Evidence map›Paper›PMID 32679894›Full record

ArticleGenes2020

Genotype-Phenotype Correlation in Children: The Impact of

Veronika C Stark, Flemming Hensen, Kerstin Kutsche, Fanny Kortüm, Jakob Olfe, Peter Wiegand, Yskert von Kodolitsch, Rainer Kozlik-Feldmann, Götz C Müller, Thomas S Mir

Open access · goldAbstract read
In one paragraph

Article in Genes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  4. Review
  5. Article
  6. The Reclassification of aCase reports in medicine · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Ocular, cardiovascular, and genetic characteristics and their associations in children with Marfan syndrome and related fibrillinopathies.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2023
    Article
  11. Article
  12. Article
  13. Review
  14. Cardiovascular manifestations in Marfan syndrome.Medicine and pharmacy reports · 2021
    Article
  15. Review
  16. Precision Medicine Approaches to Vascular Disease: JACC Focus Seminar 2/5.Journal of the American College of Cardiology · 2021
    Review
  17. Article
  18. 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

10 authors at 1 institution in 1 country.

Veronika C StarkPediatric Cardiology, University Heart and Vascular Center Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.
Flemming HensenPediatric Cardiology, University Heart and Vascular Center Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.
Kerstin KutscheInstitute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.
Fanny KortümInstitute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.
Jakob OlfePediatric Cardiology, University Heart and Vascular Center Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.ORCID 0000-0002-4449-7739
Peter WiegandPediatric Cardiology, University Heart and Vascular Center Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.
Yskert von KodolitschCardiology, University Heart and Vascular Center Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.
Rainer Kozlik-FeldmannPediatric Cardiology, University Heart and Vascular Center Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.
Götz C MüllerPediatric Cardiology, University Heart and Vascular Center Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.
Thomas S MirPediatric Cardiology, University Heart and Vascular Center Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.ORCID 0000-0002-8337-5187
Universität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, no reliable genotype-phenotype correlation is available for pediatric Marfan patients in everyday clinical practice. We investigated correlations of

Indexed as

MutationPhenotypeAdipokinesAortaChildChild, PreschoolFemaleFibrillin-1Genetic TestingGenotypeHumansMaleMarfan SyndromePrecision MedicinePulmonary ArterySternumAdipokinesFBN1 protein, humanFibrillin-1childhoodFBN1 variantgenetic testinggenotype–phenotypeMarfan syndromevariant spectrum

Identifiers

PMID32679894
PMCPMC7397236
OpenAlexW3042770477

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.