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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 3 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.

aboutno affunlabeled
A Brief History of Choline
Steven H. Zeisel
2012· article· en· Annals of Nutrition and Metabolism· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
107
citations
affunlabeled
Metabolic Myopathies: Update 2009
Brian van Adel, Mark A. Tarnopolsky
2009· review· en· Journal of Clinical Neuromuscular Disease· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
106
citations
afffundunlabeled
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in <i>GLS</i>
André B. P. Kuilenburg, Maja Tarailo‐Graovac, Phillip A. Richmond, Britt I. Drögemöller, Mahmoud A. Pouladi, René Leen +39 more
2019· article· en· New England Journal of Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
105
citations
affunlabeled
Obesity and lipid stress inhibit carnitine acetyltransferase activity
Sarah E. Seiler, Ola J. Martin, Robert C. Noland, Dorothy H. Slentz, Karen L. DeBalsi, Olga Ilkayeva +4 more
2014· article· en· Journal of Lipid Research· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
105
citations
afffundno abstractunlabeled
Arginase-1 deficiency
Yuan Yan Sin, Garrett Baron, Andreas Schulze, Colin Funk
2015· review· en· Journal of Molecular Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
103
citations
affno abstractunlabeled
LC–MS/MS progress in newborn screening
Denis C. Lehotay, Patricia Hall, Joyce Lepage, J. Eichhorst, Michele L. Etter, Cheryl R. Greenberg
2010· review· en· Clinical Biochemistry· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrow+research_integrityconsensus · none
102
citations
fundno affno abstractunlabeled
Structural and Mechanistic Studies on γ-Butyrobetaine Hydroxylase
Ivanhoe K. H. Leung, T. Krojer, Grazyna Kochan, Luc Henry, F. von Delft, Timothy D. W. Claridge +3 more
2010· article· en· Chemistry & Biology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
102
citations
affunlabeled
Treatable inherited rare movement disorders
Hyder A. Jinnah, Alberto Albanese, Kailash P. Bhatia, Francisco Cardoso, Gustavo Da Prat, Tom J. de Koning +19 more
2017· review· en· Movement Disorders· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
100
citations
afffundno abstractunlabeled
Transfer of Arginine into Lipid Bilayers Is Nonadditive
Justin L. MacCallum, William F. Bennett, D. Peter Tieleman
2011· article· en· Biophysical Journal· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
99
citations
affunlabeled
A Clinical Guide to Inherited Metabolic Diseases
Joe T.R. Clarke
2005· book· en· Cambridge University Press eBooks· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
96
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
distilled prediction:candidate · metaepi_narrowconsensus · none
94
citations
affno abstractunlabeled
Hypoglycemic brain damage
Roland N. Auer
2004· review· en· Forensic Science International· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
93
citations
affno abstractunlabeled
Tyrosinemia type II: nine cases of ocular signs and symptoms
Marian S. Macsai, Terry L. Schwartz, David M. Hinkle, Mary Beth Hummel, M. Mulhern, David Rootman
2001· article· en· American Journal of Ophthalmology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
92
citations
affno abstractunlabeled
Citrin deficiency, a perplexing global disorder
David Dimmock, Bruno Maranda, Carlo Dionisi‐Vici, Jing Wang, Soledad Kleppe, Giuseppe Fiermonte +6 more
2008· article· en· Molecular Genetics and Metabolism· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
89
citations
affunlabeled
Neonatal neuroimaging findings in inborn errors of metabolism
Andrea Poretti, Susan Blasér, Maarten H. Lequin, Ali Fatemi, Avner Meoded, Frances J. Northington +2 more
2012· review· en· Journal of Magnetic Resonance Imaging· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
89
citations
afffundaboutunlabeled
PAHdb: A locus-specific knowledgebase
Charles R. Scriver, Paula J. Waters, Christineh N. Sarkissian, Shannon Ryan, Lynne Prevost, David C�t� +3 more
2000· article· en· Human Mutation· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · insufficient_payloadconsensus · none
89
citations
affno abstractunlabeled
Adult phenylketonuria
Will Hanley
2004· review· nn· The American Journal of Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
88
citations
affunlabeled
Benzyl Alcohol Metabolism and Elimination in Neonates
Marc Lebel, Liliane A. Ferron, M. Masson, Jeanne Pichette, Charles S. Carrier
2017· article· en· Developmental Pharmacology and Therapeutics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
87
citations
affno abstractunlabeled
Hereditary and acquired diseases of acyl-coenzyme A metabolism
Grant A. Mitchell, Nicolas Gauthier, Alain Lesimple, Shu Pei Wang, Orval Mamer, Ijaz A. Qureshi
2008· review· en· Molecular Genetics and Metabolism· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
84
citations
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