|
rs12932445
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
|
29531354 |
2018 |
|
rs13143308
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
|
29531354 |
2018 |
|
rs146390073
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
|
29531354 |
2018 |
|
rs635634
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
|
29531354 |
2018 |
|
rs6891174
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
|
29531354 |
2018 |
|
rs2200733
|
|
|
0.030 |
GeneticVariation |
BEFREE |
In the Icelandic samples and the two replication sets combined, rs2200733 associated significantly with cardioembolic stroke (CES) (odds ratio [OR], 1.54; p = 8.05 x 10(-9)).
|
18991354 |
2008 |
|
rs2200733
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The rs2200733 variant on chromosome 4q25 is a risk factor for cardioembolic stroke related to atrial fibrillation in Polish patients.
|
21574119 |
2011 |
|
rs2200733
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Subsequently subgroup analysis indicated that both rs2200733 and rs10033464 conferred increased risk for cardioembolic stroke (CE stroke) (for rs2200733, OR 1.38, 95 % CI 1.26-1.51; for rs10033464, OR 1.14, 95 % CI 1.02-1.26), while rs2200733 was marginal associated with non-CE stroke (OR 1.09, 95 % CI 1.02-1.16). our results demonstrated that two SNPs (rs2200733 and rs1003346) on chromosome 4q25 were limited to the stroke of cardioembolic etiology.
|
24065534 |
2013 |
|
rs152312
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Our findings demonstrated an association between cardioembolic stroke and phosphodiesterase 4D single nucleotide polymorphisms rs152312 and 45.
|
21989204 |
2011 |
|
rs152312
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The rs152312 SNP was associated with cardioembolic stroke among whites after multiple comparison corrections.
|
16373644 |
2006 |
|
rs1003346
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Subsequently subgroup analysis indicated that both rs2200733 and rs10033464 conferred increased risk for cardioembolic stroke (CE stroke) (for rs2200733, OR 1.38, 95 % CI 1.26-1.51; for rs10033464, OR 1.14, 95 % CI 1.02-1.26), while rs2200733 was marginal associated with non-CE stroke (OR 1.09, 95 % CI 1.02-1.16). our results demonstrated that two SNPs (rs2200733 and rs1003346) on chromosome 4q25 were limited to the stroke of cardioembolic etiology.
|
24065534 |
2013 |
|
rs10033464
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Subsequently subgroup analysis indicated that both rs2200733 and rs10033464 conferred increased risk for cardioembolic stroke (CE stroke) (for rs2200733, OR 1.38, 95 % CI 1.26-1.51; for rs10033464, OR 1.14, 95 % CI 1.02-1.26), while rs2200733 was marginal associated with non-CE stroke (OR 1.09, 95 % CI 1.02-1.16). our results demonstrated that two SNPs (rs2200733 and rs1003346) on chromosome 4q25 were limited to the stroke of cardioembolic etiology.
|
24065534 |
2013 |
|
rs1205
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Three polymorphisms, rs1205 (CRP gene), rs1800779, and rs2257073 (NOS3 gene), were associated with cardioembolic stroke (p value <0.05).
|
26355258 |
2015 |
|
rs1217691063
|
|
|
0.010 |
GeneticVariation |
BEFREE |
MTHFR C677T was associated with magnetic resonance imaging-confirmed lacunar stroke, but not large artery or cardioembolic stroke.
|
26839351 |
2016 |
|
rs151091899
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The analysis of the TRPV3 gene using polymorphisms in cohort 3 and 4 revealed two polymorphisms associated with cardioembolic stroke in both cohorts, the most significant polymorphism being rs151091899 (p-value: 3.1 × 10<sup>-05</sup>; odds ratio: 5.4) in cohort 3.
|
27604134 |
2016 |
|
rs1800779
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Three polymorphisms, rs1205 (CRP gene), rs1800779, and rs2257073 (NOS3 gene), were associated with cardioembolic stroke (p value <0.05).
|
26355258 |
2015 |
|
rs1906591
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Variant rs1906591 on chromosome 4q25 confers increased risk of cardioembolic stroke in Chinese patients.
|
24932589 |
2014 |
|
rs20417
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the Boston cohort, rs20417 polymorphism was associated with increased WMHv among noncardioembolic (P = .037), but not among cardioembolic stroke patients.
|
25957909 |
2015 |
|
rs2257073
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Three polymorphisms, rs1205 (CRP gene), rs1800779, and rs2257073 (NOS3 gene), were associated with cardioembolic stroke (p value <0.05).
|
26355258 |
2015 |
|
rs2273235
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Similar results were found for m<sup>6</sup>A-SNP rs2273235 in the <i>NDST1</i> gene which was associated with cardioembolic stroke (<i>P</i> = 8.47 × 10<sup>-3</sup>).
|
31156544 |
2019 |
|
rs2910829
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Although several univariate associations were identified, only 1 SNP (rs2910829) was found to be significantly associated with cardioembolic stroke among both whites and blacks.
|
16373644 |
2006 |
|
rs505922
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Independent replication in Meta-Stroke confirmed the rs505922 association with stroke, beta (standard error, SE) = 0.066 (0.02), p = 0.001, a finding specific to large-vessel and cardioembolic stroke (p = 0.001 and p = < 0.001, respectively) but not seen with small-vessel stroke (p = 0.811).
|
23381943 |
2013 |
|
rs5065
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, in logistic analysis for Trial of Org 10172 in Acute Stroke Treatment (TOAST) classification of ischemic stroke, nonsynonymous rs5065 (STOP152Arg) and rs5067 in 3'UTR of NPPA, which were in complete linkage disequilibrium, showed significant associations with cardioembolic stroke.
|
22400494 |
2012 |
|
rs5067
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, in logistic analysis for Trial of Org 10172 in Acute Stroke Treatment (TOAST) classification of ischemic stroke, nonsynonymous rs5065 (STOP152Arg) and rs5067 in 3'UTR of NPPA, which were in complete linkage disequilibrium, showed significant associations with cardioembolic stroke.
|
22400494 |
2012 |
|
rs761740955
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The β-fibrinogen gene 455G/A polymorphism associated with cardioembolic stroke in atrial fibrillation with low CHA<sub>2</sub>DS<sub>2</sub>-VaSc score.
|
29235504 |
2017 |