inherited CNVs variant
Evidence from:
primary |
all sources
Related entities (5)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| inherited CNVs | associated_with | ASD | — | 1 |
| inherited CNVs | risk_factor_for | bipolar disorder | — | 1 |
| inherited CNVs | associated_with | epilepsy | — | 1 |
| inherited CNVs | associated_with | intellectual disability | — | 1 |
| inherited CNVs | risk_factor_for | SCZ | — | 1 |
Mentioned in (4)
Papers in which this entity is mentioned.
- Genetics and genomics of psychiatric disease. (2015)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
- BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. (2009)
Merged raw entities (2)
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 |
|---|---|---|---|
| inherited cnvs | variant | 4 | 4 |
| inherited copy number variations | variant | — | — |