rare copy number variants variant
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| rare copy number variants | risk_factor_for | bipolar disorder | — | 1 |
| rare copy number variants | risk_factor_for | schizophrenia | — | 1 |
Mentioned in (4)
Papers in which this entity is mentioned.
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
- Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
- High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
- Expanding the range of ZNF804A variants conferring risk of psychosis. (2011)
Merged raw entities (1)
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 |
|---|---|---|---|
| rare copy number variants | variant | 4 | 4 |