HapMap CEU cohort
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Related entities (21)
Mentioned in (21)
Papers in which this entity is mentioned.
- Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort. (2016)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence. (2014)
- Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. (2013)
- Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (2013)
- A comparison of approaches to account for uncertainty in analysis of imputed genotypes. (2011)
- Haplotype block structure of the genomic region of the mu opioid receptor gene. (2011)
- Expanding the range of ZNF804A variants conferring risk of psychosis. (2011)
- The neuronal transporter gene SLC6A15 confers risk to major depression. (2011)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. (2010)
- Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans. (2010)
- Genome-wide association studies in diverse populations. (2010)
- A genome-wide association study of neuroticism in a population-based sample. (2010)
- Genetic structure of Europeans: a view from the North-East. (2009)
- Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. (2009)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. (2009)
- Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. (2009)
- The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans. (2009)
- Genome-wide and candidate gene association study of cigarette smoking behaviors. (2009)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
Merged raw entities (10)
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 |
|---|---|---|---|
| hapmap ceu | cohort | 16 | 23 |
| hapmap ceu sample | cohort | 4 | 4 |
| hapmap ceu panel | cohort | 2 | 5 |
| hapmap ceu population | cohort | 2 | 3 |
| ceph sample | cohort | — | — |
| ceu panel | cohort | — | — |
| ceu sample | cohort | — | — |
| hap map ceu samples | cohort | — | — |
| hapmap european ancestry panel | cohort | — | — |
| hapmap version 2 ceu panel | cohort | — | — |