rs117834366
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
|
31473137 |
2019 |
rs429358
|
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
|
31473137 |
2019 |
rs5882
|
|
|
0.020 |
GeneticVariation |
BEFREE |
CETP I405V polymorphism is likely a risk factor for AD and VaD in our cohort, independent of APOEɛ4 status.
|
29332048 |
2018 |
rs17501010
|
|
|
0.010 |
GeneticVariation |
BEFREE |
For patients with type 2 diabetes the odds ratio of VaD increased significantly in GC+CC genotypes of rs893051 (OR=12.57, P<0.0001) and GT+TT of rs17501010 (OR=5.33, P=0.01).
|
28273404 |
2017 |
rs893051
|
|
|
0.010 |
GeneticVariation |
BEFREE |
For patients with type 2 diabetes the odds ratio of VaD increased significantly in GC+CC genotypes of rs893051 (OR=12.57, P<0.0001) and GT+TT of rs17501010 (OR=5.33, P=0.01).
|
28273404 |
2017 |
rs1217691063
|
|
|
0.040 |
GeneticVariation |
BEFREE |
We identified APOE ɛ2/ɛ3/ɛ4 and additional four genetic polymorphisms including MTHFR C677T, PON1 L55M, TGF-β1 +29C/T, and TNF-α -850C/T associated with VaD.
|
25835425 |
2015 |
rs854560
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We identified APOE ɛ2/ɛ3/ɛ4 and additional four genetic polymorphisms including MTHFR C677T, PON1 L55M, TGF-β1 +29C/T, and TNF-α -850C/T associated with VaD.
|
25835425 |
2015 |
rs662
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The interaction between PON1 genes (rs662 and rs85460) and ApoE genes showed synergistic epistasis in altering the odds of significantly having both AD and VaD.
|
24965284 |
2014 |
rs1051266
|
|
|
0.010 |
GeneticVariation |
BEFREE |
No direct association was found between variant (G) allele or genotype of rs1051266 with AD and VaD cases.
|
24554143 |
2014 |
rs290227
|
|
G |
0.810 |
GeneticVariation |
GWASDB |
We suggested a novel association of the VaD susceptibility with an intronic variant of rs290227 in the SYK gene.
|
23480133 |
2013 |
rs290227
|
|
G |
0.810 |
GeneticVariation |
GWASCAT |
We suggested a novel association of the VaD susceptibility with an intronic variant of rs290227 in the SYK gene.
|
23480133 |
2013 |
rs290227
|
|
|
0.810 |
GeneticVariation |
BEFREE |
We suggested a novel association of the VaD susceptibility with an intronic variant of rs290227 in the SYK gene.
|
23480133 |
2013 |
rs4986938
|
|
|
0.020 |
GeneticVariation |
BEFREE |
In haplotype analyses, the ERβ haplotype containing the polymorphism rs944050 variant allele and the polymorphism rs4986938 wild-type allele was associated with VaD (odds ratio = 1.70, 95% confidence interval = 1.03-2.84).
|
22183267 |
2012 |
rs944050
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The polymorphism rs944050 in the ERβ gene was associated with an increased risk of VaD in Chinese Han women.
|
22183267 |
2012 |
rs10491487
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of vascular dementia.
|
22116812 |
2012 |
rs12007229
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of vascular dementia.
|
22116812 |
2012 |
rs2497931
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of vascular dementia.
|
22116812 |
2012 |
rs26906
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of vascular dementia.
|
22116812 |
2012 |
rs4485213
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of vascular dementia.
|
22116812 |
2012 |
rs951660
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The minor allele, A, of its intronic SNP 'rs951660' might induce a delayed splicing and thus increase the susceptibility to VaD.
|
22111664 |
2013 |
rs1800795
|
|
|
0.010 |
GeneticVariation |
BEFREE |
While rs1800795 (CC or GC) genotypes alone increased the odds of developing VaD </span>by 2.2-fold, the presence of CC genotype of rs1801131 nullified this effect.
|
22015309 |
2012 |
rs1801131
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In this case-control study, we examined C677T and A1298C (rs1801133 and rs1801131) polymorphism in the methylenetetrahydrofolate reductase (MTHFR) genes and their correlation with plasma levels of homocysteine (Hcy) in AD and VaD cases and evaluated the gene-gene interaction (epistasis) with IL-6-174 G/C (rs1800795).
|
22015309 |
2012 |
rs1801133
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In this case-control study, we examined C677T and A1298C (rs1801133 and rs1801131) polymorphism in the methylenetetrahydrofolate reductase (MTHFR) genes and their correlation with plasma levels of homocysteine (Hcy) in AD and VaD cases and evaluated the gene-gene interaction (epistasis) with IL-6-174 G/C (rs1800795).
|
22015309 |
2012 |
rs140701
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The analysis of the 3 markers rs3813034, rs140701 and rs4795541 spanning the SLC6A4 locus was made in 541 consecutive patients clinically diagnosed as having VaD (n = 372) or no cognitive impairment (n = 169) attending a geriatric ward.
|
20502016 |
2010 |
rs3813034
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The analysis of the 3 markers rs3813034, rs140701 and rs4795541 spanning the SLC6A4 locus was made in 541 consecutive patients clinically diagnosed as having VaD (n = 372) or no cognitive impairment (n = 169) attending a geriatric ward.
|
20502016 |
2010 |