Evidence map›Paper›PMID 36925663›Full record

ArticleKidney medicine2023

Kidney Disease Associated With Mono-allelic

Sander Groen In 't Woud, Ilse M Rood, Eric Steenbergen, Brigith Willemsen, Henry B Dijkman, Michel van Geel, Jeroen Schoots, Jack F M Wetzels, Dorien Lugtenberg, Jeroen K J Deegens and 1 more

Open access · goldFull text read
PubMed Full text at PMC Publisher
In one paragraph

Article in Kidney medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. A Novel HomozygousKidney international reports · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. The Phenotypic Spectrum ofKidney international reports · 2023
    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

11 authors at 3 institutions in 1 country.

Sander Groen In 't WoudDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Ilse M RoodDepartment of Nephrology, Radboud University Medical Center, Nijmegen, The Netherlands.
Eric SteenbergenDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Brigith WillemsenDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Henry B DijkmanDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Michel van GeelDepartment of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.
Jeroen SchootsDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Jack F M WetzelsDepartment of Nephrology, Radboud University Medical Center, Nijmegen, The Netherlands.
Dorien LugtenbergDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Jeroen K J DeegensDepartment of Nephrology, Radboud University Medical Center, Nijmegen, The Netherlands.
Ernie M H F BongersDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Radboud University Medical Center · NLRadboud University Nijmegen · NLMaastricht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rationale & Objective: Mono-allelic variants in Study Design: Case series. Setting & Participants: We evaluated clinical and pathologic characteristics of 17 Dutch index patients with mono-allelic variants in Results: Eight different mono-allelic Limitations: Retrospective design, ascertainment bias toward severe kidney phenotypes, and familial hematuria. Conclusions: This study confirms the wide phenotypic spectrum associated with mono-allelic

Indexed as

Alport syndromeCOL4A3/COL4A4FSGSgenotype-phenotypemono-allelic variantstype IV collagen nephropathywhole exome sequencing

Identifiers

PMID36925663
PMCPMC10011433
OpenAlexW4318773542

What OpenQuestion holds

Textfull text, public
LicenceCC BY
reference markers read1
measurements read138
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.