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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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European Journal of Medical Genetics
Topic
Retraction
Abstract
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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.

112 results · 1 filter active ·
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20052025
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Machine labels · sparse coverage
Evidence
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An unlabeled work is unknown, not a negative. Label coverage is reported on every query.
112 works in the cohort · of 4,299,418page 1 of 3

Labels cover 0 of 112 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 112 of 112 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affno abstractunlabeled
Clinical and Mutational Spectrum of Mowat–Wilson Syndrome
Christiane Zweier, Christian T. Thiel, Andreas Dufke, Yanick J. Crow, Peter Meinecke, Mohnish Suri +35 more
2005· article· en· European Journal of Medical Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
137
citations
affaboutunlabeled
Attitudes of publics who are unwilling to donate DNA data for research
Anna Middleton, Richard Milne, Adrian Thorogood, Erika Kleiderman, Emilia Niemiec, Barbara Prainsack +8 more
2018· article· en· European Journal of Medical Genetics· Medicine
distilled prediction:candidate · metaresearch+research_integrityconsensus · metaresearch
91
citations
affno abstractunlabeled
Rare ACTG1 variants in fetal microlissencephaly
Karine Poirier, Jéléna Martinovic, A. Laquérrière, Mara Cavallin, Catherine Fallet‐Bianco, Isabelle Desguerre +7 more
2015· article· en· European Journal of Medical Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
32
citations
affno abstractunlabeled
Unusual 8p inverted duplication deletion with telomere capture from 8q
Karen Buysse, Francesca Antonacci, Bert Callewaert, Bart Loeys, Ulrike Fränkel, Victoria Mok Siu +3 more
2008· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
26
citations
affno abstractunlabeled
Mosaic microdeletion 18q21 as a cause of mental retardation
Dimitri J. Stavropoulos, Daune MacGregor, Grace Yoon
2010· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
19
citations
fundno affno abstractunlabeled
A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features – Is cardiac assessment necessary for all patients with 17p13.3 microduplication?
Alvin Chi Chung Ho, Anthony P. Y. Liu, Kin Shing Lun, Wing‐Fai Tang, Kelvin Y.K. Chan, Elizabeth Y.T. Lau +3 more
2012· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
16
citations
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