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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
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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 1 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
Beckwith–Wiedemann syndrome
Rosanna Weksberg, Cheryl Shuman, J. Bruce Beckwith
2009· review· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
690
citations
affno abstractunlabeled
Genomic inflation factors under polygenic inheritance
Jian Yang, Michael N. Weedon, Shaun Purcell, Guillaume Lettre, Karol Estrada, Cristen J. Willer +15 more
2011· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
642
citations
affno abstractunlabeled
Whole-genome sequencing in health care
Carla van El, Martina C. Cornel, Pascal Borry, Ros Hastings, Florence Fellmann, Shirley V. Hodgson +8 more
2013· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
383
citations
affunlabeled
The Global State of the Genetic Counseling Profession
Mary Ann R. Abacan, Lamia Alsubaie, Kristine Barlow‐Stewart, Beppy Caanen, Christophe Cordier, Eliza Courtney +32 more
2018· review· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
371
citations
affno abstractunlabeled
The mutation spectrum in RECQL4 diseases
H. Annika Siitonen, Jenni Sotkasiira, Martine Biervliet, Abdelmadjid Benmansour, Yline Capri, Valérie Cormier‐Daire +15 more
2008· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
233
citations
fundno affno abstractunlabeled
A 15q13.3 microdeletion segregating with autism
Alistair T. Pagnamenta, Kirsty Wing, Elham Sadighi Akha, Samantha J.L. Knight, Sven Bölte, Gabriele Schmötzer +7 more
2008· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
178
citations
affno abstractunlabeled
Elastin: mutational spectrum in supravalvular aortic stenosis
Kay Metcalfe, Agnes K Rucka, Leslie Smoot, Guenter Hofstadler, Gerald Tuzler, Pascal McKeown +12 more
2000· article· en· European Journal of Human Genetics· Neuroscience
distilled prediction:candidate · insufficient_payloadconsensus · none
175
citations
afffundunlabeled
Toward a roadmap in global biobanking for health
Jennifer R. Harris, Paul R. Burton, Bartha Maria Knoppers, Klaus Lindpaintner, Marianna J. Bledsoe, Anthony J. Brookes +19 more
2012· article· en· European Journal of Human Genetics· Medicine
distilled prediction:candidate · noneconsensus · none
172
citations
affno abstractunlabeled
PITX2 and FOXC1 spectrum of mutations in ocular syndromes
Linda M. Reis, Rebecca C. Tyler, Bethany A. Kloss, Kala F. Schilter, Alex V. Levin, R. Brian Lowry +5 more
2012· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
149
citations
affno abstractunlabeled
Neurofibromatosis 1
Rosalie E. Ferner
2006· review· en· European Journal of Human Genetics· Medicine
distilled prediction:candidate · metaepi_narrowconsensus · none
141
citations
afffundno abstractunlabeled
DNM1L-related mitochondrial fission defect presenting as refractory epilepsy
Jason Vanstone, Amanda M Smith, Skye McBride, Martin Holčı́k, Ghadi Antoun, Mary‐Ellen Harper +10 more
2015· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
140
citations
afffundno abstractunlabeled
Prevalence of congenital amusia
Isabelle Peretz, Dominique T. Vuvan
2017· article· en· European Journal of Human Genetics· Neuroscience
distilled prediction:candidate · noneconsensus · none
136
citations
affno abstractunlabeled
Twin study of genetic and aging effects on X chromosome inactivation
Marianne Kristiansen, Gun Peggy Knudsen, Lise Bathum, Anna K. Naumova, Thomas Heiberg Brix, Anders Jørgen Svendsen +3 more
2005· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
115
citations
fundno affno abstractunlabeled
Provision of genetic services in Europe: current practices and issues
Béatrice Godard, Helena Kääriäinen, Ulf Kristoffersson, Lisbeth Tranebjærg, Domenico Coviello, Ségolène Aymé
2003· review· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
108
citations
afffundunlabeled
De novo variants in sporadic cases of childhood onset schizophrenia
Amirthagowri Ambalavanan, Simon Girard, Kwangmi Ahn, Sirui Zhou, Alexandre Dionne‐Laporte, Dan Spiegelman +8 more
2015· article· en· European Journal of Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
100
citations

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