Evidence map›Paper›PMID 39200165›Full record

ArticleBiomedicines2024

Testing Reported Associations of Gene Variants with Non-Syndromic Orofacial Clefts in the Polish Population.

Alicja Zawiślak, Krzysztof Woźniak, Gianluca Tartaglia, Beata Kawala, Satish Gupta, Anna Znamirowska-Bajowska, Katarzyna Grocholewicz, Jan Lubiński, Anna Jakubowska

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Biomedicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Association ofGenes · 2025
    Article
  2. 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

9 authors.

Alicja ZawiślakDepartment of Maxillofacial Orthopaedics and Orthodontics, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0003-2036-2853
Krzysztof WoźniakDepartment of Orthodontics, Pomeranian Medical University, 70-111 Szczecin, Poland.
Gianluca TartagliaDepartment of Biomedical, Surgical and Dental Sciences, University of Milan, 20100 Milan, Italy.
Beata KawalaDepartment of Dentofacial Orthopaedics and Orthodontics, Wrocław Medical University, 50-425 Wroclaw, Poland.
Satish GuptaHereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland.ORCID 0009-0001-3466-5137
Anna Znamirowska-BajowskaDepartment of Dentofacial Orthopaedics and Orthodontics, Wrocław Medical University, 50-425 Wroclaw, Poland.
Katarzyna GrocholewiczDepartment of Interdisciplinary Dentistry, Pomeranian Medical University, 70-111 Szczecin, Poland.ORCID 0000-0002-1468-4664
Jan LubińskiHereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland.ORCID 0000-0003-2931-3003
Anna JakubowskaHereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland.

Funding

National Science Center 2169/B/P01/ 2011/40
6 · The paper itself

Abstract

Orofacial clefts (OFCs) are the second most common birth defect worldwide. The etiology of OFCs involves complex interactions between genetics and environment. Advances in genomic technologies have identified gene variants associated with OFCs. This study aimed to investigate whether selected SNPs in the

Indexed as

birth defectcleft lipcleft palategenetic variationMAFBMTHFRMYH9single nucleotide polymorphismSUMO1

Identifiers

PMID39200165
PMCPMC11351639

What OpenQuestion holds

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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.