Short communication: catechol-O-methyltransferase allelic variation in relation to psychological and hormonal indices of stress in children and adolescents with chromosome 22q11.2 deletion syndrome (22q11.2DS)
Author:
Funder
Foundation for the National Institutes of Health
University of New Orleans
National Institute of Mental Health
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s13353-024-00898-5.pdf
Reference20 articles.
1. Ali N, Nater UM (2020) Salivary alpha-amylase as a biomarker of stress in behavioral medicine. Int J Behav Med 27(3):337–342. https://doi.org/10.1007/s12529-019-09843-x
2. Armbruster D, Mueller A, Strobel A, Lesch K-P, Brocke B, Kirschbaum C (2012) Children under stress – COMT genotype and stressful life events predict cortisol increase in an acute social stress paradigm. Int J Neuropsychopharmacol 15(09):1229–1239. https://doi.org/10.1017/S1461145711001763
3. Baumann C, Klauke B, Weber H, Domschke K, Zwanzger P, Pauli P, Deckert J, Reif A (2013) The interaction of early life experiences with COMT val158met affects anxiety sensitivity. Genes Brain Behav 12(8):821–829
4. Beaton EA, Simon TJ (2011) How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome? J Neurodev Disord 3(1):68–75. https://doi.org/10.1007/s11689-010-9069-9
5. Du Q, de la Morena MT, van Oers NS (2020) The genetics and epigenetics of 22q112 deletion syndrome. Front Gen 10:1365
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