Evidence map›Paper›PMID 42744616›Full record

ArticlePrenatal diagnosis2026

Global Recommendations for the Use of Diagnostic Genomic Sequencing in the Prenatal Setting on Behalf of the ESHG and ISPD.

Zandra C Deans, Lina Basel Salmon, Kwong Wai Choy, Guido de Wert, Zirui Dong, Lilian Downie, Francesca Romana Grati, Sabine Hentze, Paula Jorge, Brynn Levy and 9 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Prenatal diagnosis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

19 authors.

Zandra C DeansGenQA, NHS Lothian Laboratory Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK.ORCID https://orcid.org/0000-0001-9361-6012
Lina Basel SalmonInnovation Division, Maccabi Healthcare Services, Tel Aviv, Israel.ORCID https://orcid.org/0000-0002-6327-5138
Kwong Wai ChoyDepartment of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong, China.ORCID https://orcid.org/0000-0002-3616-6200
Guido de WertDepartment of Health, Ethics and Society, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0000-0002-0410-4902
Zirui DongDepartment of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong, China.ORCID https://orcid.org/0000-0002-3626-6500
Lilian DownieVictorian Clinical Genetics Service, Murdoch Children's Research Institute, Melbourne, Australia.ORCID https://orcid.org/0000-0003-3914-5592
Francesca Romana GratiReproductive Precision Medicine Unit, Menarini Silicon Biosystems, Castel Maggiore, Italy.ORCID https://orcid.org/0000-0002-3836-5190
Sabine HentzeSynlab, Practice for Human Genetics, Mannheim, Germany.
Paula JorgeCytogenetics Laboratory, School of Medicine and Biomedical Sciences, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-6507-222X
Brynn LevyLaboratory of Personalized Genomic Medicine, Columbia University Medical Center & the New York Presbyterian Hospital, New York, New York, USA.
Luca LovrecicClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Dora MayenGenetics Clinic. Hospital Angeles Lomas. Av. Vialidad de la Barranca S/N PB, Valle de las Palmas, Huixquilucan Estado de Mexico, Mexico.
Álvaro Mendesi3S-Instituto de Investigação e Inovação em Saúde, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-8766-7646
Michael MorrisSynlab International GmbH, Munich, Germany.
Ashley PritchardNHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.ORCID https://orcid.org/0009-0002-0484-3892
Raquel Gouveia SilvaMedical Genetics Service, Local Health Unit of Santa Maria, Lisboa, Portugal.
Tina-Marié WesselsDivision Human Genetics, University of Cape Town, Cape Town, South Africa.
Francesca ForzanoGuy's and St Thomas NHS Foundation Trust, London, UK.
Natalie J ChandlerNHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0003-1396-0740

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

diagnosticfetalgenomicsprenatalsequencing

Identifiers

PMID42744616
PMCPMC13659256

What OpenQuestion holds

Textmetadata
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.