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Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
Williams NM, Franke B, Mick E, Anney RJ, Freitag CM, Gill M, Thapar A, O'Donovan MC, Owen MJ, Holmans P, Kent L, Middleton F, Zhang-James Y, Liu L, Meyer J, Nguyen TT, Romanos J, Romanos M, Seitz C, Renner TJ, Walitza S, Warnke A, Palmason H, Buitelaar J, Rommelse N, Vasquez AA, Hawi Z, Langley K, Sergeant J, Steinhausen HC, Roeyers H, Biederman J, Zaharieva I, Hakonarson H, Elia J, Lionel AC, Crosbie J, Marshall CR, Schachar R, Scherer SW, Todorov A, Smalley SL, Loo S, Nelson S, Shtir C, Asherson P, Reif A, Lesch KP, Faraone SV. Williams NM, et al. Among authors: walitza s. Am J Psychiatry. 2012 Feb;169(2):195-204. doi: 10.1176/appi.ajp.2011.11060822. Am J Psychiatry. 2012. PMID: 22420048 Free PMC article.
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
Co-morbidity of adult attention-deficit/hyperactivity disorder with focus on personality traits and related disorders in a tertiary referral center.
Jacob CP, Romanos J, Dempfle A, Heine M, Windemuth-Kieselbach C, Kruse A, Reif A, Walitza S, Romanos M, Strobel A, Brocke B, Schäfer H, Schmidtke A, Böning J, Lesch KP. Jacob CP, et al. Among authors: walitza s. Eur Arch Psychiatry Clin Neurosci. 2007 Sep;257(6):309-17. doi: 10.1007/s00406-007-0722-6. Epub 2007 Apr 1. Eur Arch Psychiatry Clin Neurosci. 2007. PMID: 17401730
299 results