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
Topic
Genetics and Neurodevelopmental Disorders
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.

1,774 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.
1,774 works in the cohort · of 4,299,418page 10 of 36

Labels cover 2 of 1,774 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 1,774 of 1,774 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affno abstractunlabeled
Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array
Laila C. Schenkel, Charles E. Schwartz, Cindy Skinner, David I. Rodenhiser, Peter Ainsworth, Guillaume Paré +1 more
2016· article· en· Journal of Molecular Diagnostics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
43
citations
affno abstractunlabeled
PRRX1 is mutated in a fetus with agnathia-otocephaly
Consolato Sergi, Deepak Kamnasaran
2011· letter· en· Clinical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrow+research_integrityconsensus · none
42
citations
afffundunlabeled
A molecular model for neurodevelopmental disorders
Carolina Oliveira Gigek, Elizabeth Chen, Vanessa Ota, Gilles Maussion, Hong Peng, Kathryn Vaillancourt +6 more
2015· article· en· Translational Psychiatry· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
41
citations
afffundaboutunlabeled
FHF1 (FGF12) epileptic encephalopathy
Sameer Al‐Mehmadi, Miranda Splitt, Venkateswaran Ramesh, Suzanne D. DeBrosse, Kimberly Dessoffy, Fan Xia +9 more
2016· article· en· Neurology Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
41
citations
affno abstractunlabeled
GRIN2B predicts attention problems among disadvantaged children
Valentina Riva, Marco Battaglia, Maria Nobile, Francesca Cattaneo, Claudio Lazazzera, Sara Mascheretti +5 more
2014· article· en· European Child & Adolescent Psychiatry· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
39
citations
afffundaboutunlabeled
New insights of altered lipid profile in Fragile X Syndrome
Artuela Çaku, Nabil G. Seidah, Audrey Lortie, Nancy Gagné, Patrice Perron, Jean Y. Dubé +1 more
2017· article· en· PLoS ONE· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
38
citations

How this was built: Screen · Findings · About