ELK3, ETS transcription factor ELK3, 2004

N. diseases: 220; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.090 Biomarker disease BEFREE In support, recent ERP studies find that, following reward feedback, a larger reward positivity (RewP) is associated with greater vulnerability for bipolar spectrum disorders, whereas a smaller RewP is associated with greater vulnerability for depression. 30443957 2019
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.090 Biomarker disease BEFREE <b>Methods:</b> We compared ERP waveforms during the processing of emotional faces in a population sample of 58 6-11-year-olds who completed self-reported measures of trait and state anxiety and depression. 29515476 2018
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.090 Biomarker disease BEFREE The CFS over other methods leads to a good overall performance in most cases, especially when KNN classifier is used for P300 component classification, illustrating that ERP component may be applied as a tool for auxiliary diagnosis of depression. 30195425 2018
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.090 Biomarker disease BEFREE The reduced task-related ERP response in individuals with depression suggests significant impairments in these individuals in stimulus integration and response functions. 30366168 2018
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.090 Biomarker disease BEFREE Abnormalities of P300 before and after antidepressant treatment in depression: an ERP-sLORETA study. 29239976 2018
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.090 GeneticVariation disease BEFREE The NET and 5-HT1A polymorphisms appear to have similar effects on hippocampal volume in patients and controls while the 5-HTTLPR polymorphism differentially affects hippocampal volume in the presence of depression. 25990886 2015
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.090 GeneticVariation disease BEFREE In conclusion, our results favor the hypothesis that monoaminergic neurotransmission in general and the F528C NET and R219L 5-HT(1A) receptor variants in particular are involved in the pathogenesis of depression. 19105200 2009
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.090 GeneticVariation disease BEFREE Since NE signaling contributes to diverse brain functions, we hypothesize that promoter variation within the human NET gene (solute carrier family 6, member 2; SLC6A2) may impact risk for NE-related disorders, including depression, attention deficit hyperactive disorder (ADHD), and autonomic dysfunction. 18591486 2008
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.090 GeneticVariation disease BEFREE MPT analyses show significant associations of the norepinephrine transporter (NET, SLC6A2) -182 T/C (rs2242446) with recurrent depression [odds ratio, OR = 4.15 (1.91-9.02)], NET -3081 A/T (rs28386840) with increase in appetite [OR = 3.58 (1.53-8.39)] and the presynaptic choline transporter (CHT, SLC5A7) rs1013940" genes_norm="60482">Ile89Val (rs1013940) with HAM-D-17 total score {i.e. overall depression severity [OR = 2.74 (1.05-7.18)]}. 18081710 2008