Evidence map›Paper›PMID 30229436›Full record

ArticleNeuromolecular medicine2018

The FOXP3 rs3761547 Gene Polymorphism in Multiple Sclerosis as a Male-Specific Risk Factor.

Natalia Wawrusiewicz-Kurylonek, Monika Chorąży, Renata Posmyk, Olga Zajkowska, Agata Zajkowska, Adam Jacek Krętowski, Joanna Tarasiuk, Jan Kochanowicz, Alina Kułakowska

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Neuromolecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 29 citations in OpenAlex.

  1. Evaluation ofCurrent protein & peptide science · 2026
    Article
  2. Revisiting Migraine Pathophysiology: from Neurons To Immune Cells Through Lens of Immune Regulatory Pathways.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. The impact ofJournal of Cancer · 2023
    Article
  7. Article
  8. Article
  9. Sex-dependent effect ofDisease models & mechanisms · 2020
    Review
  10. Review
  11. The rs3761548 FOXP3 variant is associated with multiple sclerosis and transforming growth factor β1 levels in female patients.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2019
    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

9 authors at 2 institutions in 1 country.

Natalia Wawrusiewicz-KurylonekDepartment of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Sklodowskiej-Curie 24A, 15-276, Białystok, Poland. natalia.kurylonek@gmail.com.ORCID http://orcid.org/0000-0002-1087-8154
Monika ChorążyDepartment of Neurology, Medical University of Bialystok, Białystok, Poland.
Renata PosmykDepartment of Perinatology, Medical University of Bialystok, Białystok, Poland.
Olga ZajkowskaFaculty of Applied Informatics and Mathematics, Warsaw University of Life Sciences SGGW, Warsaw, Poland.
Agata ZajkowskaDepartment of Neurology, Medical University of Bialystok, Białystok, Poland.
Adam Jacek KrętowskiDepartment of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Sklodowskiej-Curie 24A, 15-276, Białystok, Poland.
Joanna TarasiukDepartment of Neurology, Medical University of Bialystok, Białystok, Poland.
Jan KochanowiczDepartment of Neurology, Medical University of Bialystok, Białystok, Poland.
Alina KułakowskaDepartment of Neurology, Medical University of Bialystok, Białystok, Poland.
Medical University of Białystok · PLWarsaw University of Life Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The FOXP3 gene encodes a transcription factor and is predominantly expressed in the CD4

Indexed as

Polymorphism, Single NucleotideAdultFemaleForkhead Transcription FactorsGene Expression ProfilingGenetic Predisposition to DiseaseHaplotypesHumansMaleMultiple Sclerosis, Relapsing-RemittingReal-Time Polymerase Chain ReactionRisk FactorsSex FactorsForkhead Transcription FactorsFOXP3 protein, humanAutoimmune diseaseFOXP3 geneMultiple sclerosisPolymorphismTreg cells

Identifiers

PMID30229436
PMCPMC6244921
OpenAlexW2891876613

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.