Evidence map›Paper›PMID 28934398›Full record

ArticleHuman molecular genetics2017

Messenger RNA processing is altered in autosomal dominant leukodystrophy.

Anna Bartoletti-Stella, Laura Gasparini, Caterina Giacomini, Patrizia Corrado, Rossana Terlizzi, Elisa Giorgio, Pamela Magini, Marco Seri, Agostino Baruzzi, Piero Parchi and 3 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Human molecular genetics, 2017. 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
–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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Anna Bartoletti-StellaDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40123, Italy.
Laura GaspariniDepartment of Neuroscience and Brain Techonologies, Istituto Italiano di Tecnologia, Genova 16163, Italy.
Caterina GiacominiDepartment of Neuroscience and Brain Techonologies, Istituto Italiano di Tecnologia, Genova 16163, Italy.
Patrizia CorradoDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40123, Italy.
Rossana TerlizziDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40123, Italy.
Elisa GiorgioDepartment of Medical Sciences, University of Torino, Torino 10126, Italy.
Pamela MaginiMedical Genetics Unit, Department of Medical and Surgical Sciences, University of Bologna 40138, Italy.
Marco SeriMedical Genetics Unit, Department of Medical and Surgical Sciences, University of Bologna 40138, Italy.
Agostino BaruzziIRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Ospedale Bellaria, Bologna 40139, Italy.
Piero ParchiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40123, Italy.
Alfredo BruscoDepartment of Medical Sciences, University of Torino, Torino 10126, Italy.
Pietro CortelliDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40123, Italy.
Sabina CapellariDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40123, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID28934398
PMCPMC5886215

What OpenQuestion holds

Textmetadata
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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.