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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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Connective tissue disorders research
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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
fundfunder
venuejournal
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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.

1,331 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.
1,331 works in the cohort · of 4,299,418page 2 of 27

Labels cover 3 of 1,331 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 1,331 of 1,331 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundunlabeled
The liquid structure of elastin
Sarah Rauscher, Régis Pomès
2017· article· en· eLife· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
202
citations
afffundunlabeled
Mutations in WNT1 are a cause of osteogenesis imperfecta
Somayyeh Fahiminiya, Jacek Majewski, John S. Mort, Pierre Moffatt, Francis H. Glorieux, Frank Rauch
2013· article· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
196
citations
affunlabeled
Mutations in <i>SERPINF1</i> cause osteogenesis imperfecta type VI
Erica P. Homan, Frank Rauch, Ingo Grafe, Caressa Lietman, Jennifer A. Doll, Brian Dawson +11 more
2011· article· en· Journal of Bone and Mineral Research· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
190
citations
affno abstractunlabeled
Osteogenesis imperfecta
Francis H. Glorieux
2008· review· en· Best Practice & Research Clinical Rheumatology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaresearch+metaepi_narrow+research_integrity+insufficient_payloadconsensus · research_integrity
169
citations
afffundunlabeled
Fibulin-4 Deficiency Results in Ascending Aortic Aneurysms
Jianbin Huang, Elaine C. Davis, Shelby L. Chapman, Madhusudhan Budatha, Lihua Y. Marmorstein, R. Ann Word +1 more
2009· article· en· Circulation Research· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
165
citations
afffundno abstractunlabeled
Pregnancy outcome following in utero exposure to bisphosphonates
Shirley Levy, Ibrahim Fayez, Nobuko Taguchi, Jung Yeol Han, Jennifer Aiello, Doreen Matsui +3 more
2008· article· en· Bone· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
160
citations
afffundno abstractunlabeled
Impaired Elastogenesis in Hurler Disease
Aleksander Hinek, Sarah E. Wilson
2000· article· en· American Journal Of Pathology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
158
citations
afffundvenueaboutunlabeled
Structural disorder and dynamics of elastinThis paper is one of a selection of papers published in this special issue entitled “Canadian Society of Biochemistry, Molecular &amp; Cellular Biology 52nd Annual Meeting — Protein Folding: Principles and Diseases” and has undergone the Journal's usual peer review process.
Lisa D. Muiznieks, Anthony S. Weiss, Fred W. Keeley
2010· review· en· Biochemistry and Cell Biology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
156
citations
affno abstractunlabeled
Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome
Elena Belloni, Giuseppe Martucciello, Daniele Verderio, E. Ponti, Marco Seri, Vincenzo Jasonni +4 more
2000· letter· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
151
citations
afffundno abstractunlabeled
Recessive Osteogenesis Imperfecta Caused by Missense Mutations in SPARC
Roberto Mendoza‐Londono, Somayyeh Fahiminiya, Jacek Majewski, Martine Tétreault, Javad Nadaf, Pekka Kannus +14 more
2015· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
137
citations
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