Evidence map›Paper›PMID 35591945›Full record

ArticleFrontiers in molecular biosciences2022

Results from Genetic Studies in Patients Affected with Craniosynostosis: Clinical and Molecular Aspects.

Ewelina Bukowska-Olech, Anna Sowińska-Seidler, Dawid Larysz, Paweł Gawliński, Grzegorz Koczyk, Delfina Popiel, Lidia Gurba-Bryśkiewicz, Anna Materna-Kiryluk, Zuzanna Adamek, Aleksandra Szczepankiewicz and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2022. 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
1.3field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Expanding the phenotypic spectrum associated with ZIC1 variants: A neurodevelopmental disorder with and without craniosynostosis.Genetics in medicine : official journal of the American College of Medical Genetics · 2026
    Article
  2. Review
  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

14 authors at 4 institutions in 1 country.

Ewelina Bukowska-OlechDepartment of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
Anna Sowińska-SeidlerDepartment of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
Dawid LaryszDepartment of Head and Neck Surgery for Children and Adolescents, University of Warmia and Mazury in Olsztyn, Olsztyn, Poland.
Paweł GawlińskiDepartment of Medical Genetics, Institute of Mother and Child, Warsaw, Poland.
Grzegorz KoczykCenters for Medical Genetics GENESIS, Poznan, Poland.
Delfina PopielCenters for Medical Genetics GENESIS, Poznan, Poland.
Lidia Gurba-BryśkiewiczCelon Pharma S.A., Medicinal Chemistry Department, Lomianki, Poland.
Anna Materna-KirylukDepartment of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
Zuzanna AdamekPoznan University of Medical Sciences, Poznan, Poland.
Aleksandra SzczepankiewiczMolecular and Cell Biology Unit, Department of Paediatric Pulmonology, Allergy and Clinical Immunology, Poznan University of Medical Sciences, Poznan, Poland.
Paweł DominiakPoznan University of Medical Sciences, Poznan, Poland.
Filip GlistaPoznan University of Medical Sciences, Poznan, Poland.
Karolina MatuszewskaDepartment of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
Aleksander JamsheerDepartment of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
Poznan University of Medical Sciences · PLCelon Pharma (Poland) · PLInstitute of Plant Genetics, Polish Academy of Sciences · PLUniversity of Warmia and Mazury in Olsztyn · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

calvarial sutureschromosomal microarray analysiscohort screeningcraniosynostosisnext-generation sequencing

Identifiers

PMID35591945
PMCPMC9112228
OpenAlexW4224989797

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.