Elisabetta Trabetti
Overview
Explore the profile of Elisabetta Trabetti including associated specialties, affiliations and a list of published articles.
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64
Citations
2911
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Recent Articles
1.
Veschetti L, Patuzzo C, Treccani M, Moron Dalla Tor L, Deiana M, Cheri S, et al.
Scand J Med Sci Sports
. 2025 Jan;
35(1):e70018.
PMID: 39817606
Previous studies in sports science suggested that regular exercise has a positive impact on human health. However, the effects of endurance sports and their underlying mechanisms are still not completely...
2.
De Tomi E, Orlandi E, Belpinati F, Patuzzo C, Trabetti E, Gomez-Lira M, et al.
Genes (Basel)
. 2025 Jan;
15(12.
PMID: 39766913
Background/objectives: microRNAs (miRNAs) and circular RNA (circRNAs) show a close interconnection in the control of fundamental functions, such as cell proliferation and tumor development. A full understanding of this complex...
3.
Orlandi E, Ceccuzzi L, Belpinati F, Rodolfo M, Malerba G, Trabetti E, et al.
Melanoma Res
. 2024 Jun;
34(4):296-306.
PMID: 38934060
Gender disparity in melanoma is a complex issue where sex hormones could be engaged. Differences in genetic variations are important in understanding the mechanisms of sex disparity in melanoma. Post-transcriptional...
4.
Bombieri C, Corsi A, Trabetti E, Ruggiero A, Marchetto G, Vattemi G, et al.
Int J Mol Sci
. 2024 Jan;
25(2).
PMID: 38256087
Organoids are self-organized, three-dimensional structures derived from stem cells that can mimic the structure and physiology of human organs. Patient-specific induced pluripotent stem cells (iPSCs) and 3D organoid model systems...
5.
Fu J, Satterstrom F, Peng M, Brand H, Collins R, Dong S, et al.
Nat Genet
. 2022 Aug;
54(9):1320-1331.
PMID: 35982160
Some individuals with autism spectrum disorder (ASD) carry functional mutations rarely observed in the general population. We explored the genes disrupted by these variants from joint analysis of protein-truncating variants...
6.
Surendran P, Feofanova E, Lahrouchi N, Ntalla I, Karthikeyan S, Cook J, et al.
Nat Genet
. 2021 Mar;
53(5):762.
PMID: 33727701
No abstract available.
7.
Surendran P, Feofanova E, Lahrouchi N, Ntalla I, Karthikeyan S, Cook J, et al.
Nat Genet
. 2020 Nov;
52(12):1314-1332.
PMID: 33230300
Genetic studies of blood pressure (BP) to date have mainly analyzed common variants (minor allele frequency > 0.05). In a meta-analysis of up to ~1.3 million participants, we discovered 106...
8.
Wang T, Hoekzema K, Vecchio D, Wu H, Sulovari A, Coe B, et al.
Nat Commun
. 2020 Oct;
11(1):5398.
PMID: 33087701
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
9.
Wang T, Hoekzema K, Vecchio D, Wu H, Sulovari A, Coe B, et al.
Nat Commun
. 2020 Oct;
11(1):4932.
PMID: 33004838
Most genes associated with neurodevelopmental disorders (NDDs) were identified with an excess of de novo mutations (DNMs) but the significance in case-control mutation burden analysis is unestablished. Here, we sequence...
10.
Filosi M, Kam-Thong T, Essioux L, Muglia P, Trabetti E, Spooren W, et al.
Transl Psychiatry
. 2020 Apr;
10(1):106.
PMID: 32291385
Notwithstanding several research efforts in the past years, robust and replicable molecular signatures for autism spectrum disorders from peripheral blood remain elusive. The available literature on blood transcriptome in ASD...