Evidence map›Paper›PMID 41973132›Full record

ArticleHuman genetics2026

Correction: Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomalies.

Adeline Jacquinet, Lydie Flasse, Manon Dohet, Romane Vanhaeren, Hélène Pendeville, Carol Saunders, Anna Lehman, Catherine Pienkowski, Karine Morcel, Daniel Guerrier and 2 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Human genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Adeline JacquinetGIGA-Human Genetics Laboratory, University of Liège, Liège, Belgium. adeline.jacquinet@chuliege.be.
Lydie FlasseGIGA-Laboratory of Zebrafish Development and Disease Models, University of Liège, Liège , Belgium.
Manon DohetGIGA-Laboratory of Zebrafish Development and Disease Models, University of Liège, Liège , Belgium.
Romane VanhaerenGIGA-Laboratory of Zebrafish Development and Disease Models, University of Liège, Liège , Belgium.
Hélène PendevilleGIGA-Zebrafish Facility, University of Liège, Liège, Belgium.
Carol SaundersDepartment of Pathology and Laboratory Medicine, Children's Mercy Hospital, University of Missouri Kansas City, School of Medicine, Kansas City, MO, 64108, USA.
Anna LehmanDepartment of Medical Genetics, University of British Columbia, BC Children's Hospital BC Women's Hospital, Vancouver, BC, Canada.
Catherine PienkowskiCentre Reference Pathologies Gynecologiques Rares, CHU Toulouse, 31059, Toulouse Cedex9, France.
Karine MorcelUniv. Brest, Inserm, UMR1304, GETBO; Department of Obstetrics and Gynecology, CHU Brest, 29200, Brest, France.
Daniel GuerrierUniv.Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes) - UMR 6290, Rennes, France.
Vincent BoursGIGA-Human Genetics Laboratory, University of Liège, Liège, Belgium.
Bernard PeersGIGA-Laboratory of Zebrafish Development and Disease Models, University of Liège, Liège , Belgium. bpeers@uliege.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID41973132

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.