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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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American Journal of Medical Genetics Part A
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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.

974 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.
974 works in the cohort · of 4,299,418page 11 of 20

Labels cover 0 of 974 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 974 of 974 works in this cohort. Predictions are machine_predicted_unvalidated. The Gemma side is a direct model label for every work (title-only); the Codex side is a distilled, calibrated classifier. Candidate is the union; consensus is the intersection.

affno abstractunlabeled
Monozygotic twins with variable expression of Van der Woude Syndrome
Rebekah Jobling, Raechel A. Ferrier, Ross McLeod, Aline Petrin, Jeffrey C. Murray, Mary Ann Thomas
2011· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
17
citations
affunlabeled
Clinical variability of type II sialidosis by C808T mutation
Germán Rodríguez Criado, Alexey V. Pshezhetsky, A. Rodríguez Becerra, I. Gómez de Terreros
2003· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
17
citations
affno abstractunlabeled
Keppen–Lubinsky syndrome: Expanding the phenotype
Lina Basel‐Vanagaite, Lisa G. Shaffer, David Chitayat
2009· article· en· American Journal of Medical Genetics Part A· Medicine
machine prediction:candidate · noneconsensus · none
15
citations
affunlabeled
Novel cases of pediatric sudden cardiac death secondary to <scp><i>TRDN</i></scp> mutations presenting as long <scp>QT</scp> syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The <scp><i>TRDN</i></scp> arrhythmia syndrome
Bahareh Rabbani, Mohammadrafi Khorgami, Mohammad Dalili, Nasrin Zamani, Nejat Mahdieh, Michael H. Gollob
2021· article· en· American Journal of Medical Genetics Part A· Medicine
machine prediction:candidate · noneconsensus · none
15
citations
fundno affunlabeled
Sleep‐disordered breathing in children with pycnodysostosis
Sonia Khirani, Alessandro Amaddeo, Geneviève Baujat, Caroline Michot, Vincent Couloigner, Graziella Pinto +4 more
2019· article· en· American Journal of Medical Genetics Part A· Neuroscience
machine prediction:candidate · noneconsensus · none
15
citations

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