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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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European Journal of Medical 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
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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.

112 results · 1 filter active ·
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20052025
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Machine labels · sparse coverage
Evidence
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An unlabeled work is unknown, not a negative. Label coverage is reported on every query.
112 works in the cohort · of 4,299,418page 2 of 3

Labels cover 0 of 112 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 112 of 112 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundno abstractunlabeled
Intrafamilial variability of limb-girdle muscular dystrophy, LGMD1D type
Judith Zima, Alison Eaton, Endre Pál, Ágnes Till, Yoko Itō, Jodi Warman‐Chardon +5 more
2019· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
14
citations
fundno affno abstractunlabeled
Oro-dental phenotype in patients with RUNX2 duplication
Laure Merametdjian, Tony Prud’homme, Cédric Le Caignec, Bertrand Isidor, Séréna Lopez-Cazaux
2018· article· en· European Journal of Medical Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
13
citations
affno abstractunlabeled
Microdeletion 8q22.2-q22.3 in a 40-year-old male
Pierre Sinajon, Timothy Gofine, Jodi Ingram, Joyce So
2015· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
12
citations
affno abstractunlabeled
Hydranencephaly in CENPJ-related Seckel syndrome
Claudia Cuccurullo, Giuseppina Miele, Gianluca Piccolo, Leonilda Bilo, Andrea Accogli, Alessandra D’Amico +7 more
2022· article· en· European Journal of Medical Genetics· Medicine
distilled prediction:candidate · insufficient_payloadconsensus · none
8
citations
aboutno affno abstractunlabeled
A de novo BCL11B variant case manifesting with dystonic movement disorder regarding the article “BCL11B-related disorder in two canadian children: Expanding the clinical phenotype (Prasad et al., 2020).”
Philip Harrer, Verena Leppmeier, Andrea Berger, Simone Demund, Juliane Winkelmann, Steffen Berweck +1 more
2022· letter· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · research_integrityconsensus · none
8
citations
afffundno abstractunlabeled
A case of splenomegaly in CBL syndrome
Rachel R. Coe, Margaret L. McKinnon, Maja Tarailo‐Graovac, Colin J.D. Ross, Wyeth W. Wasserman, Jan M. Friedman +2 more
2017· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
8
citations
affno abstractunlabeled
Abnormal course of the corticospinal tracts in KIF5C-related encephalopathy
Alessandro Naim, Andrea Accogli, Elisabetta Amadori, Gianluca D’Onofrio, Francesca Madia, Domenico Tortora +4 more
2022· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
5
citations
fundno affno abstractunlabeled
Split hand/foot malformation associated with 20p12.1 deletion: A case report
Lyse Ruaud, Ricarda Flöttmann, Malte Spielmann, Fabienne Escande, Lionel Van Maldergem, Stefan Mundlos +1 more
2019· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
3
citations
affno abstractunlabeled
Could distal variants in ALG13 lead to atypical clinical presentation?
Andrea Accogli, Silvia Radenkovic, Wasantha Ranatunga, Anna N. Ligezka, Jean‐Baptiste Rivière, Éva Morava +1 more
2022· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
3
citations

How this was built: Screen · Findings · About