Giuseppe Novelli

38.1k total citations
636 papers, 15.5k citations indexed

About

Giuseppe Novelli is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Giuseppe Novelli has authored 636 papers receiving a total of 15.5k indexed citations (citations by other indexed papers that have themselves been cited), including 309 papers in Molecular Biology, 118 papers in Genetics and 83 papers in Cellular and Molecular Neuroscience. Recurrent topics in Giuseppe Novelli's work include Genetic Neurodegenerative Diseases (73 papers), RNA modifications and cancer (45 papers) and Mitochondrial Function and Pathology (41 papers). Giuseppe Novelli is often cited by papers focused on Genetic Neurodegenerative Diseases (73 papers), RNA modifications and cancer (45 papers) and Mitochondrial Function and Pathology (41 papers). Giuseppe Novelli collaborates with scholars based in Italy, United States and United Kingdom. Giuseppe Novelli's co-authors include Bruno Dallapiccola, Federica Sangiuolo, Paola Borgiani, Maria Rosaria D’Apice, Massimo Gennarelli, Cinzia Ciccacci, Emiliano Giardina, Francesca Amati, Annalisa Botta and Francesca Capon and has published in prestigious journals such as New England Journal of Medicine, Circulation and Journal of Clinical Investigation.

In The Last Decade

Giuseppe Novelli

617 papers receiving 15.2k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Giuseppe Novelli 8.1k 2.2k 2.1k 1.6k 1.5k 636 15.5k
Akiyoshi Fukamizu 10.8k 1.3× 1.8k 0.8× 1.6k 0.8× 1.4k 0.9× 2.4k 1.6× 365 20.9k
Mark Leppert 8.0k 1.0× 4.3k 2.0× 1.8k 0.9× 2.0k 1.3× 2.3k 1.5× 164 20.9k
Thomas J. Hudson 10.0k 1.2× 5.8k 2.6× 2.2k 1.1× 1.1k 0.7× 2.3k 1.5× 227 20.1k
Sung Ho Ryu 13.2k 1.6× 1.3k 0.6× 2.3k 1.1× 1.8k 1.1× 1.5k 1.0× 405 19.6k
Doriano Fabbro 12.4k 1.5× 799 0.4× 1.7k 0.8× 1.1k 0.7× 831 0.5× 223 20.3k
Walter Malorni 6.4k 0.8× 915 0.4× 3.4k 1.7× 727 0.5× 897 0.6× 370 14.9k
Claude Libert 6.8k 0.8× 1.9k 0.9× 5.0k 2.4× 672 0.4× 1.0k 0.7× 266 17.8k
Morley D. Hollenberg 6.9k 0.9× 1.1k 0.5× 3.3k 1.6× 2.1k 1.3× 2.0k 1.3× 425 20.8k
Yi Li 9.7k 1.2× 2.5k 1.2× 3.5k 1.7× 507 0.3× 1.7k 1.1× 695 19.1k
William A. Gahl 6.5k 0.8× 2.7k 1.2× 1.9k 0.9× 682 0.4× 805 0.5× 487 18.3k

Countries citing papers authored by Giuseppe Novelli

Since Specialization
Citations

This map shows the geographic impact of Giuseppe Novelli's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Giuseppe Novelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Giuseppe Novelli more than expected).

Fields of papers citing papers by Giuseppe Novelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Giuseppe Novelli. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Giuseppe Novelli. The network helps show where Giuseppe Novelli may publish in the future.

