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Defining the role of common variation in the genomic and biological architecture of adult human height
Why is this work in the frame?
A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.
Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Abstract
No abstract. This is not a gap in this database — OpenAlex has none either. 23.3% of the frame is in this state, and the screen finds HALF as much metaresearch here, so the absence is a measured bias rather than a missing field.
The record
- Venue
- Nature Genetics
- Topic
- Genetic Associations and Epidemiology
- Field
- Biochemistry, Genetics and Molecular Biology
- Canadian institutions
- Institut universitaire de cardiologie et de pneumologie de QuébecUniversité LavalMontreal Heart Institute
- Funders
- Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentWellcome TrustNational Human Genome Research InstituteNational Center for Advancing Translational SciencesBritish Heart FoundationNational Cancer InstituteNational Institute of Diabetes and Digestive and Kidney DiseasesNational Heart, Lung, and Blood InstituteNovo Nordisk FondenNational Institute for Health and Care ResearchNational Institute of General Medical SciencesMedical Research Council
- Keywords
- BiologyGenetic architectureGeneticsGenome-wide association studyHeritabilityPhenotypeGeneWnt signaling pathwayMissing heritability problemSingle-nucleotide polymorphismGenetic associationQuantitative trait locusGenetic variationGenomeEvolutionary biologyGenotype
- Has abstract in OpenAlex
- no