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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 & Genomic Medicine
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Retraction
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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
aboutaboutness

The four routes compose: require the funder route and exclude affiliation to get the funder-only stratum no affiliation-based frame ever sees.

103 results · 1 filter active ·
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20132025
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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.
103 works in the cohort · of 4,299,418page 1 of 3

Labels cover 0 of 103 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 103 of 103 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affunlabeled
The CLN3 gene and protein: What we know
Myriam Mirza, Anna Vainshtein, Alberto DiRonza, Uma Chandrachud, Luke J. Haslett, Michela Palmieri +6 more
2019· review· en· Molecular Genetics & Genomic Medicine· Medicine
distilled prediction:candidate · metaepi_narrowconsensus · none
76
citations
fundno affunlabeled
Metformin treatment in young children with fragile X syndrome
Hazel Maridith Barlahan Biag, Laura A. Potter, Victoria Wilkins, Sumra Afzal, Alexis Rosvall, María Jimena Salcedo‐Arellano +6 more
2019· article· en· Molecular Genetics & Genomic Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
66
citations
afffundaboutunlabeled
<i>ERCC6L2</i>‐associated inherited bone marrow failure syndrome
Iren Shabanova, Elisa Cohen, Michaela Cada, Ajoy Vincent, Ronald D. Cohn, Yigal Dror
2018· review· en· Molecular Genetics & Genomic Medicine· Medicine
distilled prediction:candidate · metaepi_narrow+research_integrity+insufficient_payloadconsensus · metaepi_narrow+insufficient_payload
37
citations
fundno affunlabeled
Defective INPP5E distribution in NPHP1‐related Senior–Loken syndrome
Ke Ning, Emilie Song, Brent E. Sendayen, Philipp P. Prosseda, Kun‐Che Chang, Alireza Ghaffarieh +6 more
2020· article· en· Molecular Genetics & Genomic Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
20
citations
affunlabeled
A‐<scp>T<sub>W</sub></scp><sub>innipeg</sub>: Pathogenesis of rare <i><scp>ATM</scp></i> missense mutation c.6200C&gt;A with decreased protein expression and downstream signaling, early‐onset dystonia, cancer, and life‐threatening radiotoxicity
Kotoka Nakamura, Francesca Fike, Sara Haghayegh, Rachel Saunders‐Pullman, Angelika J. Dawson, Thilo Dörk +1 more
2014· article· en· Molecular Genetics & Genomic Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
16
citations
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