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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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European Journal of Human Genetics
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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
fundfunder
venuejournal
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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.

513 results · 1 filter active ·
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20002025
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Machine labels · sparse coverage
Evidence
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An unlabeled work is unknown, not a negative. Label coverage is reported on every query.
513 works in the cohort · of 4,299,418page 10 of 11

Labels cover 0 of 513 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 513 of 513 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

aboutno affunlabeled
Reply to Kratz et al.
Thierry Frébourg, Svetlana Bajalica‐Lagercrantz, Carla Oliveíra, Rita Mágenheim, D. Gareth Evans, Marjolijn J. L. Ligtenberg +31 more
2020· letter· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
3
citations
afffundno abstractunlabeled
Neurobehavioral profile of individuals with pathogenic variants in CHD3
Anca Ionescu, Emmanuelle Mazur-Lainé, Mélodie Proteau-Lemieux, Inga Sophia Knoth, Keely Vachon, Kerri Whitlock +11 more
2025· article· en· European Journal of Human Genetics· Neuroscience
distilled prediction:candidate · noneconsensus · none
3
citations
affunlabeled
A second hotspot for pathogenic exon-skipping variants in CDC45
Kelly Schoch, Mischa S. G. Ruegg, Bridget J. Fellows, Joseph Cao, Sabine Uhrig, Stephanie Einsele‐Scholz +8 more
2024· article· en· European Journal of Human Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
2
citations
affno abstractunlabeled
Viewing the male-specific chromosome Y in a new light
Christian F. Deschepper
2017· letter· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
2
citations
afffundno abstractunlabeled
Identification of an episignature for the MEF2C-associated syndrome
Ananília Silva, Sadegheh Haghshenas, Liselot van der Laan, Michael A. Levy, Raissa Relator, Haley McConkey +12 more
2025· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
1
citations
affno abstractunlabeled
RICTOR variants are associated with neurodevelopmental disorders
Raphaël Carapito, Anne Molitor, Lisa Pavinato, Alaa Skeyni, M. Lambert, Angélique Pichot +31 more
2024· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
1
citations
affno abstractunlabeled
POT1 clinical risk management is an open question
Mandy L. Ballinger, David M. Thomas
2024· letter· en· European Journal of Human Genetics· Medicine
distilled prediction:candidate · metaepi_narrow+research_integrityconsensus · none
1
citations
affno abstractunlabeled
Be prepared for prenatal diagnosis
Judith G. Hall
2017· article· en· European Journal of Human Genetics· Health Professions
distilled prediction:candidate · stsconsensus · none
0
citations

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