Gene Variants Linked to Lipoprotein and Heart Disease

2010 ◽  
Vol 43 (2) ◽  
pp. 19
Author(s):  
MARY ANN MOON
Keyword(s):  
Heart Disease ◽  
Gene Variants

Effects of the PPARG P12A and C161T gene variants on serum lipids in coronary heart disease patients with and without Type 2 diabetes

2011 ◽  
Vol 358 (1-2) ◽  
pp. 355-363 ◽  
Author(s):  
Hulya Yilmaz-Aydogan ◽  
Ozlem Kurnaz ◽  
Ozlem Kurt ◽  
Basak Akadam-Teker ◽  
Ozlem Kucukhuseyin ◽  
...  
Keyword(s):  
Type 2 Diabetes ◽  
Coronary Heart Disease ◽  
Heart Disease ◽  
Serum Lipids ◽  
Gene Variants

scholarly journals Apolipoprotein A5 gene variants and the risk of coronary heart disease: A case-control study and meta-analysis

2013 ◽  
Vol 8 (4) ◽  
pp. 1175-1182 ◽  
Author(s):  
JIANQING ZHOU ◽  
LIMIN XU ◽  
RONG STEPHANIE HUANG ◽  
YI HUANG ◽  
YANPING LE ◽  
...  
Keyword(s):  
Coronary Heart Disease ◽  
Heart Disease ◽  
Case Control Study ◽  
Meta Analysis ◽  
Case Control ◽  
Gene Variants ◽  
Apolipoprotein A5 ◽  
Control Study

scholarly journals The Association of Alcohol and Alcohol Metabolizing Gene Variants with Diabetes and Coronary Heart Disease Risk Factors in a White Population

PLoS ONE ◽  
2010 ◽  
Vol 5 (8) ◽  
pp. e11735 ◽  
Author(s):  
Lise Lotte N. Husemoen ◽  
Torben Jørgensen ◽  
Knut Borch-Johnsen ◽  
Torben Hansen ◽  
Oluf Pedersen ◽  
...  
Keyword(s):  
Risk Factors ◽  
Coronary Heart Disease ◽  
Heart Disease ◽  
Coronary Heart Disease Risk ◽  
Disease Risk ◽  
Gene Variants ◽  
White Population ◽  
Heart Disease Risk Factors ◽  
Heart Disease Risk

Association between congenital heart disease and NKX2.5 gene polymorphisms: systematic review and meta-analysis

2020 ◽  
Vol 14 (18) ◽  
pp. 1747-1757
Author(s):  
Thelma B González-Castro ◽  
Carlos A Tovilla-Zárate ◽  
María L López-Narvaez ◽  
Isela E Juárez-Rojop ◽  
Juan Calderón-Colmenero ◽  
...  
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Gene Polymorphisms ◽  
Congenital Heart ◽  
Web Of Science ◽  
Meta Analysis ◽  
P Value ◽  
Gene Variants ◽  
Analysis Software ◽  
Allelic Model

Aim: To analyze the association of NKX2.5 gene with congenital heart disease (CHD), and to determine if the variants rs703752, rs3729753 and rs2277923 increase the risk for developing CHD. Materials & methods: PubMed, EBSCO and Web of Science databases were screened to identify eligible studies. Through a comprehensive meta-analysis software, the association between NKX2.5 gene variants and susceptibility of CHD was calculated by pooled odd ratio (ORs) and 95% CI. Results: We observed that the allelic model of rs703752 and rs2277923 increased the risk in the overall population: OR = 1.24; 95% CI: 1.00–1.55; Z p-value = 0.049; OR = 1.18; 95% CI: 0.01–1.37; Z p-value = 0.036; respectively. Conclusion: Our results suggested that the rs703752 and rs2277923 polymorphisms of the NKX2.5 gene are associated with CHD.

Meta-analyses of four eosinophil related gene variants in coronary heart disease

2013 ◽  
Vol 36 (4) ◽  
pp. 394-401 ◽  
Author(s):  
Jiangfang Lian ◽  
Yi Huang ◽  
R. Stephanie Huang ◽  
Limin Xu ◽  
Yanping Le ◽  
...  
Keyword(s):  
Coronary Heart Disease ◽  
Heart Disease ◽  
Gene Variants ◽  
Related Gene ◽  
Meta Analyses

scholarly journals The Association of MTHFR C677T Gene Variants and Lipid Profiles or Body Mass Index in Patients With Diabetic and Nondiabetic Coronary Heart Disease

2013 ◽  
Vol 27 (6) ◽  
pp. 427-434 ◽  
Author(s):  
Ozlem Kucukhuseyin ◽  
Ozlem Kurnaz ◽  
A. Basak Akadam-Teker ◽  
Turgay Isbir ◽  
Zehra Bugra ◽  
...  
Keyword(s):  
Body Mass Index ◽  
Coronary Heart Disease ◽  
Heart Disease ◽  
Body Mass ◽  
Mthfr C677t ◽  
Lipid Profiles ◽  
Gene Variants
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