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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: seitz c. 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
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: seitz c. Mol Psychiatry. 2007 Oct;12(10):923-33. doi: 10.1038/sj.mp.4001986. Epub 2007 Apr 10. Mol Psychiatry. 2007. PMID: 17579611
Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12.
Romanos M, Freitag C, Jacob C, Craig DW, Dempfle A, Nguyen TT, Halperin R, Walitza S, Renner TJ, Seitz C, Romanos J, Palmason H, Reif A, Heine M, Windemuth-Kieselbach C, Vogler C, Sigmund J, Warnke A, Schäfer H, Meyer J, Stephan DA, Lesch KP. Romanos M, et al. Among authors: seitz c. Mol Psychiatry. 2008 May;13(5):522-30. doi: 10.1038/mp.2008.12. Epub 2008 Feb 26. Mol Psychiatry. 2008. PMID: 18301393
Risk factors of autistic symptoms in children with ADHD.
Kröger A, Hänig S, Seitz C, Palmason H, Meyer J, Freitag CM. Kröger A, et al. Among authors: seitz c. Eur Child Adolesc Psychiatry. 2011 Dec;20(11-12):561-70. doi: 10.1007/s00787-011-0221-1. Epub 2011 Oct 16. Eur Child Adolesc Psychiatry. 2011. PMID: 22002011
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.
Elia J, Glessner JT, Wang K, Takahashi N, Shtir CJ, Hadley D, Sleiman PM, Zhang H, Kim CE, Robison R, Lyon GJ, Flory JH, Bradfield JP, Imielinski M, Hou C, Frackelton EC, Chiavacci RM, Sakurai T, Rabin C, Middleton FA, Thomas KA, Garris M, Mentch F, Freitag CM, Steinhausen HC, Todorov AA, Reif A, Rothenberger A, Franke B, Mick EO, Roeyers H, Buitelaar J, Lesch KP, Banaschewski T, Ebstein RP, Mulas F, Oades RD, Sergeant J, Sonuga-Barke E, Renner TJ, Romanos M, Romanos J, Warnke A, Walitza S, Meyer J, Pálmason H, Seitz C, Loo SK, Smalley SL, Biederman J, Kent L, Asherson P, Anney RJ, Gaynor JW, Shaw P, Devoto M, White PS, Grant SF, Buxbaum JD, Rapoport JL, Williams NM, Nelson SF, Faraone SV, Hakonarson H. Elia J, et al. Among authors: seitz c. Nat Genet. 2011 Dec 4;44(1):78-84. doi: 10.1038/ng.1013. Nat Genet. 2011. PMID: 22138692 Free PMC article.
Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated German multi-generation families.
Lin MK, Freitag CM, Schote AB, Pálmason H, Seitz C, Renner TJ, Romanos M, Walitza S, Jacob CP, Reif A, Warnke A, Cantor RM, Lesch KP, Meyer J. Lin MK, et al. Among authors: seitz c. Am J Med Genet B Neuropsychiatr Genet. 2013 Dec;162B(8):855-63. doi: 10.1002/ajmg.b.32192. Epub 2013 Sep 3. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 24038763
737 results