(Q34093571)

31 July 2017

title

Imprinted genes and mental dysfunction (English)

1 reference

31 July 2017

Davies W

1

1 reference

31 July 2017

Isles AR

series ordinal

2

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31 July 2017

Wilkinson LS

series ordinal

3

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31 July 2017

language of work or name

English

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publication date

1 September 2001

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31 July 2017

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31 July 2017

volume

33

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31 July 2017

issue

6

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31 July 2017

page(s)

428-436

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Gametic imprinting in mammals

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Role for DNA methylation in genomic imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Genomic imprinting: parental influence on the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Genomic imprinting in the brain

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

The imprinted gene and parent-of-origin effect database

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Genomic imprinting: implications for human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Completion of mouse embryogenesis requires both the maternal and paternal genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Imprinted genes, cognition and behaviour.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

On the parental origin of de novo mutation in man.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

‘Puppet’ Children A Report on Three Cases

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Angelman syndrome: a review of clinical and genetic aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Puppet-like syndrome of Angelman: a pathologic and neurochemical study

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Angelman's syndrome: a neuropathological study.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Towards a molecular understanding of Prader-Willi and Angelman syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Prader-Willi and Angelman syndromes: sister imprinted disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

UBE3A/E6-AP mutations cause Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Ubiquitin C-terminal hydrolase is an immediate-early gene essential for long-term facilitation in Aplysia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

21 January 2018

Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

A mouse model for Prader-Willi syndrome imprinting-centre mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

MR of the pituitary in patients with Prader-Willi syndrome: size determination and imaging findings

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Prader-Willi syndrome and psychoses

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

GABA-ergic neurons and the neurobiology of schizophrenia and other psychoses

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

The neuropsychology of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Hypoplasia of Cerebellar Vermal Lobules VI and VII in Autism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Parietal lobe abnormalities detected with MR in patients with infantile autism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Hippocampus in autism: a Golgi analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Development of the brainstem and cerebellum in autistic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Brainstem, cerebellar and limbic neuroanatomical abnormalities in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Mutation screening of the UBE3A/E6-AP gene in autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

A model system to study genomic imprinting of human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Genetic studies of autistic disorder and chromosome 7

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Human PEG1/MEST, an imprinted gene on chromosome 7

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

The novel gene, gamma2-COP (COPG2), in the 7q32 imprinted domain escapes genomic imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Behavioural and neurochemical effects of early social deprivation in the rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

21 January 2018

Genes and social skills

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Sex differences in higher functioning people with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Xp deletions associated with autism in three females.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Evaluating the parent-of-origin effect in bipolar affective disorder. Is a more penetrant subtype transmitted paternally?

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Mitochondrial genetic analyses suggest selection against maternal lineages in bipolar affective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Linkage of bipolar affective disorder to chromosome 18 markers in a new pedigree series.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Human homolog of the mouse imprinted gene Impact resides at the pericentric region of chromosome 18 within the critical region for bipolar affective disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Comparative genome analysis of the mouse imprinted gene impact and its nonimprinted human homolog IMPACT: toward the structural basis for species-specific imprinting.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Chromosomal aberrations and bipolar affective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Tourette syndrome, associated conditions and the complexities of treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Genome scan for linkage to Gilles de la Tourette syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Sex of parent transmission effect in Tourette's syndrome: evidence for earlier age at onset in maternally transmitted cases suggests a genomic imprinting effect.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Genes with triplet repeats: candidate mediators of neuropsychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Genomic imprinting and the strange case of the insulin-like growth factor II receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Lower Purkinje cell counts in the cerebella of four autistic subjects: initial findings of the UCLA-NSAC Autopsy Research Report.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Mitochondrial DNA Sequence Diversity in Bipolar Affective Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

Analysis of parental-origin effects in linkage data

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890108995956

10.3109/07853890108995956

21 January 2018

Identifiers

DOI

1 reference

31 July 2017

1 reference