Evidence map›Paper›PMID 29943235›Full record

ArticleNeuroscience bulletin2018

Identification of Abnormal 51 CTA/CTG Expansion as Probably the Shortest Pathogenic Allele for Spinocerebellar Ataxia-8 in China.

Minjin Wang, Shuo Guo, Wencong Yao, Jun Wang, Jianxia Tao, Yanbing Zhou, Binwu Ying

Abstract readLetter
In one paragraph

Article in Neuroscience bulletin, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Chinese abnormal compound heterozygote spinocerebellar ataxia type 8: a case report.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  6. 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

7 authors.

Minjin WangDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, 610041, China.
Shuo GuoDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, 610041, China.
Wencong YaoDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, 610041, China.
Jun WangDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, 610041, China.
Jianxia TaoDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, 610041, China.
Yanbing ZhouDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, 610041, China.
Binwu YingDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, 610041, China. binwuying@126.com.ORCID http://orcid.org/0000-0001-5334-3355

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdultChinaDNA Repeat ExpansionFemaleHumansMaleMiddle AgedPedigreeRNA, Long NoncodingSpinocerebellar DegenerationsATXN8OS gene product, humanRNA, Long Noncoding

Identifiers

PMID29943235
PMCPMC6129249

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.