Search by:Disease = BD-MDD, Source = cross-disorder study, No. of Positive Studies for BD >= 1, No. of Positive Studies for MDD >= 1
Total unique gene count: 54
Note: For BD-MDD shared genes, genes from cross-disorder studies about BD-MDD or BD-SZ-MDD were considered from cross-disorder studies, genes from
intersection analysis of BDgene and MK4MDD were considered from candidate gene intersection analysis. Some repeated genes may be both
included in cross-disorder studies and the result of candidate gene intersection analysis.
Our finding that the deleted allele of 5-HTTLPR is significa.....
More
Our finding that the deleted allele of 5-HTTLPR is significantly less common in lithium-treated unipolar probands than in controls may reflect a genuine drug response effect of this polymorphism or may simply reflect sampling variance.
Less
There was a significant difference between patients with uni.....
More
There was a significant difference between patients with unipolar disorder and controls in the proportion of individuals carrying the STin2.9 allele.The findings support the hypothesis that allelic variation in the serotonin transporter gene may contribute to susceptibility for both major depression and bipolar disorder.
Less
These results suggest that the promoter allele 2 of 5-HTT, w.....
More
These results suggest that the promoter allele 2 of 5-HTT, which has previously been shown to result in lower levels of serotonin transporter transcription, may be associated with affective disorder risk.
Less
Thus, we conclude that the SERT VNTR polymorphism may be a r.....
More
Thus, we conclude that the SERT VNTR polymorphism may be a risk factor for both schizophrenia and unipolar depression, but not for bipolar disorder, in the Han Chinese.
Less
Our data suggest that this functional transporter polymorphi.....
More
Our data suggest that this functional transporter polymorphism does not seem to play a major role in the genetics of bipolar disorder and major depression in Brazilian patients.
Less
In summary, we found an association between the less active .....
More
In summary, we found an association between the less active form of polymorphism in the serotonin transporter gene and bipolar or unipolar affective illness.
Less
Given the fact that the positive association between BDNF ge.....
More
Given the fact that the positive association between BDNF gene Val66Met polymorphism and bipolar disorder has only been demonstrated for a Caucasian population but not for a Japanese analog or our Chinese sample, it appears likely that this association is ethnicity dependent.
Less
Our findings suggest that BDNF may be a susceptibility gene .....
More
Our findings suggest that BDNF may be a susceptibility gene for MDD and schizophrenia—in particular, in a subgroup of patients with schizophrenia with a lifetime history of depressive symptoms.
Less
No association emerged between MDD cases and control subject.....
More
No association emerged between MDD cases and control subjects.But an association was found between the high-activity COMT Val allele, particularly the COMT Val/Val genotype and EO-MDD.
Less
In conclusion, we partially replicated our previous findings.....
More
In conclusion, we partially replicated our previous findings confirming a possible influence of COMT variants in MD and BD, particularly in early onset subjects, though not with the same risk genotypes.
Less
Our results support the view that COMT variation provides a .....
More
Our results support the view that COMT variation provides a weak general predisposition to neuropsychiatric disease including psychotic and affective disorders.One SNP was marginally associated in the major depressive group.
Less
We conclude that genetic variation that determines high and .....
More
We conclude that genetic variation that determines high and low activities of COMT does not have a major effect on the vulnerability to affective disorders in our sample.
Less
Our results suggest that there is a significant association .....
More
Our results suggest that there is a significant association between the dopamine D4 receptor gene and mood disorders, especially major depression, but no association between the other polymorphisms and mood disorders.
Less
DAOA genetic polymorphisms (M15, M18 andM23) were not found .....
More
DAOA genetic polymorphisms (M15, M18 andM23) were not found to confer a statistically significant increased risk of SCZ, BD or DD in the overall sample, or in Caucasians and Asians following subgroup analysis.
Less
An increase of high-activity uMAOA alleles was found in majo.....
More
An increase of high-activity uMAOA alleles was found in major depression female patients presenting a seasonal pattern (X<sup>2</sup>=3.013, P-value = 0.05) or psychotic symptoms in their episodes (X<sup>2</sup>=2.679, P-value = 0.07).. Our results suggest that MAOA gene variation may modulate the expression of some clinical aspects of severe mood disorders, especially in females, and support the existence of a genetic and aetiologic heterogeneity underlying the diagnoses of bipolar disorder and major depression.
