Evidence map›Paper›PMID 36292571›Full record

ReviewGenes2022

Identification of Two Novel

Laura Lo Riso, Gardenia Vargas-Parra, Gemma Navarro, Leonor Arenillas, Lierni Fernández-Ibarrondo, Beatriz Robredo, Carmen Ballester, Bernardo López, Albert Perez-Montaña, Antonia Sampol and 4 more

Open access · goldAbstract readReviewCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Review in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

14 authors at 2 institutions in 1 country.

Laura Lo RisoHematology and Hemotherapy Department, Hospital Universitario Son Espases, IDISBA, 07120 Palma de Mallorca, Spain.
Gardenia Vargas-ParraMolecular Biology Laboratory, Pathology Department, Hospital del Mar, 08003 Barcelona, Spain.ORCID 0000-0003-1378-736X
Gemma NavarroMolecular Biology Laboratory, Pathology Department, Hospital del Mar, 08003 Barcelona, Spain.
Leonor ArenillasHospital del Mar Medical Research Institute, IMIM, 08003 Barcelona, Spain.ORCID 0000-0002-8176-7179
Lierni Fernández-IbarrondoHospital del Mar Medical Research Institute, IMIM, 08003 Barcelona, Spain.
Beatriz RobredoHematology Department, Hospital Punta Europa, 11207 Algeciras, Spain.
Carmen BallesterHematology and Hemotherapy Department, Hospital Universitario Son Espases, IDISBA, 07120 Palma de Mallorca, Spain.
Bernardo LópezHematology and Hemotherapy Department, Hospital Universitario Son Espases, IDISBA, 07120 Palma de Mallorca, Spain.ORCID 0000-0002-2967-1874
Albert Perez-MontañaHematology and Hemotherapy Department, Hospital Universitario Son Espases, IDISBA, 07120 Palma de Mallorca, Spain.ORCID 0000-0003-2708-0090
Antonia SampolHematology and Hemotherapy Department, Hospital Universitario Son Espases, IDISBA, 07120 Palma de Mallorca, Spain.
Lourdes FlorensaHospital del Mar Medical Research Institute, IMIM, 08003 Barcelona, Spain.
Carles BessesHospital del Mar Medical Research Institute, IMIM, 08003 Barcelona, Spain.
María Antonia DuranHematology and Hemotherapy Department, Hospital Universitario Son Espases, IDISBA, 07120 Palma de Mallorca, Spain.
Beatriz BellosilloMolecular Biology Laboratory, Pathology Department, Hospital del Mar, 08003 Barcelona, Spain.
Hospital Del Mar · ESHospital Universitario Son Espases · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary familial and congenital polycythemia is a rare disease characterized by an increase in red cell mass that may be due to pathogenic variants in the EPO receptor (

Indexed as

PolycythemiaReceptors, ErythropoietinHumansReceptors, ErythropoietinEPORerythrocytosispolycythemiavariants

Identifiers

PMID36292571
PMCPMC9601602
OpenAlexW4296745849

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.