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426 results

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Association and linkage of allelic variants of the dopamine transporter gene in ADHD.
Friedel S, Saar K, Sauer S, Dempfle A, Walitza S, Renner T, Romanos M, Freitag C, Seitz C, Palmason H, Scherag A, Windemuth-Kieselbach C, Schimmelmann BG, Wewetzer C, Meyer J, Warnke A, Lesch KP, Reinhardt R, Herpertz-Dahlmann B, Linder M, Hinney A, Remschmidt H, Schäfer H, Konrad K, Hübner N, Hebebrand J. Friedel S, et al. Among authors: remschmidt h. Mol Psychiatry. 2007 Oct;12(10):923-33. doi: 10.1038/sj.mp.4001986. Epub 2007 Apr 10. Mol Psychiatry. 2007. PMID: 17579611
Transmission disequilibrium studies in early onset of obsessive-compulsive disorder for polymorphisms in genes of the dopaminergic system.
Walitza S, Scherag A, Renner TJ, Hinney A, Remschmidt H, Herpertz-Dahlmann B, Schulz E, Schafer H, Lange KW, Wewetzer C, Gerlach M. Walitza S, et al. Among authors: remschmidt h. J Neural Transm (Vienna). 2008 Jul;115(7):1071-8. doi: 10.1007/s00702-008-0051-6. Epub 2008 Apr 30. J Neural Transm (Vienna). 2008. PMID: 18446263
Familiality and molecular genetics of attention networks in ADHD.
Konrad K, Dempfle A, Friedel S, Heiser P, Holtkamp K, Walitza S, Sauer S, Warnke A, Remschmidt H, Gilsbach S, Schäfer H, Hinney A, Hebebrand J, Herpertz-Dahlmann B. Konrad K, et al. Among authors: remschmidt h. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):148-58. doi: 10.1002/ajmg.b.30967. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19418498
Mutation screen of the brain derived neurotrophic factor gene (BDNF): identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder.
Friedel S, Horro FF, Wermter AK, Geller F, Dempfle A, Reichwald K, Smidt J, Brönner G, Konrad K, Herpertz-Dahlmann B, Warnke A, Hemminger U, Linder M, Kiefl H, Goldschmidt HP, Siegfried W, Remschmidt H, Hinney A, Hebebrand J. Friedel S, et al. Among authors: remschmidt h. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):96-9. doi: 10.1002/ajmg.b.30090. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15457498
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. Among authors: remschmidt h. Mol Psychiatry. 2005 Dec;10(12):1126-32. doi: 10.1038/sj.mp.4001734. Mol Psychiatry. 2005. PMID: 16116490 Clinical Trial.
A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs.
Hebebrand J, Dempfle A, Saar K, Thiele H, Herpertz-Dahlmann B, Linder M, Kiefl H, Remschmidt H, Hemminger U, Warnke A, Knölker U, Heiser P, Friedel S, Hinney A, Schäfer H, Nürnberg P, Konrad K. Hebebrand J, et al. Among authors: remschmidt h. Mol Psychiatry. 2006 Feb;11(2):196-205. doi: 10.1038/sj.mp.4001761. Mol Psychiatry. 2006. PMID: 16222334 Clinical Trial.
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: remschmidt h. 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
426 results