Evidence map›Paper›PMID 33154736›Full record

ArticleFrontiers in neurology2020

A Han Chinese Family With Early-Onset Parkinson's Disease Carrying Novel Frameshift Mutation and Compound Heterozygous Mutation of

Chenyu Gao, Ting Huang, Rui Chen, Zhenhua Yuan, Youyong Tian, Yingdong Zhang

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

Article in Frontiers in neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

7 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. A novel variant ofFrontiers in neurology · 2024
    Article
  6. Review
  7. Case Report: A case ofFrontiers in neuroscience · 2022
    Article
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

6 authors at 1 institution in 1 country.

Chenyu GaoDepartment of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Ting HuangDepartment of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Rui ChenDepartment of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Zhenhua YuanDepartment of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Youyong TianDepartment of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Yingdong ZhangDepartment of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Around 15% of patients with Parkinson's disease (PD) have a family history, and 5-10% have confirmed genetic causes.

Indexed as

early-onsetgenetic analysisParkinson's diseasePRKN mutationswhole-exome sequence

Identifiers

PMID33154736
PMCPMC7586315
OpenAlexW3092137737

What OpenQuestion holds

Textmetadata
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.