|
rs1220000453
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found no association between CNTF null-mutation and BDNF C270T polymorphism to any depressive symptoms after exclusion of demented subjects.
|
16797081 |
2006 |
|
rs2606345
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Among Caucasian women, those with the CYP1A1 rs2606345 CC and AC genotypes had approximately 2-fold greater odds of having depressive symptoms than did those with the AA genotype (95% confidence intervals [CIs], 1.33 to 4.66 and 1.25 to 3.14, respectively).
|
16949393 |
2006 |
|
rs936306
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In Japanese women, the odds of depressive symptoms were nearly 5-fold higher among those with CYP 19 rs936306 TT genotype (95% CI, 1.10 to 22.17) than in women with the CC genotype and 9.6-fold higher (95% CI, 2.01 to 45.81) than in women with the CT genotype.
|
16949393 |
2006 |
|
rs6265
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The BDNF Val66Met polymorphism was examined in DNA samples from the mothers and daughters, and measures of depressive symptoms and rumination were also obtained.
|
17959306 |
2007 |
|
rs759834365
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The BDNF Val66Met polymorphism was examined in DNA samples from the mothers and daughters, and measures of depressive symptoms and rumination were also obtained.
|
17959306 |
2007 |
|
rs6313
|
|
|
0.040 |
GeneticVariation |
BEFREE |
Prediction of psychosis onset in Alzheimer disease: the role of depression symptom severity and the HTR2A T102C polymorphism.
|
17525976 |
2007 |
|
rs6313
|
|
|
0.040 |
GeneticVariation |
BEFREE |
Individuals carrying the T/T or T/C genotype of the T102C polymorphism of the HTR2A gene were responsive to the protective aspects of nurturing mothering, so that in the presence of high maternal nurturance, they expressed low levels of depressive symptoms, while this was not true with the carriers of the C/C genotype.
|
17339524 |
2007 |
|
rs6313
|
|
|
0.040 |
GeneticVariation |
BEFREE |
There was a significant gene-environment interaction, such that the urban residency was associated with low depressive symptoms in individuals carrying the T/T or T/C genotype of the T102C polymorphism, but not in those carrying the C/C genotype.
|
17510953 |
2007 |
|
rs6313
|
|
|
0.040 |
GeneticVariation |
BEFREE |
This study suggests a mechanism for the generation of different neuropsychiatric symptoms in AD from a single nucleotide polymorphism with reduced receptor binding in T102C 5-HT2A receptor gene homozygotes correlating with susceptibility to depressive symptoms, whereas the relative preservation of receptor binding in heterozygotes with AD correlating with susceptibility to hallucinations.
|
17481814 |
2007 |
|
rs1800497
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To examine the potential moderating role of DRD2 polymorphism (rs1800497) in the association between stressful life events and depressive symptoms among young adults.
|
17585060 |
2007 |
|
rs6265
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The BDNF Val(66)Met x 5-HTTLPR x child adversity interaction and depressive symptoms: An attempt at replication.
|
17579366 |
2008 |
|
rs759834365
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The BDNF Val(66)Met x 5-HTTLPR x child adversity interaction and depressive symptoms: An attempt at replication.
|
17579366 |
2008 |
|
rs2230912
|
|
|
0.020 |
GeneticVariation |
BEFREE |
After correcting for multiple testing, only the association of the P2RX7 Gln460Arg (rs2230912) polymorphism with depressive symptoms remained significant.
|
18801407 |
2008 |
|
rs699
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Angiotensinogen M235T polymorphism and symptoms of depression in a population-based study and a family-based study.
|
18628677 |
2008 |
|
rs6265
|
|
|
0.100 |
GeneticVariation |
BEFREE |
In addition, BDNF Val66Met and 5-HTTLPR polymorphisms seemed to moderate the effect of CSA on adult depressive symptoms.
|
19215635 |
2009 |
|
rs6265
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The low activity variants of the 5-HTT-linked polymorphic region in the serotonin transporter gene and the Met-allele of a single nucleotide polymorphism (Val66Met) in the gene encoding brain derived neurotrophic factor were independently associated with the presence of stressful life events prior to onset of depression, also when corrected for the effect of age, gender, marital status, personality disorder, neuroticism, and severity of depressive symptoms at the time of interview.
|
19339052 |
2009 |
|
rs759834365
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The low activity variants of the 5-HTT-linked polymorphic region in the serotonin transporter gene and the Met-allele of a single nucleotide polymorphism (Val66Met) in the gene encoding brain derived neurotrophic factor were independently associated with the presence of stressful life events prior to onset of depression, also when corrected for the effect of age, gender, marital status, personality disorder, neuroticism, and severity of depressive symptoms at the time of interview.
|
19339052 |
2009 |
|
rs759834365
|
|
|
0.100 |
GeneticVariation |
BEFREE |
In addition, BDNF Val66Met and 5-HTTLPR polymorphisms seemed to moderate the effect of CSA on adult depressive symptoms.
|
19215635 |
2009 |
|
rs25531
|
|
|
0.040 |
GeneticVariation |
BEFREE |
We found no evidence for an association between variants of 5-HTTLPR and rs25531 alleles, and depressive symptoms in Chinese PD patients.
|
19429111 |
2009 |
|
rs662
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The PON1 Q192R polymorphism was not associated with self-reported poor health {meta-analysis: odds ratio (OR) = 1.01 [confidence interval (CI) 0.91-1.13], P = 0.80} or depressive symptoms in either study or in meta-analyses [CES-D: OR = 1.01 (CI 0.87-1.17), P = 0.90].
|
19651761 |
2009 |
|
rs776943620
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The low activity variants of the 5-HTT-linked polymorphic region in the serotonin transporter gene and the Met-allele of a single nucleotide polymorphism (Val66Met) in the gene encoding brain derived neurotrophic factor were independently associated with the presence of stressful life events prior to onset of depression, also when corrected for the effect of age, gender, marital status, personality disorder, neuroticism, and severity of depressive symptoms at the time of interview.
|
19339052 |
2009 |
|
rs6265
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Eighty-two healthy adolescent girls were genotyped for the BDNF val66met polymorphism, and their depressive symptoms and physical activity were assessed using questionnaires.
|
20230085 |
2010 |
|
rs759834365
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Eighty-two healthy adolescent girls were genotyped for the BDNF val66met polymorphism, and their depressive symptoms and physical activity were assessed using questionnaires.
|
20230085 |
2010 |
|
rs4680
|
|
|
0.060 |
GeneticVariation |
BEFREE |
To examine the impact of the catechol-O-methyltransferase (COMT) val(158)met allele on depressive symptoms in young children exposed to early severe social deprivation as a result of being raised in institutions.
|
20403637 |
2010 |
|
rs1800795
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Epidemiologic analyses verified the health significance of those molecular interactions by documenting increased 10-year mortality risk associated with late-life depressive symptoms that occurred solely for homozygous carriers of the GATA1-sensitive G allele of rs1800795.
|
20176930 |
2010 |