Simons Simplex Collection cohort
Evidence from:
primary |
all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| de novo variant | associated_with | Simons Simplex Collection | — | 1 |
| rare CNV | associated_with | Simons Simplex Collection | — | 1 |
| Simons Simplex Collection | associated_with | autism spectrum disorder | — | 1 |
Mentioned in (8)
Papers in which this entity is mentioned.
- De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
- Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype. (2019)
- Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
- Elevated polygenic burden for autism is associated with differential DNA methylation at birth. (2018)
- 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 (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 |
|---|---|---|---|
| simons simplex collection | cohort | 8 | 24 |