Evidence map›Paper›PMID 24859875›Full record

ArticleHaematologica2014

Genome-wide genotyping of acute myeloid leukemia with translocation t(9;11)(p22;q23) reveals novel recurrent genomic alterations.

Michael W M Kühn, Lars Bullinger, Stefan Gröschel, Jan Krönke, Jennifer Edelmann, Frank G Rücker, Karina Eiwen, Peter Paschka, Verena I Gaidzik, Karlheinz Holzmann and 3 more

Abstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Haematologica, 2014. 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
–field-weighted citation impact
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.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

13 authors.

Michael W M KühnDepartment of Internal Medicine III, University of Ulm, Germany.
Lars BullingerDepartment of Internal Medicine III, University of Ulm, Germany.
Stefan GröschelDepartment of Internal Medicine III, University of Ulm, Germany.
Jan KrönkeDepartment of Internal Medicine III, University of Ulm, Germany.
Jennifer EdelmannDepartment of Internal Medicine III, University of Ulm, Germany.
Frank G RückerDepartment of Internal Medicine III, University of Ulm, Germany.
Karina EiwenDepartment of Internal Medicine III, University of Ulm, Germany.
Peter PaschkaDepartment of Internal Medicine III, University of Ulm, Germany.
Verena I GaidzikDepartment of Internal Medicine III, University of Ulm, Germany.
Karlheinz HolzmannMicroarray Core Facility, University of Ulm, Germany.
Richard F SchlenkDepartment of Internal Medicine III, University of Ulm, Germany.
Hartmut DöhnerDepartment of Internal Medicine III, University of Ulm, Germany.
Konstanze DöhnerDepartment of Internal Medicine III, University of Ulm, Germany konstanze.doehner@uniklinik-ulm.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdultChromosomes, Human, Pair 11Chromosomes, Human, Pair 9Cohort StudiesFemaleGenome-Wide Association StudyGenomicsHumansLeukemia, Myeloid, AcuteMalePolymorphism, Single NucleotideTranslocation, Geneticacute myeloid leukemiacopy number alterationsgenotypingnovel recurrent genomic alterationst(9;11)(p22;q23)

Identifiers

PMID24859875
PMCPMC4116844

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.