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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.

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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Retinal Development and 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.

2,141 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.
2,141 works in the cohort · of 4,299,418page 1 of 43

Labels cover 3 of 2,141 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 2,141 of 2,141 works in this cohort. Predictions are machine_predicted_unvalidated. The Gemma side is a direct model label for every work (title-only); the Codex side is a distilled, calibrated classifier. Candidate is the union; consensus is the intersection.

affunlabeled
Retinal Stem Cells in the Adult Mammalian Eye
Vincent Tropepe, Brenda L.K. Coles, Bernard J. Chiasson, D. Jonathan Horsford, Andrew Elia, Roderick R. McInnes +1 more
2000· article· en· Science· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
1,082
citations
affno abstractunlabeled
Leber congenital amaurosis: Genes, proteins and disease mechanisms
Anneke I. den Hollander, Ronald Roepman, Robert K. Koenekoop, Frans P.M. Cremers
2008· review· en· Progress in Retinal and Eye Research· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
824
citations
afffundunlabeled
Facile isolation and the characterization of human retinal stem cells
Brenda L.K. Coles, Brigitte Angénieux, Tomoyuki Inoue, Katia Del Rio‐Tsonis, Jason R. Spence, Roderick R. McInnes +2 more
2004· article· en· Proceedings of the National Academy of Sciences· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
411
citations
afffundno abstractunlabeled
Cell fate determination in the vertebrate retina
Erin A. Bassett, Valerie A. Wallace
2012· review· en· Trends in Neurosciences· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
321
citations
affunlabeled
How Variable Clones Build an Invariant Retina
Jie He, Gen Zhang, Alexandra D. Almeida, Michel Cayouette, Benjamin D. Simons, William A. Harris
2012· article· en· Neuron· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
243
citations
afffundunlabeled
Photoreceptors at a glance
Robert S. Molday, Orson L. Moritz
2015· review· en· Journal of Cell Science· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
225
citations
afffundno abstractunlabeled
Molecular basis for photoreceptor outer segment architecture
Andrew F.X. Goldberg, Orson L. Moritz, David S. Williams
2016· review· en· Progress in Retinal and Eye Research· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
195
citations
affunlabeled
CRB1 mutation spectrum in inherited retinal dystrophies
Anneke I. den Hollander, Jason A. Davis, Saskia D. van der Velde-Visser, Marijke N. Zonneveld, Chiara O. Pierrottet, Robert K. Koenekoop +7 more
2004· review· en· Human Mutation· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
191
citations
afffundno abstractunlabeled
Mutations in NOTCH1 Cause Adams-Oliver Syndrome
Anna‐Barbara Stittrich, Anna Lehman, Dale L. Bodian, J. R. Ashworth, Zheyuan Zong, Hong Li +13 more
2014· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
190
citations

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