Less
Our results suggest that there is no association between MAO.....
More
Our results suggest that there is no association between MAOA-LPR genotype and susceptibility to recurrent major depression, bipolar disorder, and schizophrenia in our population.
Less
There was no significant genotypic or allelic association, s.....
More
There was no significant genotypic or allelic association, suggesting that the functional VNTR polymorphism in the MAOA gene is unlikely to play a major role in the pathogenesis of bipolar disorder or unipolar depression.
Less
The risk allele rs1006737 in this gene conferred increased r.....
More
The risk allele rs1006737 in this gene conferred increased risk for recurrent major depression (P= 0.013) with similar effect sizes to those previously observed in BD (allelic odds ratio B1.15).
Less
A weak association (chi2 = 3.946, 1 df, P = 0.047; odds rati.....
More
A weak association (chi2 = 3.946, 1 df, P = 0.047; odds ratio, allele 2 vs. allele 1 = 0.71 (95% CI, 0.51-0.996)) was observed in the unipolar sample with the TH-PstI polymorphism.Our data suggest that this locus should be examined in larger samples of unipolar affective disorder.
Less
Therefore, the hypothesis that the tyrosine hydroxylase and .....
More
Therefore, the hypothesis that the tyrosine hydroxylase and the dopamine D4 receptor genes may be involved in the etiology of bipolar disorder and unipolar recurrent major depression is not supported in our study.
Less
There was no significant difference in genotype distribution.....
More
There was no significant difference in genotype distributions or allele frequencies of the MTHFR 667C>T polymorphism between controls and any of the diagnostic groups.
Less
The genotype homozygous for the T677 allele was significantl.....
More
The genotype homozygous for the T677 allele was significantly frequently observed in schizophrenics with an odds ratio of 1.9 (P = 0.0006), and in patients with major depression with an odds ratio of 2.8 (P = 0.005). Our data suggest associations of the MTHFR gene variant with schizophrenia and depression in the Japanese.
Less
The meta-analysis results suggested that east Asians have a .....
More
The meta-analysis results suggested that east Asians have a greater genetic risk from the MTHFR gene in developing schizophrenia and depression, and that the genetic effects in bipolar disorder and depression are different. A further exploration of the involvement of the MTHFR gene in the susceptibility to schizophrenia and affective disorders, with a greater number of studies with larger sample sizes, however, are needed to fully establish the role of the MTHFR gene.
Less
For unipolar depression and the MTHFR C677T polymorphism, th.....
More
For unipolar depression and the MTHFR C677T polymorphism, the fixed-effects odds ratio for homozygote variants (TT) versus the wild type (CC) was 1.36 (95%confidence interval (CI): 1.11, 1.67), with no residual between-study heterogeneity (I<sup>2</sup>= 0%)—based on 1, 280 cases and 10, 429 controls. . These results were robust to various sensitively analyses. This meta-analysis demonstrates an association between the MTHFR C677T variant and depression, schizophrenia, and bipolar disorder, raising the possibility of the use of folate in treatment and prevention.
Less
The 1298C variant was significantly associated with both Bip.....
More
The 1298C variant was significantly associated with both Bip and MD arguing that variation in the MTHFR gene contributes to the genetic risk for affective psychoses.
Less
Our results suggest that homozygosity for the T677 allele of.....
More
Our results suggest that homozygosity for the T677 allele of the MTHFR gene is unlikely to play a major role in the pathogenesis of schizophrenia or affective disorders in our sample.
Less
Haplotype-based analysis of TPH2 in patients with UP and BP .....
More
Haplotype-based analysis of TPH2 in patients with UP and BP disorder and controls from northern Swedish descent provides preliminary evidence for protective association in both disorders and thus supports a central role for TPH2 in the pathogenesis of affective disorders.
Less
Therefore, the hypothesis that the tyrosine hydroxylase and .....
More
Therefore, the hypothesis that the tyrosine hydroxylase and the dopamine D4 receptor genes may be involved in the etiology of bipolar disorder and unipolar recurrent major depression is not supported in our study.
Less
Our results suggest that there is a significant association .....
More
Our results suggest that there is a significant association between the dopamine D4 receptor gene and mood disorders, especially major depression, but no association between the other polymorphisms and mood disorders.
Less
In the case-control analysis we did not find any significant.....
