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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.

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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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Metabolism and Genetic 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.

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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.

1,813 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.
1,813 works in the cohort · of 4,299,418page 7 of 37

Labels cover 1 of 1,813 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 1,813 of 1,813 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affunlabeled
Recommendations for the use of sapropterin in phenylketonuria
Amy Cunningham, Heather Bausell, Mary M. Brown, Maggie Chapman, Kari DeFouw, Sharon L. Ernst +11 more
2012· article· en· Molecular Genetics and Metabolism· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
46
citations
afffundno abstractunlabeled
Novel homozygous PCK1 mutation causing cytosolic phosphoenolpyruvate carboxykinase deficiency presenting as childhood hypoglycemia, an abnormal pattern of urine metabolites and liver dysfunction
Päivi Vieira, Jessie M. Cameron, Elisa Rahikkala, Riikka Keski‐Filppula, Linhua Zhang, Saikat Santra +8 more
2017· article· en· Molecular Genetics and Metabolism· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
44
citations
aboutno affunlabeled
Carnitine Palmitoyltransferase-1A Deficiency
Deanna M. Dykema
2012· article· en· Advances in Neonatal Care· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
43
citations
affno abstractunlabeled
Threshold for toxicity from hyperammonemia in critically ill children
Bruno Ozanne, J. Craig Nelson, J.M. Cousineau, Marie Lambert, Véronique Phan, Grant A. Mitchell +3 more
2011· article· en· Journal of Hepatology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
42
citations
affunlabeled
Amish, Mennonite, and Hutterite Genetic Disorder Database
Michael Payne, C Anthony Rupar, Geoffrey M. Siu, Victoria Mok Siu
2011· article· en· Paediatrics & Child Health· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
41
citations
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