Prenatal Stress Exposure, Oxytocin Receptor Gene (OXTR) Methylation and Child Autistic Traits: The Moderating Role of OXTR rs53576 Genotype

LAY ABSTRACT: The gene encoding the oxytocin receptor (OXTR), localized on chromosome 3p25, is considered a promising candidate for explaining genetic vulnerability to autistic traits. Although several lines of evidence implicate OXTR SNP rs53576 (G/A) variation in social behavior, findings have bee...

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Pubblicato in:Autism Res
Autori principali: Rijlaarsdam, Jolien, van IJzendoorn, Marinus H., Verhulst, Frank C, Jaddoe, Vincent W. V., Felix, Janine F., Tiemeier, Henning, Bakermans-Kranenburg, Marian J.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2016
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5426537/
https://ncbi.nlm.nih.gov/pubmed/27520745
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/aur.1681
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