Evidence map›Paper›PMID 34136434›Full record

ArticleFrontiers in pediatrics2021

Strategies in Rapid Genetic Diagnostics of Critically Ill Children: Experiences From a Dutch University Hospital.

Miriam E Imafidon, Birgit Sikkema-Raddatz, Kristin M Abbott, Martine T Meems-Veldhuis, Morris A Swertz, K Joeri van der Velde, Gea Beunders, Dennis K Bos, Nine V A M Knoers, Wilhelmina S Kerstjens-Frederikse and 1 more

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In one paragraph

Article in Frontiers in pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

11 authors at 2 institutions in 1 country.

Miriam E ImafidonDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Birgit Sikkema-RaddatzDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Kristin M AbbottDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Martine T Meems-VeldhuisDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Morris A SwertzDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
K Joeri van der VeldeDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Gea BeundersDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Dennis K BosDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Nine V A M KnoersDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Wilhelmina S Kerstjens-FrederikseDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Cleo C van DiemenDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
University of Groningen · NLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

copy number variationgenetic diagnosticsgenetic diseaseneonatal intensive care (unit)next generation sequencing

Identifiers

PMID34136434
PMCPMC8200558
OpenAlexW3171484065

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.