trios cohort
Evidence from:
primary |
all sources
Related entities (9)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| de novo variant | associated_with | trios | — | 1 |
| European ancestry | associated_with | trios | — | 1 |
| genomic DNA | associated_with | trios | — | 1 |
| population stratification | associated_with | trios | — | 1 |
| trios | associated_with | affected offspring | — | 1 |
| trios | associated_with | families | — | 1 |
| trios | associated_with | family relationships | — | 1 |
| trios | associated_with | probands | — | 1 |
| trios | associated_with | SNP | — | 1 |
Mentioned in (15)
Papers in which this entity is mentioned.
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- A saturated map of common genetic variants associated with human height. (2022)
- Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes. (2020)
- The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. (2019)
- Structural variant calling: the long and the short of it. (2019)
- SvABA: genome-wide detection of structural variants and indels by local assembly. (2018)
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
- A general approach for haplotype phasing across the full spectrum of relatedness. (2014)
- ACMG clinical laboratory standards for next-generation sequencing. (2013)
- Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (2013)
- cn.MOPS: mixture of Poissons for discovering copy number variations in next-generation sequencing data with a low false discovery rate. (2012)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
- 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 |
|---|---|---|---|
| trios | cohort | 9 | 11 |
| trio | cohort | 6 | 8 |
| trio cohort | cohort | 3 | 3 |