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
The American Journal of Human Genetics
Topic
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.

836 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.
836 works in the cohort · of 4,299,418page 5 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 teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundno abstractunlabeled
Mutations in NOTCH1 Cause Adams-Oliver Syndrome
Anna‐Barbara Stittrich, Anna Lehman, Dale L. Bodian, J. R. Ashworth, Zheyuan Zong, Hong Li +13 more
2014· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
190
citations
afffundunlabeled
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
Saeed Al Turki, Ashok Kumar Manickaraj, Catherine L. Mercer, Sebastian S. Gerety, Marc‐Phillip Hitz, Sarah Lindsay +33 more
2014· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
187
citations
affno abstractunlabeled
Rare Mutations in XRCC2 Increase the Risk of Breast Cancer
Daniel J. Park, Fabienne Lesueur, Tú Nguyen‐Dumont, Maroulio Pertesi, FA Odefrey, Fleur Hammet +20 more
2012· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
183
citations
affno abstractunlabeled
Genomewide Linkage Analysis of Bipolar Disorder by Use of a High-Density Single-Nucleotide–Polymorphism (SNP) Genotyping Assay: A Comparison with Microsatellite Marker Assays and Finding of Significant Linkage to Chromosome 6q22
Frank A. Middleton, Michele T. Pato, Karen Gentile, Christopher P. Morley, Xinzhi Zhao, Amy F. Eisener +17 more
2004· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
173
citations
afffundno abstractunlabeled
A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis
Yee Him Cheung, Tenzin Gayden, Philippe M. Campeau, Charles A. LeDuc, Donna Russo, Văn Hùng Nguyễn +19 more
2013· article· en· The American Journal of Human Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
171
citations
afffundno abstractunlabeled
RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes
Margot R.F. Reijnders, Nurhuda Mohamad Ansor, Maria Kousi, Wyatt W. Yue, Perciliz L. Tan, Katie Clarkson +15 more
2017· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
170
citations
afffundno abstractunlabeled
Insufficient Evidence for “Autism-Specific” Genes
Scott M. Myers, Thomas D. Challman, Raphael Bernier, Thomas Bourgeron, Wendy K. Chung, John N. Constantino +7 more
2020· review· en· The American Journal of Human Genetics· Neuroscience
distilled prediction:candidate · metaepi_narrowconsensus · none
169
citations
affno abstractunlabeled
Measuring European Population Stratification with Microarray Genotype Data
Marc Bauchet, Brian McEvoy, Laurel N. Pearson, Ellen E. Quillen, Tamara Sarkisian, Kristine Hovhannesyan +3 more
2007· article· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
166
citations
affno abstractunlabeled
Mutation History of the Roma/Gypsies
Bharti Morar, David Gresham, Dora Angelicheva, Ivailo Tournev, Rebecca Gooding, Velina Guergueltcheva +16 more
2004· article· en· The American Journal of Human Genetics· Health Professions
distilled prediction:candidate · noneconsensus · none
166
citations
afffundno abstractunlabeled
Blood Pressure Loci Identified with a Gene-Centric Array
Toby Johnson, Tom R. Gaunt, Stephen Newhouse, Sandosh Padmanabhan, Maciej Tomaszewski, Meena Kumari +96 more
2011· review· en· The American Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
166
citations

How this was built: Screen · Findings · About