Dosage-sensitivity of imprinted genes expressed in the brain: 15q11-q13 and neuropsychiatric illness (Q38108660)

29 August 2017

Dosage-sensitivity of imprinted genes expressed in the brain: 15q11-q13 and neuropsychiatric illness (English)

1 reference

29 August 2017

Anthony R Isles

2

0 references

author name string

Gráinne I McNamara

series ordinal

1

1 reference

29 August 2017

1 June 2013

1 reference

Biochemical Society Transactions

29 August 2017

1 reference

29 August 2017

41

1 reference

29 August 2017

3

1 reference

29 August 2017

721-726

1 reference

Role of paternal and maternal genomes in mouse development

29 August 2017

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Completion of mouse embryogenesis requires both the maternal and paternal genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

The importance of imprinting in the human placenta.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Regulation of growth and metabolism by imprinted genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Genomic imprinting effects on brain development and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

High-resolution analysis of parent-of-origin allelic expression in the mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Increased apoptosis during neonatal brain development underlies the adult behavioral deficits seen in mice lacking a functional paternally expressed gene 3 (Peg3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Postnatal loss of Dlk1 imprinting in stem cells and niche astrocytes regulates neurogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Distinct physiological and behavioural functions for parental alleles of imprinted Grb10

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Imprinted Nesp55 influences behavioral reactivity to novel environments

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Enhanced appetitive learning and reversal learning in a mouse model for Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Urinary odour preferences in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

A possible role for imprinted genes in inbreeding avoidance and dispersal from the natal area in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Genomic imprinting: the emergence of an epigenetic paradigm.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

New insights into establishment and maintenance of DNA methylation imprints in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Developmental regulation of somatic imprints

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Dnmt3L and the establishment of maternal genomic imprints.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Dynamic CpG island methylation landscape in oocytes and preimplantation embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

PGC7/Stella protects against DNA demethylation in early embryogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

H3K9me2 attracts PGC7 in the zygote to prevent Tet3-mediated oxidation of 5-methylcytosine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Genomic imprinting: recognition and marking of imprinted loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Dosage compensation: the beginning and end of generalization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Further refinement of the critical minimal genetic region for the imprinting disorder 6q24 transient neonatal diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Gene dosage effects of the imprinted delta-like homologue 1 (dlk1/pref1) in development: implications for the evolution of imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Behavioural and cognitive profiles of mouse models for Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Angelman syndrome, a genomic imprinting disorder of the brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

The course and outcome of psychiatric illness in people with Prader-Willi syndrome: implications for management and treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Psychiatric illness in a cohort of adults with Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Prader-Willi syndrome: the psychopathological phenotype in uniparental disomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Imprinted genes and mother-offspring interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Genomic imprinting; the cost of mother's care.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Genomic imprinting and the social brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

The Angelman Syndrome protein Ube3A regulates synapse development by ubiquitinating arc.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

The Kraepelinian dichotomy - going, going... but still not gone

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Failure of neuronal homeostasis results in common neuropsychiatric phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Increased gene dosage of Ube3a results in autism traits and decreased glutamate synaptic transmission in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

In search of the psychosis gene in people with Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Independent evidence for the selective influence of GABA(A) receptors on one component of the bipolar disorder phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

Genomic imprinting as an adaptative model of developmental plasticity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20130008

21 January 2018

Identifiers

DOI

10.1042/BST20130008

1 reference

29 August 2017

1 reference

PubMed ID

23697931