clinical phenotypes phenotype
Evidence from:
primary |
all sources
Related entities (5)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| associated SNPs | associated_with | clinical phenotypes | — | 1 |
| candidate genes | associated_with | clinical phenotypes | — | 1 |
| clinical phenotypes | associated_with | genetic risk | — | 1 |
| DRD4 VNTR | associated_with | clinical phenotypes | — | 1 |
| genetic variants | associated_with | clinical phenotypes | — | 1 |
Mentioned in (10)
Papers in which this entity is mentioned.
- CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods. (2024)
- Imaging Genetics and Genomics in Psychiatry: A Critical Review of Progress and Potential. (2017)
- Guidelines for investigating causality of sequence variants in human disease. (2014)
- In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. (2014)
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
- Expansion of the human mu-opioid receptor gene architecture: novel functional variants. (2009)
- Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. (2009)
- The incentive salience of alcohol: translating the effects of genetic variant in CNR1. (2008)
- Heterogeneity in meta-analyses of genome-wide association investigations. (2007)
- Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes. (2005)
Merged raw entities (3)
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 |
|---|---|---|---|
| clinical phenotype | phenotype | 7 | 8 |
| clinical phenotypes | phenotype | 5 | 5 |
| broad clinical phenotype | phenotype | — | — |