Evidence map›Paper›PMID 37361494›Full record

ArticleAdvances in laboratory medicine2020

Prenatal screening and diagnosis of genetic abnormalities: SEGO, SEQC

Belén Prieto, Begoña Adiego, Javier Suela, Inmaculada Martín, Belén Santacruz, Javier García-Planells, Mar Gil, Concepción González, Eva Barrenechea

Open access · diamondAbstract read
In one paragraph

Article in Advances in laboratory medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 4 institutions in 1 country.

Belén PrietoDepartment of Clinical Biochemistry, Hospital Universitario Central de Asturias, Department of Biochemistry and Molecular Biochemistry, University of Oviedo, Avda Roma s/n - 33010 Oviedo, Spain.
Begoña AdiegoUnit of Gynecology and Obstetrics, Hospital de Móstoles, Universidad Juan Carlos I, Madrid, Spain.
Javier SuelaLaboratory of Genomics, NIMGenetics, Madrid, Spain.
Inmaculada MartínDepartment of Clinical Biochemistry Hospital Son Espases, Palma de Mallorca, Spain.
Belén SantacruzUnit of Gynecology and Obstetrics, Hospital Universitario de Torrejón, Madrid, Spain.
Javier García-PlanellsInstituto de Medicina Genómica, IMEGEN, Valencia, Spain.
Mar GilUnit of Gynecology and Obstetrics, Hospital Universitario de Torrejón, Madrid, Spain.
Concepción GonzálezDepartment of Clinical Analysis Hospital Universitario Virgen de la Macarena, Seville, Spain.
Eva BarrenecheaDepartment of Clinical Analysis, Hospital Universitario de Galdakao, Galdakao, Spain.
Spanish Society of Family and Community Medicine · ESHospital de Galdakao · ESHospital Universitario de Torrejón · ESInstituto de Medicina Genómica · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this paper, the scientific societies SEGO, SEQC

Indexed as

circulating cell-free DNAcombined screeninginvasive testsnuchal translucency

Identifiers

PMID37361494
PMCPMC10197315
OpenAlexW3046166130

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.