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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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Genetics and Neurodevelopmental Disorders
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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.

1,774 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.
1,774 works in the cohort · of 4,299,418page 14 of 36

Labels cover 2 of 1,774 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 1,774 of 1,774 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affvenueunlabeled
Genetic Testing of Epileptic Encephalopathies of Infancy: An Approach
Suvasini Sharma, Asuri N. Prasad
2013· review· en· Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrow+stsconsensus · none
26
citations
afffundunlabeled
Improvement of Self-Injury With Dopamine and Serotonin Replacement Therapy in a Patient With a Hemizygous <i>PAK3</i> Mutation: A New Therapeutic Strategy for Neuropsychiatric Features of an Intellectual Disability Syndrome
Gabriella Horváth, Maja Tarailo‐Graovac, Tanja Bartel, Simone Race, Margot I. Van Allen, Ingrid Blydt-Hansen +4 more
2017· article· en· Journal of Child Neurology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
25
citations
afffundaboutunlabeled
LINGO1 Variants in the French-Canadian Population
Cynthia V. Bourassa, Jean‐Baptiste Rivière, Patrick A. Dion, Geneviève Bernard, Sabrina Diab, Michel Panisset +6 more
2011· article· en· PLoS ONE· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
25
citations
affno abstractunlabeled
Associations between polymorphisms of LSAMP gene and schizophrenia
Kati Koido, Sven Janno, Tanel Traks, Madis Parksepp, Ülle Ljubajev, Peeter Veiksaar +4 more
2014· article· en· Psychiatry Research· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
24
citations
fundno affunlabeled
FMRpolyG accumulates in FMR1 premutation granulosa cells
Moran Friedman-Gohas, Shai E. Elizur, Olga Dratviman‐Storobinsky, Adva Aizer, Jigal Haas, Hila Raanani +2 more
2020· article· en· Journal of Ovarian Research· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
24
citations
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