SCIRP Mobile Website
Paper Submission

Why Us? >>

  • - Open Access
  • - Peer-reviewed
  • - Rapid publication
  • - Lifetime hosting
  • - Free indexing service
  • - Free promotion service
  • - More citations
  • - Search engine friendly

Free SCIRP Newsletters>>

Add your e-mail address to receive free newsletters from SCIRP.

 

Contact Us >>

WhatsApp  +86 18163351462(WhatsApp)
   
Paper Publishing WeChat
Book Publishing WeChat
(or Email:book@scirp.org)

Article citations

More>>

Ishak, W. W., Kahloon, M., & Fakhry, H. (2011). Oxytocin Role in Enhancing Well-Being: A Literature Review. Journal of Affective Disorders, 130, 1-9. http://dx.doi.org/10.1016/j.jad.2010.06.001

has been cited by the following article:

  • TITLE: The Oxytocin Receptor Gene (OXTR) and Gazing Behavior during Social Interaction: An Observational Study in Young Adults

    AUTHORS: Maaike Verhagen, Rutger Engels, Eeske Van Roekel

    KEYWORDS: Gazing, OXTR Gene, Rs53576, Social Inclusion, Observational Study

    JOURNAL NAME: Open Journal of Depression, Vol.3 No.4, August 26, 2014

    ABSTRACT: Background: In the present study, the relation between a polymorphic marker within the OXTR gene (rs53576) and gazing behavior during two separate social interaction tasks was examined. Gazing behavior was considered to be an integral part of belonging regulation processes. Methods: We conducted an observational interaction study (N = 116; 58 dyads) in a naturalistic setting. Participants were seated face to face with hidden cameras positioned behind them. Each couple was instructed to have two short conversations about daily topics (nightlife in the city and movies), separated by a distraction task. We studied the role of the OXTR gene in relation to gaze duration (total duration and mean duration per event) at the interaction partner, both for the total interaction and for the first and second halves of the interaction, separately. Results: Analyses showed a significant relationship between the OXTR genetic variant and mean gaze duration at the interaction partner. Individuals carrying an A-allele showed increased gaze duration. This genetic association was particularly present during the first half of the conversation. In the second interaction task, we confirmed the findings that A-allele carriers showed longer mean gaze duration. No associations were found for total gaze duration. Conclusions: The OXTR A-allele was associated with longer mean gaze duration at an unknown interaction partner, especially during the first halves of the interaction times. This might illustrate that A-carriers, compared to GG-homozygous individuals, need slightly more time to read the micro socio-emotional facial cues of a new interaction partner or need more time for social reconciliation processes. This could be indicative of a genetic liability for being less vulnerable to pick up new micro social cues.