Jessica Rosati
Overview
Explore the profile of Jessica Rosati including associated specialties, affiliations and a list of published articles.
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60
Citations
689
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Recent Articles
1.
Sollazzo R, Li Puma D, Aceto G, Paciello F, Colussi C, Vita M, et al.
Alzheimers Res Ther
. 2024 Dec;
16(1):267.
PMID: 39702316
Background: Alzheimer's Disease (AD) is a neurodegenerative disorder characterized by the accumulation of pathological proteins and synaptic dysfunction. This study aims to investigate the molecular and functional differences between human...
2.
Pietrafesa D, Casamassa A, Benassi B, Santoro M, Marano M, Consales C, et al.
Int J Mol Sci
. 2024 Nov;
25(21).
PMID: 39518995
Heterozygous mutations or genetic variants in the gene, which encodes for the β-glucocerebrosidase (GCase), a lysosomal hydrolase enzyme, may increase the risk of Parkinson's disease (PD) onset. The heterozygous E326K...
3.
Karuppasamy M, Tetreault M, Rosati J
Front Genet
. 2024 Sep;
15:1481705.
PMID: 39323868
No abstract available.
4.
Giovenale A, Turco E, Mazzoni M, Ferrone I, Torres B, Bernardini L, et al.
Stem Cell Res
. 2024 Sep;
81():103544.
PMID: 39260069
Smith-Magenis syndrome (SMS) is a complex neurodevelopmental disorder with a birth incidence of 1:25,000. SMS is caused by haploinsufficiency of the retinoic acid-induced retinoic acid1 (RAI1) gene, determined by an...
5.
Morandell J, Monziani A, Lazioli M, Donzel D, Doring J, Oss Pegorar C, et al.
Mol Ther Nucleic Acids
. 2024 Jul;
35(3):102234.
PMID: 38974999
Circular RNA (circRNA) molecules have critical functions during brain development and in brain-related disorders. Here, we identified and validated a circRNA, , stemming from the Huntington's disease (HD) gene locus...
6.
Casamassa A, Rotundo G, Ceresoni C, Turco E, Torrente I, Candido O, et al.
Stem Cell Res
. 2024 Jun;
78:103468.
PMID: 38852424
Hypomyelinating leukodystrophies (HLD) are a group of heterogeneous genetic disorders characterized by a deficit in myelin deposition during brain development. Specifically, 4H-Leukodystrophy is a recessive disease due to biallelic mutations...
7.
Manni G, Gargaro M, Ricciuti D, Fontana S, Padiglioni E, Cipolloni M, et al.
J Extracell Vesicles
. 2024 Jun;
13(6):e12446.
PMID: 38844736
Dendritic cells (DCs) are essential orchestrators of immune responses and represent potential targets for immunomodulation in autoimmune diseases. Human amniotic fluid secretome is abundant in immunoregulatory factors, with extracellular vesicles...
8.
Cipolla C, Sessa L, Rotunno G, Sodero G, Proli F, Veredice C, et al.
Children (Basel)
. 2023 Sep;
10(9).
PMID: 37761412
: Smith-Magenis syndrome (SMS) is caused by either interstitial deletions in the 17p11.2 region or pathogenic variants in the gene and is marked by a distinct set of physical, developmental,...
9.
Marano M, Rosati J, Magliozzi A, Casamassa A, Rappa A, Sergi G, et al.
Neurobiol Sleep Circadian Rhythms
. 2023 Apr;
14:100094.
PMID: 37025301
Circadian rhythm impairment may play a role in Parkinson's disease (PD) pathophysiology. Recent literature associated circadian rhythm features to the risk of developing Parkinson and to its progression through stages....
10.
Corrigendum: Deepening the understanding of CNVs on chromosome 15q11-13 by using hiPSCs: An overview
Giovenale A, Ruotolo G, Soriano A, Turco E, Rotundo G, Casamassa A, et al.
Front Cell Dev Biol
. 2023 Feb;
11:1141334.
PMID: 36819100
[This corrects the article DOI: 10.3389/fcell.2022.1107881.].