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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
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.
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 head0.028
GPT teacher head0.312
- Teacher spread
- 0.283 · 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
- Topic
- Amyotrophic Lateral Sclerosis Research
- Field
- Medicine
- Canadian institutions
- Ottawa HospitalChildren's Hospital of Eastern OntarioUniversity of Ottawa
- Funders
- National Institute on AgingNational Institute of Neurological Disorders and StrokeRobert H. Lurie Comprehensive Cancer CenterNational Cancer InstituteMND ScotlandNational Institutes of HealthBlazeman Foundation for ALSNorthwestern University
- Keywords
- Amyotrophic lateral sclerosisTARDBPNeurodegenerationFrontotemporal dementiaDementiaFrontotemporal lobar degenerationBiologyMutationSOD1C9orf72GeneticsPathologyMedicineGeneDisease
- Has abstract in OpenAlex
- no