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Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
Schumacher J, Anthoni H, Dahdouh F, König IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hülsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Körne G, Nöthen MM, Kere J. Schumacher J, et al. Among authors: warnke a. Am J Hum Genet. 2006 Jan;78(1):52-62. doi: 10.1086/498992. Epub 2005 Nov 17. Am J Hum Genet. 2006. PMID: 16385449 Free PMC article.
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
Matsson H, Huss M, Persson H, Einarsdottir E, Tiraboschi E, Nopola-Hemmi J, Schumacher J, Neuhoff N, Warnke A, Lyytinen H, Schulte-Körne G, Nöthen MM, Leppänen PH, Peyrard-Janvid M, Kere J. Matsson H, et al. Among authors: warnke a. J Hum Genet. 2015 Jul;60(7):399-401. doi: 10.1038/jhg.2015.37. Epub 2015 Apr 16. J Hum Genet. 2015. PMID: 25877001 Free PMC article.
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.
Grimm T, Garshasbi M, Puettmann L, Chen W, Ullmann R, Müller-Myhsok B, Klopocki E, Herbst L, Haug J, Jensen LR, Fischer C, Nöthen M, Ludwig K, Warnke A, Ott J, Schulte-Körne G, Ropers HH, Kuss AW. Grimm T, et al. Among authors: warnke a. Z Kinder Jugendpsychiatr Psychother. 2020 Nov;48(6):478-489. doi: 10.1024/1422-4917/a000758. Z Kinder Jugendpsychiatr Psychother. 2020. PMID: 33172359 Free article.
Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder.
Albayrak Ö, Pütter C, Volckmar AL, Cichon S, Hoffmann P, Nöthen MM, Jöckel KH, Schreiber S, Wichmann HE, Faraone SV, Neale BM, Herpertz-Dahlmann B, Lehmkuhl G, Sinzig J, Renner TJ, Romanos M, Warnke A, Lesch KP, Reif A, Schimmelmann BG, Scherag A, Hebebrand J, Hinney A; Psychiatric GWAS Consortium: ADHD Subgroup. Albayrak Ö, et al. Among authors: warnke a. Am J Med Genet B Neuropsychiatr Genet. 2013 Jun;162B(4):295-305. doi: 10.1002/ajmg.b.32144. Epub 2013 Mar 26. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23533005
Genome-wide association study in German patients with attention deficit/hyperactivity disorder.
Hinney A, Scherag A, Jarick I, Albayrak Ö, Pütter C, Pechlivanis S, Dauvermann MR, Beck S, Weber H, Scherag S, Nguyen TT, Volckmar AL, Knoll N, Faraone SV, Neale BM, Franke B, Cichon S, Hoffmann P, Nöthen MM, Schreiber S, Jöckel KH, Wichmann HE, Freitag C, Lempp T, Meyer J, Gilsbach S, Herpertz-Dahlmann B, Sinzig J, Lehmkuhl G, Renner TJ, Warnke A, Romanos M, Lesch KP, Reif A, Schimmelmann BG, Hebebrand J; Psychiatric GWAS Consortium: ADHD subgroup. Hinney A, et al. Among authors: warnke a. Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):888-97. doi: 10.1002/ajmg.b.31246. Epub 2011 Oct 19. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 22012869
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: warnke a. 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.
Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach.
Mooney MA, McWeeney SK, Faraone SV, Hinney A, Hebebrand J; IMAGE2 Consortium; German ADHD GWAS Group; Nigg JT, Wilmot B. Mooney MA, et al. Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):815-26. doi: 10.1002/ajmg.b.32446. Epub 2016 Mar 22. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 27004716 Free PMC article.
DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder.
Håvik B, Degenhardt FA, Johansson S, Fernandes CP, Hinney A, Scherag A, Lybæk H, Djurovic S, Christoforou A, Ersland KM, Giddaluru S, O'Donovan MC, Owen MJ, Craddock N, Mühleisen TW, Mattheisen M, Schimmelmann BG, Renner T, Warnke A, Herpertz-Dahlmann B, Sinzig J, Albayrak Ö, Rietschel M, Nöthen MM, Bramham CR, Werge T, Hebebrand J, Haavik J, Andreassen OA, Cichon S, Steen VM, Le Hellard S. Håvik B, et al. Among authors: warnke a. PLoS One. 2012;7(4):e35424. doi: 10.1371/journal.pone.0035424. Epub 2012 Apr 23. PLoS One. 2012. PMID: 22539971 Free PMC article.
254 results