Evidence map›Paper›PMID 29741613›Full record

ArticleBrain : a journal of neurology2018

Lysosomal storage disorder gene variants in multiple system atrophy.

Lasse Pihlstrøm, Lucia Schottlaender, Viorica Chelban, MSA Exome Consortium, Wassilios G Meissner, Monica Federoff, Andy Singleton, Henry Houlden

Open access · bronzeAbstract readLetterComment
In one paragraph

Article in Brain : a journal of neurology, 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
1.2field-weighted citation impact, top 21% 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, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. The genetic basis of multiple system atrophy.Journal of translational medicine · 2023
    Review
  4. Article
  5. Review
  6. Article
  7. ARSA variants in α-synucleinopathies.Brain : a journal of neurology · 2019
    Article
  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 5 countries.

Lasse PihlstrømDepartment of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Lucia SchottlaenderDepartment of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Viorica ChelbanDepartment of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
MSA Exome Consortium
Wassilios G MeissnerDepartment of Neurology, University Hospital Bordeaux, France.
Monica FederoffLaboratory of Neurogenetics, NIH/NIA, Bethesda, USA.
Andy SingletonLaboratory of Neurogenetics, NIH/NIA, Bethesda, USA.
Henry HouldenDepartment of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
National Hospital for Neurology and Neurosurgery · GBNational Institutes of Health · USGreat Ormond Street Hospital · GBUniversité de Bordeaux · FR

Funding

Assessment of Candidate Loci in Neurological diseasesZIAAG000957 · NIA · NATIONAL INSTITUTE ON AGING · PI SINGLETON, ANDREW · 2009 to 2024
$12.2M
Medical Research Council G0802760Medical Research Council G1001253Medical Research Council MR/J004758/1Wellcome Trust 104033
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Lysosomal Storage DiseasesMultiple System AtrophyParkinson DiseaseHumans

Identifiers

PMID29741613
PMCPMC6057515
OpenAlexW2799369868

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.