Evidence map›Paper›PMID 29967378›Full record

ArticleLeukemia2018

Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia.

Kristina B Lundin-Ström, Andrea Biloglav, Henrik Lilljebjörn, Marianne Rissler, Thoas Fioretos, Markus Hansson, Mikael Behrendtz, Anders Castor, Linda Olsson, Bertil Johansson

Open access · hybridAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Leukemia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 3 institutions in 1 country.

Kristina B Lundin-StrömDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden. Kristina.Lundin_Strom@med.lu.se.
Andrea BiloglavDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Henrik LilljebjörnDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0001-8703-1173
Marianne RisslerDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Thoas FioretosDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Markus HanssonDivision of Hematology, Skåne University Hospital and Wallenberg Centre for Molecular Medicine, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0002-7715-4548
Mikael BehrendtzDepartment of Pediatrics, Linköping University Hospital, Linköping, Sweden.
Anders CastorDepartment of Pediatrics, Skåne University Hospital, Lund, Sweden.
Linda OlssonDepartment of Clinical Genetics and Pathology, Division of Laboratory Medicine, Lund, Sweden.
Bertil JohanssonDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Lund University · SELinköping University Hospital · SESkåne University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAllelesChromosome AberrationsComputational BiologyDatabases, GeneticExome SequencingGenetic VariationGenotypeHumansPolymorphism, Single NucleotidePrecursor B-Cell Lymphoblastic Leukemia-LymphomaUniparental Disomy

Identifiers

PMID29967378
PMCPMC6127080
OpenAlexW2810401745

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.