(Q35004911)

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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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Europe PubMed Central

PubMed publication ID

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)

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Europe PubMed Central

PubMed publication ID

5 August 2017

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genetic variation

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Gerd Schulte-Körne

4

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Gerd Schulte-Körne

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Helmut Remschmidt

6

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Helmut Remschmidt

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Europe PubMed Central

PubMed publication ID

5 August 2017

Konstantin Strauch

5

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Konstantin Strauch

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Europe PubMed Central

PubMed publication ID

5 August 2017

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Anne-Kathrin Wermter

1

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Europe PubMed Central

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5 August 2017

Inge Kamp-Becker

2

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Europe PubMed Central

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5 August 2017

Philipp Hesse

3

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Europe PubMed Central

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5 August 2017

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publication date

1 March 2010

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Europe PubMed Central

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5 August 2017

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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Europe PubMed Central

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5 August 2017

153B

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Europe PubMed Central

PubMed publication ID

5 August 2017

2

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Europe PubMed Central

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5 August 2017

629-639

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Europe PubMed Central

PubMed publication ID

5 August 2017

Haploview: analysis and visualization of LD and haplotype maps

1 reference

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

1 reference

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Oxytocin and experimental therapeutics in autism spectrum disorders

1 reference

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Maximum-likelihood estimation of haplotype frequencies in nuclear families

1 reference

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

1 reference

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Oxytocin improves "mind-reading" in humans

1 reference

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Oxytocin attenuates amygdala responses to emotional faces regardless of valence

1 reference

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

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

1 reference

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Structure of the autism symptom phenotype: A proposed multidimensional model

1 reference

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Oxytocin increases gaze to the eye region of human faces

1 reference

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Oxytocin, vasopressin and pair bonding: implications for autism

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Time to give up on a single explanation for autism

1 reference

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

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

1 reference

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Understanding autism: insights from mind and brain

1 reference

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

1 reference

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Oxytocin increases retention of social cognition in autism

1 reference

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

1 reference

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

1 reference

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Oxytocin Modulates Neural Circuitry for Social Cognition and Fear in Humans

1 reference

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Oxytocin increases trust in humans

1 reference

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

1 reference

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

1 reference

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21 January 2018

Neuropeptidergic regulation of affiliative behavior and social bonding in animals

1 reference

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21 January 2018

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

1 reference

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

1 reference

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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

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

1 reference

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Genomic screen and follow-up analysis for autistic disorder

1 reference

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Rethinking the nature of genetic vulnerability to autistic spectrum disorders

1 reference

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

1 reference

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

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

1 reference

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Autism and pervasive developmental disorders

1 reference

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

1 reference

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An efficient procedure for genotyping single nucleotide polymorphisms.

1 reference

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

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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

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Transmission/disequilibrium tests using multiple tightly linked markers

1 reference

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21 January 2018

Identifiers

10.1002/AJMG.B.31032

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

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