Evidence map›Paper›PMID 38732227›Full record

ArticleInternational journal of molecular sciences2024

Ewelina Elert-Dobkowska, Iwona Stepniak, Wiktoria Radziwonik-Fraczyk, Amir Jahic, Christian Beetz, Anna Sulek

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Ewelina Elert-DobkowskaDepartment of Genetics, Institute of Psychiatry and Neurology, 02-957 Warsaw, Poland.
Iwona StepniakDepartment of Genetics, Institute of Psychiatry and Neurology, 02-957 Warsaw, Poland.
Wiktoria Radziwonik-FraczykDepartment of Genetics, Institute of Psychiatry and Neurology, 02-957 Warsaw, Poland.
Amir JahicInstitute of Diagnostic Laboratory Medicine, Clinical Chemistry and Pathobiochemistry, Charité-Universitätsmedizin, 10117 Berlin, Germany.ORCID 0000-0001-8318-0147
Christian BeetzDepartment of Chemistry and Laboratory Medicine, Jena University Hospital, 07747 Jena, Germany.ORCID 0000-0001-7061-2895
Anna SulekFaculty of Medicine, Lazarski University, 02-662 Warsaw, Poland.ORCID 0000-0003-2975-4888

Funding

National Science Center Preludium 8 UMO-2014/15/N/NZ2/00395
6 · The paper itself

Abstract

The most common form of hereditary spastic paraplegia (HSP), SPG4 is caused by single nucleotide variants and microrearrangements in the

Indexed as

HaploinsufficiencySpastic Paraplegia, HereditarySpastinAdolescentAdultAlu ElementsDNA Copy Number VariationsFemaleHumansMaleMiddle AgedNonsense Mediated mRNA DecayPedigreeYoung AdultSpastinSPAST protein, humanhereditary spastic paraplegiamicrorearrangementsSPAST deletions

Identifiers

PMID38732227
PMCPMC11084448

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.