Evidence map›Paper›PMID 38203298›Full record

ArticleInternational journal of molecular sciences2023

Expanding the Phenotype of Hereditary Congenital Facial Paresis Type 3.

Aysylu Murtazina, Artem Borovikov, Anna Kuchina, Olga Ovsova, Maria Bulakh, Alena Chukhrova, Svetlana Braslavskaya, Oksana Ryzhkova, Nikolay Skryabin, Sergey Kutsev and 1 more

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

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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

11 authors at 3 institutions in 1 country.

Aysylu MurtazinaResearch Centre for Medical Genetics, 115478 Moscow, Russia.ORCID 0000-0001-7023-7378
Artem BorovikovResearch Centre for Medical Genetics, 115478 Moscow, Russia.ORCID 0000-0001-5871-8005
Anna KuchinaResearch Centre for Medical Genetics, 115478 Moscow, Russia.
Olga OvsovaDepartment of Neurology, Neurosurgery and Medical Genetics, Ural State Medical University, 620028 Ekaterinburg, Russia.
Maria BulakhResearch Centre for Medical Genetics, 115478 Moscow, Russia.ORCID 0000-0002-8674-7230
Alena ChukhrovaResearch Centre for Medical Genetics, 115478 Moscow, Russia.ORCID 0000-0002-5474-4713
Svetlana BraslavskayaResearch Centre for Medical Genetics, 115478 Moscow, Russia.
Oksana RyzhkovaResearch Centre for Medical Genetics, 115478 Moscow, Russia.ORCID 0000-0003-1285-9093
Nikolay SkryabinResearch Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences, 634050 Tomsk, Russia.
Sergey KutsevResearch Centre for Medical Genetics, 115478 Moscow, Russia.
Elena DadaliResearch Centre for Medical Genetics, 115478 Moscow, Russia.
Research Centre for Medical Genetics · RURussian Academy of Sciences · RUUral State Medical University · RU

Funding

Ministry of Science and Higher Education of the Russian Federation Nos. 075-15-2021-1061 and RF 193021X0029
6 · The paper itself

Abstract

The

Indexed as

Facial ParalysisMuscular Dystrophy, FacioscapulohumeralAdultDendritic SpinesFemaleGenes, HomeoboxHumansPhenotypefacial paresisfacio-scapulo-humeral dystrophyHOXB1Moebius syndromeneuromuscular disorder

Identifiers

PMID38203298
PMCPMC10779017
OpenAlexW4390052925

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.