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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.

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.

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 14 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
Rett syndrome: A study of the face
Judith Allanson, Raoul C. M. Hennekam, Ute Moog, Eric Smeets
2011· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
10
citations
affunlabeled
Hydrocephaly, penoscrotal transposition, and digital anomalies associated with de novo pseudodicentric rearranged chromosome 13 characterized by classical cytogenetic methods and mBAND analysis
Denise Maria Christofolini, Maisa Yoshimoto, Jeremy A. Squire, Décio Brunoni, Maria Isabel Melaragno, Gianna Carvalheira
2006· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
10
citations
affunlabeled
Sudden infant death in a patient with <i>FGFR3</i> P250R mutation
Parag Shah, Komudi Siriwardena, Glenn Taylor, Leslie Steele, Peter N. Ray, Susan Blasér +1 more
2006· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
10
citations
afffundno abstractunlabeled
Severe connective tissue laxity including aortic dilatation in Sotos syndrome
Rebecca L. Hood, George McGillivray, Matthew F. Hunter, Stephen P. Roberston, Dennis E. Bulman, Kym M. Boycott +1 more
2015· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
10
citations
afffundunlabeled
Renpenning syndrome in a female
Raymond Y. Cho, Maria S. Peñaherrera, Christèle du Souich, Lijia Huang, Jill Mwenifumbo, Tanya N. Nelson +9 more
2019· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
10
citations
affaboutno abstractunlabeled
Robert J. Gorlin, 1923–2006: A remembrance
M. Michael Cohen
2006· article· en· American Journal of Medical Genetics Part A· Health Professions
machine prediction:candidate · noneconsensus · none
10
citations
affunlabeled
Two extraordinarily severe cases of Treacher Collins syndrome
Mislen Bauer, Wilmar Saldarriaga, S. Anthony Wolfe, J. Bruce Beckwith, Jaime L. Frías, Maimon M. Cohen
2013· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
9
citations
afffundunlabeled
Beckwith–Wiedemann syndrome in sibs discordant for IC2 methylation
Karen Y. Niederhoffer, Maria S. Peñaherrera, Denise Pugash, Rosemarie Rupps, Laura Arbour, Francine Tessier +7 more
2012· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
9
citations
affunlabeled
A rare case of trisomy 15pter‐q21.2 due to a de novo marker chromosome
Ade Nubia Xavier Pacanaro, Denise Maria Christofolini, Leslie Domenici Kulikowski, Síntia Belangero, Fernanda T. Bellucco, Monica Castro Varela +6 more
2010· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
9
citations
afffundunlabeled
Outfoxed by <i>RBFOX1</i>‐A caution about ascertainment bias
Benjamin Kamien, Anath C. Lionel, Nicole Bain, Stephen W. Scherer, Matthew F. Hunter
2014· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
9
citations
affunlabeled
Severe craniosynostosis in an infant with deletion 22q11.2 syndrome
Walla Al‐Hertani, Valerie Hastings, Jean McGowan‐Jordan, Julie Hurteau, Gail E. Graham
2012· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
8
citations
affunlabeled
Genomic analysis of “microphenotypes” in epilepsy
Kate E. Stanley, Joseph Hostyk, Linh Tran, Marta Amengual‐Gual, Patricia Dugan, Justice Clark +15 more
2021· article· en· American Journal of Medical Genetics Part A· Medicine
machine prediction:candidate · noneconsensus · none
8
citations

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