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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.

affaffiliation
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venuejournal
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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 19 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.

affunlabeled
Reply to Bagni: On BC1 RNA and the fragile X mental retardation protein
Anna Iacoangeli, Timofey S. Rozhdestvensky, Natalia Dolzhanskaya, Barthélémy Tournier, Janin Schütt, Jürgen Brosius +4 more
2008· letter· en· Proceedings of the National Academy of Sciences· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
12
citations
affvenueunlabeled
A Novel PS1 Gene Mutation in a Large Aboriginal Kindred
Rachel Butler, B. Lynn Beattie, Umamon Puang Thong, Emily Dwosh, Colleen Guimond, Howard Feldman +4 more
2010· article· en· Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
12
citations
afffundunlabeled
Experimental Autoimmune Encephalomyelitis (EAE)-Induced Elevated Expression of the E1 Isoform of Methyl CpG Binding Protein 2 (MeCP2E1): Implications in Multiple Sclerosis (MS)-Induced Neurological Disability and Associated Myelin Damage
Tina Khorshid Ahmad, Ting Zhou, Khaled Al-Taweel, Claudia Cortés, L. Ryan, Ted M. Lakowski +2 more
2017· article· en· International Journal of Molecular Sciences· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
12
citations
aboutno affunlabeled
Medication use by adolescents and adults with fragile X syndrome
Daniel J. Laxman, Jan S. Greenberg, Leann Smith DaWalt, Jinkuk Hong, M. G. Aman, Marsha R. Mailick
2017· article· en· Journal of Intellectual Disability Research· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
12
citations
affunlabeled
Excess Wnt in neurological disease
Danielle M. Pascual, Delaram Jebreili Rizi, Harsimran Kaur, Paul C. Marcogliese
2025· review· en· Biochemical Journal· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
11
citations
afffundunlabeled
Evolutionary genomics of human intellectual disability
Bernard J. Crespi, Kyle Summers, Steve Dorus
2009· article· en· Evolutionary Applications· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
11
citations
afffundvenueunlabeled
MeCP2 and CTCF: enhancing the cross-talk of silencers
Juan Ausió, Philippe T. Georgel
2017· review· en· Biochemistry and Cell Biology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
11
citations
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