Evidence map›Paper›PMID 27830186›Full record

ArticleNeurology. Genetics2016

Copy number analysis reveals a novel multiexon deletion of the

Wei Wang, Yanhong Wu, Chen Wang, Jinsong Jiao, Christopher J Klein

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

Article in Neurology. Genetics, 2016. 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 36% 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, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. IntragenicNeurology. Genetics · 2017
    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

5 authors at 1 institution in 1 country.

Wei WangDepartment of Neurology (W.W., J.J.), China-Japan Friendship Hospital, Beijing, China; Department of Neurology (W.W., C.J.K.), Department of Laboratory Medicine and Pathology (Y.W.), Department of Health Sciences Research (C.W.), and Department of Medical Genetics (C.J.K.), Mayo Clinic, Rochester, MN.
Yanhong WuDepartment of Neurology (W.W., J.J.), China-Japan Friendship Hospital, Beijing, China; Department of Neurology (W.W., C.J.K.), Department of Laboratory Medicine and Pathology (Y.W.), Department of Health Sciences Research (C.W.), and Department of Medical Genetics (C.J.K.), Mayo Clinic, Rochester, MN.
Chen WangDepartment of Neurology (W.W., J.J.), China-Japan Friendship Hospital, Beijing, China; Department of Neurology (W.W., C.J.K.), Department of Laboratory Medicine and Pathology (Y.W.), Department of Health Sciences Research (C.W.), and Department of Medical Genetics (C.J.K.), Mayo Clinic, Rochester, MN.
Jinsong JiaoDepartment of Neurology (W.W., J.J.), China-Japan Friendship Hospital, Beijing, China; Department of Neurology (W.W., C.J.K.), Department of Laboratory Medicine and Pathology (Y.W.), Department of Health Sciences Research (C.W.), and Department of Medical Genetics (C.J.K.), Mayo Clinic, Rochester, MN.
Christopher J KleinDepartment of Neurology (W.W., J.J.), China-Japan Friendship Hospital, Beijing, China; Department of Neurology (W.W., C.J.K.), Department of Laboratory Medicine and Pathology (Y.W.), Department of Health Sciences Research (C.W.), and Department of Medical Genetics (C.J.K.), Mayo Clinic, Rochester, MN.
China-Japan Friendship Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital myasthenic syndrome (CMS) is genetically and clinically heterogeneous.

Identifiers

PMID27830186
PMCPMC5089432
OpenAlexW2543116597

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.