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Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
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.
Machine scores (provisional)
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Opus teacher head0.009
GPT teacher head0.224
- Teacher spread
- 0.216 · how far apart the two teachers sit on this one work
- Validation status
score_only:v0-immature-baseline· verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it
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
- Inflammatory Bowel Disease
- Field
- Biochemistry, Genetics and Molecular Biology
- Canadian institutions
- University of TorontoMount Sinai HospitalUniversité de MontréalMontreal Heart Institute
- Funders
- National Center for Research ResourcesNational Human Genome Research InstituteCanadian Institutes of Health ResearchNational Institutes of HealthNational Institute of Allergy and Infectious DiseasesInstitut de Cardiologie de MontréalExzellenzclusters EntzündungsforschungVetenskapsrådetCrohn's and Colitis UKLeona M. and Harry B. Helmsley Charitable TrustÖrebro UniversitetCedars-Sinai Medical CenterDeutsche ForschungsgemeinschaftNational Institute of Diabetes and Digestive and Kidney DiseasesCrohn's and Colitis Foundation of CanadaUniversitetssjukhuset ÖrebroBroad InstituteCrohn's and Colitis FoundationCrohn's and Colitis Foundation of America
- Keywords
- Genome-wide association studyBiologyInflammatory bowel diseaseGenotypingGeneticsGenetic associationPTPN22Odds ratioDiseaseCase-control studyNOD2Single-nucleotide polymorphismGeneGenotypeMedicineInternal medicine
- Has abstract in OpenAlex
- no