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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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Hereditary Neurological 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
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.

522 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.
522 works in the cohort · of 4,299,418page 5 of 11

Labels cover 1 of 522 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 522 of 522 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

affvenueunlabeled
A Novel GDAP1 Mutation 439delA is Associated with Autosomal Recessive CMT Disease
Domna-Maria Georgiou, Paschalis Nicolaou, David Chitayat, Pantelitsa Koutsou, Riyana Babul‐Hirji, Jiri Vajsar +2 more
2006· article· en· Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques· Neuroscience
distilled prediction:candidate · metaresearch+metaepi_narrow+sts+scholarly_communicationconsensus · sts
11
citations
afffundunlabeled
Triple A syndrome presenting as complicated hereditary spastic paraplegia
Etienne Léveillé, Hernán Gonorazky, Marie‐France Rioux, Lili‐Naz Hazrati, Jennifer A. Ruskey, Amanda Carnevale +5 more
2018· article· en· Molecular Genetics & Genomic Medicine· Neuroscience
distilled prediction:candidate · metaepi_narrow+insufficient_payloadconsensus · insufficient_payload
11
citations
afffundunlabeled
Accumulation of Endogenous LITAF in Aggresomes
Heather E. Eaton, Julie Metcalf, Andressa Ferreira Lacerda, Craig R. Brunetti
2012· article· en· PLoS ONE· Neuroscience
distilled prediction:candidate · noneconsensus · none
11
citations
afffundaboutunlabeled
Hereditary spastic paraplegia initially diagnosed as cerebral palsy
Oksana Suchowersky, Setareh Ashtiani, Ping-Yee Billie Au, Scott McLeod, Mehrdad A. Estiar, Ziv Gan‐Or +1 more
2021· article· en· Clinical Parkinsonism & Related Disorders· Neuroscience
distilled prediction:candidate · metaresearch+metaepi_narrow+research_integrity+insufficient_payloadconsensus · insufficient_payload
9
citations
venueno affunlabeled
Two Causes of Demyelinating Neuropathy in One Patient: CMT1A and POEMS Syndrome
Nizar Chahin, Steven R. Zeldenrust, Kimberly K. Amrami, JaNean Engelstad, Pam James, B Dyck
2007· letter· en· Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques· Neuroscience
distilled prediction:candidate · metaresearch+metaepi_narrow+sts+research_integrityconsensus · sts
8
citations
fundno affno abstractunlabeled
Unusual upper limb features in <i>SORD</i> neuropathy
Christopher J. Record, Menelaos Pipis, Julian Blake, Riccardo Curró, Michael P. Lunn, Alexander M. Rossor +3 more
2022· letter· en· Journal of the Peripheral Nervous System· Neuroscience
distilled prediction:candidate · metaepi_narrow+research_integrityconsensus · none
8
citations
affno abstractunlabeled
Congenital Axonal Neuropathy and Encephalopathy
Vann Chau, Jean-François Clément, Yves Robitaille, Guy D’Anjou, Michel Vanasse
2008· article· en· Pediatric Neurology· Neuroscience
distilled prediction:candidate · metaepi_narrowconsensus · none
8
citations
afffundno abstractunlabeled
Functional and Genetic Analysis of Neuronal Isoforms of BPAG1
Anisha Lynch‐Godrei, Rashmi Kothary
2015· review· en· Methods in enzymology on CD-ROM/Methods in enzymology· Neuroscience
distilled prediction:candidate · metaresearch+metaepi_narrow+sts+research_integrityconsensus · metaepi_narrow+research_integrity
8
citations
affvenueunlabeled
Traduction française de l’échelle Charcot-Marie-Tooth Disease Pediatric Scale
Cynthia Gagnon, Rami Massie, Marjolaine Tremblay, Sylvie Darcy, Mélissa Martel, Joshua Burns
2017· article· fr· Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques· Neuroscience
distilled prediction:candidate · metaresearch+metaepi_narrow+sts+scholarly_communication+open_science+research_integrity+insufficient_payloadconsensus · sts
8
citations
affunlabeled
Hereditary Neuropathy With Liability to Pressure Palsies
Kourosh K. Jafarnia, Michael J. Sullivan, David H. Hildreth
2001· article· en· Clinical Orthopaedics and Related Research· Neuroscience
distilled prediction:candidate · metaresearch+research_integrityconsensus · none
8
citations
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