More
In the case-control analysis we did not find any significant differences between genotype frequencies of either BPD or MDD cases and controls. Our genetic association study supports the association between P2RX7 gene and severity of depressive symptoms in BPD patients.
Less
In conclusion, case-control analysis did not reveal signific.....
More
In conclusion, case-control analysis did not reveal significant results, but using a symptomseverity scale we could support the association between depressive disorder and the G-allele of the Gln460Arg polymorphism in the P2RX7 gene.
Less
When we compared the subset of bipolar cases diagnosed with .....
More
When we compared the subset of bipolar cases diagnosed with either ''manic episode with psychosis'' or/and ''major depressive disorder (MDD) with psychosis'' (N=36) against controls, we found an allelic association of rs3213207 (P1635) (P-value = 0.021, OR=2.053, 95%CI 1.103-3.82)and a haplotypic association of the same marker combination (rs16876571-rs2619539-rs3213207)(global P-value = 0.044) as in the total sample.
Less
In conclusion, our study supports the role of the WFS1 gene .....
More
In conclusion, our study supports the role of the WFS1 gene in susceptibility for MDD and BPD. By means of haplotype analysis we were able to define the GTA haplotype in the WFS1 gene related to an increased risk for mood disorders.
Less
In conclusion, we have found that both major depression and .....
More
In conclusion, we have found that both major depression and bipolar disorder are associated with HT2CR ser23 allele carrier status and that this effect is demonstrable over and above considerable inter-population variability in the frequency of this allele.
Less
ln the view of these observations, our data could be explain.....
More
ln the view of these observations, our data could be explained by assuming that allele 4 of the GABRA5 gene polymorphism confers a higher risk to UPR major depression but not necessarily to BPI disorder which combines major depression with manic episodes.
Less
The distribution of allelic frequencies of the GABRA5 locus .....
More
The distribution of allelic frequencies of the GABRA5 locus differed significantly between BP patients and controls with the 282-bp allele found to be associated with BP affective disorder, while no such difference was observed between the groups of UP patients and controls nor between the two patient groups.
Less
A significant predictive value of specific interactions betw.....
More
A significant predictive value of specific interactions between genotypes located in the investigated genes was found. We then report preliminary evidence that the epistasis between trace amine receptor 6 and heat shock protein 70 variations may compose a risk profile for major mood disorders.
Less
Our main finding is an association of FKBP5 polymorphisms (r.....
More
Our main finding is an association of FKBP5 polymorphisms (rs1360780, rs9470080, rs4713916, rs9296158 and rs9394309) with major depression but nor with bipolar disorder.
Less
The D allele was significantly more frequent in the patients.....
More
The D allele was significantly more frequent in the patients with major depression than in the controls, and the DD genotype was significantly more frequent in the patients with major depression than in the controls.
Less
Polymorphisms of CRHR1 and AVPR1b may modify susceptibility .....
More
Polymorphisms of CRHR1 and AVPR1b may modify susceptibility to mood disorders. Gene-gene interaction analysis revealed a significant epistatic interaction between AVPR1b and CRHR1 genes in susceptibility to MDD.
Less
Polymorphisms of CRHR1 and AVPR1b may modify susceptibility .....
More
Polymorphisms of CRHR1 and AVPR1b may modify susceptibility to mood disorders. Gene-gene interaction analysis revealed a significant epistatic interaction between AVPR1b and CRHR1 genes in susceptibility to MDD.
Less
Results from this expanded meta-analysis, which included our.....
More
Results from this expanded meta-analysis, which included our own new study, suggest that rs6295 (C-1019G) and rs878567 in HTR1A are related to the pathophysiology of MDs, with overlap between MDD and BP. Findings provide additional clues to the underlying biology and treatment targets in MDs.
Less
A significant predictive value of specific interactions betw.....
More
A significant predictive value of specific interactions between genotypes located in the investigated genes was found. We then report preliminary evidence that the epistasis between trace amine receptor 6 and heat shock protein 70 variations may compose a risk profile for major mood disorders.
Less
The frequency of all rare variants combined was greater than.....
More
The frequency of all rare variants combined was greater than controls in schizophrenia (OR=1.93, P-value = 0.0057) and bipolar disorder (OR=2.71, P-value = 0.00007).These data identify a candidate gene, highlight the genetic overlap between schizophrenia, bipolar disorder, and depression, and suggest that rare coding variants may contribute significantly to risk of these disorders.
