EAs cohort
Evidence from:
primary |
all sources
Related entities (25)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| 1000 Genomes Project | associated_with | EAs | — | 1 |
| Alzheimer's disease | associated_with | EAs | — | 1 |
| associated SNPs | associated_with | EAs | — | 1 |
| AUDIT-C | associated_with | EAs | — | 1 |
| auditory | associated_with | EAs | — | 1 |
| Chinese American | associated_with | EAs | — | 1 |
| Chrna7 | associated_with | EAs | — | 1 |
| cocaine-induced paranoia | associated_with | EAs | 0.0502 | 1 |
| EAs | interacts_with | AFR | — | 1 |
| EAs | associated_with | associated SNPs | — | 1 |
| EAs | associated_with | GWAS | — | 1 |
| EAs | interacts_with | His | — | 1 |
| EAs | associated_with | indel | — | 1 |
| EAs | interacts_with | SAS | — | 1 |
| EUR | interacts_with | EAs | — | 1 |
| Filipino | associated_with | EAs | — | 1 |
| Japanese American | associated_with | EAs | — | 1 |
| JPT | associated_with | EAs | — | 1 |
| novel variant | associated_with | EAs | — | 1 |
| rs16969968 | associated_with | EAs | 2.08e-06 | 1 |
| rs578776 | associated_with | EAs | — | 1 |
| rs588765 | associated_with | EAs | 0.038 | 1 |
| rs6494212 | associated_with | EAs | 0.16 | 1 |
| singletons | associated_with | EAs | — | 1 |
| SNP | associated_with | EAs | — | 1 |
Mentioned in (32)
Papers in which this entity is mentioned.
- Mapping the genetic landscape across 14 psychiatric disorders. (2026)
- Meta-analysis reveals differences in somatic alterations by genetic ancestry across common cancers. (2025)
- MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
- Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
- A harmonized public resource of deeply sequenced diverse human genomes. (2024)
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Alcohol use polygenic risk score, social support, and alcohol use among European American and African American adults. (2023)
- Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
- Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (2023)
- A saturated map of common genetic variants associated with human height. (2022)
- The complete sequence of a human genome. (2022)
- Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
- Rapid genotype imputation from sequence with reference panels. (2021)
- Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
- Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
- KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (2016)
- Dissecting ancestry genomic background in substance dependence genome-wide association studies. (2015)
- Genomewide Association Study for Maximum Number of Alcoholic Drinks in European Americans and African Americans. (2015)
- A global reference for human genetic variation. (2015)
- Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (2015)
- Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
- Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder. (2013)
- Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012)
- Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence. (2012)
- The genetics of the opioid system and specific drug addictions. (2012)
- Association of CHRNA4 polymorphisms with smoking behavior in two populations. (2011)
- Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans. (2010)
- Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
- The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans. (2009)
- Dense genomewide linkage scan for alcohol dependence in African Americans: significant linkage on chromosome 10. (2009)
- Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sample. (2009)
- Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN
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 |
|---|---|---|---|
| eas | cohort | 32 | 110 |
| original 1608 eas | cohort | — | — |