Evidence map›Paper›PMID 36071912›Full record

ArticleGlobal medical genetics2022

Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype.

Drenushe Zhuri, Hakan Gurkan, Damla Eker, Yasemin Karal, Sinem Yalcintepe, Engin Atli, Selma Demir, Emine Ikbal Atli

Open access · diamondAbstract read
In one paragraph

Article in Global medical genetics, 2022. 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
1.5field-weighted citation impact, top 16% 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, 10 citations in OpenAlex.

  1. Article
  2. [Research progress on phenotypic modifier genes in spinal muscular atrophy].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
    Review
  3. In Search of Spinal Muscular Atrophy Disease Modifiers.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. 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 1 institution in 1 country.

Drenushe ZhuriDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.ORCID 0000-0002-8370-1990
Hakan GurkanDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
Damla EkerDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
Yasemin KaralDepartment of Pediatric Neurology, Trakya University Faculty of Medicine, Edirne, Turkey.
Sinem YalcintepeDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
Engin AtliDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
Selma DemirDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
Emine Ikbal AtliDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
Trakya University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

modifying genesneuromuscular disorderSMN1SMN2spinal muscular atrophy

Identifiers

PMID36071912
PMCPMC9444347
OpenAlexW4294991817

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.