Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD

@article{Franke2010MulticenterAO,
  title={Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD},
  author={Barbara Franke and Alejandro Arias V{\'a}squez and Stefan B. Johansson and Martine Hoogman and Jasmin Romanos and Andrea Boreatti-Huemmer and Monika Heine and Christian Peter Jacob and Klaus-Peter Lesch and Miquel Casas and Marta Ribas{\'e}s and Rosa Bosch and Cristina S{\'a}nchez-Mora and N{\'u}ria G{\'o}mez-Barros and No{\`e}lia Fern{\`a}ndez-Castillo and M{\'o}nica Bay{\'e}s and Anne Halm\oy and Helene Barone Halleland and Elisabeth Toverud Landaas and Ole Bernt Fasmer and Per Morten Knappskog and Angelien J. G. A. M. Heister and Lambertus A. L. M. Kiemeney and J. J. Sandra Kooij and A. Marije Boonstra and Cees C Kan and Philip Asherson and Stephen V Faraone and Jan K. Buitelaar and Jan Haavik and Bru Cormand and Josep Antoni Ramos-Quiroga and Andreas Reif},
  journal={Neuropsychopharmacology},
  year={2010},
  volume={35},
  pages={656-664}
}
Attention deficit/hyperactivity disorder (ADHD) is one of the most common neuropsychiatric disorders with a worldwide prevalence around 4–5% in children and 1–4% in adults. Although ADHD is highly heritable and familial risk may contribute most strongly to the persistent form of the disorder, there are few studies on the genetics of ADHD in adults. In this paper, we present the first results of the International Multicentre Persistent ADHD Genetics CollaboraTion (IMpACT) that has been set up… CONTINUE READING
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