recurrent major depressive disorder phenotype
Evidence from:
primary |
all sources
Related entities (24)
Mentioned in (13)
Papers in which this entity is mentioned.
- The landscape of drug sensitivity and resistance in sarcoma. (2024)
- Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. (2023)
- ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. (2020)
- Brain Volume Abnormalities in Youth at High Risk for Depression: Adolescent Brain and Cognitive Development Study. (2020)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
- Time-varying effects of income on hippocampal volume trajectories in adolescent girls. (2018)
- 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. (2014)
- The impact of environmental factors in severe psychiatric disorders. (2014)
- A mega-analysis of genome-wide association studies for major depressive disorder. (2013)
- Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. (2011)
- The neuronal transporter gene SLC6A15 confers risk to major depression. (2011)
- Elevated inflammation levels in depressed adults with a history of childhood maltreatment. (2008)
- Amygdala volume in major depressive disorder: a meta-analysis of magnetic resonance imaging studies. (2008)
Merged raw entities (5)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| recurrent depression | phenotype | 6 | 22 |
| recurrent major depressive disorder | phenotype | 4 | 14 |
| recurrent mdd | phenotype | 4 | 5 |
| recurrent | phenotype | 1 | 1 |
| rmdd | phenotype | 1 | 8 |