rs9960767
|
|
C |
0.880 |
GeneticVariation |
GWASDB |
Common variants conferring risk of schizophrenia.
|
19571808 |
2009 |
rs9960767
|
|
C |
0.880 |
GeneticVariation |
GWASCAT |
Common variants conferring risk of schizophrenia.
|
19571808 |
2009 |
rs17594526
|
|
T |
0.800 |
GeneticVariation |
GWASDB |
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
|
19571811 |
2009 |
rs17594526
|
|
T |
0.800 |
GeneticVariation |
GWASCAT |
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
|
19571811 |
2009 |
rs9960767
|
|
|
0.880 |
GeneticVariation |
BEFREE |
Thus, we hypothesized that the disease-associated C allele of the rs9960767 polymorphism of the TCF4 gene led to impaired VDM functioning in schizophrenia patients.
|
21228604 |
2011 |
rs9960767
|
|
|
0.880 |
GeneticVariation |
BEFREE |
We therefore investigated the impact of the schizophrenia susceptibility gene TCF4 (rs9960767) on sensorimotor gating of the ASR in healthy humans and in patients with a schizophrenia spectrum disorder.
|
21543597 |
2011 |
rs9960767
|
|
|
0.880 |
GeneticVariation |
GWASDB |
Common variants at VRK2 and TCF4 conferring risk of schizophrenia.
|
21791550 |
2011 |
rs17512836
|
|
C |
0.810 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five new schizophrenia loci.
|
21926974 |
2011 |
rs17512836
|
|
C |
0.810 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies five new schizophrenia loci.
|
21926974 |
2011 |
rs9960767
|
|
|
0.880 |
GeneticVariation |
BEFREE |
As measured by prepulse inhibition, the schizophrenia risk allele C of TCF4 rs9960767 reduces sensorimotor gating.
|
21932083 |
2011 |
rs9960767
|
|
|
0.880 |
GeneticVariation |
BEFREE |
P50 suppression was significantly decreased in carriers of schizophrenia risk alleles of the TCF4 polymorphisms rs9960767, rs10401120rs, rs17597926, and 17512836 (P < 0.0002-0.00005).
|
22451930 |
2012 |
rs17597926
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
|
22688191 |
2012 |
rs2958182
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The SNP rs2958182 was reported to be significantly associated with schizophrenia (SCZ) in Han Chinese.
|
23249814 |
2013 |
rs11152369
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
|
23453885 |
2013 |
rs1261117
|
|
T |
0.800 |
GeneticVariation |
GWASDB |
A comprehensive family-based replication study of schizophrenia genes.
|
23894747 |
2013 |
rs1261117
|
|
T |
0.800 |
GeneticVariation |
GWASCAT |
A comprehensive family-based replication study of schizophrenia genes.
|
23894747 |
2013 |
rs9960767
|
|
|
0.880 |
GeneticVariation |
BEFREE |
Single nucleotide polymorphisms in TCF4 gene have been consistently associated with schizophrenia in genome wide association studies, including the C allele of rs9960767.
|
24275585 |
2014 |
rs9960767
|
|
|
0.880 |
GeneticVariation |
BEFREE |
The analyses on the 28 individual SNPs previously associated with schizophrenia found that two SNPs in TCF4 returned a significant association with the SPEQ Paranoia dimension, rs17512836 (p-value = 2.57×10⁻⁴) and rs9960767 (p-value = 6.23×10⁻⁴).
|
24718684 |
2014 |
rs17512836
|
|
|
0.810 |
GeneticVariation |
BEFREE |
The analyses on the 28 individual SNPs previously associated with schizophrenia found that two SNPs in TCF4 returned a significant association with the SPEQ Paranoia dimension, rs17512836 (p-value = 2.57×10⁻⁴) and rs9960767 (p-value = 6.23×10⁻⁴).
|
24718684 |
2014 |
rs9636107
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Biological insights from 108 schizophrenia-associated genetic loci.
|
25056061 |
2014 |
rs9636107
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study of schizophrenia in Ashkenazi Jews.
|
26198764 |
2015 |
rs2958182
|
|
|
0.020 |
GeneticVariation |
BEFREE |
This study found that the A allele of the TCF4 rs2958182 polymorphism was the risk allele of schizophrenia, and was associated with lower cognitive performance in language in schizophrenia and delayed memory in controls.
|
26343600 |
2015 |
rs1452787
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Further interaction and stratification analysis suggested that rs1452787 was notably correlated with increased SCZ risk in males (OR = 2.77, 95%CI = 1.43-5.35, P = 0.002).
|
27103199 |
2016 |
rs7235757
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that the genotype "AG" of rs9320010 and "GA" of rs7235757 decreased SCZ risk (OR = 0.70, 95%</span>CI = 0.50-0.99, P = 0.041; OR = 0.69, 95%CI = 0.49-0.97, P = 0.034, respectively).
|
27103199 |
2016 |
rs9320010
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that the genotype "AG" of rs9320010 and "GA" of rs7235757 decreased SCZ</span> risk (OR = 0.70, 95%CI = 0.50-0.99, P = 0.041; OR = 0.69, 95%CI = 0.49-0.97, P = 0.034, respectively).
|
27103199 |
2016 |