Evidence map›Paper›PMID 40004525›Full record

ArticleGenes2025

Molecular Review of Suspected Alport Syndrome Patients-A Single-Centre Experience.

Paulina Halat-Wolska, Elżbieta Ciara, Michał Pac, Łukasz Obrycki, Dorota Wicher, Katarzyna Iwanicka-Pronicka, Ewelina Bielska, Beata Chałupczyńska, Dorota Siestrzykowska, Grażyna Kostrzewa and 4 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Genes · 2026
    Article
  3. Article
  4. Article
  5. Alport Syndrome-Associated PathogenicInternational journal of genomics · 2026
    Article
  6. Article
  7. Article
  8. 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

14 authors.

Paulina Halat-WolskaDepartment of Medical Genetics, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.ORCID 0000-0002-1064-0277
Elżbieta CiaraDepartment of Medical Genetics, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.ORCID 0000-0002-1065-7968
Michał PacDepartment of Nephrology, Kidney Transplantation and Hypertension, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.
Łukasz ObryckiDepartment of Nephrology, Kidney Transplantation and Hypertension, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.ORCID 0000-0002-5134-8643
Dorota WicherDepartment of Medical Genetics, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.ORCID 0000-0002-8360-0006
Katarzyna Iwanicka-PronickaDepartment of Medical Genetics, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.
Ewelina BielskaDepartment of Medical Genetics, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.
Beata ChałupczyńskaDepartment of Medical Genetics, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.
Dorota SiestrzykowskaDepartment of Medical Genetics, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.
Grażyna KostrzewaDepartment of Medical Genetics, Warsaw Medical University, 02-106 Warsaw, Poland.
Piotr StawińskiDepartment of Medical Genetics, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.
Rafał PłoskiDepartment of Medical Genetics, Warsaw Medical University, 02-106 Warsaw, Poland.
Mieczysław LitwinDepartment of Nephrology, Kidney Transplantation and Hypertension, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.ORCID 0000-0002-5241-2483
Krystyna ChrzanowskaDepartment of Medical Genetics, The Children's Memorial Health Institute, 04-730 Warsaw, Poland.ORCID 0000-0003-3888-0624

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AutoantigensCollagen Type IVNephritis, HereditaryAdolescentAdultChildChild, PreschoolFemaleGenetic TestingHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMutationPedigreeYoung AdultAutoantigensCOL4A4 protein, humanCOL4A5 protein, humanCollagen Type IVtype IV collagen alpha3 chainAlport syndromeCOL4A3COL4A4COL4A5genetic testingnext-generation sequencingnovel molecular variants

Identifiers

PMID40004525
PMCPMC11855357

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.