Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome
0.040 GeneticVariation disease BEFREE Likewise, the higher expressing LAC haplotype (5-HTTLPR/rs25531/rs25532) was more frequent in TD probands than in controls (P = 0.024; OR, 1.33) and also in the TD alone group versus the TD plus OCD group (P = 0.0013; OR, 2.14). 23630162 2013
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome
0.040 AlteredExpression disease BEFREE To evaluate whether expression of DAT and SERT in the striatum could lead to pathophysiological change in TS rat model. 20739786 2010
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome
0.040 GeneticVariation disease BEFREE As neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls. 20010450 2010
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome
0.040 GeneticVariation disease BEFREE The lack of significance for 5-HTTLPR and COMT polymorphisms in conferring liability to TS does not exclude a role of different functional polymorphisms in genes coding for serotonergic or dopaminergic structures in the etiology of TS. 11166081 2000