Evidence map›Paper›PMID 28637621›Full record

ArticleSeminars in hematology2017

GATA2 deficiency and related myeloid neoplasms.

Marcin W Wlodarski, Matthew Collin, Marshall S Horwitz

Open access · hybridAbstract read
In one paragraph

Article in Seminars in hematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

93 citing papers in PubMed, 169 citations in OpenAlex.

  1. Review
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  3. Article
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  6. Article
  7. Review
  8. Genetic Predisposition to Hematologic Malignancies.Cold Spring Harbor perspectives in medicine · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Insights into PediatricBiomedicines · 2025
    Review
  18. Article
  19. Article
  20. Article

33 more citing papers are in PubMed but not listed here.

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

3 authors at 3 institutions in 3 countries.

Marcin W WlodarskiDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology; Medical Center; Faculty of Medicine, University of Freiburg, Germany; German Cancer Consortium (DKTK), Freiburg, Germany and German Cancer Research Center (DKFZ), Heidelberg, Germany. Electronic address: marcin.wlodarski@uniklinik-freiburg.de.
Matthew CollinInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom; Northern Centre for Bone Marrow Transplantation, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.
Marshall S HorwitzDepartment of Pathology, University of Washington School of Medicine, Seattle, WA, USA.
German Cancer Research Center · DENewcastle upon Tyne Hospitals NHS Foundation Trust · GBUniversity of Washington · US

Funding

Mistargeting of Elastase in Bone Marrow FailureR01HL079507 · NHLBI · UNIVERSITY OF WASHINGTON · PI HORWITZ, MARSHALL S. · 2004 to 2008
$1.8M
Pathogenesis of ELANE-Associated NeutropeniaR01HL130472 · NHLBI · UNIVERSITY OF WASHINGTON · PI HORWITZ, MARSHALL S. · 2016 to 2019
$1.7M
NHLBI NIH HHS R01 HL079507NHLBI NIH HHS R01 HL130472
6 · The paper itself

Abstract

The GATA2 gene codes for a hematopoietic transcription factor that through its two zinc fingers (ZF) can occupy GATA-DNA motifs in a countless number of genes. It is crucial for the proliferation and maintenance of hematopoietic stem cells. During the past 5 years, germline heterozygous mutations in GATA2 were reported in several hundred patients with various phenotypes ranging from mild cytopenia to severe immunodeficiency involving B cells, natural killer cells, CD4

Indexed as

GATA2 Transcription FactorGenetic Predisposition to DiseaseHematologic NeoplasmsHumansMyeloproliferative DisordersGATA2 Transcription FactorBone marrow failureEmberger syndromeFamilial MDSGATA2 deficiencyGenetic predispositionMonoMACMonosomy 7

Identifiers

PMID28637621
PMCPMC5650112
OpenAlexW2613566589

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.