Gene: COMT ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.060 GeneticVariation disease BEFREE To conclude, CYP1A1 m1, COMT p.H108L polymorphisms were associated with PD risk, and sexual dimorphism was observed in these associations. 24389856 2014
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.060 GeneticVariation disease BEFREE Association of monoamine oxidase B and catechol-O-methyltransferase polymorphisms with sporadic Parkinson's disease in an Iranian population. 23319194 2012
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.060 GeneticVariation disease BEFREE The catechol-O-methyltransferase and monoamine oxidase B polymorphisms and levodopa therapy in the Iranian patients with sporadic Parkinson's disease. 23093014 2012
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.060 Biomarker disease BEFREE It has been suggested that polymorphisms in monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) might increase the risk of PD. 15753616 2005
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.060 GeneticVariation disease BEFREE The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease. 15355491 2004
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.060 GeneticVariation disease BEFREE In contrast to reports in oriental populations, our results do not support a major role of APOE, PARKIN and COMT polymorphisms in PD susceptibility in the Finnish population. 12270650 2002