autosomal SNPs cohort
Evidence from:
primary |
all sources
Related entities (8)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| autosomal SNPs | interacts_with | ADHD | — | 1 |
| autosomal SNPs | associated_with | Affymetrix | — | 1 |
| autosomal SNPs | associated_with | bipolar disorder | — | 1 |
| autosomal SNPs | associated_with | GWAS | — | 1 |
| autosomal SNPs | associated_with | Illumina platform | — | 1 |
| autosomal SNPs | associated_with | major depressive disorder | — | 1 |
| autosomal SNPs | associated_with | mood disorders | — | 1 |
| Plink | interacts_with | autosomal SNPs | — | 1 |
Mentioned in (12)
Papers in which this entity is mentioned.
- The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. (2022)
- Sex differences in the genetic architecture of obsessive-compulsive disorder. (2019)
- The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
- Polygenic risk for alcohol misuse is moderated by romantic partnerships. (2019)
- Genome-wide association discoveries of alcohol dependence. (2014)
- Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence. (2014)
- A mega-analysis of genome-wide association studies for major depressive disorder. (2013)
- Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. (2012)
- Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. (2011)
- Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
- Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
- Genome-wide association studies in ADHD. (2009)
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 |
|---|---|---|---|
| autosomal snps | variant | 12 | 12 |
| autosomal snps | cohort | — | — |