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

Allele-biased expression in differentiating human neurons: implications for neuropsychiatric disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

CNVs: harbingers of a rare variant revolution in psychiatric genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

Reduced transcript expression of genes affected by inherited and de novo CNVs in autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4789165

30 September 2017

Identifiers

10.1038/NPJSCHZ.2015.19

1 reference

Europe PubMed Central

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11 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26985448%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26985448%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

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