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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.

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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Nature 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.

943 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.
943 works in the cohort · of 4,299,418page 9 of 19

Labels cover 4 of 943 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 943 of 943 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundno abstractunlabeled
Stalled developmental programs at the root of pediatric brain tumors
Selin Jessa, Alexis Blanchet-Cohen, Brian Krug, Maria Vladoiu, Marie Coutelier, Damien Faury +34 more
2019· article· en· Nature Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
299
citations
afffundno abstractunlabeled
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Kevin P. Kenna, Perry T.C. van Doormaal, Annelot M. Dekker, Nicola Ticozzi, Brendan Kenna, Frank P. Diekstra +72 more
2016· article· en· Nature Genetics· Medicine
distilled prediction:candidate · insufficient_payloadconsensus · insufficient_payload
294
citations
affno abstractunlabeled
SPTLC1 is mutated in hereditary sensory neuropathy, type 1
Khemissa Bejaoui, Chenyan Wu, Margaret Scheffler, Geoffry Haan, P. Ashby, Lianchan Wu +2 more
2001· article· en· Nature Genetics· Neuroscience
distilled prediction:candidate · noneconsensus · none
293
citations
affno abstractunlabeled
Mutations in TJP2 cause progressive cholestatic liver disease
Melissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, Peter Rushton, Barnaby Clark, David Parry +16 more
2014· article· en· Nature Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
293
citations
affno abstractunlabeled
Mutations in GJB6 cause hidrotic ectodermal dysplasia
Jérôme Lamartine, Guilherme Munhoz Essenfelder, Zoha Kibar, Isabelle Lanneluc, Edwige Callouet, Dalila Laoudj‐Chenivesse +14 more
2000· article· en· Nature Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
288
citations
affno abstractunlabeled
The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM
Johan P. de Winter, Martin A. Rooimans, Laura van der Weel, Carola G.M. van Berkel, Noa Alon, Lucine Bosnoyan-Collins +10 more
2000· article· en· Nature Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
271
citations
affno abstractunlabeled
Mutations in MKKS cause Bardet-Biedl syndrome
Anne Slavotinek, Edwin M. Stone, Kirk Mykytyn, John R. Heckenlively, Jane S. Green, Elise Héon +4 more
2000· article· en· Nature Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
270
citations

How this was built: Screen · Findings · About