Evidence map›Paper›PMID 23831919›Full record

ArticleHaematologica2013

SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype.

Valeria Visconte, Ali Tabarroki, Heesun J Rogers, Edy Hasrouni, Fabiola Traina, Hideki Makishima, Betty K Hamilton, Yang Liu, Christine O'Keefe, Alan Lichtin and 4 more

Open access · goldAbstract readLetter
In one paragraph

Article in Haematologica, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Molecular pathogenesis of myelodysplastic syndromes.Translational medicine @ UniSa · 2014
    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 2 countries.

Valeria Visconte
Ali Tabarroki
Heesun J Rogers
Edy Hasrouni
Fabiola Traina
Hideki Makishima
Betty K Hamilton
Yang Liu
Christine O'Keefe
Alan Lichtin
Leonard Horwitz
Mikkael A Sekeres
Fred H Hsieh
Ramon V Tiu
Cleveland Clinic · USUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Myelodysplastic SyndromesAdultAgedAnemia, AplasticAnemia, SideroblasticBone Marrow DiseasesBone Marrow Failure DisordersFemaleHemoglobinuria, ParoxysmalHumansMaleMastocytosisMutationPhenotypePhosphoproteinsRibonucleoprotein, U2 Small NuclearPhosphoproteinsRibonucleoprotein, U2 Small NuclearRNA Splicing FactorsSF3B1 protein, humanBMFSMCDMDSmutationsSF3B1

Identifiers

PMID23831919
PMCPMC3762110
OpenAlexW1986338223

What OpenQuestion holds

Textmetadata
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.