Evidence map›Paper›PMID 41304128›Full record

ArticleMicroorganisms2025

Evaluation of the Oral Microbiome in Patients with Alström and Bardet-Biedl Syndromes and Their Heterozygous Family Members.

Ewa Zmysłowska-Polakowska, Tomasz Płoszaj, Sebastian Skoczylas, Julia Grzybowska-Adamowicz, Aleksandra Palatyńska-Ulatowska, Monika Łukomska-Szymańska, Agnieszka Zmysłowska

Abstract read
In one paragraph

Article in Microorganisms, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

7 authors.

Ewa Zmysłowska-PolakowskaDepartment of Endodontics, Medical University of Lodz, 92-213 Lodz, Poland.ORCID 0000-0001-8959-5757
Tomasz PłoszajDepartment of Clinical Genetics, Medical University of Lodz, 92-213 Lodz, Poland.
Sebastian SkoczylasDepartment of Clinical Genetics, Medical University of Lodz, 92-213 Lodz, Poland.ORCID 0000-0003-2760-2397
Julia Grzybowska-AdamowiczDepartment of Clinical Genetics, Medical University of Lodz, 92-213 Lodz, Poland.ORCID 0009-0009-8779-3907
Aleksandra Palatyńska-UlatowskaDepartment of Endodontics, Medical University of Lodz, 92-213 Lodz, Poland.ORCID 0000-0003-0171-8594
Monika Łukomska-SzymańskaDepartment of General Dentistry, Medical University of Lodz, 92-213 Lodz, Poland.ORCID 0000-0002-6110-4298
Agnieszka ZmysłowskaDepartment of Clinical Genetics, Medical University of Lodz, 92-213 Lodz, Poland.ORCID 0000-0001-8781-4469

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alström (ALMS) and Bardet-Biedl syndromes (BBS) are rare ciliopathies characterized by obesity and hyperglycemia that lead to type 2 diabetes, but also other disorders, including neurodegeneration. However, isolated clinical manifestations can be observed in carriers of heterozygous mutations in the

Indexed as

Alström syndromeBardet-Biedl syndromegene sequencingheterozygous carriersoral microbiome

Identifiers

PMID41304128
PMCPMC12654565

What OpenQuestion holds

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LicenceCC BY
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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.