Evidence map›Paper›PMID 36292665›Full record

ArticleGenes2022

Mutation Analysis of Thin Basement Membrane Nephropathy.

Yosuke Hirabayashi, Kan Katayama, Mutsuki Mori, Hiroshi Matsuo, Mika Fujimoto, Kensuke Joh, Tomohiro Murata, Masaaki Ito, Kaoru Dohi

Open access · goldAbstract read
In one paragraph

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 21% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Understanding Better the Genetic Causes of Hematuria.Journal of the American Society of Nephrology : JASN · 2025
    Article
  5. Utility of Genetic Testing in Adults with CKD: A Systematic Review and Meta-Analysis.Clinical journal of the American Society of Nephrology : CJASN · 2025
    Article
  6. Article
  7. Article
  8. The same heterozygousFrontiers in genetics · 2023
    Article
  9. Novel Digenic Variants inCase reports in nephrology and dialysis
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Yosuke HirabayashiDepartment of Cardiology and Nephrology, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
Kan KatayamaDepartment of Cardiology and Nephrology, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.ORCID 0000-0001-6663-133X
Mutsuki MoriDepartment of Cardiology and Nephrology, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
Hiroshi MatsuoDepartment of Cardiology and Nephrology, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
Mika FujimotoDepartment of Cardiology and Nephrology, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
Kensuke JohDepartment of Pathology, The Jikei University School of Medicine, Tokyo 105-0003, Japan.ORCID 0000-0002-9334-3664
Tomohiro MurataDepartment of Cardiology and Nephrology, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
Masaaki ItoDepartment of Cardiology and Nephrology, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
Kaoru DohiDepartment of Cardiology and Nephrology, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
Mie University · JPJikei University School of Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thin basement membrane nephropathy (TBMN) is characterized by the observation of microhematuria and a thin glomerular basement membrane on kidney biopsy specimens. Its main cause is heterozygous mutations of

Indexed as

Glomerulosclerosis, Focal SegmentalNephritis, HereditaryBasement MembraneCollagen Type IVGlycineHematuriaHumansMutationNucleotidesCollagen Type IVGlycineNucleotidesautosomal dominant Alport syndromeCOL4A3COL4A4microhematuriamutationthin basement membrane nephropathyvariant

Identifiers

PMID36292665
PMCPMC9602179
OpenAlexW4303685698

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.