rs893924483
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Mann-Whitney U, t-tests, and Fisher's exact tests were used to determine if APOE4, BDNF Val66Met, or COMT Val158Met are associated with increased psychiatric symptomatology in people with epilepsy.
|
30909076 |
2019 |
rs759834365
|
|
|
0.050 |
GeneticVariation |
BEFREE |
Mann-Whitney U, t-tests, and Fisher's exact tests were used to determine if APOE4, BDNF Val66Met, or COMT Val158Met are associated with increased psychiatric symptomatology in people with epilepsy.
|
30909076 |
2019 |
rs759834365
|
|
|
0.050 |
GeneticVariation |
BEFREE |
The Val66Met polymorphism in the BDNF gene is associated with epilepsy in fragile X syndrome.
|
19394799 |
2009 |
rs759834365
|
|
|
0.050 |
GeneticVariation |
BEFREE |
However, whether BDNF Val66Met polymorphism is associated with epilepsy remains controversial.
|
26000807 |
2016 |
rs759834365
|
|
|
0.050 |
GeneticVariation |
BEFREE |
Moreover, the Val66Met polymorphisms did not influence age of epilepsy onset, duration of epilepsy, control of seizures, or extension of the irritative zone.
|
19896331 |
2010 |
rs759834365
|
|
|
0.050 |
GeneticVariation |
BEFREE |
Predisposition to epilepsy in fragile X syndrome: does the Val66Met polymorphism in the BDNF gene play a role?
|
21890420 |
2011 |
rs7127507
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Results showed significant association between rs6265 T, rs7103411 C, and rs7127507 T and cryptgenic epilepsy risk (p = 0.00003, p = 0.0002, and p = 0.002, respectively) or between rs6265 and rs7103411 and symptomatic epilepsy risk in Malaysian Indians (TT vs. CC, p = 0.004 and T vs. C, p = 0.0002, respectively) as well as between rs6265 T and risk of cryptogenic epilepsy in Malaysian Chinese (p = 0.005).
|
25876511 |
2016 |
rs7103411
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Results showed significant association between rs6265 T, rs7103411 C, and rs7127507 T and cryptgenic epilepsy risk (p = 0.00003, p = 0.0002, and p = 0.002, respectively) or between rs6265 and rs7103411 and symptomatic epilepsy risk in Malaysian Indians (TT vs. CC, p = 0.004 and T vs. C, p = 0.0002, respectively) as well as between rs6265 T and risk of cryptogenic epilepsy in Malaysian Chinese (p = 0.005).
|
25876511 |
2016 |
rs6265
|
|
|
0.070 |
GeneticVariation |
BEFREE |
The Val66Met polymorphism in the BDNF gene is associated with epilepsy in fragile X syndrome.
|
19394799 |
2009 |
rs6265
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Results showed significant association between rs6265 T, rs7103411 C, and rs7127507 T and cryptgenic epilepsy</span> risk (p = 0.00003, p = 0.0002, and p = 0.002, respectively) or between rs6265 and rs7103411 and symptomatic epilepsy risk in Malaysian Indians (TT vs. CC, p = 0.004 and T vs. C, p = 0.0002, respectively) as well as between rs6265 T and risk of cryptogenic epilepsy in Malaysian Chinese (p = 0.005).
|
25876511 |
2016 |
rs6265
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Predisposition to epilepsy in fragile X syndrome: does the Val66Met polymorphism in the BDNF gene play a role?
|
21890420 |
2011 |
rs6265
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Our meta-analysis indicated that <i>BDNF</i> rs6265 G>A polymorphism might be involved in epilepsy susceptibility, especially in the Asian population.
|
29713173 |
2018 |
rs6265
|
|
|
0.070 |
GeneticVariation |
BEFREE |
However, whether BDNF Val66Met polymorphism is associated with epilepsy remains controversial.
|
26000807 |
2016 |
rs6265
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Moreover, the Val66Met polymorphisms did not influence age of epilepsy onset, duration of epilepsy, control of seizures, or extension of the irritative zone.
|
19896331 |
2010 |
rs6265
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Mann-Whitney U, t-tests, and Fisher's exact tests were used to determine if APOE4, BDNF Val66Met, or COMT Val158Met are associated with increased psychiatric symptomatology in people with epilepsy.
|
30909076 |
2019 |