Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 Biomarker LHGDN The expression of 4-repeat MAPT, STH, and KIAA1267 was significantly increased in PD brains relative to controls. 18509094

2008
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 Biomarker LHGDN Our data provide strong evidence that the H1 clade, which contains MAPT and several other genes, is a risk factor for PD. 17514749

2007
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 GeneticVariation LHGDN To further evaluate their role in PD, we genotyped a sample set of 765 cases and controls consisting of two large European subgroups of German (n=418) and Serbian (n=347) origin for the MAPT haplotypes H1 and H2. 17637803

2007
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 Biomarker LHGDN We observed that cognitive decline and the development of PD dementia are strongly associated (p = 10(-4)) with the inversion polymorphism containing MAPT. 17683088

2007
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 GeneticVariation LHGDN We failed to demonstrate a consistent association between the MAPT H1 haplotype (delineated by intron 9 ins/del) and PD in three ethnically diverse populations. 17192721

2006
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 GeneticVariation LHGDN We investigated the association of Parkinson's disease (PD) with tau gene H1 haplotypes in the Norwegian population. 11958849

2002