(Q50313899)

2 March 2018

title

Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes. (English)

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2 March 2018

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8

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Palma Finelli

Palma Finelli

3

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Wendy Roberts

7

Wendy Roberts

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2 March 2018

Maria Teresa Bonati

1

Maria Teresa Bonati

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2 March 2018

Lidia Larizza

9

Lidia Larizza

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2 March 2018

author name string

Silvia Russo

2

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2 March 2018

Maria Rosa Valsecchi

4

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2 March 2018

Francesca Cogliati

5

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2 March 2018

Florinda Cavalleri

6

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2 March 2018

publication date

6 April 2007

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2 March 2018

published in

Neurogenetics

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2 March 2018

volume

8

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2 March 2018

issue

3

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2 March 2018

page(s)

169-178

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2 March 2018

https://scigraph.springernature.com/pub.10.1007/s10048-007-0086-0

exact match

0 references

cites work

Angelman syndrome 2005: updated consensus for diagnostic criteria.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-007-0086-0

Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-007-0086-0

Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

21 January 2018

1 reference

12 December 2020

Autism in Angelman syndrome: a population-based study

1 reference

12 December 2020

An association analysis of candidate genes on chromosome 15 q11-13 and autism spectrum disorder.

1 reference

12 December 2020

Autism in Angelman syndrome: implications for autism research.

1 reference

12 December 2020

Imprinting defects on human chromosome 15.

1 reference

12 December 2020

Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes

1 reference

12 December 2020

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

1 reference

12 December 2020

Environmental influences on the behavioral phenotype of Angelman syndrome.

1 reference

12 December 2020

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

1 reference

12 December 2020

The genetics of autism

1 reference

12 December 2020

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families

1 reference

12 December 2020

Distinct phenotypes distinguish the molecular classes of Angelman syndrome

1 reference

12 December 2020

Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review

1 reference

12 December 2020

The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders

1 reference

12 December 2020

MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression

1 reference

12 December 2020

Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations

1 reference

12 December 2020

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

1 reference

12 December 2020

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

1 reference

12 December 2020

Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region.

1 reference

12 December 2020

Case report: Angelman syndrome in an individual with a small SMC(15) and paternal uniparental disomy: a case report with reference to the assessment of cognitive functioning and autistic symptomatology.

1 reference

12 December 2020

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

1 reference

12 December 2020

Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin-proteasome pathway processes

1 reference

12 December 2020

Uniparental disomy (UPD). Genomic imprinting and a case for new genetics (prenatal and clinical implications: the "Likon" concept).

1 reference

12 December 2020

Behavioral aspects of Angelman syndrome: a case control study.

1 reference

12 December 2020

Angelman syndrome: a review of the clinical and genetic aspects

1 reference

12 December 2020

Autism as a strongly genetic disorder: evidence from a British twin study

1 reference

12 December 2020

A rapid, PCR based test for differential molecular diagnosis of Prader-Willi and Angelman syndromes

1 reference

12 December 2020

Novel mutations of ubiquitin protein ligase 3A gene in Italian patients with Angelman syndrome

1 reference

12 December 2020

Genotype and phenotype in Angelman syndrome caused by paternal UPD 15

1 reference

12 December 2020

Cognitive and adaptive behavior profiles of children with Angelman syndrome.

1 reference

12 December 2020

Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects.

1 reference

12 December 2020

Autism in Angelman syndrome: an exploration of comorbidity.

1 reference

12 December 2020

10.1007/S10048-007-0086-0

Identifiers

DOI

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2 March 2018

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2 March 2018