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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 A
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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.

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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.

974 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.
974 works in the cohort · of 4,299,418page 10 of 20

Labels cover 0 of 974 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 974 of 974 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
Achondroplasia: Really rhizomelic?
Susan C. Shelmerdine, Helen Brittain, Owen J. Arthurs, Alistair Calder
2016· review· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
20
citations
affunlabeled
Growth charts for individuals with Smith–Lemli–Opitz syndrome
Ryan W.Y. Lee, John McGready, Sandra K. Conley, Nicole M. Yanjanin, Małgorzata J.M. Nowaczyk, Forbes D. Porter
2012· article· en· American Journal of Medical Genetics Part A· Medicine
machine prediction:candidate · noneconsensus · none
20
citations
affunlabeled
<i>HIST1H1E</i> heterozygous protein‐truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30 individuals
Deepika Burkardt, Anna Zachariou, Chey Loveday, Clare L. Allen, David J. Amor, Anna Ardissone +28 more
2019· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
20
citations
affunlabeled
Pregnancy in a healthy woman with untreated citrullinemia
Murray Potter, Susan Zeesman, Barbara Brennan, Keiko Kobayashi, Hong‐Zhi Gao, Ayako Tabata +2 more
2004· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
20
citations
afffundunlabeled
Phenotypic evolution of UNC80 loss of function
Elise Valkanas, Katherine E. Schaffer, Christopher Dunham, Valerie V. Maduro, Christèle du Souich, Rosemarie Rupps +7 more
2016· article· en· American Journal of Medical Genetics Part A· Neuroscience
machine prediction:candidate · noneconsensus · none
19
citations
afffundunlabeled
<i>FGFR‐</i>associated craniosynostosis syndromes and gastrointestinal defects
Christine Elizabeth Hibberd, Sarah Bowdin, Yamini Arudchelvan, Christopher R. Forrest, Katherine A. Brakora, Ralph Marcucio +1 more
2016· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
19
citations
afffundunlabeled
Dietary intake in youth with prader‐willi syndrome
Michelle Mackenzie, Lucila Triador, Jasmeena K. Gill, Mohammadreza Pakseresht, Diana R. Mager, Catherine J. Field +1 more
2018· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
19
citations
affunlabeled
Cerebellar atrophy in Schimke‐immuno‐osseous dysplasia
Thomas Lücke, Johanna M. Clewing, Cornelius F. Boerkoel, Hans Hartmann, Anibh M. Das, Michael Knauth +2 more
2007· article· en· American Journal of Medical Genetics Part A· Immunology and Microbiology
machine prediction:candidate · noneconsensus · none
18
citations
affunlabeled
Holt‐Oram syndrome: Is there a “face”?
Judith Allanson, Ruth Newbury‐Ecob
2003· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
18
citations
afffundunlabeled
Inverted duplication with terminal deletion of 5p and no cat‐like cry
Jia‐Chi Wang, Bradley P. Coe, Brenda Lomax, Patrick MacLeod, Malcolm Parslow, Jacqueline E. Schein +2 more
2008· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
18
citations
affunlabeled
Tatton‐Brown‐Rahman syndrome: Six individuals with novel features
Tuğçe B. Balcı, Alana Strong, Jennifer M. Kalish, Elaine H. Zackai, John M. Maris, Anne F. Reilly +5 more
2020· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
18
citations

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