(Q37563075)

21 August 2017

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title

Epigenetics, genomic mutations and cognitive function (English)

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21 August 2017

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Abraham Reichenberg

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21 August 2017

Jonathan Mill

series ordinal

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21 August 2017

James H MacCabe

series ordinal

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21 August 2017

publication date

1 January 2009

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Cognitive Neuropsychiatry

21 August 2017

published in

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21 August 2017

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21 August 2017

issue

4-5

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21 August 2017

page(s)

377-390

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

21 August 2017

cites work

1 reference

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The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory.

21 January 2018

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The complex language of chromatin regulation during transcription

21 January 2018

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Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

21 January 2018

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https://api.crossref.org/works/10.1080%2F13546800902978417

Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1080%2F13546800902978417

Copy-number variations associated with neuropsychiatric conditions

21 January 2018

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FMR1 and the fragile X syndrome: human genome epidemiology review

21 January 2018

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https://api.crossref.org/works/10.1080%2F13546800902978417

22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay

21 January 2018

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https://api.crossref.org/works/10.1080%2F13546800902978417

Epigenetic gene regulation: linking early developmental environment to adult disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

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

21 January 2018

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https://api.crossref.org/works/10.1080%2F13546800902978417

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

21 January 2018

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Epigenetics in human disease and prospects for epigenetic therapy

21 January 2018

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Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements

21 January 2018

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Structural variation in the human genome

21 January 2018

1 reference

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Structural variants: changing the landscape of chromosomes and design of disease studies

21 January 2018

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Genes and the parsing of cognitive processes

21 January 2018

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COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

21 January 2018

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Molecular targets for treating cognitive dysfunction in schizophrenia.

21 January 2018

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Integration of long-term-memory-related synaptic plasticity involves bidirectional regulation of gene expression and chromatin structure

21 January 2018

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Two classes of short interfering RNA in RNA silencing

21 January 2018

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Exploring and explaining epigenetic effects.

21 January 2018

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Subtle chromosomal rearrangements in children with unexplained mental retardation

21 January 2018

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Angelman syndrome: a review of clinical and genetic aspects

21 January 2018

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Epigenetic mechanisms in memory formation.

21 January 2018

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Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

21 January 2018

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Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour

21 January 2018

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Molecular studies of major depressive disorder: the epigenetic perspective

21 January 2018

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Epigenomic profiling reveals DNA-methylation changes associated with major psychosis

21 January 2018

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High rates of schizophrenia in adults with velo-cardio-facial syndrome.

21 January 2018

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The pathophysiology of fragile x syndrome.

21 January 2018

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Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Neuropsychological impairments in schizophrenia: Integration of performance-based and brain imaging findings

21 January 2018

1 reference

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A population-based cohort study of premorbid intellectual, language, and behavioral functioning in patients with schizophrenia, schizoaffective disorder, and nonpsychotic bipolar disorder.

21 January 2018

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Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Prevalence estimation of Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Epistasis between catechol-O-methyltransferase and type II metabotropic glutamate receptor 3 genes on working memory brain function

21 January 2018

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Epigenetic regulation in psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Rett syndrome: clinical review and genetic update

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Molecular genetics of human cognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Is COMT a susceptibility gene for schizophrenia?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Genetic abnormalities of chromosome 22 and the development of psychosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

Strong association of de novo copy number mutations with sporadic schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13546800902978417

10.1080/13546800902978417

21 January 2018

Identifiers

DOI

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21 August 2017

1 reference