(Q34602621)

3 August 2017

title

Insights on the functional impact of microRNAs present in autism-associated copy number variants (English)

1 reference

3 August 2017

0 references

1 reference

Varadarajan Vaishnavi

1

1 reference

3 August 2017

Mayakannan Manikandan

2

1 reference

3 August 2017

Basant K Tiwary

3

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3 August 2017

Arasambattu Kannan Munirajan

4

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3 August 2017

language of work or name

English

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publication date

25 February 2013

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3 August 2017

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3 August 2017

volume

8

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3 August 2017

issue

2

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3 August 2017

page(s)

e56781

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Creative Commons Attribution 4.0 International

3 August 2017

copyright license

start time

25 February 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

Cytoscape

object named as

Cytoscape

2 references

9 June 2022

https://europepmc.org/search?query=(METHODS:'Cytoscape')

based on heuristic

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

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7 July 2018

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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

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7 July 2018

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Epilepsy and Tsc2 Haploinsufficiency Lead to Autistic-Like Social Deficit Behaviors in Rats

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Structural variation of chromosomes in autism spectrum disorder

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

Global variation in copy number in the human genome

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

The neuronal microRNA system

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

Severe expressive-language delay related to duplication of the Williams-Beuren locus

7 July 2018

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Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

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7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

Brain overgrowth in autism during a critical time in development: implications for frontal pyramidal neuron and interneuron development and connectivity

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

7 July 2018

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Long-range control of gene expression: emerging mechanisms and disruption in disease

7 July 2018

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Autism as a paradigmatic complex genetic disorder

7 July 2018

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Brain development in autism: early overgrowth followed by premature arrest of growth

7 July 2018

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Network biology: understanding the cell's functional organization

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

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7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

Autism as a strongly genetic disorder: evidence from a British twin study

7 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

7 July 2018

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0056781

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

Common deletion polymorphisms in the human genome.

7 July 2018

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Spastic paraplegia type 2 associated with axonal neuropathy and apparent PLP1 position effect.

21 January 2018

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Heterogeneous dysregulation of microRNAs across the autism spectrum.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0056781

Participation of microRNAs in human interactome: extraction of microRNA-microRNA regulations.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0056781

Computing topological parameters of biological networks.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0056781

Haploinsufficiency of CMIP in a girl with autism spectrum disorder and developmental delay due to a de novo deletion on chromosome 16q23.2.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3581547

Phenotype of FOXP2 haploinsufficiency in a mother and son.

26 October 2018

1 reference

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10.1371/JOURNAL.PONE.0056781

26 October 2018

Identifiers

DOI

1 reference

3 August 2017

0 references

1 reference

3 August 2017

1 reference