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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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Genetics in Medicine
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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.

568 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.
568 works in the cohort · of 4,299,418page 6 of 12

Labels cover 2 of 568 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 568 of 568 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundunlabeled
Public variant databases: liability?
Adrian Thorogood, Robert Cook‐Deegan, Bartha Maria Knoppers
2016· article· en· Genetics in Medicine· Medicine
distilled prediction:candidate · metaresearch+insufficient_payloadconsensus · none
32
citations
affno abstractunlabeled
Carrier testing for spinal muscular atrophy
Jonathan M. Gitlin, Kenneth H. Fischbeck, Thomas O. Crawford, Valerie Cwik, Alan R. Fleischman, Karla Gonye +16 more
2010· article· en· Genetics in Medicine· Medicine
distilled prediction:candidate · noneconsensus · none
31
citations
afffundno abstractunlabeled
DOORS syndrome and a recurrent truncating ATP6V1B2 variant
Éliane Beauregard‐Lacroix, G. Pacheco-Cuellar, Norbert Fonya Ajeawung, Jessica Tardif, Klaus Dieterich, Tabib Dabir +16 more
2020· article· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
30
citations
afffundno abstractunlabeled
Mobility in osteogenesis imperfecta: a multicenter North American study
Karen M. Kruger, Angela Caudill, Mercedes Rodriguez Celin, Sandesh C.S. Nagamani, Jay R. Shapiro, Robert D. Steiner +13 more
2019· article· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
30
citations
afffundno abstractunlabeled
Assessing non-Mendelian inheritance in inherited axonopathies
Dana M. Bis‐Brewer, Ziv Gan‐Or, Patrick Sleiman, Aixa Rodríguez, Alexa Bacha, Ashley Kosikowski +60 more
2020· article· en· Genetics in Medicine· Neuroscience
distilled prediction:candidate · noneconsensus · none
27
citations
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