Evidence map›Paper›PMID 38337829›Full record

ArticleDiagnostics (Basel, Switzerland)2024

Exome Sequencing Reveals Biallelic Mutations in

Víctor Raggio, Soledad Rodríguez, Sandra Feder, Rosario Gueçaimburú, Lucía Spangenberg

Open access · goldAbstract readCase Reports
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Chromosomal Location and Identification ofDiagnostics (Basel, Switzerland) · 2025
    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

5 authors at 3 institutions in 1 country.

Víctor RaggioDepartamento de Genética, Facultad de Medicina, Universidad de la República, Montevideo 11800, Uruguay.ORCID 0000-0001-5389-5002
Soledad RodríguezDepartamento de Genética, Facultad de Medicina, Universidad de la República, Montevideo 11800, Uruguay.
Sandra FederLaboratorio de Genética Clínica Genodiagnosis, Montevideo 11600, Uruguay.
Rosario GueçaimburúCentro de Referencia Nacional de Defectos Congénitos y Enfermedades Raras (CRENADECER), Av. Agraciada 2989, Montevideo 11800, Uruguay.
Lucía SpangenbergDepartamento Básico de Medicina, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo 11600, Uruguay.
Universidad de la República de Uruguay · UYCentro Uruguayo de Imagenología Molecular · UYHospital Británico · UY

Funding

Agencia Nacional de Investigación e Innovación FSS_X_2022_1_173209Inter-American Development Bank ATN/KK-L4584-"Fortalecimiento de las capacidades técnicas y humanas para las exportaciones de servicios genómicos"
6 · The paper itself

Abstract

The Kondo-Fu type of spondyloepiphyseal dysplasia (SEDKF) is a rare skeletal dysplasia caused by homozygous or compound heterozygous mutations in the

Indexed as

diagnostic odysseymassive sequencingmedical genomicsmolecular geneticsosseous dysplasiasrare diseases

Identifiers

PMID38337829
PMCPMC10855125
OpenAlexW4391404178

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.