← all works
A case of hypocholesterolemia and steatosis in a carrier of a PCSK9 loss-of-function mutation and polymorphisms predisposing to nonalcoholic fatty liver 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.
The three-model screen
all 1,000 screened works →All three models called this out of scope.
stratum: aff_core · design weight: 5595.24 (the sample is stratified; any rate computed without the weight is wrong)
Claude Opus 4.8OUT
genre: empirical
about Canada: no
confidence: high
Clinical case report of a PCSK9 mutation carrier.
GPT-5.6 (high)OUT
genre: empirical
about Canada: no
confidence: high
This reports a clinical case involving a genetic mutation and liver disease, not research itself.
Grok 4.5OUT
genre: empirical
about Canada: no
confidence: medium
Clinical genetics case of PCSK9 mutation and steatosis; title-domain clear despite empty abstract.
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
- Journal of clinical lipidology
- Topic
- Lipoproteins and Cardiovascular Health
- Field
- Medicine
- Canadian institutions
- Université de MontréalMontreal Clinical Research Institute
- Funders
- —
- Keywords
- MedicineSteatosisHypocholesterolemiaNonalcoholic fatty liver diseaseFatty liverInternal medicineLoss functionDiseaseMutationGastroenterologyGeneticsGeneCholesterolPhenotypeBiology
- Has abstract in OpenAlex
- no