Evidence map›Paper›PMID 36960056›Full record

ArticleFrontiers in immunology2023

Degradation of collagen I by activated C1s in periodontal Ehlers-Danlos Syndrome.

Albert Amberger, Johanna Pertoll, Pia Traunfellner, Ines Kapferer-Seebacher, Heribert Stoiber, Lars Klimaschewski, Nicole Thielens, Christine Gaboriaud, Johannes Zschocke

Open access · goldFull text read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Genetic diagnosis of the Ehlers-Danlos syndromes.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2024
    Article
  5. 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 2 countries.

Albert AmbergerInstitute of Human Genetics, Med. Univ. Innsbruck, Innsbruck, Austria.
Johanna PertollInstitute of Human Genetics, Med. Univ. Innsbruck, Innsbruck, Austria.
Pia TraunfellnerInstitute of Human Genetics, Med. Univ. Innsbruck, Innsbruck, Austria.
Ines Kapferer-SeebacherDepartment of Conservative Dentistry and Periodontology, Med. Univ. Innsbruck, Innsbruck, Austria.
Heribert StoiberInstitute of Virology, Med. Univ. Innsbruck, Innsbruck, Austria.
Lars KlimaschewskiInstitute of Neuroanatomie, Med. Univ. Innsbruck., Innsbruck, Austria.
Nicole ThielensUniv. Grenoble Alpes, Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Structurale (IBS), Grenoble, France.
Christine GaboriaudUniv. Grenoble Alpes, Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Structurale (IBS), Grenoble, France.
Johannes ZschockeInstitute of Human Genetics, Med. Univ. Innsbruck, Innsbruck, Austria.
Innsbruck Medical University · ATCEA Grenoble · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Periodontal Ehlers-Danlos syndrome (pEDS) is an autosomal dominant disorder characterized by early-onset periodontitis leading to premature loss of teeth, lack of attached gingiva and thin and fragile gums leading to gingival recession. Connective tissue abnormalities of pEDS typically include easy bruising, pretibial plaques, distal joint hypermobility, hoarse voice, and less commonly manifestations such as organ or vessel rupture. pEDS is caused by heterozygous missense mutations in

Indexed as

Complement C1sEhlers-Danlos SyndromeCollagen Type IHumansMutation, MissenseCollagen Type IComplement C1sC1r proteasecollagen Icomplement activationEhlers-Danlos Syndromeperiodontites

Identifiers

PMID36960056
PMCPMC10028100
OpenAlexW4323363413

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read43
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.