Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.400 AlteredExpression disease BEFREE After treatment with E2, NOS III, ER alpha, and ER beta mRNA expression was enhanced in arterial vessels of postmenopausal women with CAD. 16207548 2005
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.400 GeneticVariation disease LHGDN This study seeks to investigate the association between the ESR1 haplotype created by the c.454-397 T>C and c.454-351 A>G polymorphisms, the length of the (TA)n repeats, and the angiographic extent of CAD. 16159931 2005
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.400 GeneticVariation disease BEFREE Estrogen receptor alpha (ESR1) gene variation is associated with a range of important estrogen-dependent characteristics, including responses of lipid profile and atherosclerotic severity to hormone replacement therapy, coronary heart disease risk, and migraine. 16179580 2005
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.400 GeneticVariation disease BEFREE The (TA)(n)length in the ER-alpha gene promoter region is associated with the angiographic severity of CAD in young patients. 14972425 2004
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.400 GeneticVariation disease BEFREE Molecular analysis of the estrogen receptor alpha gene in men with coronary artery disease: association with disease status. 12691862 2003
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.400 GeneticVariation disease BEFREE Estrogen-receptor polymorphisms and effects of estrogen replacement on high-density lipoprotein cholesterol in women with coronary disease. 11919305 2002
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.400 GeneticVariation disease BEFREE We conclude that -1989T/G or its linked polymorphisms in the ER-alpha gene may confer risk for CAD and that the G/G genotype may be an independent predictor for CAD in patients with familial hypercholesterolemia. 12006396 2002
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.400 Biomarker disease CTD_human Premature coronary artery disease associated with a disruptive mutation in the estrogen receptor gene in a man. 9396482 1997