Evidence map›Paper›PMID 36101818›Full record

ArticleJIMD reports2022

Glycosaminoglycan linkage region of urinary bikunin as a potentially useful biomarker for β3GalT6-deficient spondylodysplastic Ehlers-Danlos syndrome.

Mahnaz Nikpour, Fredrik Noborn, Jonas Nilsson, Tim Van Damme, Olivier Kaye, Delfien Syx, Fransiska Malfait, Göran Larson

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in JIMD reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. The Role of Clinical Glyco(proteo)mics in Precision Medicine.Molecular & cellular proteomics : MCP · 2023
    Article
  6. 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

8 authors at 3 institutions in 2 countries.

Mahnaz NikpourDepartment of Laboratory Medicine, Sahlgrenska Academy University of Gothenburg Gothenburg Sweden.
Fredrik NobornDepartment of Laboratory Medicine, Sahlgrenska Academy University of Gothenburg Gothenburg Sweden.
Jonas NilssonProteomics Core Facility, Sahlgrenska Academy University of Gothenburg Gothenburg Sweden.
Tim Van DammeDepartment of Biomolecular Medicine, Center for Medical Genetics Ghent University Hospital Ghent Belgium.ORCID https://orcid.org/0000-0002-6424-4421
Olivier KayeCentre de Rheumatologie Liège Belgium.
Delfien SyxDepartment of Biomolecular Medicine, Center for Medical Genetics Ghent University Hospital Ghent Belgium.
Fransiska MalfaitDepartment of Biomolecular Medicine, Center for Medical Genetics Ghent University Hospital Ghent Belgium.
Göran LarsonDepartment of Laboratory Medicine, Sahlgrenska Academy University of Gothenburg Gothenburg Sweden.ORCID https://orcid.org/0000-0002-2616-0366
Ghent University Hospital · BEUniversity of Gothenburg · SESahlgrenska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spondylodysplastic type of Ehlers-Danlos syndrome (spEDS) is caused by genetic defects in the

Indexed as

bikuninEhlers–Danlos syndromeglycopeptidesglycoproteomicsglycosaminoglycan linkage regionlinkeropathiesliquid chromatographytandem mass spectrometryβ3GalT6

Identifiers

PMID36101818
PMCPMC9458601
OpenAlexW4283688041

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.