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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 10 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
De Novo Mutations in YWHAG Cause Early-Onset Epilepsy
Ilaria Guella, Marna B. McKenzie, Daniel M. Evans, Sarah E. Buerki, Eric Toyota, Margot I. Van Allen +21 more
2017· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
86
citations
afffundno abstractunlabeled
Genetic Analysis of 103 Candidate Genes for Coronary Artery Disease and Associated Phenotypes in a Founder Population Reveals a New Association between Endothelin-1 and High-Density Lipoprotein Cholesterol
Guillaume Paré, David Serre, Diane Brisson, Sonia S. Anand, Alexandre Montpetit, G Tremblay +3 more
2007· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
85
citations
affno abstractunlabeled
A Novel Locus for Leber Congenital Amaurosis Maps to Chromosome 6q
Sharola Dharmaraj, Yingying Li, Johane M. Robitaille, Eduardo Silva, Danping Zhu, Thomas N. Mitchell +3 more
2000· letter· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
83
citations
affno abstractunlabeled
Mutations in the NHEJ Component XRCC4 Cause Primordial Dwarfism
Jennie Murray, Mirjam van der Burg, Hanna IJspeert, Paula Carroll, Qian Wu, Takashi Ochi +16 more
2015· article· en· The American Journal of Human Genetics· Physics and Astronomy
machine prediction:candidate · noneconsensus · none
83
citations
affunlabeled
Imputation of KIR Types from SNP Variation Data
Damjan Vukcevic, James A. Traherne, Sigrid Næss, Eva Ellinghaus, Alexander Dilthey, Mark Lathrop +8 more
2015· article· en· The American Journal of Human Genetics· Immunology and Microbiology
machine prediction:candidate · noneconsensus · none
82
citations
affno abstractunlabeled
Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome
Yline Capri, Elisabetta Flex, Oliver H.F. Krumbach, Giovanna Carpentieri, Serena Cecchetti, Christina Lißewski +27 more
2019· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
81
citations
affno abstractunlabeled
Mutations in IMPG1 Cause Vitelliform Macular Dystrophies
Gaël Manès, Isabelle Meunier, Almudena Ávila‐Fernández, Sandro Banfi, Guylène Le Meur, Xavier Zanlonghi +21 more
2013· article· en· The American Journal of Human Genetics· Medicine
machine prediction:candidate · noneconsensus · none
81
citations
afffundunlabeled
Shifting landscapes of human MTHFR missense-variant effects
Jochen Weile, Nishka Kishore, Song Sun, Ranim Maaieh, Marta Verby, Roujia Li +15 more
2021· article· en· The American Journal of Human Genetics· Medicine
machine prediction:candidate · noneconsensus · none
80
citations
affno abstractunlabeled
The Metabolic Map into the Pathomechanism and Treatment of PGM1-CDG
Silvia Radenkovic, Matthew Bird, Tim L. Emmerzaal, Sunnie Wong, Catarina Felgueira, Kyle M. Stiers +19 more
2019· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
80
citations
afffundno abstractunlabeled
De Novo Mutations in EBF3 Cause a Neurodevelopmental Syndrome
Hannah Sleven, Seth J. Welsh, Jing Yu, Mair E. A. Churchill, Caroline F. Wright, Alex Henderson +15 more
2016· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
78
citations
afffundno abstractunlabeled
Hypomorphic Temperature-Sensitive Alleles of NSDHL Cause CK Syndrome
Keith W. McLarren, Tesa Severson, Christèle du Souich, David W. Stockton, Lisa E. Kratz, David Cunningham +34 more
2010· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
74
citations

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