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4,299,418 works, Canadian by any of four routes.

Every filter state is a URL; the URL is the query; the query is citable via /q/⟨hash⟩. The page, the API and the export parse the same parameters.

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The current cohort, streamed from the database: every work column, the machine labels, the provisional scores, and the per-row validation status. Exports are capped at 100,000 rows. Mints a permanent /q/ link for this exact query. The same filters always produce the same link, whoever asks.

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Human Mutation
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Direct Codex and Gemma labels are unvalidated and sparse. Distilled predictions cover the full frame and are also unvalidated. Choose the evidence source explicitly; absence of a direct label is never a negative label.

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The four routes compose: require the funder route and exclude affiliation to get the funder-only stratum no affiliation-based frame ever sees.

366 results · 1 filter active ·
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20002025
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Machine labels · sparse coverage
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An unlabeled work is unknown, not a negative. Label coverage is reported on every query.
366 works in the cohort · of 4,299,418page 3 of 8

Labels cover 0 of 366 works in this cohort. The rest are unlabeled, which is not a negative label: the label table is sparse today and grows as labeling rounds land.

Distilled predictions cover 366 of 366 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundunlabeled
Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA Synthetase<i>IARS2</i>in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome
Jeremy Schwartzentruber, Daniela Buhaş, Jacek Majewski, Florin Sasarman, Simon Papillon‐Cavanagh, Isabelle Thiffaut +12 more
2014· article· en· Human Mutation· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
78
citations
affunlabeled
Evidence for genetic heterogeneity in D-2-hydroxyglutaric aciduria
Martijn Kranendijk, Eduard A. Struys, K. Michael Gibson, Wjera V. Wickenhagen, José E. Abdenur, Jochen Buechner +17 more
2009· article· en· Human Mutation· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
74
citations
fundno affunlabeled
<i>MERTK</i> mutation update in inherited retinal diseases
Isabelle Audo, Saddek Mohand‐Saïd, Élise Boulanger-Scemama, Xavier Zanlonghi, Christel Condroyer, Vanessa Démontant +6 more
2018· review· en· Human Mutation· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
70
citations
afffundunlabeled
The molecular basis of glutamate formiminotransferase deficiency
John Hilton, Karen E. Christensen, David Watkins, Benjamin A. Raby, Yannick Renaud, Xavier Estivill +3 more
2003· article· en· Human Mutation· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
68
citations
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How this was built: Screen · Findings · About