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Association of the tumor necrosis factor -308 A/ G promoter polymorphism with Tourette syndrome.
Published in:
International Journal of Immunogenetics, 2014, v. 41, n. 6, p. 493, doi. 10.1111/iji.12147
By:
- Keszler, G.;
- Kruk, E.;
- Kenezloi, E.;
- Tarnok, Z.;
- Sasvari‐Szekely, M.;
- Nemoda, Z.
Publication type:
Article
Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.
Published in:
Molecular Psychiatry, 2012, v. 17, n. 7, p. 665, doi. 10.1038/mp.2011.151
By:
- Karagiannidis, I;
- Rizzo, R;
- Tarnok, Z;
- Wolanczyk, T;
- Hebebrand, J;
- Nöthen, M M;
- Lehmkuhl, G;
- Farkas, L;
- Nagy, P;
- Barta, C;
- Szymanska, U;
- Panteloglou, G;
- Miranda, D M;
- Feng, Y;
- Sandor, P;
- Barr, C;
- Paschou, P
Publication type:
Article
The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
Published in:
Molecular Psychiatry, 2010, v. 15, n. 2, p. 216, doi. 10.1038/mp.2008.64
By:
- Mukherjee, N.;
- Kidd, K. K.;
- Pakstis, A. J.;
- Speed, W. C.;
- Li, H.;
- Tarnok, Z.;
- Barta, C.;
- Kajuna, S. L. B.;
- Kidd, J. R.
Publication type:
Article
Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome.
Published in:
Genes, Brain & Behavior, 2012, v. 11, n. 4, p. 444, doi. 10.1111/j.1601-183X.2012.00778.x
By:
- Paschou, P.;
- Stylianopoulou, E.;
- Karagiannidis, I.;
- Rizzo, R.;
- Tarnok, Z.;
- Wolanczyk, T.;
- Hebebrand, J.;
- Nöthen, M. M.;
- Lehmkuhl, G.;
- Farkas, L.;
- Nagy, P.;
- Szymanska, U.;
- Lykidis, D.;
- Androutsos, C.;
- Tsironi, V.;
- Koumoula, A.;
- Barta, C.;
- Klidonas, S.;
- Ypsilantis, P.;
- Simopoulos, C.
Publication type:
Article

Found: 4

Association of the tumor necrosis factor -308 A/ G promoter polymorphism with Tourette syndrome.

Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.

The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.

Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome.