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Common genetic determinants of vitamin D insufficiency: a genome-wide association study
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.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.
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
- The Lancet
- Topic
- Vitamin D Research Studies
- Field
- Medicine
- Canadian institutions
- Public Health Agency of CanadaHealth CanadaMcGill University Health CentreMcGill UniversityJewish General Hospital
- Funders
- National Human Genome Research InstituteNational Institute of Mental HealthNational Heart, Lung, and Blood InstituteNational Institute of Child Health and Human DevelopmentNational Institute of Arthritis and Musculoskeletal and Skin DiseasesNational Institute of Diabetes and Digestive and Kidney DiseasesBiocenter, University of OuluDirectorate for Biological SciencesNational Institutes of HealthMedical Research CouncilNational Center for Research ResourcesNational Institute of Allergy and Infectious DiseasesVersus ArthritisErasmus Medisch CentrumNational Eye InstituteAgricultural Research ServiceAcademy of FinlandNational Institute on AgingNational Institute for Health and Care ResearchNederlandse Organisatie voor Wetenschappelijk OnderzoekUniversity College LondonBiotechnology and Biological Sciences Research CouncilWellcome TrustOulun YliopistoHelsingin YliopistoSchool of Medicine, Boston UniversityEuropean CommissionZonMwJohns Hopkins UniversityU.S. Department of AgricultureKing's College LondonJuvenile Diabetes Research Foundation InternationalCanadian Institutes of Health ResearchAmerican Heart Association
- Keywords
- Vitamin D and neurologyGenome-wide association studyGenotypeBiologyGeneticsLocus (genetics)vitamin D deficiencyHeritabilityGenetic associationCYP24A1Calcitriol receptorInternal medicineMedicineSingle-nucleotide polymorphismEndocrinologyGene
- Has abstract in OpenAlex
- no