Evidence map›Paper›PMID 29535392›Full record

ArticleScientific reports2018

Prevalence of the single-nucleotide polymorphism rs11554137 (IDH1

Giorgia Acquaviva, Michela Visani, Dario de Biase, Gianluca Marucci, Enrico Franceschi, Alicia Tosoni, Alba A Brandes, Kerry J Rhoden, Annalisa Pession, Giovanni Tallini

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

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

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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 4 institutions in 1 country.

Giorgia AcquavivaDepartment of Medicine (Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale) - Molecular Diagnostic Unit, Azienda USL di Bologna, University of Bologna School of Medicine, Bologna, Italy.
Michela VisaniDepartment of Medicine (Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale) - Molecular Diagnostic Unit, Azienda USL di Bologna, University of Bologna School of Medicine, Bologna, Italy.
Dario de BiaseDepartment of Pharmacy and Biotechnology (Dipartimento di Farmacia e Biotecnologie) - Molecular Diagnostic Unit, Azienda USL di Bologna, University of Bologna, Bologna, Italy. dario.debiase@unibo.it.ORCID 0000-0002-0609-8817
Gianluca MarucciAnatomic Pathology Unit, AUSL of Bologna, Bologna, Italy (currently at Department of Neuropathology, IRCCS Foundation Carlo Besta Neurological Institute, Milan, Italy.
Enrico FranceschiDepartment of Oncology, AUSL Bologna - IRCCS Institute of Neurological Sciences, Bologna, Italy.
Alicia TosoniDepartment of Oncology, AUSL Bologna - IRCCS Institute of Neurological Sciences, Bologna, Italy.
Alba A BrandesDepartment of Oncology, AUSL Bologna - IRCCS Institute of Neurological Sciences, Bologna, Italy.
Kerry J RhodenMedical Genetics Unit, Department of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Annalisa PessionDepartment of Pharmacy and Biotechnology (Dipartimento di Farmacia e Biotecnologie) - Molecular Diagnostic Unit, Azienda USL di Bologna, University of Bologna, Bologna, Italy.
Giovanni TalliniDepartment of Medicine (Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale) - Molecular Diagnostic Unit, Azienda USL di Bologna, University of Bologna School of Medicine, Bologna, Italy.
Azienda USL di Bologna · ITInstitute of Neurological Sciences · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IDH mutational status is required for proper diagnosis according to the WHO criteria revised in 2016. The single nucleotide polymorphism (SNP) rs11554137 (IDH1

Indexed as

Polymorphism, Single NucleotideAdolescentAdultAgedAged, 80 and overBrain NeoplasmsFemaleGenetic Predisposition to DiseaseHigh-Throughput Nucleotide SequencingHumansIsocitrate DehydrogenaseItalyMaleMiddle AgedMutation, MissenseNeoplasm GradingIDH1 protein, humanIsocitrate Dehydrogenase

Identifiers

PMID29535392
PMCPMC5849696
OpenAlexW2790545043

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.