Evidence map›Paper›PMID 40225151›Full record

ArticleHuman mutation2023

Unexpected Inheritance Patterns in a Large Cohort of Patients with a Suspected Ciliopathy.

Aurélie Gouronc, Elodie Javey, Anne-Sophie Leuvrey, Elsa Nourisson, Sylvie Friedmann, Valérie Reichert, Nicolas Derive, Christine Francannet, Boris Keren, Jonathan Lévy and 6 more

Abstract read
In one paragraph

Article in Human mutation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

16 authors.

Aurélie GouroncGenetics Diagnostic Laboratory, Strasbourg University Hospital, Strasbourg, France.ORCID 0000-0003-0758-8882
Elodie JaveyGenetics Diagnostic Laboratory, Strasbourg University Hospital, Strasbourg, France.
Anne-Sophie LeuvreyGenetics Diagnostic Laboratory, Strasbourg University Hospital, Strasbourg, France.
Elsa NourissonGenetics Diagnostic Laboratory, Strasbourg University Hospital, Strasbourg, France.
Sylvie FriedmannGenetics Diagnostic Laboratory, Strasbourg University Hospital, Strasbourg, France.
Valérie ReichertGenetics Diagnostic Laboratory, Strasbourg University Hospital, Strasbourg, France.
Nicolas DeriveMedical Biology Laboratory SeqOIA-PFMG2025, Paris, France.
Christine FrancannetMedical Genetics Service, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.
Boris KerenMedical Biology Laboratory SeqOIA-PFMG2025, Paris, France.
Jonathan LévyGenetics Department, Robert Debré University Hospital, APHP Nord, Paris, France.
Marc PlanesClinical Genetics Service, CHRU Morvan, 29609 Brest, France.
Lyse RuaudGenetics Department, Robert Debré University Hospital, APHP Nord, Paris, France.
Jeanne AmielMedical Genomics Service for Rare Diseases, Necker-Sick children Hospital, AP-HP, Paris, France.
Hélène DollfusMedical Genetics Laboratory, UMRS_1112, Alsace Medical Genetics Institute (IGMA), Strasbourg University and INSERM, Strasbourg, France.ORCID 0000-0002-2249-895X
Sophie ScheideckerGenetics Diagnostic Laboratory, Strasbourg University Hospital, Strasbourg, France.ORCID 0000-0003-0902-8926
Jean MullerGenetics Diagnostic Laboratory, Strasbourg University Hospital, Strasbourg, France.ORCID 0000-0002-7682-559X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ciliopathies are rare genetic disorders caused by dysfunction of the primary or motile cilia. Their mode of inheritance is mostly autosomal recessive with biallelic pathogenic variants inherited from the parents. However, exceptions exist such as uniparental disomy (UPD) or the appearance of a

Indexed as

CiliopathiesInheritance PatternsBardet-Biedl SyndromeCiliaCohort StudiesFemaleHigh-Throughput Nucleotide SequencingHumansMaleMutationPedigreePolymorphism, Single NucleotideUniparental Disomy

Identifiers

PMID40225151
PMCPMC11918889

What Socratic 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 Socratic graph.