|
rs6265
|
|
|
0.020 |
GeneticVariation |
BEFREE |
As a whole, the BDNF Val66Met polymorphism was not associated with learning and memory performance in patients recovering from SAH.
|
18797348 |
2008 |
|
rs759834365
|
|
|
0.020 |
GeneticVariation |
BEFREE |
As a whole, the BDNF Val66Met polymorphism was not associated with learning and memory performance in patients recovering from SAH.
|
18797348 |
2008 |
|
rs6265
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The Met allele of the BDNF Val66Met polymorphism predicts poor outcome among survivors of aneurysmal subarachnoid hemorrhage.
|
17761923 |
2007 |
|
rs759834365
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The Met allele of the BDNF Val66Met polymorphism predicts poor outcome among survivors of aneurysmal subarachnoid hemorrhage.
|
17761923 |
2007 |
|
rs1217691063
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, frequency of MTHFR C677T genotype, CT (53% vs. 20%; p < 0.001) and TT (15% vs. 2%; p < 0.05) was significantly higher in SAH group as compared to healthy controls.
|
29926428 |
2018 |
|
rs144757781
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We identified 2 different variants in exon 38 from the <i>PCNT</i> gene shared between affected members from 2 different families with either IA or SAH (p.R2728C and p.V2811L).
|
30413633 |
2018 |
|
rs17576
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our study showed that the rs3918242 (T) and rs17576 (G), the cross reaction between rs3918242 and smoking increased the risk of subarachnoid hemorrhage.
|
29763368 |
2018 |
|
rs17577
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, after adjusting for covariates, we did not find any direct association between rs17577 and subarachnoid hemorrhage risk.
|
29763368 |
2018 |
|
rs3918242
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our study showed that the rs3918242 (T) and rs17576 (G), the cross reaction between rs3918242 and smoking increased the risk of subarachnoid hemorrhage.
|
29763368 |
2018 |
|
rs762890408
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We identified 2 different variants in exon 38 from the <i>PCNT</i> gene shared between affected members from 2 different families with either IA or SAH (p.R2728C and p.V2811L).
|
30413633 |
2018 |
|
rs73933023
|
|
|
0.010 |
GeneticVariation |
BEFREE |
For the fourth variant, p.Pro4501Leu (RS73933023), the results of the prediction programs were discrepant and the prevalence in the general population was high, i.e. almost 0.5%, which is too frequent to be associated with the rare SAH phenotype.
|
28750945 |
2017 |
|
rs77375493
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We report the case of an untreated 32-year-old woman with a history of JAK2 V617F-positive ET with cerebellar and subarachnoid hemorrhages without evidence of sinus vein thrombosis.
|
24582788 |
2015 |
|
rs10986769
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The chi-square test, multivariable logistic regression analysis with adjustment for covariates, as well as a stepwise forward selection procedure revealed that the C->T polymorphism (rs1324694) of ERLIN1, the C->T polymorphism (rs12679196) of TRAPPC9, and the G->T polymorphism (rs16936752) of WNK2 were significantly (P<0.05) associated with the prevalence of intracerebral hemorrhage, and that the A->G polymorphism (rs3111754) of ITM2C and the A->G polymorphism (rs10986769) of MAPKAP1 were significantly associated with the prevalence of subarachnoid hemorrhage.
|
20198315 |
2010 |
|
rs12679196
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The chi-square test, multivariable logistic regression analysis with adjustment for covariates, as well as a stepwise forward selection procedure revealed that the C->T polymorphism (rs1324694) of ERLIN1, the C->T polymorphism (rs12679196) of TRAPPC9, and the G->T polymorphism (rs16936752) of WNK2 were significantly (P<0.05) associated with the prevalence of intracerebral hemorrhage, and that the A->G polymorphism (rs3111754) of ITM2C and the A->G polymorphism (rs10986769) of MAPKAP1 were significantly associated with the prevalence of subarachnoid hemorrhage.
|
20198315 |
2010 |
|
rs1324694
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The chi-square test, multivariable logistic regression analysis with adjustment for covariates, as well as a stepwise forward selection procedure revealed that the C->T polymorphism (rs1324694) of ERLIN1, the C->T polymorphism (rs12679196) of TRAPPC9, and the G->T polymorphism (rs16936752) of WNK2 were significantly (P<0.05) associated with the prevalence of intracerebral hemorrhage, and that the A->G polymorphism (rs3111754) of ITM2C and the A->G polymorphism (rs10986769) of MAPKAP1 were significantly associated with the prevalence of subarachnoid hemorrhage.
|
20198315 |
2010 |
|
rs16936752
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The chi-square test, multivariable logistic regression analysis with adjustment for covariates, as well as a stepwise forward selection procedure revealed that the C->T polymorphism (rs1324694) of ERLIN1, the C->T polymorphism (rs12679196) of TRAPPC9, and the G->T polymorphism (rs16936752) of WNK2 were significantly (P<0.05) associated with the prevalence of intracerebral hemorrhage, and that the A->G polymorphism (rs3111754) of ITM2C and the A->G polymorphism (rs10986769) of MAPKAP1 were significantly associated with the prevalence of subarachnoid hemorrhage.
|
20198315 |
2010 |
|
rs200525645
|
|
|
0.010 |
GeneticVariation |
BEFREE |
This suggests that carriers of the subunit B His95Arg factor XIII polymorphism have an increased risk of aneurysmal SAH.
|
19826759 |
2010 |
|
rs3111754
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The chi-square test, multivariable logistic regression analysis with adjustment for covariates, as well as a stepwise forward selection procedure revealed that the C->T polymorphism (rs1324694) of ERLIN1, the C->T polymorphism (rs12679196) of TRAPPC9, and the G->T polymorphism (rs16936752) of WNK2 were significantly (P<0.05) associated with the prevalence of intracerebral hemorrhage, and that the A->G polymorphism (rs3111754) of ITM2C and the A->G polymorphism (rs10986769) of MAPKAP1 were significantly associated with the prevalence of subarachnoid hemorrhage.
|
20198315 |
2010 |
|
rs777785946
|
|
|
0.010 |
GeneticVariation |
BEFREE |
This suggests that carriers of the subunit B His95Arg factor XIII polymorphism have an increased risk of aneurysmal SAH.
|
19826759 |
2010 |
|
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 |
|
rs1799983
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Endothelial nitric oxide synthase gene [G894T] polymorphism as a possible risk factor in aneurysmal subarachnoid haemorrhage.
|
18046500 |
2008 |
|
rs1800977
|
|
|
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 |
|
rs3027898
|
|
|
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 |
|
rs55951658
|
|
|
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 |
|
rs619203
|
|
|
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 |