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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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The American Journal of Human Genetics
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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.

836 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.
836 works in the cohort · of 4,299,418page 8 of 17

Labels cover 0 of 836 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 836 of 836 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.

affno abstractunlabeled
ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions
Hao Hu, Katinka Eggers, Wei Chen, Masoud Garshasbi, M. Mahdi Motazacker, Klaus Wrogemann +10 more
2011· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
111
citations
afffundno abstractunlabeled
GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies
Mika Asai-Coakwell, Curtis R. French, K. Berry, Ming Ye, Ron Koss, Martin J. Somerville +4 more
2007· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
109
citations
affno abstractunlabeled
CRYBA4, a Novel Human Cataract Gene, Is Also Involved in Microphthalmia
Gail Billingsley, Sathiyavedu Thyagarajan Santhiya, Andrew D. Paterson, Koji Ogata, Shoshana J. Wodak, Sayed Mohsen Hosseini +5 more
2006· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
108
citations
fundno affno abstractunlabeled
Autozygosity Mapping of a Seckel Syndrome Locus to Chromosome 3q22.1-q24
Judith Goodship, Harinder Gill, Joan Carter, Andrew P. Jackson, Miranda Splitt, Michael Wright
2000· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
107
citations
afffundno abstractunlabeled
Cole-Carpenter Syndrome Is Caused by a Heterozygous Missense Mutation in P4HB
Frank Rauch, Somayyeh Fahiminiya, Jacek Majewski, Jian Carrot‐Zhang, Sergei P. Boudko, Francis H. Glorieux +3 more
2015· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
106
citations
affno abstractunlabeled
DNA Microarrays: A Molecular Cloning Manual
Alain E. Lagarde
2003· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
102
citations
affno abstractunlabeled
Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome
Machteld M. Oud, Paul Tuijnenburg, Maja Hempel, Naomi van Vlies, Zemin Ren, Sacha Ferdinandusse +32 more
2017· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
101
citations
afffundno abstractunlabeled
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
Carol-Anne Martin, Kata Sarlós, Clare V. Logan, Roshan Singh Thakur, David Parry, Anna H. Bizard +45 more
2018· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
99
citations

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