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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.

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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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American Journal of Medical Genetics Part A
Topic
Retraction
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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
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.

974 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.
974 works in the cohort · of 4,299,418page 2 of 20

Labels cover 0 of 974 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 974 of 974 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affunlabeled
Investigation of<i>NRXN1</i>deletions: Clinical and molecular characterization
Mindy Preston Dabell, Jill A. Rosenfeld, Patricia I. Bader, Luis Escobar, Dima El‐Khechen, Stephanie E. Vallee +27 more
2013· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
111
citations
affunlabeled
A novel missense mutation in the galactosyltransferase‐I (<i>B4GALT7</i>) gene in a family exhibiting facioskeletal anomalies and Ehlers–Danlos syndrome resembling the progeroid type
Muhammad Faiyaz‐Ul‐Haque, Syed Hassan Ejaz Zaidi, Mariam Al‐Ali, Mariam Al‐Mureikhi, Shelley Kennedy, Ghalia M.H Al-Thani +2 more
2004· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
109
citations
affunlabeled
A mutation in <i>TGFB</i><i>3</i> associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with marfan and loeys–dietz syndrome
Hugh Young Rienhoff, Chang‐Yeol Yeo, Rachel Morissette, Irina Khrebtukova, Jonathan S. Melnick, Shujun Luo +8 more
2013· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
107
citations
affunlabeled
Further delineation of Kabuki syndrome in 48 well‐defined new individuals
Linlea Armstrong, Azza Abd El Monéim, Kirk Aleck, David J. Aughton, Clarisse Baumann, Stephen R. Braddock +22 more
2004· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
103
citations
affunlabeled
Quality of life in osteogenesis imperfecta: A mixed‐methods systematic review
Noémi Dahan‐Oliel, Sarah Oliel, Argerie Tsimicalis, Kathleen Montpetit, Frank Rauch, Maman Joyce Dogba
2015· review· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaresearch+metaepi_narrowconsensus · none
101
citations
affunlabeled
The AKT genes and their roles in various disorders
M. Michael Cohen
2013· review· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
95
citations
afffundunlabeled
The adult phenotype in Costello syndrome
Susan M. White, J. M. Graham, Bronwyn Kerr, Karen W. Gripp, Rosanna Weksberg, Cheryl Cytrynbaum +5 more
2005· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
91
citations
affunlabeled
Complex II deficiency—A case report and review of the literature
Shailly Jain‐Ghai, Jessie M. Cameron, Almundher Al‐Maawali, Susan Blasér, Nevena MacKay, Brian Robinson +1 more
2013· review· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
89
citations
affunlabeled
Paternal transmission of fragile X syndrome
Susan Zeesman, Lonnie Zwaigenbaum, Donald T. Whelan, Randi J. Hagerman, Flora Tassone, Sherryl A. Taylor
2004· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
81
citations
affunlabeled
Ocular phenotypes of three genetic variants of Bardet–Biedl syndrome
Elise Héon, Carol A. Westall, Rivka Carmi, Khalil Elbedour, Carole M. Panton, Leslie MacKeen +2 more
2004· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
79
citations
affaboutunlabeled
Cranial nerve manifestations in CHARGE syndrome
Kim Blake, Timothy S Hartshorne, Christopher Lawand, A. Nichole Dailor, James W. Thelin
2008· article· en· American Journal of Medical Genetics Part A· Medicine
distilled prediction:candidate · noneconsensus · none
78
citations
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