Wellcome Trust case control consortium cohort
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Related entities (14)
Mentioned in (17)
Papers in which this entity is mentioned.
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence. (2012)
- A comparison of approaches to account for uncertainty in analysis of imputed genotypes. (2011)
- A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. (2011)
- Using public control genotype data to increase power and decrease cost of case-control genetic association studies. (2010)
- i-GSEA4GWAS: a web server for identification of pathways/gene sets associated with traits by applying an improved gene set enrichment analysis to genome-wide association study. (2010)
- Genome-wide association study of bipolar disorder in European American and African American individuals. (2009)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. (2009)
- Genome-wide association studies in ADHD. (2009)
- The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA. (2009)
- Marker selection for genetic case-control association studies. (2009)
- Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk. (2009)
- Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
- Heterogeneity in meta-analyses of genome-wide association investigations. (2007)
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 |
|---|---|---|---|
| wellcome trust case control consortium | cohort | 17 | 22 |