Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function (Q35591685)

9 August 2017

title

Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function (English)

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9 August 2017

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9 August 2017

Marzena Gajecka

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9 August 2017

Renzo Guerrini

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9 August 2017

Alex R Paciorkowski

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9 August 2017

Liu Lin Thio

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9 August 2017

Jill A Rosenfeld

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9 August 2017

Christina A Gurnett

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9 August 2017

Shashikant Kulkarni

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9 August 2017

Wendy K Chung

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9 August 2017

Eric D Marsh

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9 August 2017

Mattia Gentile

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9 August 2017

James D Reggin

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9 August 2017

James W Wheless

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9 August 2017

Sandhya Balasubramanian

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9 August 2017

Ravinesh Kumar

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9 August 2017

Susan L Christian

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9 August 2017

Carla Marini

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9 August 2017

Natalia Maltsev

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9 August 2017

Lisa G Shaffer

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9 August 2017

publication date

22 June 2011

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European Journal of Human Genetics

9 August 2017

published in

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9 August 2017

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9 August 2017

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9 August 2017

page(s)

1238-1245

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Characterising and predicting haploinsufficiency in the human genome.

9 August 2017

cites work

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Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment

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CHL1 is a selective organizer of the presynaptic machinery chaperoning the SNARE complex

27 July 2018

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Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome

27 July 2018

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Dominant-negative mutations in alpha-II spectrin cause West syndrome with severe cerebral hypomyelination, spastic quadriplegia, and developmental delay

27 July 2018

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Zebrafish gene knockdowns imply roles for human YWHAG in infantile spasms and cardiomegaly

27 July 2018

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4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment

27 July 2018

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27 July 2018

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Selective populations of hippocampal interneurons express ErbB4 and their number and distribution is altered in ErbB4 knockout mice

27 July 2018

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Arx acts as a regional key selector gene in the ventral telencephalon mainly through its transcriptional repression activity

27 July 2018

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MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations

27 July 2018

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A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment

27 July 2018

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27 July 2018

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Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females

27 July 2018

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The genetics of early telencephalon patterning: some assembly required

27 July 2018

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

27 July 2018

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Identification of Arx transcriptional targets in the developing basal forebrain

27 July 2018

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Distinct molecular pathways for development of telencephalic interneuron subtypes revealed through analysis of Lhx6 mutants

27 July 2018

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GABA and neuroligin signaling: linking synaptic activity and adhesion in inhibitory synapse development

27 July 2018

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A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

27 July 2018

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Identification and expression analysis of novel Jakmip1 transcripts

27 July 2018

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Neurexin-neuroligin signaling in synapse development

27 July 2018

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Evaluation of clustering algorithms for protein-protein interaction networks

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Actinfilin is a Cul3 substrate adaptor, linking GluR6 kainate receptor subunits to the ubiquitin-proteasome pathway

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Stargazin and other transmembrane AMPA receptor regulating proteins interact with synaptic scaffolding protein MAGI-2 in brain

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Are early myoclonic encephalopathy (EME) and the Ohtahara syndrome (EIEE) independent of each other?

27 July 2018

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Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy

27 July 2018

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Pathogenesis of infantile spasms: a model based on developmental desynchronization

27 July 2018

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Munc18-1 regulates early and late stages of exocytosis via syntaxin-independent protein interactions

27 July 2018

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A proposal for case definitions and outcome measures in studies of infantile spasms and West syndrome: consensus statement of the West Delphi group

27 July 2018

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Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.

27 July 2018

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Phosphorylation of syntaphilin by cAMP-dependent protein kinase modulates its interaction with syntaxin-1 and annuls its inhibitory effect on vesicle exocytosis

27 July 2018

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Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX

27 July 2018

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Actinfilin, a brain-specific actin-binding protein in postsynaptic density

27 July 2018

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Laminar organization of the NMDA receptor complex within the postsynaptic density.

27 July 2018

1 reference

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Microtubule binding by CRIPT and its potential role in the synaptic clustering of PSD-95

27 July 2018

1 reference

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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

N-methyl-D-aspartate receptor subunit- and neuronal-type dependence of excitotoxic signaling through post-synaptic density 95.

26 September 2018

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A possible association of responsiveness to adrenocorticotropic hormone with specific GRIN1 haplotypes in infantile spasms

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Array-CGH detection of a de novo 0.7-Mb deletion in 19p13.13 including CACNA1A associated with mental retardation and epilepsy with infantile spasms

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Molecular characterization of a monosomy 1p36 presenting as an Aicardi syndrome phenocopy.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

STRING 8--a global view on proteins and their functional interactions in 630 organisms

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Electroencephalographic evolution of hypsarrhythmia: toward an early treatment option

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Risk of autism spectrum disorders after infantile spasms: a population-based study nested in a cohort with seizures in the first year of life

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Which GABA(A) receptor subunits are necessary for tonic inhibition in the hippocampus?

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Docking of axonal mitochondria by syntaphilin controls their mobility and affects short-term facilitation

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Spectrum of epilepsy in terminal 1p36 deletion syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

alphaII-spectrin is essential for assembly of the nodes of Ranvier in myelinated axons.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Classical West "syndrome" phenotype with a subtelomeric 4p trisomy.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Common recurrent microduplication syndromes: diagnosis and management in clinical practice

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3230360

Left-ventricular non-compaction in a patient with monosomy 1p36

15 November 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2011.121

Deletion of 7q11.21-q11.23 and infantile spasms without deletion of MAGI2

21 January 2018

1 reference

12 December 2020

Polyalanine expansion of ARX associated with cryptogenic West syndrome

1 reference

12 December 2020

Infantile spasms in a patient with partial duplication of chromosome 2p

1 reference

12 December 2020

Characterization of a complex rearrangement with interstitial deletions and inversion on human chromosome 1

1 reference

12 December 2020

Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia

1 reference

12 December 2020

Identifiers

DOI

10.1038/EJHG.2011.121

1 reference

9 August 2017

1 reference

9 August 2017

1 reference