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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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Genomics and Rare Diseases
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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.

1,801 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.
1,801 works in the cohort · of 4,299,418page 4 of 37

Labels cover 4 of 1,801 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 1,801 of 1,801 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affno abstractunlabeled
Human monogenic disorders — a source of novel drug targets
Ryan R. Brinkman, Marie‐Pierre Dubé, Guy A. Rouleau, Andrew Orr, Mark Samuels
2006· review· en· Nature Reviews Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
94
citations
fundno affunlabeled
De novo <i>GABRA1</i> mutations in Ohtahara and West syndromes
Hirofumi Kodera, Chihiro Ohba, Mitsuhiro Kato, Toshiyuki Maeda, Kaoru Araki, Daisuke Tajima +16 more
2016· article· en· Epilepsia· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
92
citations
affno abstractunlabeled
Contemplating effects of genomic structural variation
Janet A. Buchanan, Stephen W. Scherer
2008· review· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
92
citations
affaboutunlabeled
Availability and funding of clinical genomic sequencing globally
Kathryn A. Phillips, Michael P. Douglas, Sarah Wordsworth, James Buchanan, Deborah A. Marshall
2021· review· en· BMJ Global Health· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
92
citations
affunlabeled
Whole-Genome Sequencing in Newborn Screening Programs
Bartha Maria Knoppers, Karine Sénécal, Pascal Borry, Denise Avard
2014· article· en· Science Translational Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
86
citations
affunlabeled
RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome
Nina Bögershausen, I-Chun Tsai, Esther Pohl, Pelin Özlem Şimşek‐Kiper, Filippo Beleggia, E. Ferda Perçin +22 more
2015· article· en· Journal of Clinical Investigation· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
86
citations
afffundunlabeled
PhenCode: connecting ENCODE data with mutations and phenotype
Belinda Giardine, Cathy Riemer, Tim Hefferon, Daryl J. Thomas, Fan Hsu, Julian Zielenski +20 more
2007· article· en· Human Mutation· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
82
citations
affunlabeled
Clinical utility of genomic sequencing: a measurement toolkit
Robin Z. Hayeems, David Dimmock, David Bick, John W. Belmont, Robert C. Green, Brendan C. Lanpher +6 more
2020· review· en· npj Genomic Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
81
citations
afffundno abstractunlabeled
De Novo Mutations in EBF3 Cause a Neurodevelopmental Syndrome
Hannah Sleven, Seth J. Welsh, Jing Yu, Mair E. A. Churchill, Caroline F. Wright, Alex Henderson +15 more
2016· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
78
citations
afffundunlabeled
A Draft Human Pangenome Reference
Wen‐Wei Liao, Mobin Asri, Jana Ebler, Daniel Doerr, Marina Haukness, Glenn Hickey +49 more
2022· preprint· en· bioRxiv (Cold Spring Harbor Laboratory)· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
74
citations

How this was built: Screen · Findings · About