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Title: Parent of origin effects in attention/deficit hyperactivity disorder (ADHD) : analysis of data from the international multicenter ADHD genetics (IMAGE) program
Author(s): Anney, R.J.
Hawi, Z.
Sheehan, K.
Mulligan, A.
Pinto, C.
Brookes, K.J.
Xu, X.
Zhou, K.
Franke, B. (182880869)
Buitelaar, J.K. (081545622)
Vermeulen, H.H.M. (298981033)
Banaschewski, T.
Sonuga-Barke, E.
Ebstein, R.
Manor, I.
Miranda, A.
Mulas, F.
Oades, R.D.
Roeyers, H.
Lambregts-Rommelse, N.N.J. (316004480)
Rothenberger, A.
Sergeant, J.A.
Steinhausen, H.C.
Taylor, E.
Thompson, M.
Asherson, P.
Faraone, S.V.
Gill, M.
Publication year: 2008
Document type: Article / Letter to editor
Journal: American Journal of Medical Genetics Part B : Neuropsychiatric Genetics
ISSN: 1552-4841
Volume: vol. 147B
Issue: iss. 8
Start page: p. 1495
End page: p. 1500
Abstract: There are conflicting reports suggesting that the parental origin of transmitted risk alleles may play a role in the etiology of attention deficit/hyperactivity disorder (ADHD). A recent report by Hawi and colleagues observed a generalized paternal over-transmission of alleles associated with ADHD. This was not replicated in more recent studies. Using data from a large multicenter study we examined the overall and gene-specific parent of origin effect in 554 independent SNPs across 47 genes. Transmission disequilibrium and explicit parent of origin test were performed using PLINK. Overall parent of origin effect was tested by Chi-square. There was no overall parent of origin effect in the IMAGE sample (chi(1)(2) = 1.82, P = 0.117). Five markers in three genes, DDC, TPH2, and SLC6A2 showed nominal association (P < 0.01) with ADHD combined subtype when restricted to maternal or paternal transmission only. Following the initial report by Hawi and co-workers three studies, including this one, found no evidence to support an overall parent of origin effect for markers associated with ADHD. We cannot however, exclude gene-specific parent of origin effect in the etiology ADHD.
Subject: UMCN 3.2: Cognitive neurosciences
UMCN 5.1: Genetic defects of metabolism
UMCN 5.2: Endocrinology and reproduction
Organization: Psychiatry
UMCN Extern
Human Genetics
Epidemiology, Biostatistics & HTA
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/71540

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