Evidence map›Paper›PMID 31667458›Full record

ArticleJBMR plus2019

Despite Genetic Iron Overload,

Alessa Wagner, Betül Alan, Dilay Yilmaz, Mubashir Ahmad, Peng Liu, Naveen Kumar Tangudu, Jan P Tuckermann, Maja Vujic Spasic

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Bone phenotyping of murine hemochromatosis models with deficiencies of Hjv, Alk2, or Alk3: The influence of sex and the bone compartment.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Iron at the Interface of Hepatocellular Carcinoma.International journal of molecular sciences · 2021
    Review
  8. Review
  9. 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 1 country.

Alessa WagnerInstitute of Comparative Molecular Endocrinology, University of Ulm Ulm Germany.
Betül AlanInstitute of Comparative Molecular Endocrinology, University of Ulm Ulm Germany.
Dilay YilmazInstitute of Comparative Molecular Endocrinology, University of Ulm Ulm Germany.
Mubashir AhmadInstitute of Comparative Molecular Endocrinology, University of Ulm Ulm Germany.
Peng LiuInstitute of Comparative Molecular Endocrinology, University of Ulm Ulm Germany.
Naveen Kumar TanguduInstitute of Comparative Molecular Endocrinology, University of Ulm Ulm Germany.
Jan P TuckermannInstitute of Comparative Molecular Endocrinology, University of Ulm Ulm Germany.
Maja Vujic SpasicInstitute of Comparative Molecular Endocrinology, University of Ulm Ulm Germany.
Technische Hochschule Ulm · DEUniversität Ulm · DEUniversity Hospital Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the most prevalent genetic iron overload disorders in Caucasians is caused by mutations in the

Indexed as

BONEHFE‐HEMOCHROMATOSISIRONOSTEOBLAST/OSTEOCLASTSOSTEOPOROSIS

Identifiers

PMID31667458
PMCPMC6808227
OpenAlexW2947793435

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.