Evidence map›Paper›PMID 27653456›Full record

ArticleScientific reports2016

Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson's disease.

Lamei Yuan, Zhi Song, Xiong Deng, Wen Zheng, Yi Guo, Zhijian Yang, Hao Deng

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

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Cathepsin B p.Gly284Val Variant in Parkinson's Disease Pathogenesis.International journal of molecular sciences · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. DnaJ/Hsp40 Family and Parkinson's Disease.Frontiers in neuroscience · 2017
    Review
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

7 authors at 2 institutions in 1 country.

Lamei YuanCenter for Experimental Medicine, the Third Xiangya Hospital, Central South University, Changsha, China.
Zhi SongDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.
Xiong DengCenter for Experimental Medicine, the Third Xiangya Hospital, Central South University, Changsha, China.
Wen ZhengDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.
Yi GuoDepartment of Medical Information, Information Security and Big Data Research Institute, Central South University, Changsha, China.
Zhijian YangCenter for Experimental Medicine, the Third Xiangya Hospital, Central South University, Changsha, China.
Hao DengCenter for Experimental Medicine, the Third Xiangya Hospital, Central South University, Changsha, China.
Central South University · CNThird Xiangya Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is one of the most common neurodegenerative disorders. Accumulated evidence confirms that genetic factors play a considerable role in PD pathogenesis. To examine whether point variants or haplotypes are associated with PD development, genotyping of 35 variants in 22 PD-related genes was performed in a well-characterized cohort of 512 Han Chinese PD patients and 512 normal controls. Both Pearson's χ

Identifiers

PMID27653456
PMCPMC5032117
OpenAlexW2521953218

What OpenQuestion holds

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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.