Evidence map›Paper›PMID 38318288›Full record

ArticleFrontiers in genetics2023

The value of genome-wide analysis in craniosynostosis.

Alexandra Topa, Anna Rohlin, André Fehr, Lovisa Lovmar, Göran Stenman, Peter Tarnow, Giovanni Maltese, Madiha Bhatti-Søfteland, Lars Kölby

Abstract read
In one paragraph

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. The role of pathogenic TCF12 variants in children with coronal craniosynostosis-a systematic review with addition of two novel cases.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Pooled it
  2. Review
  3. Article
  4. Review
  5. 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

9 authors.

Alexandra TopaDepartment of Laboratory Medicine, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden.
Anna RohlinDepartment of Laboratory Medicine, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden.
André FehrDepartment of Laboratory Medicine, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden.
Lovisa LovmarDepartment of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden.
Göran StenmanDepartment of Laboratory Medicine, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden.
Peter TarnowDepartment of Plastic Surgery, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden.
Giovanni MalteseDepartment of Plastic Surgery, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden.
Madiha Bhatti-SøftelandDepartment of Plastic Surgery, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden.
Lars KölbyDepartment of Plastic Surgery, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

craniofacialgenegeneticskullsuturesyndromesynostosis

Identifiers

PMID38318288
PMCPMC10839781

What OpenQuestion holds

Textmetadata
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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.