Publications

Detailed Information

Association study between single nucleotide polymorphisms in promoter region of AVPR1A and Korean autism spectrum disorders

Cited 33 time in Web of Science Cited 34 time in Scopus
Authors

Yang, So Young; Cho, Soo-Churl; Yoo, Hee Jeong; Cho, In Hee; Kim, Boong-Nyun; Shin, Min-Sup; Son, Jung-Woo; Kim, Hyo-Won; Kang, Je-Ouk; Kim, Soon Ae; Yang, Young-Hui; Chung, Un-Sun; Park, Tae-Won; Kim, Jae-Won; Park, Mira

Issue Date
2010-08-02
Publisher
ELSEVIER IRELAND LTD
Citation
NEUROSCIENCE LETTERS; Vol.479 3; 197-200
Keywords
Autism spectrum disorders (ASD)Single nucleotide polymorphisms (SNPs)Arginine vasopressin receptor 1A (AVPR1A)Family-base association study
Abstract
To determine the association between arginine vasopressin receptor 1A gene (AVPR1A)and autism spectrum disorders (ASDs), we examined 3 single nucleotide polymorphisms (SNPs), namely, rs7294536, rs3759292, and rs10877969, in the promoter region of AVPR1A by using a family-based association test (FBAT) in 151 Korean trios. Our results demonstrated a statistically significant association between autism and SNPs (additive model: rs7294536, chi(2)=9.328, df=2, P=0.002: rs10877969, chi(2)=11.529, df=2, P<0.001) as well as between autism and haplotype analysis (additive model: chi(2)=14.122, df=3,P=0.003). In addition, we found that ADI-R scores calculated by using a diagnostic algorithm for failure to develop peer relationships (A2) were higher in subjects having the AA genotype than in subjects having the AG and GG genotypes of rs7294536. Thus, our study provides evidence for a possible association between these SNPs and the phenotype of ASDs. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
ISSN
0304-3940
Language
English
URI
https://hdl.handle.net/10371/78442
DOI
https://doi.org/10.1016/j.neulet.2010.05.050
Files in This Item:
There are no files associated with this item.
Appears in Collections:

Altmetrics

Item View & Download Count

  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Share