Evidence map›Paper›PMID 31068669›Full record

ReviewEuropean journal of human genetics : EJHG2019

Population genetic screening: current issues in a European country.

Laurent Pasquier, Bertrand Isidor, Emmanuelle Rial-Sebbag, Sylvie Odent, Guy Minguet, Grégoire Moutel

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in European journal of human genetics : EJHG, 2019. 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

6 authors.

Laurent PasquierService de Génétique Clinique, Centre Référence "Déficiences Intellectuelles de causes rares" (CRDI), Centre Hospitalier Universitaire Rennes, 16 boulevard de Bulgarie, F-35203, Rennes, France. laurent.pasquier@chu-rennes.fr.ORCID http://orcid.org/0000-0003-3985-1286
Bertrand IsidorService de Génétique Médicale, Centre Hospitalier Universitaire Nantes, 9 quai Moncousu, F-44093, Nantes cedex 1, France.
Emmanuelle Rial-SebbagINSERM UMR 1027, Toulouse Université, 37 allée Jules Guesde, F-31000, Toulouse, France.
Sylvie OdentService de Génétique Clinique, Centre Référence Anomalies du Développement CLAD Ouest, Centre Hospitalier Universitaire Rennes, 16 boulevard de Bulgarie, F-35203, Rennes, France.
Guy MinguetInstitut Mines Télécom Atlantique, Département Sciences Sociales et de Gestion, 4 rue Alfred Kastler, F-44307, Nantes Cedex 3, France.
Grégoire MoutelINSERM U1086, Anticipe, Normandie Université, 3 avenue du Général Harris, F-14076, Caen, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetics, PopulationGenetic TestingEuropeGenetic Diseases, InbornGenome, HumanGenomicsHumans

Identifiers

PMID31068669
PMCPMC6777526

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.