disease status phenotype
Evidence from:
primary |
all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| ancestry | risk_factor_for | disease status | — | 1 |
| genetic liability | biomarker_for | disease status | — | 1 |
| study cohort | associated_with | disease status | — | 1 |
Mentioned in (24)
Papers in which this entity is mentioned.
- Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
- Large-scale collaboration in ENIGMA-EEG: A perspective on the meta-analytic approach to link neurological and psychiatric liability genes to electrophysiological brain activity. (2021)
- Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data. (2021)
- Detection and characterization of lung cancer using cell-free DNA fragmentomes. (2021)
- Polygenic risk scores: from research tools to clinical instruments. (2020)
- Tutorial: a guide to performing polygenic risk score analyses. (2020)
- Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
- Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data (2020)
- Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
- PDGFRA gene, maternal binge drinking and obstructive heart defects. (2018)
- Fragment Length of Circulating Tumor DNA. (2016)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- An introductory review of parallel independent component analysis (p-ICA) and a guide to applying p-ICA to genetic data and imaging phenotypes to identify disease-associated biological pathways and systems in common complex disorders. (2015)
- Guidelines for investigating causality of sequence variants in human disease. (2014)
- Dietary intake, nutrition, and fetal alcohol spectrum disorders in the Western Cape Province of South Africa. (2014)
- Within-subject template estimation for unbiased longitudinal image analysis. (2012)
- Detectable clonal mosaicism from birth to old age and its relationship to cancer. (2012)
- Gene set analysis of genome-wide association studies: methodological issues and perspectives. (2011)
- MicroRNA expression aberration as potential peripheral blood biomarkers for schizophrenia. (2011)
- Discovering genetic ancestry using spectral graph theory. (2010)
- The genetic interpretation of area under the ROC curve in genomic profiling. (2010)
- A hybrid design: case-parent triads supplemented by control-mother dyads. (2009)
- WGCNA: an R package for weighted correlation network analysis. (2008)
Merged raw entities (1)
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 |
|---|---|---|---|
| disease status | phenotype | 24 | 30 |