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Pilot study on HTR2A promoter polymorphism, -1438G/A (rs6311) and a nearby copy number variation showed association with onset and severity in early onset obsessive-compulsive disorder.
Walitza S, Bové DS, Romanos M, Renner T, Held L, Simons M, Wewetzer C, Fleischhaker C, Remschmidt H, Warnke A, Grünblatt E. Walitza S, et al. Among authors: fleischhaker c. J Neural Transm (Vienna). 2012 Apr;119(4):507-15. doi: 10.1007/s00702-011-0699-1. Epub 2011 Aug 28. J Neural Transm (Vienna). 2012. PMID: 21874579
Transmission disequilibrium studies in children and adolescents with obsessive-compulsive disorders pertaining to polymorphisms of genes of the serotonergic pathway.
Walitza S, Wewetzer C, Gerlach M, Klampfl K, Geller F, Barth N, Hahn F, Herpertz-Dahlmann B, Gössler M, Fleischhaker C, Schulz E, Hebebrand J, Warnke A, Hinney A. Walitza S, et al. Among authors: fleischhaker c. J Neural Transm (Vienna). 2004 Jul;111(7):817-25. doi: 10.1007/s00702-004-0134-y. Epub 2004 Apr 13. J Neural Transm (Vienna). 2004. PMID: 15206000
Brain-derived neurotrophic factor V66M polymorphism in childhood-onset obsessive-compulsive disorder.
Mössner R, Walitza S, Lesch KP, Geller F, Barth N, Remschmidt H, Hahn F, Herpertz-Dahlmann B, Fleischhaker C, Schulz E, Warnke A, Hinney A, Wewetzer C. Mössner R, et al. Among authors: fleischhaker c. Int J Neuropsychopharmacol. 2005 Mar;8(1):133-6. doi: 10.1017/S146114570400495X. Epub 2005 Jan 10. Int J Neuropsychopharmacol. 2005. PMID: 15638951 Free article. No abstract available.
87 results