Evidence map›Paper›PMID 35286699›Full record

ArticleAdvances in experimental medicine and biology2022

The Immunogenetics of Systemic Sclerosis.

Begüm Ünlü, Ümit Türsen, Zeynab Rajabi, Navid Jabalameli, Fateme Rajabi

Abstract read
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In one paragraph

Article in Advances in experimental medicine and biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
19.6field-weighted citation impact, top 1% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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 2 countries.

Begüm ÜnlüDepartment of Dermatology, Mersin University, Mersin, Turkey.
Ümit TürsenDepartment of Dermatology, Mersin University, Mersin, Turkey. utursen@mersin.edu.tr.ORCID http://orcid.org/0000-0002-5807-6759
Zeynab RajabiTehran University of Medical Sciences, Tehran, Iran.
Navid JabalameliNetwork of Dermatology Research (NDR), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
Fateme RajabiNetwork of Dermatology Research (NDR), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
Mersin Üniversitesi · TRUniversal Scientific Education and Research Network · IRTehran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic sclerosis (SSc) is a rare disease with a prevalence ranging from 7 to 700 cases per million. Like with most autoimmune diseases, both environmental and genetic factors are involved in the pathogenesis of the SSc. Though the incidence of SSc in the family members of those affected and the concordance rate in twins is very low, inheritance is still the strongest risk factor of SSc. Thus, multiple studies have been conducted to identify the genes responsible for this inheritance including candidate gene association studies and genome-wide analyses. Variations and mutations in the genes encoding cytokines, adhesion molecules, and signaling proteins involved in the interaction between endothelial cells, fibroblasts, and immune cells have been found to be associated with SSc susceptibility. In this chapter, these genes and their contribution to the pathogenesis of the SSc are discussed in detail. These genes are categorized into five major groups of HLA genes, genes involved in the innate immune responses, genes affecting adaptive immune responses, genes with a role in the fibrogenesis pathways, and apoptosis, autophagy, and pyroptosis-related genes.

Indexed as

Autoimmune DiseasesScleroderma, SystemicEndothelial CellsGenome-Wide Association StudyHumansImmunogeneticsFibrosisGenetic polymorphismsImmunogeneticsSusceptibilitySystemic sclerosis

Identifiers

PMID35286699
OpenAlexW4226152806

What OpenQuestion holds

Textmetadata
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.