Less
Our results suggest that shared common risk factors for schi.....
More
Our results suggest that shared common risk factors for schizophrenia, major depressive disorder and bipolar disorder exist in the CTLA-4 gene in the Chinese Han population.
Less
These findings indicate that common variations in the BCL9 g.....
More
These findings indicate that common variations in the BCL9 gene confer risk of schizophrenia and may also be associated with bipolar disorder and major depressive disorder in the Chinese Han population.
Less
TDT <sub>linkage</sub> P-value = 0.011, RR (95% .....
More
TDT <sub>linkage</sub> P-value = 0.011, RR (95% CI)=2.1(1.2-3.8) in NIMH study; TDT <sub>linkage</sub> P-value = 0.629, RR (95% CI)=1.1(0.5-2.6) in pittsburgh study. Combined TDT <sub>linkage</sub> P-value = 0.066, RR (95% CI)=1.3(0.7-2.6). We detected a significant linkage disequilibrium (LD) indicated by preferential maternal transmission of the GluR7 S310 allele to R-MDD patients. We performed a second independent study by applying the TDT in 81 parent-offspring triads from families that inherit recurrent early-onset major depressive disorder (RE-MDD). The results from this second study showed only a suggestive maternal association
Less
Our finding that the deleted allele of 5-HTTLPR is significa.....
More
Our finding that the deleted allele of 5-HTTLPR is significantly less common in lithium-treated unipolar probands than in controls may reflect a genuine drug response effect of this polymorphism or may simply reflect sampling variance.
Less
There was a significant difference between patients with uni.....
More
There was a significant difference between patients with unipolar disorder and controls in the proportion of individuals carrying the STin2.9 allele.The findings support the hypothesis that allelic variation in the serotonin transporter gene may contribute to susceptibility for both major depression and bipolar disorder.
Less
These results suggest that the promoter allele 2 of 5-HTT, w.....
More
These results suggest that the promoter allele 2 of 5-HTT, which has previously been shown to result in lower levels of serotonin transporter transcription, may be associated with affective disorder risk.
Less
Thus, we conclude that the SERT VNTR polymorphism may be a r.....
More
Thus, we conclude that the SERT VNTR polymorphism may be a risk factor for both schizophrenia and unipolar depression, but not for bipolar disorder, in the Han Chinese.
Less
Our data suggest that this functional transporter polymorphi.....
More
Our data suggest that this functional transporter polymorphism does not seem to play a major role in the genetics of bipolar disorder and major depression in Brazilian patients.
Less
In summary, we found an association between the less active .....
More
In summary, we found an association between the less active form of polymorphism in the serotonin transporter gene and bipolar or unipolar affective illness.
Less
Given the fact that the positive association between BDNF ge.....
More
Given the fact that the positive association between BDNF gene Val66Met polymorphism and bipolar disorder has only been demonstrated for a Caucasian population but not for a Japanese analog or our Chinese sample, it appears likely that this association is ethnicity dependent.
Less
Our findings suggest that BDNF may be a susceptibility gene .....
More
Our findings suggest that BDNF may be a susceptibility gene for MDD and schizophrenia—in particular, in a subgroup of patients with schizophrenia with a lifetime history of depressive symptoms.
Less
No association emerged between MDD cases and control subject.....
More
No association emerged between MDD cases and control subjects.But an association was found between the high-activity COMT Val allele, particularly the COMT Val/Val genotype and EO-MDD.
Less
In conclusion, we partially replicated our previous findings.....
More
In conclusion, we partially replicated our previous findings confirming a possible influence of COMT variants in MD and BD, particularly in early onset subjects, though not with the same risk genotypes.
Less
Our results support the view that COMT variation provides a .....
More
Our results support the view that COMT variation provides a weak general predisposition to neuropsychiatric disease including psychotic and affective disorders.One SNP was marginally associated in the major depressive group.
Less
We conclude that genetic variation that determines high and .....
More
We conclude that genetic variation that determines high and low activities of COMT does not have a major effect on the vulnerability to affective disorders in our sample.
Less
Our results suggest that there is a significant association .....
More
Our results suggest that there is a significant association between the dopamine D4 receptor gene and mood disorders, especially major depression, but no association between the other polymorphisms and mood disorders.
