MétaCan
Menu
Cohort builder

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.

Search term
Author
Year range
Sort
Language
Type
Field
Venue
Topic
Genomic variations and chromosomal abnormalities
Retraction
Abstract
Evidence source
Study design
Label agreement
Label status

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.

1,322 results · 1 filter active ·
Results by year
20002025
Publication date
Categories
Machine labels · sparse coverage
Evidence
Language
Type
Citations
An unlabeled work is unknown, not a negative. Label coverage is reported on every query.
1,322 works in the cohort · of 4,299,418page 12 of 27

Labels cover 3 of 1,322 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 1,322 of 1,322 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affunlabeled
Duplication of the STS region in males is a benign copy‐number variant
Aubry Furrow, Aaron Theisen, Lea Velsher, Erawati V. Bawle, Sujatha Sastry, Nancy J. Mendelsohn +3 more
2011· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
21
citations
afffundunlabeled
HD-CNV: hotspot detector for copy number variants
Jenna Butler, M Elizabeth O Locke, Kathleen A. Hill, Mark Daley
2012· article· en· Bioinformatics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
21
citations
affno abstractunlabeled
Where are the missing pieces of the schizophrenia genetics puzzle?
Simon Girard, Lan Xiong, Patrick A. Dion, Guy A. Rouleau
2011· review· en· Current Opinion in Genetics & Development· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
20
citations
affno abstractunlabeled
The use of cytogenetics in understanding ovarian cancer
Marcus Q. Bernardini, J. Weberpals, Jeremy A. Squire
2003· review· en· Biomedicine & Pharmacotherapy· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
20
citations
affunlabeled
Copy number variation in metabolic phenotypes
Matthew B. Lanktree, Robert A. Hegele
2008· review· en· Cytogenetic and Genome Research· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
20
citations
affunlabeled
Genome Mapping Nomenclature
Sarah J. Moore, Jean McGowan‐Jordan, Adam C. Smith, Katrina Rack, Udo Koehler, Marian Stevens‐Kroef +3 more
2023· review· en· Cytogenetic and Genome Research· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
20
citations
affno abstractunlabeled
Mosaic microdeletion 18q21 as a cause of mental retardation
Dimitri J. Stavropoulos, Daune MacGregor, Grace Yoon
2010· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
19
citations
fundno affunlabeled
The psychiatric phenotypes of 1q21 distal deletion and duplication
Stefanie C. Linden, Cameron Watson, Jacqueline Smith, Samuel J. R. A. Chawner, T. Lancaster, Ffion Evans +11 more
2021· article· en· Translational Psychiatry· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
19
citations
affno abstractunlabeled
Mosaic copy number variation in schizophrenia
Douglas M. Ruderfer, Kim Chambert, Jennifer L. Moran, Michael E. Talkowski, Elizabeth Chen, Carolina Oliveira Gigek +15 more
2013· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
19
citations
affunlabeled
The Hunter–McAlpine syndrome results from duplication 5q35–qter
AGW Hunter, Barbara R. DuPont, Margaret E. McLaughlin, Lyn Hinton, Elizabeth Baker, Lesley C. Adès +2 more
2004· article· en· Clinical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
19
citations
afffundunlabeled
Inverted duplication with terminal deletion of 5p and no cat‐like cry
Jia‐Chi Wang, Bradley P. Coe, Brenda Lomax, Patrick MacLeod, Malcolm Parslow, Jacqueline E. Schein +2 more
2008· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
18
citations
affunlabeled
A Case Report of Monozygotic Twins with Smith-Magenis Syndrome
Matthew Hicks, Susan A. Ferguson, François P. Bernier, Jean-François Lemay
2008· article· en· Journal of Developmental & Behavioral Pediatrics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
18
citations

How this was built: Screen · Findings · About