Evidence map›Paper›PMID 35895135›Full record

ArticleJournal of neurology2022

DCTN1 mutation associated parkinsonism: case series of three new families with perry syndrome.

Thomas B Stoker, Vaclav Dostal, Jeffrey Cochius, Caroline H Williams-Gray, Clemens R Scherzer, Junhao Wang, Ganqiang Liu, Ian Coyle-Gilchrist

Open access · hybridAbstract readLetter
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Perry Disease: Expanding the Genetic Basis.Movement disorders clinical practice · 2023
    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

8 authors at 4 institutions in 3 countries.

Thomas B StokerDepartment of Neurology, Norfolk and Norwich University Hospital, Colney Lane, Norwich, UK. tbs26@cantab.net.ORCID 0000-0001-5186-7630
Vaclav DostalDepartment of Neurology, Norfolk and Norwich University Hospital, Colney Lane, Norwich, UK.
Jeffrey CochiusDepartment of Neurology, Norfolk and Norwich University Hospital, Colney Lane, Norwich, UK.
Caroline H Williams-GrayJohn Van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Clemens R ScherzerADPA Center for Advanced Parkinson Research, Harvard Medical School, Brigham and Women's Hospital, Boston, MA, USA.
Junhao WangNeurobiology Research Center, School of Medicine, Shenzhen Campus of Sun Yat-Sen University, Shenzhen, 518107, Guangdong, China.
Ganqiang LiuNeurobiology Research Center, School of Medicine, Shenzhen Campus of Sun Yat-Sen University, Shenzhen, 518107, Guangdong, China.
Ian Coyle-GilchristDepartment of Neurology, Norfolk and Norwich University Hospital, Colney Lane, Norwich, UK.
Norfolk and Norwich University Hospital · GBSun Yat-sen University · CNBrigham and Women's Hospital · USUniversity of Cambridge · GB

Funding

Genome-Wide Prediction of Dementia in Parkinson's DiseaseR01NS115144 · NINDS · YALE UNIVERSITY · PI SCHERZER, CLEMENS R · 2019 to 2025
$4.4M
Medical Research Council MR/R007446/1NINDS NIH HHS R01NS115144
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

HypoventilationParkinsonian DisordersDepressionDynactin ComplexHumansMutationTDP-43 ProteinopathiesDCTN1 protein, humanDynactin Complex

Identifiers

PMID35895135
OpenAlexW4288178078

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.