Evidence map›Paper›PMID 36051068›Full record

ArticleEJHaem2022

Variants in the new E1' cryptic exon of the

Catarina Dantas Rodrigues, Rita Pombal, Janet Pereira, Luís Relvas, Elizabete Cunha, José Carlos Almeida, Tabita Maia, Helena Silva, Celeste Bento

Open access · diamondAbstract readCase Reports
In one paragraph

Article in EJHaem, 2022. 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
0.2field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  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

9 authors at 3 institutions in 1 country.

Catarina Dantas RodriguesServiço de Hematologia Centro Hospitalar de Tondela Viseu Viseu Portugal.ORCID https://orcid.org/0000-0002-7714-0488
Rita PombalServiço de Imunohemoterapia Centro Hospitalar de Vila Nova de Gaia/Espinho Gaia Portugal.
Janet PereiraEritropatologia e Metabolismo do Ferro, Serviço de Hematologia Clínica Centro Hospitalar Universitário de Coimbra Coimbra Portugal.
Luís RelvasEritropatologia e Metabolismo do Ferro, Serviço de Hematologia Clínica Centro Hospitalar Universitário de Coimbra Coimbra Portugal.
Elizabete CunhaEritropatologia e Metabolismo do Ferro, Serviço de Hematologia Clínica Centro Hospitalar Universitário de Coimbra Coimbra Portugal.
José Carlos AlmeidaEritropatologia e Metabolismo do Ferro, Serviço de Hematologia Clínica Centro Hospitalar Universitário de Coimbra Coimbra Portugal.
Tabita MaiaEritropatologia e Metabolismo do Ferro, Serviço de Hematologia Clínica Centro Hospitalar Universitário de Coimbra Coimbra Portugal.
Helena SilvaServiço de Hematologia Centro Hospitalar de Tondela Viseu Viseu Portugal.
Celeste BentoEritropatologia e Metabolismo do Ferro, Serviço de Hematologia Clínica Centro Hospitalar Universitário de Coimbra Coimbra Portugal.
Hospitais da Universidade de Coimbra · PTCentro Hospitalar Tondela-Viseu · PTCentro Hospitalar de Vila Nova de Gaia · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital erythrocytosis (CE) represents a rare and heterogeneous group of hereditary disorders. The molecular basis of

Indexed as

congenital erythrocytosiserythrocytosispolycythaemiaVHLvon Hippel–Lindau

Identifiers

PMID36051068
PMCPMC9421959
OpenAlexW4283767348

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.