Evidence map›Paper›PMID 35054877›Full record

ArticleInternational journal of molecular sciences2022

De Novo

Mateusz Dawidziuk, Anna Kutkowska-Kazmierczak, Ewelina Bukowska-Olech, Marta Jurek, Ewa Kalka, Dorothy Lys Guilbride, Mariusz Ireneusz Furmanek, Monika Bekiesinska-Figatowska, Jerzy Bal, Pawel Gawlinski

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

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 40% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. 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

10 authors at 3 institutions in 2 countries.

Mateusz DawidziukDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0001-5102-8722
Anna Kutkowska-KazmierczakDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0001-5295-7363
Ewelina Bukowska-OlechDepartment of Medical Genetics, Poznan University of Medical Sciences, 60-806 Poznan, Poland.ORCID 0000-0003-0509-1696
Marta JurekDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
Ewa KalkaUnit of Anthropology, Institute of Mother and Child, 01-211 Warsaw, Poland.
Dorothy Lys GuilbrideIndependent Researcher, Manhiça MPT 1122, Mozambique.
Mariusz Ireneusz FurmanekDepartment of Radiology and Diagnostic Imaging, Centre for Postgraduate Medical Education, 02-507 Warsaw, Poland.
Monika Bekiesinska-FigatowskaDepartment of Diagnostic Imaging, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0003-1787-3425
Jerzy BalDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
Pawel GawlinskiDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0002-3672-5834
Manhiça Health Research Centre · MZPostgraduate School of Molecular Medicine · PLPoznan University of Medical Sciences · PL

Funding

National Science Centre, Poland 2015/19/B/NZ2/01824
6 · The paper itself

Abstract

Actin molecules are fundamental for embryonic structural and functional differentiation; γ-actin is specifically required for the maintenance and function of cytoskeletal structures in the ear, resulting in hearing. Baraitser-Winter Syndrome (B-WS, OMIM #243310, #614583) is a rare, multiple-anomaly genetic disorder caused by mutations in either cytoplasmically expressed actin gene,

Indexed as

ActinsAdultAlgorithmsBase SequenceDeafnessFaciesGenotypeGrowth DisordersHumansHydrocephalusMagnetic Resonance ImagingMutationObesityPedigreePhenotypeX-Linked Intellectual DisabilityACTG1 protein, humanActinsACTG1 geneactinopathyBaraitser–Winter syndromepartial deafness

Identifiers

PMID35054877
PMCPMC8776155
OpenAlexW4205735168

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.