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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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Genomics and Rare Diseases
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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.

1,801 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.
1,801 works in the cohort · of 4,299,418page 3 of 37

Labels cover 4 of 1,801 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 1,801 of 1,801 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundunlabeled
New Diagnostic Approaches for Undiagnosed Rare Genetic Diseases
Taila Hartley, Gabrielle Lemire, Kristin D. Kernohan, Heather Howley, David R. Adams, Kym M. Boycott
2020· review· en· Annual Review of Genomics and Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
104
citations
affunlabeled
Further delineation of Kabuki syndrome in 48 well‐defined new individuals
Linlea Armstrong, Azza Abd El Monéim, Kirk Aleck, David J. Aughton, Clarisse Baumann, Stephen R. Braddock +22 more
2004· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
103
citations
afffundunlabeled
De novo variants in sporadic cases of childhood onset schizophrenia
Amirthagowri Ambalavanan, Simon Girard, Kwangmi Ahn, Sirui Zhou, Alexandre Dionne‐Laporte, Dan Spiegelman +8 more
2015· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
100
citations
fundno affunlabeled
The role of protein complexes in human genetic disease
L. Therese Bergendahl, Lukas Gerasimavicius, Jamilla Miles, Lewis Macdonald, Jonathan N. Wells, Julie P. I. Welburn +1 more
2019· review· en· Protein Science· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
100
citations
afffundaboutunlabeled
Exome Sequencing as a Diagnostic Tool for Pediatric‐Onset Ataxia
Sarah L. Sawyer, Jeremy Schwartzentruber, Chandree L. Beaulieu, David A. Dyment, Amanda Smith, Jodi Warman‐Chardon +11 more
2013· article· en· Human Mutation· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
100
citations
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