Evidence map›Paper›PMID 32026430›Full record

ReviewAging clinical and experimental research2021

The contribution of CNVs to the most common aging-related neurodegenerative diseases.

Giulia Gentile, Valentina La Cognata, Sebastiano Cavallaro

Abstract readReview
PubMed Publisher
In one paragraph

Review in Aging clinical and experimental research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  6. Genetic Study of Early Onset Parkinson's Disease in Cyprus.International journal of molecular sciences · 2022
    Article
  7. Article
  8. Review
  9. Review
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  12. Copy Number Variation in Parkinson's Disease: An Update from Sub-Saharan Africa.Movement disorders : official journal of the Movement Disorder Society · 2021
    Article
  13. Review
  14. Article
  15. 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

3 authors at 1 institution in 1 country.

Giulia Gentile *Institute for Biomedical Research and Innovation, National Research Council of Italy, Via Paolo Gaifami 18, 95125, Catania, Italy.ORCID http://orcid.org/0000-0003-0180-3481
Valentina La Cognata *Institute for Biomedical Research and Innovation, National Research Council of Italy, Via Paolo Gaifami 18, 95125, Catania, Italy.ORCID http://orcid.org/0000-0003-4066-0655
Sebastiano CavallaroInstitute for Biomedical Research and Innovation, National Research Council of Italy, Via Paolo Gaifami 18, 95125, Catania, Italy. sebastiano.cavallaro@cnr.it.ORCID https://orcid.org/0000-0001-7590-1792
Institute for Biomedical Research and Innovation · IT

Funding

Consiglio Nazionale delle Ricerche DSB.AD009.001.018European Social Fund CIP 2014.IT.05.SFOP.014/3/10.4/9.2.10/0008
6 · The paper itself

Abstract

Alzheimer and Parkinson's diseases are neurodegenerative aging-related pathological conditions, mainly caused by the interplay of genetic and non-genetic factors and whose incidence rate is going to drastically increase given the growing life expectancy. To address these complex multifactorial traits, a systems biology strategy is needed to highlight genotype-phenotype correlations as well as overlapping gene signatures. Copy number variants (CNVs) are structural chromosomal imbalances that can have pathogenic nature causing or contributing to the disease onset or progression. Moreover, neurons affected by CNVs have been found to decline in number depending on age in healthy controls and may be selectively vulnerable to aging-related cell-death. In this review, we aim to update the reader on the role of these variations in the pathogenesis of Alzheimer and Parkinson diseases. To widen the comprehension of pathogenic mechanisms underlying them, we discuss variations detected from blood or brain specimens, as well as overlapped signatures between the two pathologies.

Indexed as

Neurodegenerative DiseasesParkinson DiseaseAgingBrainDNA Copy Number VariationsHumansAgingAlzheimer’s diseaseCopy number variationGermlineParkinson’s diseaseSomatic mosaicism

Identifiers

PMID32026430
OpenAlexW3005044033

What OpenQuestion holds

Textmetadata
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.