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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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Muscle Physiology and Disorders
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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.

2,525 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.
2,525 works in the cohort · of 4,299,418page 37 of 51

Labels cover 2 of 2,525 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 2,525 of 2,525 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.

affno abstractunlabeled
Duchenne muscular dystrophy: Ringo to the rescue?
Ronald D. Cohn, Victor Dubowitz
2016· editorial· en· Neuromuscular Disorders· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
2
citations
afffundunlabeled
Isolation of a persistently quiescent muscle satellite cell population
Alexandra P. Steele, Anika L. Syroid, Cassandra Mombo, Shathana Raveetharan, Irena A. Rebalka, Thomas J. Hawke
2024· article· en· American Journal of Physiology-Cell Physiology· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
2
citations
aboutno affno abstractunlabeled
DUCHENNE MUSCULAR DYSTROPHY - GENETICS
Sara Passos, Patrícia Tavares, Thiago Junqueira Ribeiro de Rezende, L. Souza, Tábada Samantha Marques Rosa, C. Iwabe-Marchese +2 more
2018· article· en· Neuromuscular Disorders· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
2
citations
affaboutunlabeled
Muscle loss: does one size fit all? A comment on Bozzetti's paper
Marı́a Cristina González, Alfonso J. Cruz‐Jentoft, Stuart M. Phillips, Carla M. Prado
2024· letter· en· Current Opinion in Clinical Nutrition & Metabolic Care· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
2
citations
affunlabeled
Cardiac MRI in Duchenne and Becker Muscular Dystrophy
Manu Santhappan Girija, Deepak Menon, Kiran Polavarapu, Veeramani Preethish‐Kumar, Seena Vengalil, Saraswati Nashi +10 more
2024· article· en· Annals of Indian Academy of Neurology· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
2
citations
affno abstractunlabeled
Molecular Diagnosis of Myopathies
Andrew Gómez-Vargas, Steven K. Baker
2011· review· en· Rheumatic Disease Clinics of North America· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
2
citations
affunlabeled
A rare case of myopathy with fatigability due to <i>PYROXD1</i> variation
Dipti Baskar, Aneesha Thomas, Vijay Kumar Boddu, Rashmi Santhoshkumar, Ram Murthy Anjanappa, Saraswati Nashi +8 more
2024· article· en· Journal of Neuromuscular Diseases· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
2
citations

How this was built: Screen · Findings · About