(Q35004911)

English

Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level

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scholarly article

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Europe PubMed Central

5 August 2017

Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level (English)

1 reference

Europe PubMed Central

5 August 2017

0 references

1 reference

based on heuristic

inferred from title

genetic variation

1 reference

based on heuristic

inferred from title

Gerd Schulte-Körne

4

object named as

Gerd Schulte-Körne

0 references

Helmut Remschmidt

6

object named as

Helmut Remschmidt

1 reference

Europe PubMed Central

5 August 2017

Konstantin Strauch

5

object named as

Konstantin Strauch

1 reference

Europe PubMed Central

5 August 2017

author name string

Anne-Kathrin Wermter

1

1 reference

Europe PubMed Central

5 August 2017

Inge Kamp-Becker

2

1 reference

Europe PubMed Central

5 August 2017

Philipp Hesse

3

1 reference

Europe PubMed Central

5 August 2017

language of work or name

1 reference

based on heuristic

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publication date

1 March 2010

1 reference

Europe PubMed Central

5 August 2017

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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Europe PubMed Central

5 August 2017

153B

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Europe PubMed Central

5 August 2017

2

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Europe PubMed Central

5 August 2017

629-639

1 reference

Europe PubMed Central

5 August 2017

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

The neuroscience of affiliation: forging links between basic and clinical research on neuropeptides and social behavior

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Oxytocin and experimental therapeutics in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Maximum-likelihood estimation of haplotype frequencies in nuclear families

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

A powerful strategy to account for multiple testing in the context of haplotype analysis

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Oxytocin improves "mind-reading" in humans

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Oxytocin attenuates amygdala responses to emotional faces regardless of valence

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

DNA binding specificity of different STAT proteins. Comparison of in vitro specificity with natural target sites

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Structure of the autism symptom phenotype: A proposed multidimensional model.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Oxytocin increases gaze to the eye region of human faces

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Oxytocin, vasopressin and pair bonding: implications for autism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Time to give up on a single explanation for autism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Neuropeptides and social behaviour: effects of oxytocin and vasopressin in humans

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Understanding autism: insights from mind and brain

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Serotonin transporter gene-linked polymorphic region: allele distributions in relationship to body weight and in anorexia nervosa

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Oxytocin increases retention of social cognition in autism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Dimensional structure of the autism phenotype: relations between early development and current presentation.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Oxytocin Modulates Neural Circuitry for Social Cognition and Fear in Humans

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Oxytocin increases trust in humans

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Neuropeptidergic regulation of affiliative behavior and social bonding in animals

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Oxytocin receptors in brain cortical regions are reduced in haploinsufficient (+/-) reeler mice

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Search for potential autism treatments turns to 'trust hormone'

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Defining the phenotype in human genetic studies: forward genetics and reverse phenotyping

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Genomic screen and follow-up analysis for autistic disorder.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Rethinking the nature of genetic vulnerability to autistic spectrum disorders

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Pervasive social deficits, but normal parturition, in oxytocin receptor-deficient mice

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Structural equation analysis of a hypothesised symptom model in the autism spectrum.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Autism and pervasive developmental disorders

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

An efficient procedure for genotyping single nucleotide polymorphisms.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Genes controlling affiliative behavior as candidate genes for autism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Transmission/disequilibrium tests using multiple tightly linked markers

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31032

21 January 2018

Identifiers

10.1002/AJMG.B.31032

1 reference

Europe PubMed Central

5 August 2017

1 reference

Europe PubMed Central

5 August 2017

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