lead SNP cohort
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Related entities (24)
Mentioned in (19)
Papers in which this entity is mentioned.
- Associations between common genetic variants and income provide insights about the socio-economic health gradient. (2025)
- Functional analysis of cancer-associated germline risk variants. (2025)
- Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
- Global impact of unproductive splicing on human gene expression. (2024)
- Guidelines for Evaluating the Comparability of Down-Sampled GWAS Summary Statistics. (2023)
- Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
- Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
- Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. (2021)
- Interpretation of risk loci from genome-wide association studies of Alzheimer's disease. (2020)
- Sex differences in the genetic architecture of obsessive-compulsive disorder. (2019)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. (2019)
- Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. (2018)
- Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. (2017)
- Genome-wide association study identifies 74 loci associated with educational attainment. (2016)
- Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (2013)
- Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. (2012)
- Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. (2010)
Merged raw entities (8)
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 |
|---|---|---|---|
| lead snp | variant | 15 | 20 |
| lead snps | variant | 11 | 24 |
| 579 ext snps | cohort | — | — |
| lead single nucleotide polymorphism | cohort | — | — |
| lead single nucleotide polymorphisms | cohort | — | — |
| lead snp | cohort | — | — |
| lead snps | cohort | — | — |
| lead variants | cohort | — | — |