Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 288
Gene Symbol: ANK3
ANK3
0.700 GeneticVariation disease BEFREE Variants in the ANK3 gene encoding ankyrin-G are associated with neurodevelopmental disorders, including intellectual disability, autism, schizophrenia, and bipolar disorder. 31813652 2020
Entrez Id: 775
Gene Symbol: CACNA1C
CACNA1C
0.700 GeneticVariation disease BEFREE Our findings suggest a role of rs1034936 CACNA1C gene variant in BD-AA group. 31634677 2020
Entrez Id: 5649
Gene Symbol: RELN
RELN
0.570 AlteredExpression disease BEFREE Prefrontal fatty acid composition in schizophrenia and bipolar disorder: Association with reelin expression. 28583708 2020
Entrez Id: 91752
Gene Symbol: ZNF804A
ZNF804A
0.500 GeneticVariation disease BEFREE In model 2, ZNF804A rs1344706 was significantly associated with BD; however, this association did not predict diagnosis when entered into the weighted model. 31727397 2020
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.400 AlteredExpression disease BEFREE This task was used to delineate systems-level neural deficits in BD contributing to inattentive performance in human subjects with BD as well as mouse models with either parietal cortex (PC) lesions or reduced dopamine transporter (DAT) expression. 31025493 2020
Entrez Id: 7124
Gene Symbol: TNF
TNF
0.400 Biomarker disease BEFREE A search strategy was developed using the terms: "Mood disorder" OR "Depressive Disorder" OR "Bipolar disorder" AND "Infliximab" OR "tumor necrosis factor antagonist" as text words and Medical Subject Headings (i.e., MeSH and EMTREE). 31837338 2020
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
0.390 AlteredExpression disease BEFREE Using mature miRNA profiling and quantitative real-time PCR (qRT-PCR) in the orbitofrontal cortex (OFC) of SCZ (N = 29; 20 male and 9 female), BD (N = 26; 12 male and 14 female), and unaffected control (N = 25; 21 male and 4 female) subjects, we uncovered that miR-223, an exosome-secreted miRNA that targets glutamate receptors, was increased at the mature miRNA level in the OFC of SCZ and BD patients with positive history of psychosis at the time of death and was inversely associated with deficits in the expression of its targets glutamate ionotropic receptor NMDA-type subunit 2B (GRIN2B) and glutamate ionotropic receptor AMPA-type subunit 2 (GRIA2). 31775160 2020
Entrez Id: 207
Gene Symbol: AKT1
AKT1
0.390 Biomarker disease BEFREE We conclude AKT1 is less likely to be a vulnerability gene in BD. 31810747 2020
Entrez Id: 2891
Gene Symbol: GRIA2
GRIA2
0.320 AlteredExpression disease BEFREE Using mature miRNA profiling and quantitative real-time PCR (qRT-PCR) in the orbitofrontal cortex (OFC) of SCZ (N = 29; 20 male and 9 female), BD (N = 26; 12 male and 14 female), and unaffected control (N = 25; 21 male and 4 female) subjects, we uncovered that miR-223, an exosome-secreted miRNA that targets glutamate receptors, was increased at the mature miRNA level in the OFC of SCZ and BD patients with positive history of psychosis at the time of death and was inversely associated with deficits in the expression of its targets glutamate ionotropic receptor NMDA-type subunit 2B (GRIN2B) and glutamate ionotropic receptor AMPA-type subunit 2 (GRIA2). 31775160 2020
Entrez Id: 266727
Gene Symbol: MDGA1
MDGA1
0.320 Biomarker disease BEFREE MDGA1 (MAM domain-containing glycosylphosphatidylinositol anchor) has recently been linked to schizophrenia and bipolar disorder. 31812551 2020
Entrez Id: 1769
Gene Symbol: DNAH8
DNAH8
0.310 Biomarker disease BEFREE Interestingly, SERCA-mediated Ca<sup>2+</sup> dyshomeostasis has been associated with neuropathological conditions, such as bipolar disorder, schizophrenia, Parkinson's disease and Alzheimer's disease. 31646509 2020
Entrez Id: 431708
Gene Symbol: MDD1
MDD1
0.030 Biomarker disease BEFREE OCD prevalence in BD was not significantly different than in MDD. 31818777 2020
Entrez Id: 5225
Gene Symbol: PGC
PGC
