Evidence map›Paper›PMID 37107549›Full record

ArticleGenes2023

The Role of Genetic Testing in Children Requiring Surgery for Ectopia Lentis.

Mohammud Musleh, Adam Bull, Emma Linton, Jingshu Liu, Sarah Waller, Claire Hardcastle, Jill Clayton-Smith, Vinod Sharma, Graeme C Black, Susmito Biswas and 2 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. 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
1.9field-weighted citation impact, top 13% 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, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  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

12 authors at 5 institutions in 2 countries.

Mohammud MuslehEye Department, St. James's University Hospital, Leeds LS9 7TF, UK.
Adam BullManchester Royal Eye Hospital, Manchester M13 9WL, UK.
Emma LintonManchester Royal Eye Hospital, Manchester M13 9WL, UK.
Jingshu LiuDivision of Evolution, Infection and Genomics, School of Biological Sciences, University of Manchester, Manchester M13 9PL, UK.
Sarah WallerManchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester M13 9WL, UK.
Claire HardcastleManchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester M13 9WL, UK.
Jill Clayton-SmithDivision of Evolution, Infection and Genomics, School of Biological Sciences, University of Manchester, Manchester M13 9PL, UK.
Vinod SharmaManchester Royal Eye Hospital, Manchester M13 9WL, UK.ORCID 0000-0001-6035-4773
Graeme C BlackDivision of Evolution, Infection and Genomics, School of Biological Sciences, University of Manchester, Manchester M13 9PL, UK.
Susmito BiswasManchester Royal Eye Hospital, Manchester M13 9WL, UK.
Jane L AshworthManchester Royal Eye Hospital, Manchester M13 9WL, UK.
Panagiotis I SergouniotisManchester Royal Eye Hospital, Manchester M13 9WL, UK.ORCID 0000-0003-0986-4123
Manchester Royal Eye Hospital · GBUniversity of Manchester · GBSt Mary's Hospital · GBSt James's University Hospital · GBUniversity of Ljubljana · SI

Funding

Department of Health CL-2017-06-001Wellcome TrustWellcome Trust 200990/Z/16/ZWellcome Trust 224643/Z/21/Z
6 · The paper itself

Abstract

Non-traumatic ectopia lentis can be isolated or herald an underlying multisystemic disorder. Technological advances have revolutionized genetic testing for many ophthalmic disorders, and this study aims to provide insights into the clinical utility of genetic analysis in paediatric ectopia lentis. Children that underwent lens extraction for ectopia lentis between 2013 and 2017 were identified, and gene panel testing findings and surgical outcomes were collected. Overall, 10/11 cases received a probable molecular diagnosis. Genetic variants were identified in four genes:

Indexed as

Ectopia LentisLens, CrystallineMarfan SyndromeChildChild, PreschoolGenetic TestingHumansLatent TGF-beta Binding ProteinsRetrospective StudiesLatent TGF-beta Binding ProteinsLTBP2 protein, humanectopia lentisgenetic testingMarfan syndrome

Identifiers

PMID37107549
PMCPMC10137664
OpenAlexW4361006546

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.