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Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families.
Karagiannidis I, Dehning S, Sandor P, Tarnok Z, Rizzo R, Wolanczyk T, Madruga-Garrido M, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Szymanska U, Anastasiou Z, Stathias V, Androutsos C, Tsironi V, Koumoula A, Barta C, Zill P, Mir P, Müller N, Barr C, Paschou P. Karagiannidis I, et al. Among authors: paschou p. J Med Genet. 2013 Nov;50(11):760-4. doi: 10.1136/jmedgenet-2013-101637. Epub 2013 Jul 3. J Med Genet. 2013. PMID: 23825391
The distribution and most recent common ancestor of the 17q21 inversion in humans.
Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Mehdi SQ, Kajuna SL, Barta C, Kungulilo S, Karoma NJ, Lu RB, Zhukova OV, Kim JJ, Comas D, Siniscalco M, New M, Li P, Li H, Manolopoulos VG, Speed WC, Rajeevan H, Pakstis AJ, Kidd JR, Kidd KK. Donnelly MP, et al. Among authors: paschou p. Am J Hum Genet. 2010 Feb 12;86(2):161-71. doi: 10.1016/j.ajhg.2010.01.007. Epub 2010 Jan 28. Am J Hum Genet. 2010. PMID: 20116045 Free PMC article.
A global view of the OCA2-HERC2 region and pigmentation.
Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Barta C, Lu RB, Zhukova OV, Kim JJ, Siniscalco M, New M, Li H, Kajuna SL, Manolopoulos VG, Speed WC, Pakstis AJ, Kidd JR, Kidd KK. Donnelly MP, et al. Among authors: paschou p. Hum Genet. 2012 May;131(5):683-96. doi: 10.1007/s00439-011-1110-x. Epub 2011 Nov 8. Hum Genet. 2012. PMID: 22065085 Free PMC article.
Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.
Karagiannidis I, Rizzo R, Tarnok Z, Wolanczyk T, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Barta C, Szymanska U, Panteloglou G, Miranda DM, Feng Y, Sandor P, Barr C; TSGeneSEE; Paschou P. Karagiannidis I, et al. Among authors: paschou p. Mol Psychiatry. 2012 Jul;17(7):665-8. doi: 10.1038/mp.2011.151. Epub 2011 Nov 15. Mol Psychiatry. 2012. PMID: 22083730 No abstract available.
Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome.
Paschou P, Stylianopoulou E, Karagiannidis I, Rizzo R, Tarnok Z, Wolanczyk T, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Szymanska U, Lykidis D, Androutsos C, Tsironi V, Koumoula A, Barta C, Klidonas S, Ypsilantis P, Simopoulos C; TSGeneSEE Consortium; Skavdis G, Grigoriou M. Paschou P, et al. Genes Brain Behav. 2012 Jun;11(4):444-51. doi: 10.1111/j.1601-183X.2012.00778.x. Epub 2012 Apr 11. Genes Brain Behav. 2012. PMID: 22435649 Free article.
Exploring genomic structure differences and similarities between the Greek and European HapMap populations: implications for association studies.
Stathias V, Sotiris GR, Karagiannidis I, Bourikas G, Martinis G, Papazoglou D, Tavridou A, Papanas N, Maltezos E, Theodoridis M, Vargemezis V, Manolopoulos VG, Speed WC, Kidd JR, Kidd KK, Drineas P, Paschou P. Stathias V, et al. Among authors: paschou p. Ann Hum Genet. 2012 Nov;76(6):472-83. doi: 10.1111/j.1469-1809.2012.00730.x. Ann Hum Genet. 2012. PMID: 23061745
87 results