Evidence map›Paper›PMID 31749804›Full record

ArticleFrontiers in immunology2019

Rebekka Gröbner, Ines Kapferer-Seebacher, Albert Amberger, Rita Redolfi, Fabien Dalonneau, Erik Björck, Di Milnes, Isabelle Bally, Veronique Rossi, Nicole Thielens and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

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  18. The Ehlers-Danlos syndromes.Nature reviews. Disease primers · 2020
    Review
  19. Two Different MissenseFrontiers in immunology · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 7 institutions in 4 countries.

Rebekka GröbnerInstitute for Human Genetics, Medical University Innsbruck, Innsbruck, Austria.
Ines Kapferer-SeebacherDepartment for Operative and Restorative Dentistry, Medical University Innsbruck, Innsbruck, Austria.
Albert AmbergerInstitute for Human Genetics, Medical University Innsbruck, Innsbruck, Austria.
Rita RedolfiInstitute for Human Genetics, Medical University Innsbruck, Innsbruck, Austria.
Fabien DalonneauUniversity of Grenoble Alpes, CEA, CNRS, IBS, Grenoble, France.
Erik BjörckDepartment of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden.
Di MilnesGenetic Health Queensland, Royal Brisbane and Women's Hospital, Herston, QLD, Australia.
Isabelle BallyUniversity of Grenoble Alpes, CEA, CNRS, IBS, Grenoble, France.
Veronique RossiUniversity of Grenoble Alpes, CEA, CNRS, IBS, Grenoble, France.
Nicole ThielensUniversity of Grenoble Alpes, CEA, CNRS, IBS, Grenoble, France.
Heribert StoiberInstitute of Virology, Medical University Innsbruck, Innsbruck, Austria.
Christine GaboriaudUniversity of Grenoble Alpes, CEA, CNRS, IBS, Grenoble, France.
Johannes ZschockeInstitute for Human Genetics, Medical University Innsbruck, Innsbruck, Austria.
Innsbruck Medical University · ATCentre National de la Recherche Scientifique · FRCEA Grenoble · FRInstitut de Biologie Structurale · FRKarolinska University Hospital · SERoyal Brisbane and Women's Hospital · AUUniversité Grenoble Alpes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heterozygous missense or in-frame insertion/deletion mutations in complement 1 subunits C1r and C1s cause periodontal Ehlers-Danlos Syndrome (pEDS), a specific EDS subtype characterized by early severe periodontal destruction and connective tissue abnormalities like easy bruising, pretibial haemosiderotic plaques, and joint hypermobility. We report extensive functional studies of 16

Indexed as

Cells, CulturedComplement ActivationComplement C1Complement C1rEhlers-Danlos SyndromeFibroblastsHumansMutationPeriodontal DiseasesComplement C1Complement C1rC1r/scomplement systemconnective tissueEhlers-Danlos syndromeperiodontitis

Identifiers

PMID31749804
PMCPMC6848165
OpenAlexW2981546930

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.