In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery (Q28274728)

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Language	Label	Description	Also known as
English	In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery	scientific article

Statements

instance of

scholarly article

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title

In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery (English)

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main subject

prioritization

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based on heuristic

inferred from title

in silico

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based on heuristic

inferred from title

gene discovery

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based on heuristic

inferred from title

author

Ingrid Scheffer

series ordinal

4

object named as

Ingrid E Scheffer

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Samuel Berkovic

series ordinal

5

object named as

Samuel F Berkovic

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author name string

Karen L Oliver

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1

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Vesna Lukic

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2

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Saskia Freytag

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3

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Melanie Bahlo

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6

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language of work or name

English

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publication date

February 2016

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published in

Neurology. Genetics

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stated in

Crossref

volume

2

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issue

1

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page(s)

e51

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cites work

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20 March 2017

De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathy

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Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

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20 March 2017

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20 March 2017

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20 March 2017

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Systematic noise degrades gene co-expression signals but can be corrected

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29 September 2017

Novel Genes of Early-Onset Epileptic Encephalopathies: From Genotype to Phenotypes.

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29 September 2017

GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders

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29 September 2017

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De novo KCNB1 mutations in epileptic encephalopathy

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29 September 2017

Harnessing gene expression networks to prioritize candidate epileptic encephalopathy genes

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29 September 2017

GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy

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29 September 2017

De novo mutations in SLC35A2 encoding a UDP-galactose transporter cause early-onset epileptic encephalopathy

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29 September 2017

Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability.

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Diagnostic yield of genetic testing in epileptic encephalopathy in childhood

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retrieved

27 November 2018

Identifiers

DOI

10.1212/NXG.0000000000000051

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PMC publication ID

4817907

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PubMed publication ID

27066588

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