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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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American Journal of Medical Genetics Part B Neuropsychiatric 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.

affaffiliation
fundfunder
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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.

221 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.
221 works in the cohort · of 4,299,418page 4 of 5

Labels cover 0 of 221 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 221 of 221 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.

affunlabeled
Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to<i>SH3TC2</i>,<i>ADRB2</i>, and<i>HTR4</i>on 5q, and within the desmocollin gene cluster on 18q
John B. Vincent, Abdul Noor, Christian Windpassinger, Peter J. Gianakopoulos, Thomas Schwarzbraun, Simon E. Alfred +6 more
2008· article· en· American Journal of Medical Genetics Part B Neuropsychiatric Genetics· Medicine
machine prediction:candidate · noneconsensus · none
13
citations
afffundunlabeled
Dermatoglyphic profile in 22q deletion syndrome
Beatriz Martín, Lourdes Fañanás, Blanca Gutiérrez, Eva W. C. Chow, Anne S. Bassett
2004· article· en· American Journal of Medical Genetics Part B Neuropsychiatric Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
12
citations
affunlabeled
Blood‐based dynamic genomic signature for obsessive–compulsive disorder
Yuan Wang, Changming Cheng, Zongfeng Zhang, Jianyu Wang, Yao Wang, Xiaoping Li +10 more
2018· article· en· American Journal of Medical Genetics Part B Neuropsychiatric Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
7
citations
fundno affunlabeled
Expanded RED products and loci containing CAG/CTG repeats on chromosome 17 (ERDA1) and chromosome 18 (CTG18.1) in trans‐generational pairs with bipolar affective disorder
Julien Mendlewicz, Daniel Souery, Jurgen Del‐Favero, Isabelle Massat, Kerstin Lindblad, Christer Engström +4 more
2004· article· en· American Journal of Medical Genetics Part B Neuropsychiatric Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
6
citations
affno abstractunlabeled
Novel histamine H1 gene polymorphism and clozapine-induced weight gain
Vincenzo S. Basile, Mario Masellis, Vural Özdemir, S M Quiterio, Herbert Y. Meltzer, Jeffrey A. Lieberman +4 more
2000· article· en· American Journal of Medical Genetics Part B Neuropsychiatric Genetics· Immunology and Microbiology
machine prediction:candidate · noneconsensus · none
2
citations

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