ArticleAmerican journal of human genetics2021
Rare and de novo coding variants in chromodomain genes in Chiari I malformation.
Article in American journal of human genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04856839 (Phenotypes, Biomarkers and Pathophysiology in Syringomyelia), which is not on this map. Cited by 2 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.
Phenotypes, Biomarkers and Pathophysiology in Syringomyelia
Who cites it
2 citing papers in PubMed.
- Exploring pathogenesis, prevalence, and genetic associations in Chiari malformation type 1: a contemporary perspective.Asian biomedicine : research, reviews and news · 2024Review
- Childhood-onset progressive dystonia associated with pathogenic truncating variants in CHD8.Annals of clinical and translational neurology · 2021Article
Corrections and comments
- Erratum for
Authors and funding
31 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Identifiers
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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.