Less
DAOA genetic polymorphisms (M15, M18 andM23) were not found .....
More
DAOA genetic polymorphisms (M15, M18 andM23) were not found to confer a statistically significant increased risk of SCZ, BD or DD in the overall sample, or in Caucasians and Asians following subgroup analysis.
Less
An increase of high-activity uMAOA alleles was found in majo.....
More
An increase of high-activity uMAOA alleles was found in major depression female patients presenting a seasonal pattern (X<sup>2</sup>=3.013, P-value = 0.05) or psychotic symptoms in their episodes (X<sup>2</sup>=2.679, P-value = 0.07).. Our results suggest that MAOA gene variation may modulate the expression of some clinical aspects of severe mood disorders, especially in females, and support the existence of a genetic and aetiologic heterogeneity underlying the diagnoses of bipolar disorder and major depression.
Less
Our results suggest that there is no association between MAO.....
More
Our results suggest that there is no association between MAOA-LPR genotype and susceptibility to recurrent major depression, bipolar disorder, and schizophrenia in our population.
Less
There was no significant genotypic or allelic association, s.....
More
There was no significant genotypic or allelic association, suggesting that the functional VNTR polymorphism in the MAOA gene is unlikely to play a major role in the pathogenesis of bipolar disorder or unipolar depression.
Less
There was no significant difference in genotype distribution.....
More
There was no significant difference in genotype distributions or allele frequencies of the MTHFR 667C>T polymorphism between controls and any of the diagnostic groups.
Less
The genotype homozygous for the T677 allele was significantl.....
More
The genotype homozygous for the T677 allele was significantly frequently observed in schizophrenics with an odds ratio of 1.9 (P = 0.0006), and in patients with major depression with an odds ratio of 2.8 (P = 0.005). Our data suggest associations of the MTHFR gene variant with schizophrenia and depression in the Japanese.
Less
The meta-analysis results suggested that east Asians have a .....
More
The meta-analysis results suggested that east Asians have a greater genetic risk from the MTHFR gene in developing schizophrenia and depression, and that the genetic effects in bipolar disorder and depression are different. A further exploration of the involvement of the MTHFR gene in the susceptibility to schizophrenia and affective disorders, with a greater number of studies with larger sample sizes, however, are needed to fully establish the role of the MTHFR gene.
Less
For unipolar depression and the MTHFR C677T polymorphism, th.....
More
For unipolar depression and the MTHFR C677T polymorphism, the fixed-effects odds ratio for homozygote variants (TT) versus the wild type (CC) was 1.36 (95%confidence interval (CI): 1.11, 1.67), with no residual between-study heterogeneity (I<sup>2</sup>= 0%)—based on 1, 280 cases and 10, 429 controls. . These results were robust to various sensitively analyses. This meta-analysis demonstrates an association between the MTHFR C677T variant and depression, schizophrenia, and bipolar disorder, raising the possibility of the use of folate in treatment and prevention.
Less
The 1298C variant was significantly associated with both Bip.....
More
The 1298C variant was significantly associated with both Bip and MD arguing that variation in the MTHFR gene contributes to the genetic risk for affective psychoses.
Less
Our results suggest that homozygosity for the T677 allele of.....
More
Our results suggest that homozygosity for the T677 allele of the MTHFR gene is unlikely to play a major role in the pathogenesis of schizophrenia or affective disorders in our sample.
Less
Haplotype-based analysis of TPH2 in patients with UP and BP .....
More
Haplotype-based analysis of TPH2 in patients with UP and BP disorder and controls from northern Swedish descent provides preliminary evidence for protective association in both disorders and thus supports a central role for TPH2 in the pathogenesis of affective disorders.
Less
Therefore, the hypothesis that the tyrosine hydroxylase and .....
More
Therefore, the hypothesis that the tyrosine hydroxylase and the dopamine D4 receptor genes may be involved in the etiology of bipolar disorder and unipolar recurrent major depression is not supported in our study.
Less
Our results suggest that there is a significant association .....
More
Our results suggest that there is a significant association between the dopamine D4 receptor gene and mood disorders, especially major depression, but no association between the other polymorphisms and mood disorders.
Less
In the case-control analysis we did not find any significant.....
More
In the case-control analysis we did not find any significant differences between genotype frequencies of either BPD or MDD cases and controls. Our genetic association study supports the association between P2RX7 gene and severity of depressive symptoms in BPD patients.
