Evidence map›Paper›PMID 20372188›Full record

ArticleEuropean journal of human genetics : EJHG2010

Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1].

Mine Arslan-Kirchner, Eloisa Arbustini, Catherine Boileau, Anne Child, Gwenaelle Collod-Beroud, Anne De Paepe, Jörg Epplen, Guillaume Jondeau, Bart Loeys, Laurence Faivre

Abstract readValidation Study
In one paragraph

Article in European journal of human genetics : EJHG, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. A Novel Heterozygous Intronic Mutation in theBioMed research international · 2018
    Article
  4. Non-cardiac manifestations of Marfan syndrome.Annals of cardiothoracic surgery · 2017
    Review
  5. Athletes and the Aorta: Normal Adaptations and the Diagnosis and Management of Pathology.Current treatment options in cardiovascular medicine · 2017
    Review
  6. De Novo Paternal FBN1 Mutation Detected in Embryos Before Implantation.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  7. Article
  8. 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.

Mine Arslan-KirchnerInstitute of Human Genetics, Hannover Medical School, Hannover, Germany. arslan.mine@mh-hannover.de
Eloisa Arbustini
Catherine Boileau
Anne Child
Gwenaelle Collod-Beroud
Anne De Paepe
Jörg Epplen
Guillaume Jondeau
Bart Loeys
Laurence Faivre

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdipokinesChromatography, High Pressure LiquidFibrillin-1FibrillinsHumansMarfan SyndromeMicrofilament ProteinsPhenotypeSensitivity and SpecificityAdipokinesFBN1 protein, humanFibrillin-1FibrillinsMicrofilament Proteins

Identifiers

PMID20372188
PMCPMC2987429

What OpenQuestion holds

Textmetadata
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.