Evidence map›Paper›PMID 35765406›Full record

ReviewCureus2022

A Systematic Review of the Role of Runt-Related Transcription Factor 1 (RUNX1) in the Pathogenesis of Hematological Malignancies in Patients With Inherited Bone Marrow Failure Syndromes.

Janan Illango, Archana Sreekantan Nair, Rajvi Gor, Ransirini Wijeratne Fernando, Mushrin Malik, Nabeel A Siddiqui, Pousette Hamid

Open access · diamondAbstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Cureus, 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
0.5field-weighted citation impact, top 34% 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, 3 citations in OpenAlex.

  1. Article
  2. [Clinical characteristics of RUNX1-mutated acute myeloid leukemia patients].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2026
    Article
  3. Article
  4. Humanized mouse models in MDS.Cell death & disease · 2025
    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

7 authors at 1 institution in 1 country.

Janan IllangoResearch, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Archana Sreekantan NairInternal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Rajvi GorResearch, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Ransirini Wijeratne FernandoResearch, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Mushrin MalikResearch, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Nabeel A SiddiquiResearch, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Pousette HamidNeurology, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
California Institute of Behavioral Neurosciences and Psychology (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatic

Indexed as

hematological malignanciesinherited bone marrow failure syndromesmutations and polymorphismspathogenesisrunx1 gene

Identifiers

PMID35765406
PMCPMC9233622
OpenAlexW4281950255

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.