Evidence map›Paper›PMID 32219094›Full record

ArticleFrontiers in medicine2020

Prevalence of Non-psychiatric Comorbidities in Pre-symptomatic and Symptomatic Huntington's Disease Gene Carriers in Poland.

Daniel Zielonka, Grzegorz Witkowski, Elzbieta A Puch, Marta Lesniczak, Iwona Mazur-Michalek, Mark Isalan, Michal Mielcarek

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

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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 4 institutions in 2 countries.

Daniel ZielonkaDepartment of Public Health, Poznan University of Medical Sciences, Poznan, Poland.
Grzegorz WitkowskiFirst Department of Neurology, Institute of Psychiatry and Neurology, Warsaw, Poland.
Elzbieta A PuchDepartment of Human Evolutionary Biology, Adam Mickiewicz University, Poznan, Poland.
Marta LesniczakDepartment of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland.
Iwona Mazur-MichalekDepartment of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland.
Mark IsalanDepartment of Life Sciences, Imperial College London, London, United Kingdom.
Michal MielcarekDepartment of Life Sciences, Imperial College London, London, United Kingdom.
Poznan University of Medical Sciences · PLImperial College London · GBAdam Mickiewicz University in Poznań · PLInstitute of Psychiatry and Neurology · PL

Funding

Medical Research Council MC_PC_18050Wellcome Trust 102944/Z/13/Z
6 · The paper itself

Abstract

Huntington's disease (HD) is monogenic neurodegenerative disorder caused by CAG expansions within the Huntingtin gene (

Indexed as

comorbiditieshuntington's diseasemultimorbidityperipheral pathologypre-symptomatic stagesymptomatic stage

Identifiers

PMID32219094
PMCPMC7078243
OpenAlexW3012270469

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.