INSR, insulin receptor, 3643

N. diseases: 452; N. variants: 109
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.070 GeneticVariation disease BEFREE This study postulates that this reflects a common genetic cause, and investigates whether the INSR rs2059806 single nucleotide polymorphism (SNP) (a risk factor for essential hypertension, type 2 diabetes and metabolic syndrome) is also associated with pre-eclampsia. 28117222 2017
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.070 Biomarker disease BEFREE Insulin receptor number is reduced in healthy offspring of patients with essential hypertension. 15485753 2004
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.070 GeneticVariation disease BEFREE The first molecular genetic association with human essential hypertension (HT) involved the insulin receptor gene (INSR). 9247738 1997
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.070 Biomarker disease BEFREE Thus, the results from this study do not support a role for the INSR gene in the genesis of essential hypertension in the population studied. 8523386 1995
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.070 GeneticVariation disease BEFREE The present study examined genotypes for the obesity-associated ApaLI restriction fragment length polymorphism of LDLR, and genotypes for a hypertension-associated RsaI restriction fragment length polymorphism at the insulin receptor gene (INSR) locus, which is linked to LDLR, in relation to plasma lipids, body mass index and blood pressure in 27 obese and 57 non-obese Caucasians with severe essential hypertension, selected on the basis of having parents who were both hypertensive, and in 25 obese and 45 non-obese normotensive subjects selected on the basis of having parents who were both normotensive after the age of 50 years.2. 7913431 1994
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.070 GeneticVariation disease BEFREE Short report: insertion variant in intron 9, but not microsatellite in intron 2, of the insulin receptor gene is associated with essential hypertension. 8301111 1993
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.070 GeneticVariation disease BEFREE Independent, marked associations of alleles of the insulin receptor and dipeptidyl carboxypeptidase-I genes with essential hypertension. 8104754 1993