individuals cohort
Evidence from:
primary |
all sources
Related entities (5)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| individuals | associated_with | damaging variants | — | 1 |
| individuals | associated_with | de novo variant | — | 1 |
| individuals | associated_with | families | — | 1 |
| individuals | associated_with | missense variants | — | 1 |
| individuals | associated_with | rare variant | — | 1 |
Mentioned in (23)
Papers in which this entity is mentioned.
- Cell-Free DNA Fragmentomics: The Novel Promising Biomarker. (2023)
- Factors associated with phosphatidylethanol (PEth) sensitivity for detecting unhealthy alcohol use: An individual patient data meta-analysis. (2021)
- ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing. (2020)
- Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data (2020)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
- RNentropy: an entropy-based tool for the detection of significant variation of gene expression across multiple RNA-Seq experiments. (2018)
- Statistical algorithms improve accuracy of gene fusion detection. (2017)
- Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. (2017)
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
- Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
- Heritability and genomics of gene expression in peripheral blood. (2014)
- Temporal specification and bilaterality of human neocortical topographic gene expression. (2014)
- Ethanol metabolism and osmolarity modify behavioral responses to ethanol in C. elegans. (2012)
- An integrated map of genetic variation from 1,092 human genomes. (2012)
- A longitudinal study of the long-term consequences of drinking during pregnancy: heavy in utero alcohol exposure disrupts the normal processes of brain development. (2012)
- Quantitative tract-based white matter development from birth to age 2years. (2012)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- The FaceBase Consortium: a comprehensive program to facilitate craniofacial research. (2011)
- Discovering genetic ancestry using spectral graph theory. (2010)
- Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966. (2009)
- Neurodevelopmental trajectories of the human cerebral cortex. (2008)
- Population structure and eigenanalysis. (2006)
- Discriminating power of localized three-dimensional facial morphology. (2005)
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 |
|---|---|---|---|
| individuals | cohort | 23 | 26 |