complex diseases phenotype
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Mentioned in (20)
Papers in which this entity is mentioned.
- Associations between common genetic variants and income provide insights about the socio-economic health gradient. (2025)
- Genome-wide association testing beyond SNPs. (2025)
- Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
- Principles and methods for transferring polygenic risk scores across global populations. (2024)
- Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
- Single-cell RNA sequencing of peripheral blood links cell-type-specific regulation of splicing to autoimmune and inflammatory diseases. (2024)
- Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
- Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
- The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
- Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
- Designing combination therapies with modeling chaperoned machine learning. (2019)
- The impact of structural variation on human gene expression. (2017)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- HLAreporter: a tool for HLA typing from next generation sequencing data. (2015)
- Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
- Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate. (2013)
- DELLY: structural variant discovery by integrated paired-end and split-read analysis. (2012)
- An integrated encyclopedia of DNA elements in the human genome. (2012)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data. (2011)
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 |
|---|---|---|---|
| complex diseases | phenotype | 28 | 35 |
| complex disease | phenotype | 22 | 32 |
| common diseases | phenotype | 19 | 23 |
| common disease | phenotype | 9 | 10 |
| common complex disease | phenotype | 3 | 3 |
| common complex diseases | phenotype | 3 | 3 |
| complex human diseases | phenotype | 3 | 3 |
| common variant common disease scenario | phenotype | — | — |
| complex disease liability loci | phenotype | — | — |