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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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Journal of Medical 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.

449 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.
449 works in the cohort · of 4,299,418page 1 of 9

Labels cover 0 of 449 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 449 of 449 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundunlabeled
Apoptosis and cancer: mutations within caspase genes
Saeid Ghavami, Mohammad Hashemi, Sudharsana Rao Ande, Behzad Yeganeh, Wenyan Xiao, Mohsen Eshraghi +4 more
2009· review· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
708
citations
afffundunlabeled
The molecular genetics of Marfan syndrome and related disorders
Peter N. Robinson, Emilio Arteaga‐Solis, Clair Baldock, Gwenaëlle Collod‐Béroud, Patrick Booms, Anne De Paepe +13 more
2006· review· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
431
citations
afffundunlabeled
What can exome sequencing do for you?
Jacek Majewski, Jeremy Schwartzentruber, Emilie Lalonde, Alexandre Montpetit, Nada Jabado
2011· review· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
382
citations
affunlabeled
The cardiofaciocutaneous syndrome
Amy E. Roberts, Judith Allanson, Suzanne K. Jadico, Maria Inês Kavamura, Jacqueline A. Noonan, John M. Opitz +2 more
2006· review· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
270
citations
affunlabeled
<i>SMAD4</i> mutations found in unselected HHT patients
Carol J. Gallione, Jjais Richards, Tom G.W. Letteboer, Diane Rushlow, Nadia L. Prigoda, Tracey P. Leedom +6 more
2006· article· en· Journal of Medical Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
256
citations
affunlabeled
Kabuki syndrome: international consensus diagnostic criteria
Margaret P Adam, Siddharth Banka, Hans T. Björnsson, Olaf A. Bodamer, Albert E. Chudley, Jaqueline Harris +8 more
2018· article· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
248
citations
affunlabeled
<i>NOTCH2</i> mutations in Alagille syndrome
Binita M. Kamath, Robert C. Bauer, Kathleen M. Loomes, Grace F. Chao, Jennifer Gerfen, Anne Hutchinson +11 more
2011· article· en· Journal of Medical Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
219
citations
affunlabeled
Rett syndrome: clinical review and genetic update
Linda S. Weaving
2005· review· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
213
citations
affunlabeled
Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia
Kathleen Kaiser‐Rogers, Deborah E. McFadden, Chad Livasy, Jerome Dansereau, Ruby Jiang, Judith Knops +3 more
2005· letter· en· Journal of Medical Genetics· Medicine
distilled prediction:candidate · metaepi_narrow+research_integrity+insufficient_payloadconsensus · none
197
citations
afffundunlabeled
Mutations in WNT1 are a cause of osteogenesis imperfecta
Somayyeh Fahiminiya, Jacek Majewski, John S. Mort, Pierre Moffatt, Francis H. Glorieux, Frank Rauch
2013· article· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
196
citations
affunlabeled
Germline E-cadherin mutations in familial lobular breast cancer
Serena Masciari, Nils‐Göran Larsson, Janine Senz, Niki Boyd, Pardeep Kaurah, M. Kandel +10 more
2007· letter· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrow+research_integrityconsensus · none
187
citations
affunlabeled
High frequency of de novo mutations in Li–Fraumeni syndrome
Kelly Gonzalez, Carolyn H. Buzin, Katie Noltner, Dongqing Gu, W Li, David Malkin +1 more
2009· letter· en· Journal of Medical Genetics· Medicine
distilled prediction:candidate · research_integrityconsensus · research_integrity
169
citations
affunlabeled
Clinical course of sly syndrome (mucopolysaccharidosis type VII)
Adriana M. Montaño, Robert D. Steiner, Brett H. Graham, Marina Szlago, Robert M. Greenstein, Mercédes Pineda +21 more
2016· article· en· Journal of Medical Genetics· Medicine
distilled prediction:candidate · insufficient_payloadconsensus · none
165
citations
affunlabeled
Phenotype of triploid embryos: Table 1
Deborah E. McFadden
2005· article· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
160
citations

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