|
rs9722
|
|
|
0.010 |
GeneticVariation |
BEFREE |
No association of the rs9722 C >T in the S100B gene and susceptibility to major depression in a Chinese population.
|
18939940 |
2008 |
|
rs6265
|
|
|
0.100 |
GeneticVariation |
BEFREE |
To conclude, we did not replicate the Val66Met effect on hippocampal volume in neither patients with major depression nor in healthy participants.
|
19668114 |
2009 |
|
rs6313
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Six polymorphisms in four genes related to the serotonin system, including the HTTLPR and HTTVNTR in the SLC6A4 gene, rs6295 in the HTR1A gene, rs11568817 and rs130058 in the HTR1B gene, and rs6313 in the HTR2A gene, were studied in 420 patients with MD to investigate the relationship between these genes and suicidal ideation in MD.
|
19897250 |
2009 |
|
rs759834365
|
|
|
0.100 |
GeneticVariation |
BEFREE |
To conclude, we did not replicate the Val66Met effect on hippocampal volume in neither patients with major depression nor in healthy participants.
|
19668114 |
2009 |
|
rs6295
|
|
|
0.050 |
GeneticVariation |
BEFREE |
Six polymorphisms in four genes related to the serotonin system, including the HTTLPR and HTTVNTR in the SLC6A4 gene, rs6295 in the HTR1A gene, rs11568817 and rs130058 in the HTR1B gene, and rs6313 in the HTR2A gene, were studied in 420 patients with MD to investigate the relationship between these genes and suicidal ideation in MD.
|
19897250 |
2009 |
|
rs2230912
|
|
|
0.040 |
GeneticVariation |
BEFREE |
A non-synonymous single nucleotide polymorphism, rs2230912 (P2RX7-E13A, G allele) and a microsatellite marker NBG6 were both previously found to be associated with bipolar disorder (P=0.00071 and 0.008, respectively). rs2230912 has also been found to show association with unipolar depression.
|
18268501 |
2009 |
|
rs2230912
|
|
|
0.040 |
GeneticVariation |
BEFREE |
We found no allelic or genotypic association between rs2230912 and BPI or Mdd-UP both in the national samples and in the combined European patient sample.
|
19330776 |
2009 |
|
rs11568817
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A haplotype association study suggested that the rs11568817-rs130058 haplotype of the HTR1B gene is significantly associated with suicidal ideation in MD.
|
19897250 |
2009 |
|
rs130058
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A haplotype association study suggested that the rs11568817-rs130058 haplotype of the HTR1B gene is significantly associated with suicidal ideation in MD.
|
19897250 |
2009 |
|
rs6691840
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In order to test whether the functional Ser310Ala polymorphism is involved in the development of specific personality traits, and thus to MD, we conducted the first association study on 195 selected healthy Italian individuals.
|
19221446 |
2009 |
|
rs772335034
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A non-synonymous single nucleotide polymorphism, rs2230912 (P2RX7-E13A, G allele) and a microsatellite marker NBG6 were both previously found to be associated with bipolar disorder (P=0.00071 and 0.008, respectively). rs2230912 has also been found to show association with unipolar depression.
|
18268501 |
2009 |
|
rs945032
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Remarkably, a functional SNP, rs945032, located in the promoter region of the bradykinin receptor B2 gene (BDKRB2) was associated to three disorders (panic disorder, substance abuse, and bipolar disorder), and two additional BDKRB2 SNPs to obsessive-compulsive disorder and major depression, providing evidence for common variants of susceptibility to several related psychiatric disorders.
|
19086053 |
2009 |
|
rs4680
|
|
|
0.100 |
GeneticVariation |
BEFREE |
This effect of rs4680 is similar to its observed influence on response to serotonergic and noradrenergic drug treatments in major depressive disorder.
|
19520435 |
2010 |
|
rs4680
|
|
|
0.100 |
GeneticVariation |
BEFREE |
In the present study, the effect of COMT val158met on response to electroconvulsive therapy (ECT) was analyzed in a sample of 104 Caucasian patients (f = 71, m = 33) with pharmacologically treatment-resistant Major Depression.
|
19309019 |
2010 |
|
rs6265
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Meta-analysis of the BDNF Val66Met polymorphism in major depressive disorder: effects of gender and ethnicity.
|
18852698 |
2010 |
|
rs6265
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Meta-analysis of BDNF Val66Met polymorphism association with treatment response in patients with major depressive disorder.
|
20167454 |
2010 |
|
rs6265
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Brain derived neurotrophic factor gene polymorphism (Val66Met) and short-term antidepressant response in major depressive disorder.
|
20674983 |
2010 |
|
rs759834365
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Brain derived neurotrophic factor gene polymorphism (Val66Met) and short-term antidepressant response in major depressive disorder.
|
20674983 |
2010 |
|
rs759834365
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Meta-analysis of the BDNF Val66Met polymorphism in major depressive disorder: effects of gender and ethnicity.
|
18852698 |
2010 |
|
rs759834365
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Meta-analysis of BDNF Val66Met polymorphism association with treatment response in patients with major depressive disorder.
|
20167454 |
2010 |
|
rs1006737
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Recent genetic studies found the A allele of the variant rs1006737 in the alpha 1C subunit of the L-type voltage-gated calcium channel (CACNA1C) gene to be overrepresented in patients suffering from bipolar disorder, schizophrenia or major depression.
|
19781653 |
2010 |
|
rs1006737
|
|
|
0.070 |
GeneticVariation |
BEFREE |
The single nucleotide polymorphisms FKBP5:rs1360780, BDNF:rs6265 (Val66Met), P2RX7:2230912 (Gln460Arg) and CACNA1C:rs1006737 were genotyped in DNA from 457 depression cases (major depression, dysthymia, and mixed anxiety depression) and 2286 healthy controls with no symptom of psychopathology.
|
20226536 |
2010 |
|
rs6311
|
|
|
0.050 |
GeneticVariation |
BEFREE |
No relationship found between -1438A/G polymorphism of the serotonin 2A receptor gene (rs6311) and major depression susceptibility in a northeastern Thai population.
|
20589614 |
2010 |
|
rs1049353
|
|
|
0.040 |
GeneticVariation |
BEFREE |
We assessed the CB1 receptor gene (CNR1) single nucleotide polymorphism (SNP) rs1049353 (1359 G/A) and the fatty acid amide hydrolase (FAAH) gene rs324420 SNP (cDNA 385C to A) for their associations with MD and/or BD in 83 Caucasian patients with recurrent MD, 134 Caucasian individuals with BD, and 117 Caucasian healthy subjects.
|
20080186 |
2010 |
|
rs2230912
|
|
|
0.040 |
GeneticVariation |
BEFREE |
The single nucleotide polymorphisms FKBP5:rs1360780, BDNF:rs6265 (Val66Met), P2RX7:2230912 (Gln460Arg) and CACNA1C:rs1006737 were genotyped in DNA from 457 depression cases (major depression, dysthymia, and mixed anxiety depression) and 2286 healthy controls with no symptom of psychopathology.
|
20226536 |
2010 |