Evidence map›Paper›PMID 41392321›Full record

ArticleEuropean journal of human genetics : EJHG2026

Cascade counselling and testing. Recommendations of the European Society of Human Genetics.

Guido de Wert, Carla G van El, Angus Clarke, Christophe Cordier, Florence Fellmann, Maurizio Genuardi, Sabine Hentze, Hülya Kayserili, Milan Macek, Rhona MacLeod and 7 more

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2026. 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. Article
  2. Mainstreaming genetic testing in community oncology settings.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. 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

17 authors.

Guido de WertDepartment of Health, Ethics and Society, Faculty of Health, Medicine and Life Sciences, CAPHRI Care and Public Health Research Institute, GROW School for Oncology and Reproduction, Maastricht University, Maastricht, The Netherlands. g.dewert@maastrichtuniversity.nl.ORCID 0000-0002-0410-4902
Carla G van ElSection Community Genetics, Department of Human Genetics, and Amsterdam Public Health research institute, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-2201-2320
Angus ClarkeDivision of Cancer and Genetics, Cardiff University School of Medicine, Cardiff, UK.ORCID 0000-0002-1200-9286
Christophe CordierSonic Suisse SA, Genesupport, Lausanne, Switzerland.
Florence FellmannFeelGood Onco, Clarens, Switzerland.ORCID 0000-0003-3156-4768
Maurizio GenuardiDepartment of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0002-7410-8351
Sabine HentzeSynlab, Practice for Human Genetics, Heidelberg, Germany.
Hülya KayseriliKoc University School of Medicine (KUSOM) Medical Genetics Department, Istanbul, Turkey.ORCID 0000-0003-0376-499X
Milan MacekMotol University Hospital-2nd Faculty of Medicine, Charles University, Prague, Czechia.ORCID 0000-0002-5173-5280
Rhona MacLeodManchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Manchester, UK.
Béla MeleghUniversity of Pécs, Pécs, Hungary.
Álvaro MendesCGPP-Centre for Predictive and Preventive Genetics, IBMC - Institute for Molecular and Cell Biology, University of Porto, Porto, Portugal.ORCID 0000-0002-8766-7646
Emmanuelle Rial-SebbagCERPOP, Bioethics team, Inserm, Université de Toulouse, Toulouse, France.
Vigdís StefánsdóttirDepartment of Genetics and Molecular Medicine, Landspitali University Hospital, Reykjavik, Iceland.ORCID 0000-0003-4451-3126
Lisbeth TranebjærgThe Kennedy Centre, Department of Clinical Genetics, University Hospital, Copenhagen, Denmark.
Fiona UlphUniversity of Manchester Division of Psychology & Mental Health, School of Health Sci, Manchester, UK.ORCID 0000-0003-3590-6542
Francesca ForzanoGuy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0001-5632-0052

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cascade testing (CT) is an effective instrument for identifying an index patient's relatives at high risk of a heritable condition enabling informed decision-making on preventive interventions and reproductive choice. However, CT remains underutilised and faces barriers. Discussions are ongoing on how to optimise informing family members and testing uptake in a responsible manner. The European Society of Human Genetics (ESHG) contributes to this debate and provides recommendations based on an ethical analysis of when CT is justified, or may be less compelling, considering proportionality and the judicious use of finite resources. ESHG underscores the strong consensus regarding the 'moral architecture' of CT in cases of a high risk of serious, avoidable harm. In such cases, a more active approach towards CT is suggested, including a more directive approach in counselling, more active support for the proband, direct contacting, and balancing confidentiality when this is necessary to avoid a high risk of serious harm, taking account of national regulations and jurisdictions. In contrast, more caution is advised in more complex cases where the balance of benefits and harms of CT is less clear, such as when penetrance is low, and actionability or medical treatment is limited. This more cautious approach does not call for directivity, direct contact or the relaxing of medical confidentiality. The focus, then, shifts to cascade counselling, rather than cascade testing. In some cases, CT may not be proportional or appropriate given the balance between benefits and harms, also in view of available resources.

Indexed as

Genetic CounselingGenetic TestingHuman GeneticsEuropeHumans

Identifiers

PMID41392321
PMCPMC12858827

What OpenQuestion holds

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LicenceCC BY
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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.