Literature DB >> 12092907

Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.

M M Menold1, Y Shao, C M Wolpert, S L Donnelly, K L Raiford, E R Martin, S A Ravan, R K Abramson, H H Wright, G R Delong, M L Cuccaro, M A Pericak-Vance, J R Gilbert.   

Abstract

Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the brain, acting via the GABAA receptors. The GABAA receptors are comprised of several different homologous subunits, forming a group of receptors that are both structurally and functionally diverse. Three of the GABAA receptor subunit genes (GABRB3, GABRA5 and GABRG3) form a cluster on chromosome 15q11-q13, in a region that has been genetically associated with autistic disorder (AutD). Based on these data, we examined 16 single nucleotide polymorphisms (SNPs) located within GABRB3, GABRA5 and GABRG3 for linkage disequilibrium (LD) in 226 AutD families (AutD patients and parents). Genotyping was performed using either OLA (oligonucleotide ligation assay), or SSCP (single strand conformation polymorphism) followed by DNA sequencing. We tested for LD using the Pedigree Disequilibrium Test (PDT). PDT results gave significant evidence that AutD is associated with two SNPs located within the GABRG3 gene (exon5_539T/C, p=0.02 and intron5_687T/C, p=0.03), suggesting that the GABRG3 gene or a gene nearby contributes to genetic risk in AutD.

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Year:  2001        PMID: 12092907     DOI: 10.3109/01677060109167380

Source DB:  PubMed          Journal:  J Neurogenet        ISSN: 0167-7063            Impact factor:   1.250


  55 in total

Review 1.  The neurobiology of autism: new pieces of the puzzle.

Authors:  Maria T Acosta; Phillip L Pearl
Journal:  Curr Neurol Neurosci Rep       Date:  2003-03       Impact factor: 5.081

2.  Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.

Authors:  Dorota A Kwasnicka-Crawford; Wendy Roberts; Stephen W Scherer
Journal:  J Autism Dev Disord       Date:  2007-04

3.  No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese population.

Authors:  Mamoru Tochigi; Chieko Kato; Shinko Koishi; Yuki Kawakubo; Kenji Yamamoto; Hideo Matsumoto; Ohiko Hashimoto; Soo-Yung Kim; Keiichiro Watanabe; Yukiko Kano; Eiji Nanba; Nobumasa Kato; Tsukasa Sasaki
Journal:  J Hum Genet       Date:  2007-10-24       Impact factor: 3.172

Review 4.  Role of GABA in the mechanism of the onset of puberty in non-human primates.

Authors:  Ei Terasawa
Journal:  Int Rev Neurobiol       Date:  2005       Impact factor: 3.230

Review 5.  Using genetic findings in autism for the development of new pharmaceutical compounds.

Authors:  Jacob A S Vorstman; Will Spooren; Antonio M Persico; David A Collier; Stefan Aigner; Ravi Jagasia; Jeffrey C Glennon; Jan K Buitelaar
Journal:  Psychopharmacology (Berl)       Date:  2013-11-30       Impact factor: 4.530

Review 6.  Emerging drugs for the treatment of symptoms associated with autism spectrum disorders.

Authors:  Logan K Wink; Martin H Plawecki; Craig A Erickson; Kimberly A Stigler; Christopher J McDougle
Journal:  Expert Opin Emerg Drugs       Date:  2010-09       Impact factor: 4.191

Review 7.  Ionotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases.

Authors:  Hongjie Yuan; Chian-Ming Low; Olivia A Moody; Andrew Jenkins; Stephen F Traynelis
Journal:  Mol Pharmacol       Date:  2015-04-22       Impact factor: 4.436

Review 8.  Early pharmacological treatment of autism: a rationale for developmental treatment.

Authors:  Terrence C Bethea; Linmarie Sikich
Journal:  Biol Psychiatry       Date:  2007-02-15       Impact factor: 13.382

Review 9.  Meta-Analysis of the Association between GABA Receptor Polymorphisms and Autism Spectrum Disorder (ASD).

Authors:  Manijeh Mahdavi; Majid Kheirollahi; Roya Riahi; Fariborz Khorvash; Mehdi Khorrami; Maryam Mirsafaie
Journal:  J Mol Neurosci       Date:  2018-05-03       Impact factor: 3.444

10.  Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential model of autism spectrum disorder.

Authors:  Timothy M DeLorey; Peyman Sahbaie; Ezzat Hashemi; Gregg E Homanics; J David Clark
Journal:  Behav Brain Res       Date:  2007-09-14       Impact factor: 3.332

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