Evidence map›Paper›PMID 28017548›Full record

ArticleParkinsonism & related disorders2017

Evaluating the role of TMEM230 variants in Parkinson's disease.

Hauke Baumann, Simone Wolff, Alexander Münchau, Johann M Hagenah, Katja Lohmann, Christine Klein

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in Parkinsonism & related disorders, 2017. 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
2.0field-weighted citation impact, top 13% 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, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. The Role of TMEM230 Gene in Parkinson's Disease.Journal of Parkinson's disease · 2018
    Review
  4. Article
  5. Article
  6. New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.Current neurology and neuroscience reports · 2017
    Review
  7. TMEM230 in Parkinson's disease.Neurobiology of aging · 2017
    Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Hauke BaumannInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Simone WolffDepartment of Neurology, University Hospital Schleswig Holstein, Lübeck, Germany.
Alexander MünchauInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany; Department of Neurology, University Hospital Schleswig Holstein, Lübeck, Germany.
Johann M HagenahInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany; Department of Neurology, Westküstenklinikum Heide, Heide, Germany.
Katja LohmannInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany. Electronic address: katja.lohmann@neuro.uni-luebeck.de.
Christine KleinInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
University of Lübeck · DE

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 StudiesParkinson DiseaseHumansMutation

Identifiers

PMID28017548
OpenAlexW2567373376

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.