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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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Retraction
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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.

affaffiliation
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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 4 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 teacher distillation outputs. Candidate is the union; consensus is the intersection.

affunlabeled
Mutation analysis of <i>B3GALTL</i> in Peters Plus syndrome
Linda M. Reis, Rebecca C. Tyler, Omar Abdul‐Rahman, Pamela Trapane, Robert Wallerstein, Diane L. Broome +6 more
2008· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
61
citations
affunlabeled
Genetic heterogeneity in Usher syndrome
Bronya J.B. Keats, Sevtap Savas
2004· review· en· American Journal of Medical Genetics Part A· Neuroscience
distilled prediction:candidate · metaepi_narrow+research_integrityconsensus · none
57
citations
affunlabeled
The ontogeny of Robin sequence
Robrecht J. H. Logjes, Corstiaan C. Breugem, Gijs van Haaften, Emma C. Paes, G.H. Sperber, Marie‐José H. van den Boogaard +1 more
2018· review· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
56
citations
afffundunlabeled
Clinical and genetic aspects of trigonocephaly: A study of 25 cases
Cyrus Azimi, Shelley Kennedy, David Chitayat, Pranesh Chakraborty, Joe T.R. Clarke, Christopher R. Forrest +1 more
2002· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
55
citations
affunlabeled
<i>FOXE3</i> plays a significant role in autosomal recessive microphthalmia
Linda M. Reis, Rebecca C. Tyler, Adele Schneider, Tanya Bardakjian, Joan M. Stoler, Serge B. Melançon +1 more
2010· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
55
citations
affunlabeled
Overview of German, Nazi, and Holocaust medicine
M. Michael Cohen
2010· review· en· American Journal of Medical Genetics Part A· Arts and Humanities
distilled prediction:candidate · sts+insufficient_payloadconsensus · none
54
citations
affunlabeled
Cornelia de Lange syndrome in diverse populations
Leah Dowsett, Antonio R. Porras, Paul Kruszka, Brandon Davis, Tommy Hu, Engela Honey +60 more
2019· article· en· American Journal of Medical Genetics Part A· Medicine
distilled prediction:candidate · insufficient_payloadconsensus · none
53
citations
affunlabeled
The face signature of fibrodysplasia ossificans progressiva
Peter Hammond, Michael Suttie, Raoul C. M. Hennekam, Judith Allanson, Eileen M. Shore, Frederick S. Kaplan
2012· article· en· American Journal of Medical Genetics Part A· Medicine
distilled prediction:candidate · noneconsensus · none
51
citations
affunlabeled
The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew‐Wood syndrome): Report of eight cases including a living child and further evidence for autosomal recessive inheritance
David Chitayat, Hana Sroka, Sarah Keating, Randall S. Colby, Greg Ryan, Ants Toi +9 more
2007· article· en· American Journal of Medical Genetics Part A· Medicine
distilled prediction:candidate · noneconsensus · none
51
citations

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