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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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Orphanet Journal of Rare Diseases
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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.

328 results · 1 filter active ·
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20062025
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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.
328 works in the cohort · of 4,299,418page 1 of 7

Labels cover 0 of 328 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 328 of 328 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
CHARGE syndrome
Kim Blake, Chitra Prasad
2006· review· en· Orphanet Journal of Rare Diseases· Medicine
machine prediction:candidate · noneconsensus · none
274
citations
affunlabeled
Recommendations for the management of tyrosinaemia type 1
Corinne De Laet, Carlo Dionisi‐Vici, James V. Leonard, Patrick McKiernan, Grant A. Mitchell, Lidia Monti +3 more
2013· review· en· Orphanet Journal of Rare Diseases· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
226
citations
afffundunlabeled
A novel recurrent mutation in ATP1A3 causes CAPOS syndrome
Michelle Demos, Clara DM van Karnebeek, Colin J.D. Ross, Shelin Adam, Yaoqing Shen, Shing H. Zhan +6 more
2014· article· en· Orphanet Journal of Rare Diseases· Neuroscience
machine prediction:candidate · noneconsensus · none
192
citations
affunlabeled
Primary biliary cirrhosis
Teru Kumagi, EJenny Heathcote
2008· review· en· Orphanet Journal of Rare Diseases· Medicine
machine prediction:candidate · noneconsensus · none
174
citations
affunlabeled
Walker-Warburg syndrome
Jiri Vajsar, Harry Schachter
2006· review· en· Orphanet Journal of Rare Diseases· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
162
citations
afffundunlabeled
Cirrhotic cardiomyopathy
Soon Koo Baik, Tamer Fouad, Samuel S. Lee
2007· review· en· Orphanet Journal of Rare Diseases· Medicine
machine prediction:candidate · noneconsensus · none
149
citations
affunlabeled
Genotype-phenotype correlations in recessive RYR1-related myopathies
Kimberly Amburgey, Angela M. Bailey, J.H. Hwang, Mark A. Tarnopolsky, Carsten G. Bönnemann, Līvija Medne +5 more
2013· article· en· Orphanet Journal of Rare Diseases· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
126
citations
aboutno affunlabeled
Global epidemiology of amyloid light-chain amyloidosis
Nishant Kumar, Nicole Zhang, Dasha Cherepanov, Dorothy Romanus, Michael E. Hughes, Douglas V. Faller
2022· review· en· Orphanet Journal of Rare Diseases· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
95
citations
aboutno affunlabeled
The hyperornithinemia–hyperammonemia-homocitrullinuria syndrome
Diego Martinelli, Daria Diodato, Emanuela Ponzi, Magnus Monné, Sara Boenzi, Enrico Bertini +2 more
2015· review· en· Orphanet Journal of Rare Diseases· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
94
citations
affunlabeled
Alstrom syndrome (OMIM 203800): a case report and literature review
Tisha Joy, Henian Cao, Graeme C. Black, Rayaz A. Malik, Valentine Charlton-Menys, Robert A. Hegele +1 more
2007· review· en· Orphanet Journal of Rare Diseases· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
89
citations
fundno affunlabeled
Comparing access to orphan medicinal products in Europe
Bernarda Zamora, F. Maignen, P. O’Neill, Jorge Mestre‐Ferrandiz, Martina Garau
2019· article· en· Orphanet Journal of Rare Diseases· Economics, Econometrics and Finance
machine prediction:candidate · noneconsensus · none
87
citations
afffundunlabeled
The genotypic and phenotypic spectrum of PIGA deficiency
Maja Tarailo‐Graovac, Graham Sinclair, Sylvia Stöckler‐Ipsiroglu, Margot Van Allen, Jacob Rozmus, Casper Shyr +9 more
2015· article· en· Orphanet Journal of Rare Diseases· Immunology and Microbiology
machine prediction:candidate · noneconsensus · none
87
citations
affunlabeled
Hypersensitivity pneumonitis
Yves Lacasse, Yvon Cormier
2006· review· en· Orphanet Journal of Rare Diseases· Medicine
machine prediction:candidate · noneconsensus · none
77
citations

How this was built: Screen · Findings · About