0.020 GeneticVariation disease BEFREE Our objectives were: (i) to test the ability of polygenic risk scores (PRS) derived from the latest PGC ADHD-GWAS (Demontis et al., 2019) to predict the presence of cADHD in BP patients; (ii) to examine the hypothesis that BP preceded by cADHD is a BP subtype with particular clinical traits and (iii) partially shares its molecular basis with ADHD. 31791676 2020
Entrez Id: 3693
Gene Symbol: ITGB5
ITGB5
0.010 GeneticVariation disease BEFREE We found a significant overexpression of the gene ITGB5 at 3q25 in SZ and BD after multiple testing p value adjustment. 31695175 2020
Entrez Id: 283
Gene Symbol: ANG
ANG
0.010 Biomarker disease BEFREE By comparing the differences between the three groups, we obtained the following results: (1) both the BD and MDD patients showed shared weaker intra-network FC in the left mPFC and right precuneus within the DMN as well as weaker inter-ROI FC between the left AI and right AI compared with the healthy controls; (2) the BD had weaker while the MDD had stronger intra-network FC in the right dlPFC within the rCEN as well as stronger inter-ROI FC between the right dlPFC and right ANG compared with the healthy controls; (3) the BD showed specific, stronger inter-ROI FC between the left PPC and right AI as well as stronger inter-network FC between the lCEN and SN compared with either the MDD or the control group. 30382529 2020
Entrez Id: 163782
Gene Symbol: KANK4
KANK4
0.010 GeneticVariation disease BEFREE A linkage and exome study implicates rare variants of KANK4 and CAP2 in bipolar disorder in a multiplex family. 31400178 2020
Entrez Id: 5640
Gene Symbol: PRS
PRS
0.010 Biomarker disease BEFREE An interaction between BD-PRS and childhood maltreatment was observed for the risk of rapid cycling (P = .01). 31628696 2020
Entrez Id: 6445
Gene Symbol: SGCG
SGCG
0.010 Biomarker disease BEFREE MDGA1 (MAM domain-containing glycosylphosphatidylinositol anchor) has recently been linked to schizophrenia and bipolar disorder. 31812551 2020
Entrez Id: 10486
Gene Symbol: CAP2
CAP2
0.010 GeneticVariation disease BEFREE A linkage and exome study implicates rare variants of KANK4 and CAP2 in bipolar disorder in a multiplex family. 31400178 2020
Entrez Id: 407008
Gene Symbol: MIR223
MIR223
0.010 Biomarker disease BEFREE Using mature miRNA profiling and quantitative real-time PCR (qRT-PCR) in the orbitofrontal cortex (OFC) of SCZ (N = 29; 20 male and 9 female), BD (N = 26; 12 male and 14 female), and unaffected control (N = 25; 21 male and 4 female) subjects, we uncovered that miR-223, an exosome-secreted miRNA that targets glutamate receptors, was increased at the mature miRNA level in the OFC of SCZ and BD patients with positive history of psychosis at the time of death and was inversely associated with deficits in the expression of its targets glutamate ionotropic receptor NMDA-type subunit 2B (GRIN2B) and glutamate ionotropic receptor AMPA-type subunit 2 (GRIA2). 31775160 2020
Entrez Id: 5176
Gene Symbol: SERPINF1
SERPINF1
0.010 AlteredExpression disease BEFREE PEDF levels were especially lower in MDD patients than in HCs and patients with bipolar disorder (BD) and schizophrenia (SCZ), and elevated PEDF were consistent with decreased HAM-D scores in patients given antidepressant therapy (ADT). 31676463 2020
Entrez Id: 775
Gene Symbol: CACNA1C
CACNA1C
0.700 Biomarker disease CTD_human Genome-wide association study identifies 30 loci associated with bipolar disorder. 31043756 2019
Entrez Id: 775
Gene Symbol: CACNA1C
CACNA1C
0.700 GeneticVariation disease BEFREE Genome-wide association studies have suggested that allelic variations in the CACNA1C gene confer susceptibility to schizophrenia and bipolar disorder only in women. 30124797 2019
Entrez Id: 1312
Gene Symbol: COMT
COMT
0.700 GeneticVariation disease BEFREE These findings seem to indicate a role of COMT polymorphisms in regulating cognitive functioning in patients with BD. 30146088 2019
Entrez Id: 775
Gene Symbol: CACNA1C
CACNA1C
0.700 GeneticVariation disease BEFREE The CACNA1C polymorphism rs1006737 is associated with the mean thickness of cortical brain areas that have been shown to be altered in bipolar disorder. 31829002 2019