Weber H, Scholz CJ, Jacob CP, Heupel J, Kittel-Schneider S, Erhardt A, Hempel S, Schmidt B, Kiel T, Gessner A, Lesch KP, Reif A (2014)
Publication Type: Journal article
Publication year: 2014
Book Volume: 264
Pages Range: 409-421
Journal Issue: 5
DOI: 10.1007/s00406-013-0476-2
Attention-deficit/hyperactivity disorder (ADHD) is the most frequent psychiatric disorder in children, where it displays a global prevalence of 5 %. In up to 50 % of the cases, ADHD may persist into adulthood (aADHD), where it is often comorbid with personality disorders. Due to a potentially heritable nature of this comorbidity, we hypothesized that their genetic framework may contain common risk-modifying genes. SPOCK3, a poorly characterized, putatively Ca(2+)-binding extracellular heparan/chondroitin sulfate proteoglycan gene encoded by the human chromosomal region 4q32.3, was found to be associated with polymorphisms among the top ranks in a genome-wide association study (GWAS) on ADHD and a pooled GWAS on personality disorder (PD). We therefore genotyped 48 single nucleotide polymorphisms (SNPs) representative of the SPOCK3 gene region in 1,790 individuals (n
APA:
Weber, H., Scholz, C.J., Jacob, C.P., Heupel, J., Kittel-Schneider, S., Erhardt, A.,... Reif, A. (2014). SPOCK3, a risk gene for adult ADHD and personality disorders. European archives of psychiatry and clinical neuroscience, 264(5), 409-421. https://doi.org/10.1007/s00406-013-0476-2
MLA:
Weber, Heike, et al. "SPOCK3, a risk gene for adult ADHD and personality disorders." European archives of psychiatry and clinical neuroscience 264.5 (2014): 409-421.
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