Evidence map›Paper›PMID 36013501›Full record

ReviewMedicina (Kaunas, Lithuania)2022

Genetic Polymorphism of

Kalthoum Tizaoui, Jae Il Shin, Gwang Hun Jeong, Jae Won Yang, Seoyeon Park, Ji Hong Kim, Soo Young Hwang, Se Jin Park, Ai Koyanagi, Lee Smith

Open access · goldAbstract readReview
In one paragraph

Review in Medicina (Kaunas, Lithuania), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Endocrine-Metabolic Crosstalk Between Diabetes Mellitus and Hypothyroidism: From Network Mechanisms to Translational Stratification.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. Genetics of Vitiligo: A Review.Clinical, cosmetic and investigational dermatology · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Acquired drivers of C3 glomerulopathy.Clinical kidney journal · 2025
    Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Genes · 2024
    Article
  19. Article
  20. SNP inInternational journal of molecular sciences · 2023
    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

10 authors at 6 institutions in 4 countries.

Kalthoum TizaouiDepartment of Basic Sciences, Division of Histology and Immunology, Faculty of Medicine Tunis, Tunis El Manar University, Tunis 2092, Tunisia.ORCID 0000-0001-8524-6058
Jae Il ShinDepartment of Pediatrics, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID 0000-0003-2326-1820
Gwang Hun JeongCollege of Medicine, Gyeongsang National University, Jinju 52727, Korea.
Jae Won YangDepartment of Nephrology, Yonsei University Wonju College of Medicine, Wonju 26426, Korea.
Seoyeon ParkYonsei University College of Medicine, Seoul 06273, Korea.
Ji Hong KimDepartment of Pediatrics, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID 0000-0001-5352-5423
Soo Young HwangYonsei University College of Medicine, Seoul 06273, Korea.
Se Jin ParkDepartment of Pediatrics, Eulji University School of Medicine, Daejeon 35233, Korea.ORCID 0000-0002-7650-5393
Ai KoyanagiResearch and Development Unit, Parc Sanitari Sant Joan de Déu, CIBERSAM, Dr. Antoni Pujadas, 42, Sant Boi de Llobregat, 08830 Barcelona, Spain.ORCID 0000-0002-9565-5004
Lee SmithCentre for Health Performance and Wellbeing, Anglia Ruskin University, Cambridge CB1 1PT, UK.ORCID 0000-0002-5340-9833
Yonsei University · KRAnglia Ruskin University · GBEulji University · KRGyeongsang National University · KRInstitució Catalana de Recerca i Estudis Avançats · ESTunis El Manar University · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is known that the etiology and clinical outcomes of autoimmune diseases are associated with a combination of genetic and environmental factors. In the case of the genetic factor, the SNPs of the

Indexed as

Autoimmune DiseasesLupus Erythematosus, SystemicProtein Tyrosine Phosphatase, Non-Receptor Type 22Genetic Predisposition to DiseaseGenotypeHumansImmune SystemPolymorphism, Single NucleotideProtein Tyrosine Phosphatase, Non-Receptor Type 22PTPN22 protein, humanautoimmune diseasesgenetic associationLyp proteinPTPN22single nucleotide polymorphisms (SNPs)

Identifiers

PMID36013501
PMCPMC9415475
OpenAlexW4289523720

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.