Evidence map›Paper›PMID 25728710›Full record

ArticleInternational journal of hematology2015

Somatic thrombopoietin (THPO) gene mutations in childhood myeloid leukemias.

Maite E Houwing, Eva A Koopman-Coenen, Rogier Kersseboom, Saskia Gooskens, Inge M Appel, Susan T C J M Arentsen-Peters, Andrica C H de Vries, Dirk Reinhardt, Jan Stary, André Baruchel and 6 more

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In one paragraph

Article in International journal of hematology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

16 authors at 8 institutions in 4 countries.

Maite E HouwingDepartment of Pediatric Oncology/Hematology, Erasmus MC-Sophia Children's Hospital, Dr Molewaterplein 60, Room Na 16.13, 3015 GJ, Rotterdam, The Netherlands.
Eva A Koopman-Coenen
Rogier Kersseboom
Saskia Gooskens
Inge M Appel
Susan T C J M Arentsen-Peters
Andrica C H de Vries
Dirk Reinhardt
Jan Stary
André Baruchel
Valerie de Haas
Marjolein Blink
Rob H Lopes Cardozo
Rob Pieters
C Michel Zwaan
Marry M van den Heuvel-Eibrink
Erasmus MC - Sophia Children’s Hospital · NLPrincess Máxima Center · NLErasmus MC · NLHaga Hospital · NLHôpital Robert-Debré · FRKardiologie Frankfurt-Sachsenhausen · DEStichting Kinderoncologie Nederland · NLUniversity Hospital in Motol · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report, for the first time, a non-syndromic infant with a reversible myeloproliferative disease that harbors a germline hereditary thrombopoietin (THPO) gene mutation, a condition that is known to induce familial thrombocytosis at increasing age. In order to investigate whether somatic THPO gene mutations play a role in sporadic pediatric myeloproliferative diseases, we performed a mutation screening of a large representative cohort of pediatric acute myeloid leukemia, myeloid leukemia of Down syndrome, and juvenile myelomonocytic leukemia samples and show that gain-of-function THPO mutations are extremely rare in sporadic pediatric myeloproliferative diseases.

Indexed as

MutationFemaleGerm-Line MutationHumansInfantLeukemia, MyeloidMalePedigreeRNA Splice SitesThrombopoietinRNA Splice SitesThrombopoietin

Identifiers

PMID25728710
OpenAlexW2461719898

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.