Lasky-Su, Jessica; Anney, Richard J.L.; Neale, Benjamin M.; Franke, Barbara; Zhou, Kaixin; Maller, Julian B.; Vasquez, Alejandro Arias; Chen, Wai; Asherson, Philip; Buitelaar, Jan; Banaschewski, Tobias; Ebstein, Richard; Gill, Richard; Miranda, Ana; Mulas, Fernando; Faraone, Stephen V. et al:
Genome-wide association scan of the time to onset of Attention Deficit Hyperactivity Disorder
In: American Journal of Medical Genetics, Part B : Neuropsychiatric Genetics, Jg. 147 (2008), Heft 8, S. 1355 - 1358
2008Artikel/Aufsatz in ZeitschriftOA Grün
MedizinMedizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters
Damit verbunden: 1 Publikation(en)
Titel in Englisch:
Genome-wide association scan of the time to onset of Attention Deficit Hyperactivity Disorder
Autor*in:
Lasky-Su, Jessica;Anney, Richard J.L.;Neale, Benjamin M.;Franke, Barbara;Zhou, Kaixin;Maller, Julian B.;Vasquez, Alejandro Arias;Chen, Wai;Asherson, Philip;Buitelaar, Jan;Banaschewski, Tobias;Ebstein, Richard;Gill, Richard;Miranda, Ana;Mulas, Fernando;Oades, Robert D.UDE
GND
1208788639
LSF ID
29685
ORCID
0000-0001-6151-5559ORCID iD
Sonstiges
der Hochschule zugeordnete*r Autor*in
;
Roeyers, Herbert;Rothenberger, Aribert;Sergeant, Joseph;Sonuga-Barke, Edmund;Steinhausen, Hans-Christoph;Taylor, Eric;Daly, Mark;Laird, Nan;Lange, Christroph;Faraone, Stephen V.
Erscheinungsjahr:
2008
Open Access?:
OA Grün
DuEPublico 1 ID
Sprache des Textes:
Englisch

Abstract:

A time-to-onset analysis for family-based samples was performed on the genomewide association (GWAS) data for attention deficit hyperactivity disorder (ADHD) to determine if associations exist with the age at onset of ADHD. The initial dataset consisted of 958 parent-offspring trios that were genotyped on the Perlegen 600,000 SNP array. After data cleaning procedures, 429,981 autosomal SNPs and 930 parent-offspring trios were used found suitable for use and a family-based logrank analysis was performed using that age at first ADHD symptoms as the quantitative trait of interest. No SNP achieved genome-wide significance, and the lowest P-values had a magnitude of 10−7. Several SNPs among a pre-specified list of candidate genes had nominal associations including SLC9A9, DRD1, ADRB2, SLC6A3, NFIL3, ADRB1, SYT1, HTR2A, ARRB2, and CHRNA4. Of these findings SLC9A9 stood out as a promising candidate, with nominally significant SNPs in six distinct regions of the gene.