Evidence map›Paper›PMID 25414040›Full record

ArticleBrain : a journal of neurology2015

Reply: PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease.

Tsz Hang Wong, Annemieke J M H Verkerk, Annemieke J Rozemuller, Rob Willemsen, Manuela Neumann, Vincenzo Bonifati, John van Swieten

Open access · bronzeAbstract readLetterComment
PubMed Full text at PMC Publisher
In one paragraph

Article in Brain : a journal of neurology, 2015. 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
0.2field-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, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Tsz Hang Wong1 Department of Neurology, Erasmus Medical Centre, 3015 CE Rotterdam, The Netherlands.
Annemieke J M H Verkerk2 Department of Internal Medicine, Erasmus Medical Centre, 3015 CE Rotterdam, The Netherlands.
Annemieke J Rozemuller3 Department of Pathology, VU University Medical Centre, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands.
Rob Willemsen4 Department of Clinical Genetics, Erasmus Medical Centre, 3015 CE Rotterdam, The Netherlands.
Manuela Neumann5 DZNE, German Centre for Neurodegenerative Disease, 72076 Tübingen, Germany 6 Department of Neuropathology, University of Tübingen, 72076 Tübingen, Germany.
Vincenzo Bonifati4 Department of Clinical Genetics, Erasmus Medical Centre, 3015 CE Rotterdam, The Netherlands.
John van Swieten1 Department of Neurology, Erasmus Medical Centre, 3015 CE Rotterdam, The Netherlands 7 Alzheimer Centre, Neuroscience Campus Amsterdam, 1007 MB Amsterdam, The Netherlands 8 Department of Neurology, Neuroscience Campus Amsterdam, 1007 MB Amsterdam, The Netherlands j.c.vanswieten@erasmusmc.nl.
Erasmus University Rotterdam · NLAmsterdam Neuroscience · NLAmsterdam UMC Location VUmc · NLGerman Center for Neurodegenerative Diseases · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Cyclic AMP-Dependent Protein Kinase RIbeta SubunitFemaleHumansMaleNeurodegenerative DiseasesPolymorphism, Single NucleotideCyclic AMP-Dependent Protein Kinase RIbeta Subunit

Identifiers

PMID25414040
PMCPMC4614125
OpenAlexW2110627460

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.