AGRE cohort
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| AGRE | associated_with | autism | — | 1 |
Mentioned in (6)
Papers in which this entity is mentioned.
- Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
- Identification of common genetic risk variants for autism spectrum disorder. (2019)
- Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. (2012)
- Plasma cytokine levels in children with autistic disorder and unrelated siblings. (2012)
- A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. (2009)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
Merged raw entities (3)
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 |
|---|---|---|---|
| agre | cohort | 6 | 13 |
| autism genetic resource exchange | cohort | 3 | 5 |
| agre collection | cohort | 1 | 2 |