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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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Journal of Medical Genetics
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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.

449 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.
449 works in the cohort · of 4,299,418page 5 of 9

Labels cover 0 of 449 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 449 of 449 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

aboutno affunlabeled
Longevity in Schimke immuno-osseous dysplasia
Shu Lou
2002· letter· en· Journal of Medical Genetics· Immunology and Microbiology
distilled prediction:candidate · metaepi_narrow+research_integrity+insufficient_payloadconsensus · research_integrity
47
citations
affunlabeled
A <i>PCSK9</i> variant and familial combined hyperlipidaemia
Marianne Abifadel, L. Bernier, Geneviève Dubuc, Grégory Nuel, Jessica Bonneau, Ana Paula Marques +8 more
2008· article· en· Journal of Medical Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
46
citations
affunlabeled
<i>GPR98</i> mutations cause Usher syndrome type 2 in males
Inga Ebermann, Martin H. J. Wiesen, Eberhart Zrenner, I. López, Renée Pigeon, Susanne Kohl +3 more
2009· article· en· Journal of Medical Genetics· Neuroscience
distilled prediction:candidate · noneconsensus · none
42
citations
affunlabeled
Homozygosity mapping of a third Joubert syndrome locus to 6q23
Clotilde Lagier‐Tourenne, Eugen Boltshauser, Noralv Breivik, Moez Gribaa, Christine Bétard, Clara Barbot
2004· article· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
42
citations
afffundunlabeled
Current status of human chromosome 14
Deepak Kamnasaran
2002· review· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
38
citations
fundno affunlabeled
Mutations in IRS4 are associated with central hypothyroidism
Charlotte A. Heinen, Emmely M. de Vries, Mariëlle Alders, Hennie Bikker, Nitash Zwaveling‐Soonawala, Erica L T van den Akker +7 more
2018· article· en· Journal of Medical Genetics· Neuroscience
distilled prediction:candidate · noneconsensus · none
37
citations
afffundaboutunlabeled
<i>SETD1B</i>-associated neurodevelopmental disorder
Alexandra Roston, Dan Evans, Harinder Gill, Margaret L. McKinnon, Bertrand Isidor, Benjamin Cogné +8 more
2020· article· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
35
citations
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