Co-authorship network of co-authors of Giuseppe Novelli

This figure shows the co-authorship network connecting the top 25 collaborators of Giuseppe Novelli. A scholar is included among the top collaborators of Giuseppe Novelli based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Giuseppe Novelli. Giuseppe Novelli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Caputo, Valerio, Clara Balsano, Leonardo Calò, et al.. (2025). The Diagnostic Value of Copy Number Variants in Genetic Cardiomyopathies and Channelopathies. Journal of Cardiovascular Development and Disease. 12(7). 258–258.
2.
Cappa, Marco, Gabriella Pozzobon, Massimiliano Orso, et al.. (2024). The economic burden of pediatric growth hormone deficiency in Italy: a cost of illness study. Journal of Endocrinological Investigation. 47(7). 1743–1750.
3.
Latini, Andrea, Carlo Perricone, Fulvia Ceccarelli, et al.. (2024). The dysregulation of mitochondrial homeostasis–related genes could be involved in the decrease of mtDNA copy number in systemic lupus erythematosus patients. Immunologic Research. 72(6). 1384–1392. 4 indexed citations
4.
Cocciadiferro, Dario, Tommaso Mazza, Nicola Ullmann, et al.. (2024). Two Novel Biallelic Variants in the FARSA Gene: The First Italian Case and a Literature Review. Genes. 15(12). 1573–1573.
5.
Latini, Andrea, et al.. (2024). Low Expression Levels of miRNA-155 and miRNA-499a are Associated with Obesity in Type 2 Diabetes. Epigenomics. 16(2). 85–91. 3 indexed citations
6.
Centofanti, Federica, Tonino Alonzi, Andrea Latini, et al.. (2022). Indole-3-carbinol in vitro antiviral activity against SARS-Cov-2 virus and in vivo toxicity. Cell Death Discovery. 8(1). 491–491. 13 indexed citations
7.
Belmonte, Beatrice, et al.. (2021). Genetic and Epigenetic Factors of Takotsubo Syndrome: a Systematic Review. Preprints.org. 7 indexed citations
8.
Ciccacci, Cinzia, et al.. (2021). Emerging Role of microRNAs and Long Non-Coding RNAs in Sjögren’s Syndrome. Genes. 12(6). 903–903. 17 indexed citations
9.
Mbarek, Hamdi, Massimiliano Cocca, Yasser Al‐Sarraj, et al.. (2021). Poking COVID-19: Insights on Genomic Constraints among Immune-Related Genes between Qatari and Italian Populations. Genes. 12(11). 1842–1842.
10.
Murdocca, Michela, Francesco Torino, Sabina Pucci, et al.. (2021). Urine LOX-1 and Volatilome as Promising Tools towards the Early Detection of Renal Cancer. Cancers. 13(16). 4213–4213. 23 indexed citations
11.
Caputo, Valerio, Claudia Strafella, Andrea Termine, et al.. (2020). RNAseq-Based Prioritization Revealed COL6A5, COL8A1, COL10A1 and MIR146A as Common and Differential Susceptibility Biomarkers for Psoriasis and Psoriatic Arthritis: Confirmation from Genotyping Analysis of 1417 Italian Subjects. International Journal of Molecular Sciences. 21(8). 2740–2740. 16 indexed citations
12.
Salehi, Leila, et al.. (2020). An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene. SHILAP Revista de lepidopterología. 8(8). 1445–1451. 2 indexed citations
13.
Salehi, Leila, et al.. (2020). Neurovascular manifestations in connective tissue diseases: The case of Marfan Syndrome. Mechanisms of Ageing and Development. 191. 111346–111346. 5 indexed citations
14.
Spitalieri, Paola, Annalisa Botta, Michela Murdocca, et al.. (2015). Generation of Human Induced Pluripotent Stem Cells from Extraembryonic Tissues of Fetuses Affected by Monogenic Diseases. Cellular Reprogramming. 17(4). 275–287. 18 indexed citations
15.
Ciafrè, Silvia Anna, Michela Murdocca, Andrea Masotti, et al.. (2015). A Perturbed MicroRNA Expression Pattern Characterizes Embryonic Neural Stem Cells Derived from a Severe Mouse Model of Spinal Muscular Atrophy (SMA). International Journal of Molecular Sciences. 16(8). 18312–18327. 21 indexed citations
16.
Spitalieri, Paola, Giancarlo Cortese, Adalgisa Pietropolli, et al.. (2009). Identification of Multipotent Cytotrophoblast Cells from Human First Trimester Chorionic Villi. Cloning and Stem Cells. 11(4). 535–556. 22 indexed citations
17.
Conte, Chiara, Stefano Gambardella, Fabrizio Rinaldi, et al.. (2008). Screening of EDA1 Gene in X-Linked Anhidrotic Ectodermal Dysplasia Using DHPLC: Identification of 14 Novel Mutations in Italian Patients. Genetic Testing. 12(3). 437–442. 11 indexed citations
18.
Salehi, Leila, E. Bonifazi, Enrico Di Stasio, et al.. (2007). Risk Prediction for Clinical Phenotype in Myotonic Dystrophy Type 1: Data from 2,650 Patients. Genetic Testing. 11(1). 84–90. 46 indexed citations
19.
Semprini, Sabrina, Alessandra Tacconelli, Francesca Capon, et al.. (2001). A Single Strand Conformation Polymorphism-Based Carrier Test for Spinal Muscular Atrophy. Genetic Testing. 5(1). 33–37. 11 indexed citations
20.
Novelli, Giuseppe, et al.. (1993). Identification of Three Novel Cystic Fibrosis Mutations in a Sample of Italian Cystic Fibrosis Patients. Human Heredity. 43(5). 295–300. 16 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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