Evidence map›Paper›PMID 31595045›Full record

ArticleEuropean journal of human genetics : EJHG2020

ESHG PPPC Comments on postmortem use of genetic data for research purposes.

Florence Fellmann, Emmanuelle Rial-Sebbag, Christine Patch, Sabine Hentze, Vigdis Stefandottir, Álvaro Mendes, Carla G van El, Martina C Cornel, Francesca Forzano, Public and Professional Committee (PPPC) of the European Society of Human Genetics (ESHG)

Abstract read
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In one paragraph

Article in European journal of human genetics : EJHG, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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

10 authors.

Florence FellmannThe ColLaboratory, University of Lausanne, Lausanne, Switzerland. florence.fellmann@gmail.com.
Emmanuelle Rial-SebbagUMR 1027, Inserm, Université Paul Sabatier-Toulouse III, Toulouse Cedex, France.
Christine PatchGenomics England, Queen Mary University of London, London, United Kingdom.
Sabine HentzeHuman Genetics, Heidelberg, Germany.
Vigdis StefandottirDepartment of Genetics and Molecular Medicine, Landspitali University Hospital, Reykjavik, Iceland.
Álvaro MendesUnIGENe and CGPP-Centre for Predictive and Preventive Genetics, IBMC-Institute for Molecular and Cell Biology, i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Carla G van ElSection Community Genetics, Department of Clinical Genetics and Amsterdam Public Health research institute, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Martina C CornelSection Community Genetics, Department of Clinical Genetics and Amsterdam Public Health research institute, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-5397-5544
Francesca ForzanoClinical Genetics Department, Guy's & St Thomas' NHS Foundation Trust, London, United Kingdom. Francesca.Forzano@gstt.nhs.uk.
Public and Professional Committee (PPPC) of the European Society of Human Genetics (ESHG)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AutopsyBiological Specimen BanksEuropeExpert TestimonyGenetic PrivacyHuman GeneticsHumansPublic PolicySocieties, Medical

Identifiers

PMID31595045
PMCPMC6974591

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.