Population differences in the International Multi-Centre ADHD Gene Project

Benjamin M Neale, Pak C Sham, Shaun Purcell, Tobias Banaschewski, Jan Buitelaar, Barbara Franke, Edmund Sonuga-Barke, Richard Ebstein, Jacques Eisenberg, Aisling Mulligan, Michael Gill, Iris Manor, Ana Miranda, Fernando Mulas, Robert D Oades, Herbert Roeyers, Aribert Rothenberger, Joseph Sergeant, Hans-Christoph Steinhausen, Eric TaylorMargaret Thompson, Wai Chen, Kaixin Zhou, Philip Asherson, Stephen V Faraone

Research output: Contribution to journalArticlepeer-review

19 Citations (Scopus)


The International Multi-Centre ADHD Gene sample consists of 674 families from eight countries (Belgium, England, Germany, Holland, Ireland, Israel, Spain, and Switzerland) ascertained from clinics for combined-type attention definity hyperactivity disorder in an offspring. 863 SNPs were successfully genotyped across 47 autosomal genes implicated in psychiatric disorders yielding a single nucleotide polymorphism (SNP) density of approximately one SNP per 2.5 kb. A global test of heterogeneity showed 269 SNPs nominally significant (expected 43). Inclusion of the Israeli population accounted for approximately 70% of these nominally significant tests. Hardy-Weinberg equilibrium tests suggest that combining all these populations would induce stratification, but that the Northern European populations (Belgium, England, Germany, Holland, and Ireland) could be appropriate. Tag SNPs were generated using pair-wise and aggressive tagging from Carlson et al. [2004] and de Bakker et al. [2005], respectively, in each population and applied to the other populations. Cross-population performance across Northern Europe was consistent with within population comparisons. Smaller sample size for each population tended to yield more problems for the generation of aggressive tags and the application of pair-wise tags. Any case-control sample employing an Israeli sample with Northern Europeans must consider stratification. A Northern European tag set, however, appears to be appropriate for capturing the variation across populations.

Original languageEnglish
Pages (from-to)98-107
Number of pages10
JournalGenetic Epidemiology
Issue number2
Publication statusPublished - Feb 2008


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