Autism Genome Project cohort
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| Autism Genome Project | associated_with | copy number variant | — | 1 |
| Autism Genome Project | associated_with | rare CNVs | — | 1 |
Mentioned in (4)
Papers in which this entity is mentioned.
- Identification of common genetic risk variants for autism spectrum disorder. (2019)
- Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism. (2016)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
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 |
|---|---|---|---|
| autism genome project | cohort | 3 | 4 |
| agp | cohort | 1 | 1 |