Less
In conclusion, case-control analysis did not reveal signific.....
More
In conclusion, case-control analysis did not reveal significant results, but using a symptomseverity scale we could support the association between depressive disorder and the G-allele of the Gln460Arg polymorphism in the P2RX7 gene.
Less
When we compared the subset of bipolar cases diagnosed with .....
More
When we compared the subset of bipolar cases diagnosed with either ''manic episode with psychosis'' or/and ''major depressive disorder (MDD) with psychosis'' (N=36) against controls, we found an allelic association of rs3213207 (P1635) (P-value = 0.021, OR=2.053, 95%CI 1.103-3.82)and a haplotypic association of the same marker combination (rs16876571-rs2619539-rs3213207)(global P-value = 0.044) as in the total sample.
Less
In conclusion, our study supports the role of the WFS1 gene .....
More
In conclusion, our study supports the role of the WFS1 gene in susceptibility for MDD and BPD. By means of haplotype analysis we were able to define the GTA haplotype in the WFS1 gene related to an increased risk for mood disorders.
Less
In conclusion, we have found that both major depression and .....
More
In conclusion, we have found that both major depression and bipolar disorder are associated with HT2CR ser23 allele carrier status and that this effect is demonstrable over and above considerable inter-population variability in the frequency of this allele.
Less
ln the view of these observations, our data could be explain.....
More
ln the view of these observations, our data could be explained by assuming that allele 4 of the GABRA5 gene polymorphism confers a higher risk to UPR major depression but not necessarily to BPI disorder which combines major depression with manic episodes.
Less
The distribution of allelic frequencies of the GABRA5 locus .....
More
The distribution of allelic frequencies of the GABRA5 locus differed significantly between BP patients and controls with the 282-bp allele found to be associated with BP affective disorder, while no such difference was observed between the groups of UP patients and controls nor between the two patient groups.
Less
Our main finding is an association of FKBP5 polymorphisms (r.....
More
Our main finding is an association of FKBP5 polymorphisms (rs1360780, rs9470080, rs4713916, rs9296158 and rs9394309) with major depression but nor with bipolar disorder.
Less
The D allele was significantly more frequent in the patients.....
More
The D allele was significantly more frequent in the patients with major depression than in the controls, and the DD genotype was significantly more frequent in the patients with major depression than in the controls.
Less
Polymorphisms of CRHR1 and AVPR1b may modify susceptibility .....
More
Polymorphisms of CRHR1 and AVPR1b may modify susceptibility to mood disorders. Gene-gene interaction analysis revealed a significant epistatic interaction between AVPR1b and CRHR1 genes in susceptibility to MDD.
Less
Polymorphisms of CRHR1 and AVPR1b may modify susceptibility .....
More
Polymorphisms of CRHR1 and AVPR1b may modify susceptibility to mood disorders. Gene-gene interaction analysis revealed a significant epistatic interaction between AVPR1b and CRHR1 genes in susceptibility to MDD.
Less
Results from this expanded meta-analysis, which included our.....
More
Results from this expanded meta-analysis, which included our own new study, suggest that rs6295 (C-1019G) and rs878567 in HTR1A are related to the pathophysiology of MDs, with overlap between MDD and BP. Findings provide additional clues to the underlying biology and treatment targets in MDs.
Less
Our results suggest that shared common risk factors for schi.....
More
Our results suggest that shared common risk factors for schizophrenia, major depressive disorder and bipolar disorder exist in the CTLA-4 gene in the Chinese Han population.
Less
TDT <sub>linkage</sub> P-value = 0.011, RR (95% .....
More
TDT <sub>linkage</sub> P-value = 0.011, RR (95% CI)=2.1(1.2-3.8) in NIMH study; TDT <sub>linkage</sub> P-value = 0.629, RR (95% CI)=1.1(0.5-2.6) in pittsburgh study. Combined TDT <sub>linkage</sub> P-value = 0.066, RR (95% CI)=1.3(0.7-2.6). We detected a significant linkage disequilibrium (LD) indicated by preferential maternal transmission of the GluR7 S310 allele to R-MDD patients. We performed a second independent study by applying the TDT in 81 parent-offspring triads from families that inherit recurrent early-onset major depressive disorder (RE-MDD). The results from this second study showed only a suggestive maternal association
Less