Giuseppe Novelli
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Explore the profile of Giuseppe Novelli including associated specialties, affiliations and a list of published articles.
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415
Citations
8907
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Recent Articles
1.
Belardi R, Pacifici F, Baldetti M, Velocci S, Minieri M, Pieri M, et al.
Int J Mol Sci
. 2025 Mar;
26(5).
PMID: 40076585
Kidney transplantation is currently the treatment of choice for patients with end-stage kidney diseases. Although significant advancements in kidney transplantation have been achieved over the past decades, the host's immune...
2.
De Benedittis G, Latini A, Morgante C, Bonini C, Cela E, Kroegler B, et al.
Autoimmunity
. 2025 Mar;
58(1):2473741.
PMID: 40035723
Interstitial lung disease (ILD) is a common extra-articular manifestation of rheumatoid arthritis (RA). The inflammatory response in lung disease is characterized by severe oxidative stress, which enhances cellular senescence. Telomeric...
3.
Infante M, Silvestri F, Padilla N, Pacifici F, Pastore D, Pinheiro M, et al.
J Clin Med
. 2025 Feb;
14(4).
PMID: 40004833
Type 1 diabetes mellitus (T1D) is a chronic autoimmune disease caused by the immune-mediated destruction of insulin-producing pancreatic beta cells, resulting in the lifelong need for exogenous insulin. Over the...
4.
Latini A, De Benedittis G, Morgante C, Gasperini B, DIppolito I, Lauro D, et al.
Acta Diabetol
. 2025 Feb;
PMID: 39976627
Aims: We aimed to analyse Sirtuin 1 (SIRT1) and Vitamin D receptor (VDR) expression levels in the peripheral blood of patients with type 2 diabetes (T2D), characterized for the presence...
5.
Morgante C, Latini A, De Benedittis G, Novelli G, Spallone V, Ciccacci C, et al.
Gene
. 2025 Feb;
945:149289.
PMID: 39921046
The aim of this study was to investigate possible associations between the KCNJ11 rs2285676 and T2D susceptibility and/or clinical manifestations. The KCNJ11 rs2285676 genotypic/allelic distribution and the case/control association analysis...
6.
Malaspina P, Jodice C, Ciminelli B, Biancolella M, Colona V, Latini A, et al.
Hum Genomics
. 2025 Jan;
19(1):7.
PMID: 39885568
Background: The Immunoglobulin Heavy Chain (IGH) genomic region is responsible for the production of circulating antibodies and warrants careful investigation for its association with COVID-19 characteristics. Multiple allelic variants within...
7.
Lomuscio S, Cocciadiferro D, Petrizzelli F, Liorni N, Mazza T, Allegorico A, et al.
Genes (Basel)
. 2025 Jan;
15(12.
PMID: 39766840
: The gene encodes for the catalytic α subunit of Cytoplasmic phenylalanine-tRNA synthetase (FARS1), an essential enzyme for protein biosynthesis in transferring its amino acid component to tRNAs. Biallelic pathogenic...
8.
Ranucci G, Page C, Marchionni E, Minotti C, Silvestrini G, Gastaldi S, et al.
Ann Hematol
. 2024 Dec;
103(12):5999-6002.
PMID: 39672944
Recently, germline variants have also been found as contributors of disease etiology in myeloproliferative neoplasms (MPN). The consideration of such inherited traits is crucial for clinical management of patients, particularly...
9.
Stellacci E, Martinelli S, Carbone P, Demuru E, Genuardi M, Ghiorzo P, et al.
Front Med (Lausanne)
. 2024 Dec;
11:1422163.
PMID: 39640978
Background: Genetic and genomic literacy of health professionals is of utmost importance to realize the full potential of personalized medicine. As part of a European Union project, we piloted an...
10.
Graziani L, Carriero M, Ferradini V, Conte C, Bengala M, Sangiuolo F, et al.
Clin Genet
. 2024 Nov;
107(3):369-370.
PMID: 39614649
WDFY3 (MIM#617485) defects may manifest neurodevelopmental disorders (NDDs) and opposite effects on brain size based on allelic effect. This case highlights a heterozygous WDFY3 nonsense variant linked to mild-to-moderate NDDs,...