combined cohort cohort
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| de novo variant | associated_with | combined cohort | — | 1 |
| SNP | associated_with | combined cohort | — | 1 |
Mentioned in (14)
Papers in which this entity is mentioned.
- Genome-wide association testing beyond SNPs. (2025)
- Osteoclasts in Osteosarcoma: Mechanisms, Interactions, and Therapeutic Prospects. (2023)
- Copy number signatures and mutational processes in ovarian carcinoma. (2018)
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
- How effective are brief interventions in reducing alcohol consumption: do the setting, practitioner group and content matter? Findings from a systematic review and metaregression analysis. (2016)
- A global reference for human genetic variation. (2015)
- Experiences with workflows for automating data-intensive bioinformatics. (2015)
- A global reference for human genetic variation. (2015)
- Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
- Recurrent somatic structural variations contribute to tumorigenesis in pediatric osteosarcoma. (2014)
- Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
- Association of CHRNA4 polymorphisms with smoking behavior in two populations. (2011)
- Investigation of the Dynamic Gait Index in children: a pilot study. (2011)
- Can we identify genes for alcohol consumption in samples ascertained for heterogeneous purposes? (2009)
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 |
|---|---|---|---|
| combined cohort | cohort | 9 | 10 |
| phase 3 | cohort | 5 | 7 |
| combined samples | cohort | 1 | 1 |