Haplotype Reference Consortium cohort
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Related entities (10)
Mentioned in (16)
Papers in which this entity is mentioned.
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- A harmonized public resource of deeply sequenced diverse human genomes. (2024)
- Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
- A saturated map of common genetic variants associated with human height. (2022)
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
- Polygenic risk scores for alcohol involvement relate to brain structure in substance-naïve children: Results from the ABCD study. (2021)
- Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. (2021)
- Rapid genotype imputation from sequence with reference panels. (2021)
- Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
- Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts. (2019)
- Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. (2018)
- Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. (2018)
- The Immune Landscape of Cancer. (2018)
- Fast and accurate long-range phasing in a UK Biobank cohort. (2016)
- A global reference for human genetic variation. (2015)
- A global reference for human genetic variation. (2015)
Merged raw entities (1)
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 |
|---|---|---|---|
| haplotype reference consortium | cohort | 16 | 20 |