Evidence map›Paper›PMID 32922396›Full record

ReviewFrontiers in immunology2020

T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical Features.

Giuliana Giardino, Carla Borzacchiello, Martina De Luca, Roberta Romano, Rosaria Prencipe, Emilia Cirillo, Claudio Pignata

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Informed clinical decisions by outfoxing human FOXN1 variants.The Journal of allergy and clinical immunology · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Comprehensive phenotypic analysis of diverse FOXN1 variants.The Journal of allergy and clinical immunology · 2023
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Inborn errors of immunity associated with defects of thymic development.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2022
    Review
  13. Article
  14. Review
  15. Article
  16. Thymus and autoimmunity.Seminars in immunopathology · 2021
    Review
  17. Article
  18. Thymus Degeneration and Regeneration.Frontiers in immunology · 2021
    Review
  19. Combined immunodeficiencies.Jornal de pediatria
    Review
  20. Short histological kaleidoscope - recent findings in histology. Part II.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

7 authors.

Giuliana GiardinoDepartment of Translational Medical Sciences, Pediatric Section, Federico II University of Naples, Naples, Italy.
Carla BorzacchielloDepartment of Translational Medical Sciences, Pediatric Section, Federico II University of Naples, Naples, Italy.
Martina De LucaDepartment of Translational Medical Sciences, Pediatric Section, Federico II University of Naples, Naples, Italy.
Roberta RomanoDepartment of Translational Medical Sciences, Pediatric Section, Federico II University of Naples, Naples, Italy.
Rosaria PrencipeDepartment of Translational Medical Sciences, Pediatric Section, Federico II University of Naples, Naples, Italy.
Emilia CirilloDepartment of Translational Medical Sciences, Pediatric Section, Federico II University of Naples, Naples, Italy.
Claudio PignataDepartment of Translational Medical Sciences, Pediatric Section, Federico II University of Naples, Naples, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Combined Immunodeficiencies (CID) are rare congenital disorders characterized by defective T-cell development that may be associated with B- and NK-cell deficiency. They are usually due to alterations in genes expressed in hematopoietic precursors but in few cases, they are caused by impaired thymic development. Athymia was classically associated with DiGeorge Syndrome due to

Indexed as

HumansSevere Combined ImmunodeficiencyThymus GlandT-LymphocytesCHARGECHD7 geneDiGeorge anomalyFOXN1 genePax 1/9PAX1 geneTBX1 geneThymus

Identifiers

PMID32922396
PMCPMC7457079
OpenAlexW3049277810

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.