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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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Molecular Genetics and Metabolism
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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.

642 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.
642 works in the cohort · of 4,299,418page 3 of 13

Labels cover 0 of 642 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 642 of 642 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affno abstractunlabeled
X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism
Ying Wang, Rachel Busin, Catherine Reeves, Lena Bezman, Gerald V. Raymond, Cicely J. Toomer +13 more
2011· article· en· Molecular Genetics and Metabolism· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
56
citations
afffundno abstractunlabeled
Disease specific therapies in leukodystrophies and leukoencephalopathies
Guy Helman, Keith Van Haren, Joshua L. Bonkowsky, Geneviève Bernard, Amy Pizzino, Nancy Braverman +17 more
2015· article· en· Molecular Genetics and Metabolism· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
55
citations
affno abstractunlabeled
Vitamin B12 and birth defects
Fei Li, David Watkins, David S. Rosenblatt
2009· review· en· Molecular Genetics and Metabolism· Medicine
distilled prediction:candidate · metaepi_narrowconsensus · none
51
citations
affaboutno abstractunlabeled
Hepatic Carnitine Palmitoyl Transferase 1 (CPT1 A) Deficiency in North American Hutterites (Canadian and American): Evidence for a Founder Effect and Results of a Pilot Study on a DNA-Based Newborn Screening Program
C. Prasad, John P. Johnson, Jean‐Paul Bonnefont, Louise A. Dilling, A. Micheil Innes, J. C. Haworth +8 more
2001· article· en· Molecular Genetics and Metabolism· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
50
citations
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
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