non-European ancestry cohort
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| polygenic risk score | associated_with | non-European ancestry | — | 2 |
Mentioned in (17)
Papers in which this entity is mentioned.
- BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
- MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
- Alcohol Use Disorder Polygenic Score Compared With Family History and ADH1B. (2024)
- Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. (2024)
- Principles and methods for transferring polygenic risk scores across global populations. (2024)
- The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (2024)
- Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
- Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. (2024)
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Alcohol use polygenic risk score, social support, and alcohol use among European American and African American adults. (2023)
- Polygenic scoring accuracy varies across the genetic ancestry continuum. (2023)
- Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
- Parsing genetically influenced risk pathways: genetic loci impact problematic alcohol use via externalizing and specific risk. (2022)
- Sibling comparisons elucidate the associations between educational attainment polygenic scores and alcohol, nicotine and cannabis. (2020)
- Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019)
- A SNP panel for identification of DNA and RNA specimens. (2018)
- A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
Merged raw entities (9)
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 |
|---|---|---|---|
| non-european ancestry | cohort | 14 | 18 |
| non-european populations | cohort | 12 | 18 |
| non-european ancestry | phenotype | 6 | 6 |
| non-european | cohort | 3 | 5 |
| non-european ancestries | cohort | 3 | 4 |
| non-european cohorts | cohort | 2 | 2 |
| non-european individuals | cohort | 2 | 2 |
| individuals of non-european ancestry | cohort | 1 | 1 |
| non-europeans | cohort | 1 | 1 |