Genetic association analysis of ATG16L1 rs2241880, rs6758317 and ATG16L2 rs11235604 polymorphisms with rheumatoid arthritis in a Chinese population

2021 ◽  
Vol 93 ◽  
pp. 107378
Author(s):  
Ji-Jun Mo ◽  
Wei Zhang ◽  
Qin-Wen Wen ◽  
Ting-Hui Wang ◽  
Wen Qin ◽  
...  
Keyword(s):  
Rheumatoid Arthritis ◽  
Genetic Association ◽  
Association Analysis ◽  
Chinese Population ◽  
Genetic Association Analysis

Genetic association analysis of myocardial infarction with thrombospondin-1 N700S variant in a Chinese population

2004 ◽  
Vol 113 (3-4) ◽  
pp. 181-186 ◽  
Author(s):  
Xiaoyang Zhou ◽  
Jianfeng Huang ◽  
Jianhong Chen ◽  
Jiangong Zhao ◽  
Dongliang Ge ◽  
...  
Keyword(s):  
Myocardial Infarction ◽  
Genetic Association ◽  
Association Analysis ◽  
Chinese Population ◽  
Genetic Association Analysis ◽  
Thrombospondin 1

scholarly journals Genetic Association Analysis of Common Variants in FOXO3 Related to Longevity in a Chinese Population

PLoS ONE ◽  
2016 ◽  
Vol 11 (12) ◽  
pp. e0167918 ◽  
Author(s):  
Rong Lin ◽  
Yunxia Zhang ◽  
Dongjing Yan ◽  
Xiaoping Liao ◽  
Xianshou Wang ◽  
...  
Keyword(s):  
Genetic Association ◽  
Association Analysis ◽  
Chinese Population ◽  
Common Variants ◽  
Genetic Association Analysis

Genetic association analysis between IL9 and coronary artery disease in a Chinese Han population

Cytokine ◽  
2022 ◽  
Vol 150 ◽  
pp. 155761
Author(s):  
Lingfeng Zha ◽  
Jiangtao Dong ◽  
Qianwen Chen ◽  
Yuhua Liao ◽  
Hongsong Zhang ◽  
...  
Keyword(s):  
Coronary Artery Disease ◽  
Coronary Artery ◽  
Genetic Association ◽  
Association Analysis ◽  
Chinese Han Population ◽  
Chinese Han ◽  
Genetic Association Analysis ◽  
Han Population ◽  
Artery Disease

scholarly journals Prevalence, Patterns, and Genetic Association Analysis of Modic Vertebral Endplate Changes

2017 ◽  
Vol 11 (4) ◽  
pp. 594-600 ◽  
Author(s):  
Rishi Mugesh Kanna ◽  
Rajasekaran Shanmuganathan ◽  
Veera Ranjani Rajagopalan ◽  
Senthil Natesan ◽  
Raveendran Muthuraja ◽  
...  
Keyword(s):  
Candidate Genes ◽  
Genetic Association ◽  
Association Analysis ◽  
Disc Degeneration ◽  
Lumbar Disc ◽  
Nucleotide Polymorphisms ◽  
Lumbar Disc Degeneration ◽  
Vertebral Endplate ◽  
Genetic Association Analysis ◽  
Study Population

<sec><title>Study Design</title><p>A prospective genetic association study.</p></sec><sec><title>Purpose</title><p>The etiology of Modic changes (MCs) is unclear. Recently, the role of genetic factors in the etiology of MCs has been evaluated. However, studies with a larger patient subset are lacking, and candidate genes involved in other disc degeneration phenotypes have not been evaluated. We studied the prevalence of MCs and genetic association of 41 candidate genes in a large Indian cohort.</p></sec><sec><title>Overview of Literature</title><p>MCs are vertebral endplate signal changes predominantly observed in the lumbar spine. A significant association between MCs and lumbar disc degeneration and nonspecific low back pain has been described, with the etiopathogenesis implicating various mechanical, infective, and biochemical factors.</p></sec><sec><title>Methods</title><p>We studied 809 patients using 1.5-T magnetic resonance imaging to determine the prevalence, patterns, distribution, and type of lumbar MCs. Genetic association analysis of 71 single nucleotide polymorphisms (SNPs) of 41 candidate genes was performed based on the presence or absence of MCs. SNPs were genotyped using the Sequenome platform, and an association test was performed using PLINK software.</p></sec><sec><title>Results</title><p>The mean age of the study population (n=809) was 36.7±10.8 years. Based on the presence of MCs, the cohort was divided into 702 controls and 107 cases (prevalence, 13%). MCs were more commonly present in the lower (149/251, 59.4%) than in the upper (102/251, 40.6%) endplates. L4–5 endplates were the most commonly affected levels (30.7%). Type 2 MCs were the most commonly observed pattern (n=206, 82%). The rs2228570 SNP of VDR (<italic>p</italic>=0.02) and rs17099008 SNP of MMP20 (<italic>p</italic>=0.03) were significantly associated with MCs.</p></sec><sec><title>Conclusions</title><p>Genetic polymorphisms of SNPs of VDR and MMP20 were significantly associated with MCs. Understanding the etiopathogenetic mechanisms of MCs is important for planning preventive and therapeutic strategies.</p></sec>

scholarly journals Bioinformatic and Genetic Association Analysis of MicroRNA Target Sites in One-Carbon Metabolism Genes

PLoS ONE ◽  
2011 ◽  
Vol 6 (7) ◽  
pp. e21851 ◽  
Author(s):  
Nicole Stone ◽  
Faith Pangilinan ◽  
Anne M. Molloy ◽  
Barry Shane ◽  
John M. Scott ◽  
...  
Keyword(s):  
Genetic Association ◽  
Association Analysis ◽  
Carbon Metabolism ◽  
Microrna Target ◽  
Genetic Association Analysis ◽  
Target Sites ◽  
One Carbon Metabolism

scholarly journals Genetic Association Analysis of Cell Cycle Regulators Reveals YWHAZ Has Prognostic Significance in Prostate Cancer

2020 ◽  
Vol 17 (2) ◽  
pp. 209-216 ◽  
Author(s):  
CHIA-CHENG YU ◽  
LIH-CHYANG CHEN ◽  
WEN-HSIN LIN ◽  
VICTOR C. LIN ◽  
CHAO-YUAN HUANG ◽  
...  
Keyword(s):  
Prostate Cancer ◽  
Cell Cycle ◽  
Genetic Association ◽  
Association Analysis ◽  
Prognostic Significance ◽  
Cell Cycle Regulators ◽  
Genetic Association Analysis
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