Evidence map›Paper›PMID 36316491›Full record

ArticleEuropean journal of human genetics : EJHG2023

The genetic counsellor role in the United Kingdom : Position on behalf of the Association of Genetic Nurses and Counsellors (AGNC), Endorsed by the Genetic Counsellor Registration Board (GCRB) and Academy for Healthcare Science (AHCS).

Anna Middleton, Nicola Taverner, Natalie Moreton, Roberta Rizzo, Catherine Houghton, Catherine Watt, Esther Horton, Sara Levene, Phil Leonard, Athalie Melville and 4 more

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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  19. New year, new genes.European journal of human genetics : EJHG · 2023
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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

14 authors.

Anna MiddletonEngagement and Society, Wellcome Connecting Science, Wellcome Genome Campus, Hinxton, Cambridge, UK. Am2624@cam.ac.uk.ORCID 0000-0003-3103-8098
Nicola TavernerSchool of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0001-5456-597X
Natalie MoretonManchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Manchester, UK.
Roberta RizzoUniversity Hospital Southampton NHS Foundation Trust, Southampton, UK.
Catherine HoughtonLiverpool Centre for Genomic Medicine, Liverpool Women's NHS Foundation Trust, Liverpool, UK.
Catherine WattDepartment of Clinical Genetics, West of Scotland Genetic Services, Glasgow, UK.
Esther HortonNottingham University Hospitals, Nottingham, UK.
Sara LeveneThe Centre for Reproductive & Genetic Health, London, UK.
Phil LeonardBirmingham Women's NHS Foundation Trust, Birmingham, UK.
Athalie MelvilleWessex Clinical Genetics Service, Southampton, UK.
Somya EllisManchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Manchester, UK.
Vishakha TripathiGuy's and St Thomas' Clinical Genetics Service, Guy's Hospital, London, UK.
Christine PatchEngagement and Society, Wellcome Connecting Science, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-4191-0663
Elaine JenkinsHead of Standards, Academy for Healthcare Science, London, UK.

Funding

Wellcome Trust 108413/A/15/D
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

CounselorsNursesDelivery of Health CareGenetic CounselingHumansUnited Kingdom

Identifiers

PMID36316491
PMCPMC9822947

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.