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Page 1
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. 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: walitza s. 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.
Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder.
Walitza S, Renner TJ, Dempfle A, Konrad K, Wewetzer Ch, Halbach A, Herpertz-Dahlmann B, Remschmidt H, Smidt J, Linder M, Flierl L, Knölker U, Friedel S, Schäfer H, Gross C, Hebebrand J, Warnke A, Lesch KP. Walitza S, et al. Mol Psychiatry. 2005 Dec;10(12):1126-32. doi: 10.1038/sj.mp.4001734. Mol Psychiatry. 2005. PMID: 16116490 Clinical Trial.
Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder.
Mössner R, Walitza S, Geller F, Scherag A, Gutknecht L, Jacob C, Bogusch L, Remschmidt H, Simons M, Herpertz-Dahlmann B, Fleischhaker C, Schulz E, Warnke A, Hinney A, Wewetzer C, Lesch KP. Mössner R, et al. Among authors: walitza s. Int J Neuropsychopharmacol. 2006 Aug;9(4):437-42. doi: 10.1017/S1461145705005997. Epub 2005 Sep 7. Int J Neuropsychopharmacol. 2006. PMID: 16146581 Free article.
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample.
Heiser P, Dempfle A, Friedel S, Konrad K, Hinney A, Kiefl H, Walitza S, Bettecken T, Saar K, Linder M, Warnke A, Herpertz-Dahlmann B, Schäfer H, Remschmidt H, Hebebrand J. Heiser P, et al. Among authors: walitza s. J Neural Transm (Vienna). 2007;114(4):513-21. doi: 10.1007/s00702-006-0584-5. Epub 2006 Nov 10. J Neural Transm (Vienna). 2007. PMID: 17093889
No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD.
Schimmelmann BG, Friedel S, Dempfle A, Warnke A, Lesch KP, Walitza S, Renner TJ, Romanos M, Herpertz-Dahlmann B, Linder M, Schäfer H, Seitz C, Palmason H, Freitag C, Meyer J, Konrad K, Hinney A, Hebebrand J. Schimmelmann BG, et al. Among authors: walitza s. J Neural Transm (Vienna). 2007;114(4):523-6. doi: 10.1007/s00702-006-0616-1. Epub 2007 Jan 15. J Neural Transm (Vienna). 2007. PMID: 17219016
306 results