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Page 1
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. 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
Genetic association signal near NTN4 in Tourette syndrome.
Paschou P, Yu D, Gerber G, Evans P, Tsetsos F, Davis LK, Karagiannidis I, Chaponis J, Gamazon E, Mueller-Vahl K, Stuhrmann M, Schloegelhofer M, Stamenkovic M, Hebebrand J, Noethen M, Nagy P, Barta C, Tarnok Z, Rizzo R, Depienne C, Worbe Y, Hartmann A, Cath DC, Budman CL, Sandor P, Barr C, Wolanczyk T, Singer H, Chou IC, Grados M, Posthuma D, Rouleau GA, Aschauer H, Freimer NB, Pauls DL, Cox NJ, Mathews CA, Scharf JM. Paschou P, et al. Among authors: karagiannidis i. Ann Neurol. 2014 Aug;76(2):310-5. doi: 10.1002/ana.24215. Epub 2014 Jul 21. Ann Neurol. 2014. PMID: 25042818 Free PMC article.
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. Among authors: karagiannidis i. 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: karagiannidis i. Ann Hum Genet. 2012 Nov;76(6):472-83. doi: 10.1111/j.1469-1809.2012.00730.x. Ann Hum Genet. 2012. PMID: 23061745
Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort.
Bertelsen B, Stefánsson H, Riff Jensen L, Melchior L, Mol Debes N, Groth C, Skov L, Werge T, Karagiannidis I, Tarnok Z, Barta C, Nagy P, Farkas L, Brøndum-Nielsen K, Rizzo R, Gulisano M, Rujescu D, Kiemeney LA, Tosato S, Nawaz MS, Ingason A, Unnsteinsdottir U, Steinberg S, Ludvigsson P, Stefansson K, Kuss AW, Paschou P, Cath D, Hoekstra PJ, Müller-Vahl K, Stuhrmann M, Silahtaroglu A, Pfundt R, Tümer Z. Bertelsen B, et al. Among authors: karagiannidis i. Biol Psychiatry. 2016 Mar 1;79(5):383-391. doi: 10.1016/j.biopsych.2015.08.027. Epub 2015 Sep 3. Biol Psychiatry. 2016. PMID: 26444075
Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology.
Alexander J, Potamianou H, Xing J, Deng L, Karagiannidis I, Tsetsos F, Drineas P, Tarnok Z, Rizzo R, Wolanczyk T, Farkas L, Nagy P, Szymanska U, Androutsos C, Tsironi V, Koumoula A, Barta C; TSGeneSEE; Sandor P, Barr CL, Tischfield J, Paschou P, Heiman GA, Georgitsi M. Alexander J, et al. Among authors: karagiannidis i. Front Neurosci. 2016 Sep 21;10:428. doi: 10.3389/fnins.2016.00428. eCollection 2016. Front Neurosci. 2016. PMID: 27708560 Free PMC article.
Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome.
Pagliaroli L, Vereczkei A, Padmanabhuni SS, Tarnok Z, Farkas L, Nagy P, Rizzo R, Wolanczyk T, Szymanska U, Kapisyzi M, Basha E, Koumoula A, Androutsos C, Tsironi V, Karagiannidis I, Paschou P, Barta C. Pagliaroli L, et al. Among authors: karagiannidis i. Front Neurol. 2020 Aug 14;11:803. doi: 10.3389/fneur.2020.00803. eCollection 2020. Front Neurol. 2020. PMID: 32922348 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. 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.
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.
Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, Khalifa N, Dahl N, Huang AY, Neale BM, Coppola G, Mathews CA, Scharf JM; Tourette International Collaborative Genetics Study (TIC Genetics); Tourette Syndrome Genetics Southern and Eastern Europe Initiative (TSGENESEE); Tourette Association of America International Consortium for Genetics (TAAICG); Fernandez TV, Buxbaum JD, De Rubeis S, Grice DE, Xing J, Heiman GA, Tischfield JA, Paschou P, Willsey AJ, State MW. Wang S, et al. Cell Rep. 2018 Sep 25;24(13):3441-3454.e12. doi: 10.1016/j.celrep.2018.08.082. Cell Rep. 2018. PMID: 30257206 Free PMC article.
45 results