Evidence map›Paper›PMID 39652411›Full record

ArticleJournal of the American Society of Nephrology : JASN2025

Using VNtyper from Whole Exome Sequencing Data to Detect Pathogenic Variants in the MUC1 Gene.

Hassan Saei, Cécile Masson, Vincent Morinière, Jessica Kachmar, Laurence Heidet, Olivier Gribouval, Corinne Antignac, Guillaume Dorval

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Chronic Kidney Disease of unexplained cause (CKDx): a consensus statement by the Genes & Kidney Working Group of the ERA.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Article
  3. Long-Read Sequencing of thebioRxiv : the preprint server for biology · 2025
    Article
  4. 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

8 authors.

Hassan SaeiLaboratory of Hereditary Kidney Diseases, Inserm UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.
Cécile MassonBioinformatics Platform, Inserm UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.ORCID 0000-0001-7870-7821
Vincent MorinièreDepartment of Genomic Medicine for Rare Diseases, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
Jessica KachmarLaboratory of Hereditary Kidney Diseases, Inserm UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.ORCID 0009-0007-0543-0025
Laurence HeidetLaboratory of Hereditary Kidney Diseases, Inserm UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.ORCID 0000-0002-1362-5515
Olivier GribouvalLaboratory of Hereditary Kidney Diseases, Inserm UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.ORCID 0000-0003-0238-8224
Corinne AntignacLaboratory of Hereditary Kidney Diseases, Inserm UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.
Guillaume DorvalLaboratory of Hereditary Kidney Diseases, Inserm UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.ORCID 0000-0003-3883-1398

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID39652411
PMCPMC11801743

What OpenQuestion holds

Textmetadata
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.