All of Us Research Program cohort
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Mentioned in (12)
Papers in which this entity is mentioned.
- Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. (2026)
- Genome-wide association testing beyond SNPs. (2025)
- A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2025)
- Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (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)
- A harmonized public resource of deeply sequenced diverse human genomes. (2024)
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Variant interpretation using population databases: Lessons from gnomAD. (2022)
- The Data Use Ontology to streamline responsible access to human biomedical datasets. (2021)
Merged raw entities (2)
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 |
|---|---|---|---|
| all of us research program | cohort | 11 | 21 |
| all of us | cohort | 7 | 17 |