ArticleKidney international reports2026
Database of
Article in Kidney international reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Molecular Basis of Rare Inherited Tubulopathies of the Kidney: A Primer for Clinicians.International journal of molecular sciences · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Dent disease type 1 is an X-linked proximal tubulopathy caused by pathogenic variants in Methods: Potentially pathogenic Results: We identified 524 unique pathogenic or likely pathogenic variants, exceeding all existing databases. Variant types included missense (31%), InDel insertions and deletions (37%), nonsense (14%), splicing defects (13%), and large deletions (5%). Most variants (74%) were reported only once. Exon 10 (NM_001127898.4) showed the highest density of pathogenic variants, driven by missense and in-frame insertions and deletions (InDel). Structural mapping revealed functional restrained regions in Helix H and O-Q helices. Source-variant counts indicated a minimum of 880 affected families, suggesting approximately 3520 globally. Conclusion: This uniformly annotated catalog-the most comprehensive to date-enhances interpretation of
Indexed as
Identifiers
What Socratic 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 Socratic graph.