Evidence map›Paper›PMID 38177407›Full record

ArticleEuropean journal of human genetics : EJHG2024

Informed consent for whole genome sequencing in mainstream clinics: logistical constraints and possible solutions.

Amina Chaouch, Fiona Ulph, James Alder, Hisham Hamdalla, John Ealing, Tara Clancy, Rhona Macleod, Angus John Clarke

Open access · hybridAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 100% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 4 institutions in 1 country.

Amina ChaouchManchester Centre for Clinical Neurosciences, Salford Royal NHS Foundation Trust, Manchester, M8 6HD, UK. amina.chaouch@manchester.ac.uk.ORCID 0009-0005-4340-6400
Fiona UlphSchool of Psychological Sciences, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.ORCID 0000-0003-3590-6542
James AlderManchester Medical School, Manchester University, Manchester, M13 9PL, UK.
Hisham HamdallaManchester Centre for Clinical Neurosciences, Salford Royal NHS Foundation Trust, Manchester, M8 6HD, UK.
John EalingManchester Centre for Clinical Neurosciences, Salford Royal NHS Foundation Trust, Manchester, M8 6HD, UK.
Tara ClancyUniversity of Manchester, Manchester, UK.
Rhona MacleodSt Mary's Hospital, Manchester University Hospitals NHS Foundation Trust, Manchester Centre for Genomic Medicine, Manchester, UK.
Angus John ClarkeCardiff University School of Medicine, Institute of Medical Genetics, University Hospital of Wales, Cardiff, UK.ORCID 0000-0002-1200-9286
Salford Royal NHS Foundation Trust · GBUniversity of Manchester · GBSt Mary's Hospital · GBUniversity Hospital of Wales · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Informed ConsentHumansWhole Genome Sequencing

Identifiers

PMID38177407
PMCPMC10924082
OpenAlexW4390586096

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.