ArticleNeurology2012
Exome sequencing identifies a novel TRPV4 mutation in a CMT2C family.
Article in Neurology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06677502 (The Usefulness of Cerebrolysin in Alleviating the Severity of Delirium in Critically Ill Patients), which is not on this map. Cited by 17 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
The Usefulness of Cerebrolysin in Alleviating the Severity of Delirium in Critically Ill Patients
Who cites it
17 citing papers in PubMed.
- Single-bacterial cell insights into mechanisms of ceftriaxone resistance in Neisseria subflava.Nature communications · 2026Article
- The Evolution of Gene Sequencing Technologies: Unveiling Genetic Architecture of Nonsyndromic Orofacial Clefts.Genetics research · 2026Review
- Combined clinical, structural and cellular studies discriminate pathogenic and benign TRPV4 variants.Brain : a journal of neurology · 2025Article
- TRPV4 neuromuscular disease registry highlights bulbar, skeletal and proximal limb manifestations.Brain : a journal of neurology · 2025Article
- Review
- Sensory Innervation of the Larynx and the Search for Mucosal Mechanoreceptors.Journal of speech, language, and hearing research : JSLHR · 2021Article
- TRPing to the Point of Clarity: Understanding the Function of the Complex TRPV4 Ion Channel.Cells · 2021Review
- Hearing loss in inherited peripheral neuropathies: Molecular diagnosis by NGS in a French series.Molecular genetics & genomic medicine · 2019Article
- Gene regulation and genetics in neurochemistry, past to future.Journal of neurochemistry · 2016Review
- Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathy.Neurology. Genetics · 2015Article
- The genetics of Charcot-Marie-Tooth disease: current trends and future implications for diagnosis and management.The application of clinical genetics · 2015Review
- Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy.Neurology · 2014Article
- Structural biology of TRP channels.Handbook of experimental pharmacology · 2014Review
- Clinical implications of genetic advances in Charcot-Marie-Tooth disease.Nature reviews. Neurology · 2013Review
- The puzzle of TRPV4 channelopathies.EMBO reports · 2013Review
- Molecular genetics of charcot-marie-tooth disease: from genes to genomes.Molecular syndromology · 2012Article
- Whole-exome sequencing improves genetic testing accuracy in pulmonary artery hypertension.Pulmonary circulationArticle
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Authors and funding
13 authors.
Funding
Abstract
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.