Evidence map›Paper›PMID 33261141›Full record

ReviewInternational journal of molecular sciences2020

Impact of Genetic Variations and Epigenetic Mechanisms on the Risk of Obesity.

Martina Chiurazzi, Mauro Cozzolino, Roberta Clara Orsini, Martina Di Maro, Matteo Nicola Dario Di Minno, Antonio Colantuoni

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 32 citations in OpenAlex.

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  11. Genes · 2022
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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

6 authors at 2 institutions in 3 countries.

Martina ChiurazziDepartment of Clinical Medicine and Surgery, University of Naples "Federico II", 80131 Naples, Italy.
Mauro CozzolinoDepartment of Obstetrics, Gynecology and Reproductive Sciences, Yale School of Medicine, New Haven, CT 06511, USA.
Roberta Clara OrsiniDepartment of Clinical Medicine and Surgery, University of Naples "Federico II", 80131 Naples, Italy.
Martina Di MaroDepartment of Clinical Medicine and Surgery, University of Naples "Federico II", 80131 Naples, Italy.
Matteo Nicola Dario Di MinnoDepartment of Translational Medical Sciences, University of Naples "Federico II", 80131 Naples, Italy.ORCID 0000-0001-8059-3819
Antonio ColantuoniDepartment of Clinical Medicine and Surgery, University of Naples "Federico II", 80131 Naples, Italy.
University of Naples Federico II · ITUniversidad Rey Juan Carlos · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rare genetic obesity disorders are characterized by mutations of genes strongly involved in the central or peripheral regulation of energy balance. These mutations are effective in causing the early onset of severe obesity and insatiable hunger (hyperphagia), suggesting that the genetic component can contribute to 40-70% of obesity. However, genes' roles in the processes leading to obesity are still unclear. This review is aimed to summarize the current knowledge of the genetic causes of obesity, especially monogenic obesity, describing the role of epigenetic mechanisms in obesity and metabolic diseases. A comprehensive understanding of the underlying genetic and epigenetic mechanisms, with the metabolic processes they control, will permit adequate management and prevention of obesity.

Indexed as

Epigenesis, GeneticGenetic Predisposition to DiseaseGenetic VariationBody WeightHumansObesityRisk Factorsepigeneticsmonogenic obesityobesitypolygenic obesitysyndromic obesity

Identifiers

PMID33261141
PMCPMC7729759
OpenAlexW3108911025

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.