Evidence map›Paper›PMID 35991542›Full record

ArticleFrontiers in genetics2022

COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts.

Tommi Välikangas, Sini Junttila, Kalle T Rytkönen, Anu Kukkonen-Macchi, Tomi Suomi, Laura L Elo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  4. The peptidoglycan ofScience translational medicine · 2025
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  11. SARS-CoV-2 and the DNA damage response.The Journal of general virology · 2023
    Review
  12. 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

6 authors at 3 institutions in 1 country.

Tommi VälikangasTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Sini JunttilaTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Kalle T RytkönenTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Anu Kukkonen-MacchiTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Tomi SuomiTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Laura L EloTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Turku Centre for Computer Science · FIÅbo Akademi University · FIUniversity of Turku · FI

Funding

European Research Council 677943
6 · The paper itself

Abstract

The coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is spreading across the world despite vast global vaccination efforts. Consequently, many studies have looked for potential human host factors and immune mechanisms associated with the disease. However, most studies have focused on comparing COVID-19 patients to healthy controls, while fewer have elucidated the specific host factors distinguishing COVID-19 from other infections. To discover genes specifically related to COVID-19, we reanalyzed transcriptome data from nine independent cohort studies, covering multiple infections, including COVID-19, influenza, seasonal coronaviruses, and bacterial pneumonia. The identified COVID-19-specific signature consisted of 149 genes, involving many signals previously associated with the disease, such as induction of a strong immunoglobulin response and hemostasis, as well as dysregulation of cell cycle-related processes. Additionally, potential new gene candidates related to COVID-19 were discovered. To facilitate exploration of the signature with respect to disease severity, disease progression, and different cell types, we also offer an online tool for easy visualization of the selected genes across multiple datasets at both bulk and single-cell levels.

Indexed as

COVID-19infectionRNA-seqseveritysignaturesingle-cell

Identifiers

PMID35991542
PMCPMC9388772
OpenAlexW4289889046

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.