SSC cohort
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| de novo variant | associated_with | SSC | — | 2 |
| probands | associated_with | SSC | — | 1 |
| SSC | associated_with | Tween-20 | — | 1 |
| TIC Genetics | associated_with | SSC | — | 1 |
Mentioned in (7)
Papers in which this entity is mentioned.
- Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder. (2021)
- De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
- Identification of common genetic risk variants for autism spectrum disorder. (2019)
- Case-control meta-analysis of blood DNA methylation and autism spectrum disorder. (2018)
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- Facial phenotypes in subgroups of prepubertal boys with autism spectrum disorders are correlated with clinical phenotypes. (2011)
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 |
|---|---|---|---|
| ssc | cohort | 7 | 33 |
| ssc control trios | cohort | 1 | 2 |
| ssc sample | cohort | — | — |