simplex families cohort
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| copy number variant | associated_with | simplex families | — | 1 |
| de novo variant | associated_with | simplex families | — | 1 |
Mentioned in (8)
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)
- Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
- Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019)
- Environmental factors influencing the risk of autism. (2017)
- Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism. (2016)
- Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
- 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 (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 |
|---|---|---|---|
| simplex families | cohort | 7 | 9 |
| simplex | cohort | 1 | 1 |
| simplex asd families | cohort | 1 | 2 |