MétaCan
Menu
Cohort builder

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.

Search term
Author
Year range
Sort
Language
Type
Field
Venue
Genetics in Medicine
Topic
Retraction
Abstract
Evidence source
Study design
Label agreement
Label status

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
aboutaboutness

The four routes compose: require the funder route and exclude affiliation to get the funder-only stratum no affiliation-based frame ever sees.

568 results · 1 filter active ·
Results by year
20002025
Publication date
Categories
Machine labels · sparse coverage
Evidence
Language
Type
Citations
An unlabeled work is unknown, not a negative. Label coverage is reported on every query.
568 works in the cohort · of 4,299,418page 1 of 12

Labels cover 2 of 568 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 568 of 568 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affno abstractunlabeled
Phenylalanine hydroxylase deficiency: diagnosis and management guideline
Jerry Vockley, Hans C. Andersson, Kevin M. Antshel, Nancy Braverman, Barbara K. Burton, Dianne M. Frazier +4 more
2014· article· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
722
citations
affunlabeled
Loeys–Dietz syndrome: a primer for diagnosis and management
Gretchen MacCarrick, James H. Black, Sarah Bowdin, Ismaı̈l El-Hamamsy, Pamela A. Frischmeyer‐Guerrerio, Anthony L. Guerrerio +3 more
2014· review· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
579
citations
affno abstractunlabeled
Phenylalanine hydroxylase deficiency
John J. Mitchell, Yannis Trakadis, Charles R. Scriver
2011· review· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
535
citations
afffundno abstractunlabeled
Practical guidelines for managing adults with 22q11.2 deletion syndrome
Wai Lun Alan Fung, Nancy J. Butcher, Gregory Costain, Danielle M. Andrade, Erik Boot, Eva W.C. Chow +14 more
2015· review· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
314
citations
affno abstractunlabeled
Recommendations for returning genomic incidental findings? We need to talk!
Wylie Burke, Armand H. Matheny Antommaria, Robin L. Bennett, Jeffrey R. Botkin, Ellen Wright Clayton, Gail E. Henderson +12 more
2013· review· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
288
citations
affno abstractunlabeled
A proposed nosology of inborn errors of metabolism
Carlos R. Ferreira, Clara van Karnebeek, Jerry Vockley, Nenad Blau
2018· article· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
270
citations
affunlabeled
The landscape of epilepsy-related GATOR1 variants
Sara Baldassari, Fabienne Picard, Nienke E. Verbeek, Marjan van Kempen, Eva H. Brilstra, Gaëtan Lesca +82 more
2018· article· en· Genetics in Medicine· Medicine
distilled prediction:candidate · noneconsensus · none
239
citations
affno abstractunlabeled
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)
Peter Horak, Malachi Griffith, Arpad Danos, Beth A. Pitel, Subha Madhavan, Xue‐Lu Liu +41 more
2022· article· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
239
citations
affno abstractunlabeled
Initial report from the Hunter Outcome Survey
J. E. Wraith, Michael Beck, Roberto Giugliani, Joe T.R. Clarke, Rick Martin, Joseph Muenzer
2008· article· en· Genetics in Medicine· Medicine
distilled prediction:candidate · insufficient_payloadconsensus · none
190
citations
affno abstractunlabeled
Low risk of solid tumors in persons with Down syndrome
Henrik Hasle, Jan M. Friedman, Jørgen H. Olsen, Sonja A. Rasmussen
2016· article· en· Genetics in Medicine· Medicine
distilled prediction:candidate · insufficient_payloadconsensus · none
184
citations

How this was built: Screen · Findings · About