Evidence map›Paper›PMID 38073170›Full record

ArticleJournal of genetics2023

Why are you hitting yourself? Whole-exome sequencing diagnosis of monogenic autoimmunity.

Lina M Castano-Jaramillo, Francisco Rivas Larrauri, Selma C Scheffler-Mendoza, Alonso Gutierrez-Hernandez, Juan Carlos Bustamante Ogando, Paulina Colin, Margarita Ortega Cisneros, Sandra Rajme-López, Edgar Alejandro Medina-Torres, Laura Berron Ruiz and 4 more

Abstract read
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In one paragraph

Article in Journal of genetics, 2023. 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, top 59% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 4 institutions in 1 country.

Lina M Castano-JaramilloClinical Immunology Department, Instituto Nacional de Pediatria, Mexico City, Mexico.dr.lugo.reyes@gmail.com.
Francisco Rivas Larrauri
Selma C Scheffler-Mendoza
Alonso Gutierrez-Hernandez
Juan Carlos Bustamante Ogando
Paulina Colin
Margarita Ortega Cisneros
Sandra Rajme-López
Edgar Alejandro Medina-Torres
Laura Berron Ruiz
Ana Luisa Rodriguez-Lozano
Sara Elva Espinosa Padilla
Marco Antonio Yamazaki-Nakashimada
Saul O Lugo Reyes
Instituto Nacional de Pediatria · MXNational Institute of Genomic Medicine · MXHospital de Especialidades · MXInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inborn errors of immunity may present with autoimmunity and autoinflammation as hallmark clinical manifestations. We aimed to identify the potential monogenic causes of autoimmune disorders in 26 patients from a pediatric reference hospital in Mexico through whole-exome sequencing. We specifically selected patients with a family history of autoimmune diseases, early-onset symptoms, and difficult-to-control autoimmune disorders or autoimmunity associated with infection predisposition. We identified the genetic variants that were compatible with the patients' phenotype in 54% of the patients. Autoimmune diseases are often caused by a combination of genetic factors, but cases that appear at a young age are resistant to treatment or occur in clusters, as well as the presence of autoimmune symptoms alongside infectious diseases should raise suspicion for an underlying inborn error of immunity.

Indexed as

Autoimmune DiseasesAutoimmunityChildExome SequencingGenotypeHumansPhenotype

Identifiers

PMID38073170
OpenAlexW4389001575

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.