Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

I. Jarick, A-L Volckmar, C. Puetter, S. Pechlivanis, T. T. Nguyen, M. R. Dauvermann, S. Beck, Oe Albayrak, S. Scherag, S. Gilsbach, S. Cichon, P. Hoffmann, F. Degenhardt, M. M. Noethen, S. Schreiber, H-E Wichmann, K-H Joeckel, J. Heinrich, C. M. T. Tiesler, S. V. FaraoneS. Walitza, J. Sinzig, C. Freitag, J. Meyer, B. Herpertz-Dahlmann, G. Lehmkuhl, T. J. Renner, A. Warnke, M. Romanos, K-P Lesch, A. Reif, B. G. Schimmelmann, J. Hebebrand, A. Scherag, A. Hinney

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)115-121
JournalMolecular Psychiatry
Volume19
Issue number1
DOIs
Publication statusPublished - Jan 2014

Keywords

  • ADHD
  • children
  • CNVs
  • GWAS
  • PARK2

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