Evidence map›Paper›PMID 33672002›Full record

ArticleGenes2021

Acceptability of Telegenetics for Families with Genetic Eye Diseases.

Suzannah Bell, Urvi Karamchandani, Kirsten Malcolmson, Mariya Moosajee

Abstract read
In one paragraph

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Commentary: An eye on the genes.Indian journal of ophthalmology · 2022
    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

4 authors.

Suzannah BellMoorfields Eye Hospital NHS Foundation Trust, London EC1V 2PD, UK.ORCID 0000-0002-3328-3698
Urvi KaramchandaniMoorfields Eye Hospital NHS Foundation Trust, London EC1V 2PD, UK.ORCID 0000-0002-7571-2059
Kirsten MalcolmsonMoorfields Eye Hospital NHS Foundation Trust, London EC1V 2PD, UK.
Mariya MoosajeeMoorfields Eye Hospital NHS Foundation Trust, London EC1V 2PD, UK.ORCID 0000-0003-1688-5360

Funding

Wellcome Trust 205174/Z/16/Z
6 · The paper itself

Abstract

Healthcare providers around the world have implemented remote routine consultations to minimise disruption during the COVID-19 pandemic. Virtual clinics are particularly suitable for patients with genetic eye diseases as they rely on detailed histories with genetic counselling. During April-June 2019, the opinion of carers of children with inherited eye disorders attending the ocular genetics service at Moorfields Eye Hospital NHS Foundation Trust (MEH) were canvassed. Sixty-five percent of families (

Indexed as

COVID-19Eye DiseasesGenetic CounselingPandemicsSARS-CoV-2Surveys and QuestionnairesTelemedicineChildFemaleHumansInfantgenetic eye diseaseophthalmologyrare diseaseremote consultationsservice deliverytelegeneticstelemedicine

Identifiers

PMID33672002
PMCPMC7919280

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.