|
rs1024611
|
|
|
0.010 |
GeneticVariation |
BEFREE |
This meta-analysis was performed to evaluate the relationships between the monocyte chemoattractant protein-1 (MCP-1) -2518A>G (rs1024611 A>G) polymorphism and its serum levels, and the risk of cerebral infarction.
|
24720638 |
2014 |
|
rs10304
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The genotypic distribution of rs10304 for men showed a significant difference between the control and CI groups.
|
23033319 |
2012 |
|
rs1042579
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Thrombomodulin Ala455Val Polymorphism and the risk of cerebral infarction in a biracial population: the Stroke Prevention in Young Women Study.
|
15574195 |
2004 |
|
rs1044006
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Statistical analyses showed that rs1044009 and rs1044006 were associated with the risk of cerebral infarction disease in the Chinese Han agedness population.
|
27370894 |
2016 |
|
rs1044009
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Statistical analyses showed that rs1044009 and rs1044006 were associated with the risk of cerebral infarction disease in the Chinese Han agedness population.
|
27370894 |
2016 |
|
rs1050283
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Association of the LOX-1 rs1050283 Polymorphism with Risk for Atherosclerotic Cerebral Infarction and its Effect on sLOX-1 and LOX-1 Expression in a Chinese Population.
|
27840386 |
2017 |
|
rs10507391
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The results of the meta-analysis indicate that ALOX5AP rs10507391/SG13S114 A>T polymorphism is not associated with the risk of cerebral infarction in the Chinese population.
|
25242267 |
2015 |
|
rs1051266
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We selected three known RFC-1 polymorphisms (-43C>T, 80A>G, 696T>C) and investigated their relationship to cerebral infarction in the Korean population.
|
25659099 |
2015 |
|
rs1057335
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our findings suggest that the α2AP Arg407Lys polymorphism could be involved in the pathogenesis of cerebral ischemia and its outcomes.
|
29306602 |
2019 |
|
rs1059703
|
|
|
0.010 |
GeneticVariation |
BEFREE |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regression analysis with adjustment for conventional risk factors (P<0.05) revealed that the -14C-->T polymorphism (rs1800977) of ABCA1, the A-->C (rs3027898) and C-->T (Ser532Leu, rs1059703) polymorphisms of IRAK1, and the G-->C (Cys2229Ser) polymorphism (rs619203) of ROS1 were significantly associated with atherothrombotic cerebral infarction; that the -428G-->A polymorphism (rs710968) of LIMK1 was significantly associated with intracerebral hemorrhage; and that the 13989A-->G (Ile118Val) polymorphism (NC_000007.12) of CYP3A4 was significantly associated with subarachnoid hemorrhage.
|
18566305 |
2008 |
|
rs10780199
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Furthermore, the C-C-G and G-G-G haplotypes of rs7042521-rs11137351-rs10780199 were significantly more frequent in the CI group than in the control group (p = 0.024 and p < 0.000).
|
21166801 |
2010 |
|
rs10846744
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The frequency of the C allele for rs10846744 and that of the T allele for rs2278986 appeared to be significantly increased in the CHD group (OR: 1.416, 95%CI: 1.128-1.778, P=0.0058 and OR: 1.681, 95%CI: 1.327-2.130, P<0.0001, respectively).
|
28552715 |
2017 |
|
rs10898909
|
|
|
0.010 |
GeneticVariation |
BEFREE |
For all subjects, the frequency of the T-A-G haplotype (rs1783596-rs4382936-rs10898909) was also significantly higher (P=0.031), whereas the frequency of the T-C-G haplotype (rs1783596-rs4382936-rs10898909) was significantly lower (P=0.029) in the CI patients than in the control 1 group.
|
19763137 |
2009 |
|
rs11053646
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The study indicated that the G501C variant in LOX-1 gene may be associated with susceptibility to cerebral infarction, independent of other common risk factors, in northern Chinese Han population.
|
24661313 |
2014 |
|
rs11137351
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Furthermore, the C-C-G and G-G-G haplotypes of rs7042521-rs11137351-rs10780199 were significantly more frequent in the CI group than in the control group (p = 0.024 and p < 0.000).
|
21166801 |
2010 |
|
rs112735431
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Diseases associated with the RNF213 gene include moyamoya disease, with the p.R4810K (c.14429G>A, rs112735431) homozygous variant thought to be the most pathogenic and significantly associated with severe manifestation such as early onset or cerebral infarction at onset.
|
31806452 |
2020 |
|
rs1131882
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that rs768963 polymorphism was significantly more frequent in the CI group than in the non-CI group and the T-T-G-T haplotype of C795T-T924C-G1686A-rs768963 was significantly less frequent in the CI subjects (0.238 versus 0.339; OR 0.617 [95%CI 0.444-0.856]).
|
25557379 |
2015 |
|
rs11614913
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Thus, the SNP rs11614913 is significantly associated with moyamoya disease, as well as cerebral infarction and adult age in patients with moyamoya disease.
|
22659075 |
2012 |
|
rs11833579
|
|
|
0.010 |
GeneticVariation |
BEFREE |
This is the first study to show an association of rs11833579 with multiple episodes of cerebral ischemia of atherothrombotic origin, and of rs11833579 and rs12425791 with short duration of ischemia.
|
22011019 |
2012 |
|
rs1188383936
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The aim of this study is to determine the role of hereditary thrombophilic factors including factor V Leiden A1691G (FVL), prothrombin G20210A, and methylenetetrahydrofolate reductase (MTHFR) C677T gene mutations in patients with stroke because of cerebral infarct.
|
19263510 |
2009 |
|
rs1188383936
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The mutant MTHFR heterozygous 677C/T</span> carriers were increased in patients with cerebral infarction compared with controls (53.9% vs. 36.9%, 0.01 < P < 0.025).
|
10929044 |
2000 |
|
rs1207570776
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The aim of this study is to determine the role of hereditary thrombophilic factors including factor V Leiden A1691G (FVL), prothrombin G20210A, and methylenetetrahydrofolate reductase (MTHFR) C677T gene mutations in patients with stroke because of cerebral infarct.
|
19263510 |
2009 |
|
rs1217691063
|
|
|
0.040 |
GeneticVariation |
BEFREE |
The methylenetetrahydrofolate reductase (MTHFR) 677C>T and 1298A>C polymorphisms, which are associated with hyperhomocysteinemia and nitric oxide (NO) deficiency (which is related to atherothrombosis and cerebral ischemia), have not been studied in moyamoya disease.
|
25098357 |
2014 |
|
rs1217691063
|
|
|
0.040 |
GeneticVariation |
BEFREE |
The mutant MTHFR heterozygous 677C/T</span> carriers were increased in patients with cerebral infarction compared with controls (53.9% vs. 36.9%, 0.01 < P < 0.025).
|
10929044 |
2000 |
|
rs1217691063
|
|
|
0.040 |
GeneticVariation |
BEFREE |
The aim of this study is to determine the role of hereditary thrombophilic factors including factor V Leiden A1691G (FVL), prothrombin G20210A, and methylenetetrahydrofolate reductase (MTHFR) C677T gene mutations in patients with stroke because of cerebral infarct.
|
19263510 |
2009 |