Evidence map›Paper›PMID 34135841›Full record

ArticleFrontiers in neurology2021

Genetic Determinants Highlight the Existence of Shared Etiopathogenetic Mechanisms Characterizing Age-Related Macular Degeneration and Neurodegenerative Disorders.

Claudia Strafella, Valerio Caputo, Andrea Termine, Carlo Fabrizio, Paola Ruffo, Saverio Potenza, Andrea Cusumano, Federico Ricci, Carlo Caltagirone, Emiliano Giardina and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

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  10. Bioinformatic Tools for the Analysis and Prediction of ncRNA Interactions.International journal of molecular sciences · 2021
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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

11 authors at 3 institutions in 2 countries.

Claudia StrafellaGenomic Medicine Laboratory UILDM, IRCCS Santa Lucia Foundation, Rome, Italy.
Valerio CaputoGenomic Medicine Laboratory UILDM, IRCCS Santa Lucia Foundation, Rome, Italy.
Andrea TermineGenomic Medicine Laboratory UILDM, IRCCS Santa Lucia Foundation, Rome, Italy.
Carlo FabrizioGenomic Medicine Laboratory UILDM, IRCCS Santa Lucia Foundation, Rome, Italy.
Paola RuffoGenomic Medicine Laboratory UILDM, IRCCS Santa Lucia Foundation, Rome, Italy.
Saverio PotenzaDepartment of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.
Andrea CusumanoUOSD of Ophthalmology PTV Foundation "Policlinico Tor Vergata", Rome, Italy.
Federico RicciUNIT Retinal Diseases PTV Foundation "Policlinico Tor Vergata", Rome, Italy.
Carlo CaltagironeDepartment of Clinical and Behavioral Neurology, IRCCS Fondazione Santa Lucia, Rome, Italy.
Emiliano GiardinaGenomic Medicine Laboratory UILDM, IRCCS Santa Lucia Foundation, Rome, Italy.
Raffaella CascellaMedical Genetics Laboratory, Department of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.
Fondazione Santa Lucia · ITUniversity of Rome Tor Vergata · ITPoliclinico Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related macular degeneration (AMD) showed several processes and risk factors in common with neurodegenerative disorders (NDDs). The present work explored the existence of genetic determinants associated with AMD, which may provide insightful clues concerning its relationship with NDDs and their possible application into the clinical practice. In this study, 400 AMD patients were subjected to the genotyping analysis of 120 genetic variants by OpenArray technology. As the reference group, 503 samples representative of the European general population were utilized. Statistical analysis revealed the association of 23 single-nucleotide polymorphisms (SNPs) with AMD risk. The analysis of epistatic effects revealed that

Indexed as

age-related macular degenerationetiopathogenesisgenetic networkmiRNAsneurodegenerative disorderssusceptibility

Identifiers

PMID34135841
PMCPMC8200556
OpenAlexW3167874033

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.