Evidence map›Paper›PMID 36291092›Full record

ArticleCells2022

A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger.

José M Bastida, Stefano Malvestiti, Doris Boeckelmann, Verónica Palma-Barqueros, Mira Wolter, María L Lozano, Hannah Glonnegger, Rocío Benito, Carlo Zaninetti, Felix Sobotta and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. A novelHaematologica · 2026
    Article
  2. Article
  3. GATA1 in Normal and Pathologic Megakaryopoiesis and Platelet Development.Advances in experimental medicine and biology · 2024
    Review
  4. 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

15 authors at 8 institutions in 5 countries.

José M BastidaDepartmento de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), 37007 Salamanca, Spain.ORCID 0000-0002-8007-3909
Stefano MalvestitiDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Faculty of Medicine, Medical Center-University of Freiburg, 79106 Freiburg, Germany.ORCID 0000-0003-1595-2365
Doris BoeckelmannDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Faculty of Medicine, Medical Center-University of Freiburg, 79106 Freiburg, Germany.ORCID 0000-0001-9238-2904
Verónica Palma-BarquerosServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Pascual Parrilla, CIBERER-U765, 30003 Murcia, Spain.ORCID 0000-0002-5699-0053
Mira WolterDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Faculty of Medicine, Medical Center-University of Freiburg, 79106 Freiburg, Germany.
María L LozanoServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Pascual Parrilla, CIBERER-U765, 30003 Murcia, Spain.ORCID 0000-0003-3148-7037
Hannah GlonneggerDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Faculty of Medicine, Medical Center-University of Freiburg, 79106 Freiburg, Germany.
Rocío BenitoInstituto de Investigación Biomédica de Salamanca (IBSAL), Instituto de Biología Molecular y Cellular del Cáncer (IBMCC), Centro de Investigación del Cáncer (CIC), Universidad de Salamanca-Consejo Superior de Investigaciones Cientificas (CSIC), 37007 Salamanca, Spain.ORCID 0000-0001-9781-4198
Carlo ZaninettiInstitut für Transfusionsmedizin, Universitätsmedizin Greifswald, 17475 Greisfwald, Germany.
Felix SobottaDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Faculty of Medicine, Medical Center-University of Freiburg, 79106 Freiburg, Germany.
Freimut H SchillingChildren's Hospital, Kantonsspital Luzern, 6000 Lucerne, Switzerland.
Neil V MorganInstitute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TT, UK.ORCID 0000-0001-6433-5692
Kathleen FresonDepartment of Cardiovascular Sciences, Center for Molecular and Vascular Biology, KU Leuven, 3000 Leuven, Belgium.ORCID 0000-0002-4381-2442
José RiveraServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Pascual Parrilla, CIBERER-U765, 30003 Murcia, Spain.ORCID 0000-0003-4225-6840
Barbara ZiegerDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Faculty of Medicine, Medical Center-University of Freiburg, 79106 Freiburg, Germany.
University of Freiburg · DECentro Regional de Hemodonación · ESConsejo Superior de Investigaciones Científicas · ESKU Leuven · BELuzerner Kantonsspital · CHUniversidad de Salamanca · ESUniversitätsmedizin Greifswald · DEUniversity of Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The GATA1 transcription factor is essential for normal erythropoiesis and megakaryocytic differentiation. Germline GATA1 pathogenic variants in the N-terminal zinc finger (N-ZF) are typically associated with X-linked thrombocytopenia, platelet dysfunction, and dyserythropoietic anemia. A few variants in the C-terminal ZF (C-ZF) domain are described with normal platelet count but altered platelet function as the main characteristic. Independently performed molecular genetic analysis identified a

Indexed as

Anemia, Dyserythropoietic, CongenitalGATA1 Transcription FactorGenetic Diseases, X-LinkedGenetic VariationThrombocytopeniaZinc FingersBlood PlateletsHumansIntegrinsMalePhenotypeGATA1 protein, humanGATA1 Transcription FactorIntegrinsbleedingGATA1inherited platelet defectsplatelet pathophysiology

Identifiers

PMID36291092
PMCPMC9600848
OpenAlexW4306366887

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.