Htr1b gene
Evidence from:
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Related entities (10)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| Htr1b | risk_factor_for | ADHD | — | 1 |
| Htr1b | risk_factor_for | aggression | — | 1 |
| Htr1b | risk_factor_for | alcohol | — | 1 |
| Htr1b | associated_with | alcoholism | — | 1 |
| Htr1b | associated_with | antisocial alcoholism | — | 1 |
| Htr1b | associated_with | drinking | — | 1 |
| Htr1b | associated_with | high line | — | 1 |
| Htr1b | associated_with | low line | — | 1 |
| Htr1b | associated_with | mood disorders | — | 1 |
| serotonin | interacts_with | Htr1b | — | 1 |
Mentioned in (11)
Papers in which this entity is mentioned.
- A review on neuroimaging studies of genetic and environmental influences on early brain development. (2019)
- Regional Differences and Similarities in the Brain Transcriptome for Mice Selected for Ethanol Preference From HS-CC Founders. (2018)
- Genome-wide association analysis identifies common variants influencing infant brain volumes. (2017)
- Clinically relevant genetic biomarkers from the brain in alcoholism with representation on high resolution chromosome ideograms. (2015)
- Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned. (2012)
- The genetic basis of alcoholism: multiple phenotypes, many genes, complex networks. (2012)
- Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence. (2012)
- Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. (2011)
- Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation. (2008)
- Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
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 |
|---|---|---|---|
| htr1b | gene | 11 | 13 |
| 5-ht1b receptor | gene | — | — |