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
The American Journal of Human Genetics
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.

836 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.
836 works in the cohort · of 4,299,418page 14 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. The Gemma side is a direct model label for every work (title-only); the Codex side is a distilled, calibrated classifier. Candidate is the union; consensus is the intersection.

fundno affno abstractunlabeled
DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation
Ronen Schneider, Konstantin Deutsch, Gregory J. Hoeprich, Jonathan Marquez, Tobias Hermle, Daniela A. Braun +27 more
2020· article· en· The American Journal of Human Genetics· Medicine
machine prediction:candidate · noneconsensus · none
34
citations
afffundno abstractunlabeled
Parental Genotypes in the Risk of a Complex Disease
Damian Labuda, Maja Krajinović, Audrey Sabbagh, Claire Infante‐Rivard, Daniel Sinnett
2002· article· en· The American Journal of Human Genetics· Medicine
machine prediction:candidate · noneconsensus · none
34
citations
affno abstractunlabeled
Role of CAMK2D in neurodevelopment and associated conditions
Pomme M.F. Rigter, Charlotte de Konink, Matthew J. Dunn, Martina Proietti Onori, Jennifer B. Humberson, Matthew Thomas +36 more
2024· article· en· The American Journal of Human Genetics· Medicine
machine prediction:candidate · noneconsensus · none
32
citations
afffundunlabeled
Trio RNA sequencing in a cohort of medically complex children
Ashish R. Deshwar, Kyoko E. Yuki, Huayun Hou, Yijing Liang, Tayyaba Khan, Alper Celik +13 more
2023· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
32
citations
afffundunlabeled
RetiGene, a comprehensive gene atlas for inherited retinal diseases
Carlo Rivolta, Elifnaz Çelik, Dhryata Kamdar, Francesca Cancellieri, Karolina Kamińska, Mukhtar Ullah +25 more
2025· review· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
25
citations
affno abstractunlabeled
De novo variants in ATP2B1 lead to neurodevelopmental delay
Meer Jacob Rahimi, Nicole Urban, Meret Wegler, Heinrich Sticht, Michael Schaefer, Bernt Popp +30 more
2022· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
24
citations

How this was built: Screen · Findings · About