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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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European 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.

affaffiliation
fundfunder
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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.

513 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.
513 works in the cohort · of 4,299,418page 3 of 11

Labels cover 0 of 513 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 513 of 513 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affno abstractunlabeled
Five children with deletions of 1p34.3 encompassing AGO1 and AGO3
Mari Tokita, Penny Chow, Ghayda Mirzaa, Nicola Dikow, Bianca Maas, Bertrand Isidor +9 more
2014· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
62
citations
afffundaboutunlabeled
Life insurance: genomic stratification and risk classification
Yann Joly, Hilary Burton, Bartha Maria Knoppers, Ida Ngueng Feze, Tom Dent, Nora Pashayan +8 more
2013· letter· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
57
citations
aboutno affunlabeled
Future-proofing biobanks’ governance
Felix Gille, Effy Vayena, Alessandro Blasimme
2020· review· en· European Journal of Human Genetics· Medicine
distilled prediction:candidate · metaepi_narrow+research_integrityconsensus · none
57
citations
affno abstractunlabeled
Genotype and phenotype spectrum of NRAS germline variants
Franziska Altmüller, Christina Lißewski, Débora Romeo Bertola, Elisabetta Flex, Zornitza Stark, Stephanie Spranger +20 more
2017· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
56
citations
affno abstractunlabeled
Identification and functional analysis of novel THAP1 mutations
Katja Lohmann, Nils Uflacker, Alev Erogullari, Thora Lohnau, Susen Winkler, Andreas Dendorfer +18 more
2011· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
54
citations
afffundno abstractunlabeled
HLA-DQB1*02 and DQB1*06:03P are associated with peanut allergy
Anne‐Marie Madore, Vanessa T. Vaillancourt, Yuka Asai, Reza Alizadehfar, Moshe Ben‐Shoshan, Déborah Michel +8 more
2013· article· en· European Journal of Human Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
51
citations
afffundunlabeled
Registered access: authorizing data access
Stephanie O. M. Dyke, Mikael Lindén, Ilkka Lappalainen, Jordi Rambla, Knox Carey, David Lloyd +40 more
2018· article· en· European Journal of Human Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
48
citations
afffundno abstractunlabeled
Retrospective access to data: the ENGAGE consent experience
Anne Marie Tassé, Isabelle Budin‐Ljøsne, Bartha Maria Knoppers, Jennifer R. Harris
2010· article· en· European Journal of Human Genetics· Medicine
distilled prediction:candidate · metaresearch+research_integrityconsensus · none
47
citations
affno abstractunlabeled
TSEN54 mutations cause pontocerebellar hypoplasia type 5
Yasmin Namavar, David Chitayat, P. G. Barth, Fred van Ruissen, Marit B. de Wissel, Bwee Tien Poll‐The +2 more
2011· article· en· European Journal of Human Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
47
citations
affno abstractunlabeled
Patient mutations alter ATRX targeting to PML nuclear bodies
Nathalie G. Bérubé, Jasmine Healy, Chantal Médina, Shaobo Wu, Todd R Hodgson, Magdalena Jagla +1 more
2007· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
47
citations
afffundno abstractunlabeled
Expansion of phenotype and genotypic data in CRB2-related syndrome
Ryan E. Lamont, Wen‐Hann Tan, A. Micheil Innes, Jillian S. Parboosingh, Dina Schneidman‐Duhovny, Aleksandar Rajkovic +14 more
2016· review· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
46
citations

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