Evidence map›Paper›PMID 35453856›Full record

ArticleDiagnostics (Basel, Switzerland)2022

Genetic Testing for Rare Diseases.

José M Millán, Gema García-García

Abstract readEditorial
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

  1. Pooled it
  2. Review
  3. Review
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

2 authors.

José M MillánInstituto de Investigación Sanitaria La Fe, Molecular, Cellular and Genomics Biomedicine, 46026 Valencia, Spain.ORCID 0000-0002-7211-9129
Gema García-GarcíaInstituto de Investigación Sanitaria La Fe, Molecular, Cellular and Genomics Biomedicine, 46026 Valencia, Spain.ORCID 0000-0002-2113-0600

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The term rare disease was coined in the 1970s to refer to diseases that have a low prevalence [...].

Identifiers

PMID35453856
PMCPMC9028486

What OpenQuestion holds

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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.