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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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The American 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.

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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.

836 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.
836 works in the cohort · of 4,299,418page 2 of 17

Labels cover 0 of 836 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 836 of 836 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affno abstractunlabeled
Long Runs of Homozygosity Are Enriched for Deleterious Variation
Zachary A. Szpiech, Jishu Xu, Trevor J. Pemberton, Weiping Peng, Sebastian Zöllner, Noah A. Rosenberg +1 more
2013· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
367
citations
affno abstractunlabeled
Mutations in STRA6 Cause a Broad Spectrum of Malformations Including Anophthalmia, Congenital Heart Defects, Diaphragmatic Hernia, Alveolar Capillary Dysplasia, Lung Hypoplasia, and Mental Retardation
Francesca Pasutto, Heinrich Sticht, G. Hammersen, Gabriele Gillessen‐Kaesbach, David Fitzpatrick, Gudrun Nürnberg +17 more
2007· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
359
citations
afffundno abstractunlabeled
Mutations in EZH2 Cause Weaver Syndrome
William T. Gibson, Rebecca L. Hood, Shing H. Zhan, Dennis E. Bulman, Anthony P. Fejes, Richard A. Moore +9 more
2011· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
328
citations
afffundno abstractunlabeled
SHANK1 Deletions in Males with Autism Spectrum Disorder
Daisuke Sato, Anath C. Lionel, Claire S. Leblond, Aparna Prasad, Dalila Pinto, Susan Walker +25 more
2012· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
325
citations
affno abstractunlabeled
Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
Marie‐Christine Chartier‐Harlin, Justus C. Dächsel, Carles Vilariño‐Güell, Sarah Lincoln, Frédéric Leprêtre, Mary Hulihan +44 more
2011· article· en· The American Journal of Human Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
304
citations
affno abstractunlabeled
Genomic Disorders on 22q11
Heather E. McDermid, Bernice E. Morrow
2002· review· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
281
citations

How this was built: Screen · Findings · About