Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4129
Gene Symbol: MAOB
MAOB
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.600 GeneticVariation LHGDN In conclusion, variants in FGF20 and MAOB show evidence of statistical interactions, which emphasizes the importance of considering them jointly in genetic analysis of PD and illustrates potential patterns of biological interaction contributing to PD risk. 18205889

2008
Entrez Id: 4129
Gene Symbol: MAOB
MAOB
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.600 GeneticVariation LHGDN Polymorphisms of catechol-0-methyltransferase (COMT), monoamine oxidase B (MAOB), N-acetyltransferase 2 (NAT2) and cytochrome P450 2D6 (CYP2D6) gene in patients with early onset of Parkinson's disease. 17270484

2007
Entrez Id: 4129
Gene Symbol: MAOB
MAOB
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.600 GeneticVariation LHGDN These results suggest that a strong gender difference exists with respect to the modifying effect of MAO-B genotype on the smoking association with PD. 12428723

2002