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

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	The Diagnostic Value of Copy Number Variants in Genetic Cardiomyopathies and Channelopathies 2025 ·Journal of Cardiovascular Development and Disease ·Valerio Caputo, (unknown), (unknown), (unknown), Clara Balsano, (unknown), Leonardo Calò, Ruggiero Mango, Giuseppe Novelli, Federica Sangiuolo	0
2	The economic burden of pediatric growth hormone deficiency in Italy: a cost of illness study 2024 ·Journal of Endocrinological Investigation ·Marco Cappa, Gabriella Pozzobon, Massimiliano Orso, Mohamad Maghnie, Giuseppa Patti, Federico Spandonaro, (unknown), Giuseppe Novelli, (unknown), Mariacarolina Salerno, (unknown)	0
3	The dysregulation of mitochondrial homeostasis–related genes could be involved in the decrease of mtDNA copy number in systemic lupus erythematosus patients 2024 ·Immunologic Research ·(unknown), Andrea Latini, (unknown), Carlo Perricone, Fulvia Ceccarelli, Giuseppe Novelli, Lucia Novelli, Cinzia Ciccacci, Paola Borgiani	4
4	Two Novel Biallelic Variants in the FARSA Gene: The First Italian Case and a Literature Review 2024 ·Genes ·(unknown), Dario Cocciadiferro, (unknown), (unknown), Tommaso Mazza, (unknown), Nicola Ullmann, Giuseppe Novelli, Renato Cutrera, Antonio Novelli	0
5	Implementing the Risk Stratification and Clinical Management of Breast Cancer Families Using Polygenic Risk Score Evaluation: A Pilot Study 2024 ·Journal of Personalized Medicine ·(unknown), (unknown), (unknown), Chiara Conte, Leila Salehi, Miriam Lucia Carriero, (unknown), Vincenzo Cirigliano, (unknown), (unknown), Ilaria Portarena, Oreste Claudio Buonomo, Giuseppe Novelli, Michela Biancolella	1
6	In Cis Effect of DMPK Expanded Alleles in Myotonic Dystrophy Type 1 Patients Carrying Variant Repeats at 5′ and 3′ Ends of the CTG Array 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), Maria Rosaria D’Apice, Federica Centofanti, Roberto Massa, Giuseppe Novelli, Annalisa Botta	1
7	Indole-3-carbinol in vitro antiviral activity against SARS-Cov-2 virus and in vivo toxicity 2022 ·Cell Death Discovery ·Federica Centofanti, Tonino Alonzi, Andrea Latini, Paola Spitalieri, Michela Murdocca, Xiaohong Chen, (unknown), Qianwen Shang, Delia Goletti, Yufang Shi, Andrea Duranti, Carlo Tomino, Michela Biancolella, Federica Sangiuolo, Maria Rosaria Capobianchi, Suresh Kumar Jain, Giuseppe Novelli, Pier Paolo Pandolfi	13
8	Emerging Role of microRNAs and Long Non-Coding RNAs in Sjögren’s Syndrome 2021 ·Genes ·(unknown), Cinzia Ciccacci, Andrea Latini, Lucia Novelli, Giuseppe Novelli, Paola Borgiani	17
9	Peptide Platform as a Powerful Tool in the Fight against COVID-19 2021 ·Viruses ·Michela Murdocca, Gennaro Citro, Isabella Romeo, Antonio Lupia, Shane Miersch, (unknown), (unknown), Antonio Rossi, Sachdev S. Sidhu, Pier Paolo Pandolfi, Stefano Alcaro, Federica Sangiuolo, Giuseppe Novelli	14
10	Genetic and Epigenetic Factors of Takotsubo Syndrome: a Systematic Review 2021 ·Preprints.org ·(unknown), (unknown), Beatrice Belmonte, Ruggiero Mango, Giuseppe Novelli, Carmela Rita Balistreri, Federica Sangiuolo	7
11	Breast cancer in West Africa: molecular analysis of BRCA genes in early-onset breast cancer patients in Burkina Faso 2021 ·Human Genomics ·Michela Biancolella, (unknown), (unknown), Théodora Mahoukèdè Zohoncon, (unknown), (unknown), Andrea Latini, Chiara Conte, Tégwindé Rébeca Compaore, Charlemagne Ouédraogo, (unknown), Jacques Simporè, Giuseppe Novelli	10
12	Carrier frequency of CFTR variants in the non‐Caucasian populations by genome aggregation database (gnomAD)‐based analysis 2020 ·Annals of Human Genetics ·(unknown), L. Mannucci, Giuseppe Novelli, Federica Sangiuolo, Maria Rosaria D’Apice, Annalisa Botta	8
13	The differential response to anti IL-6 treatment in COVID-19: the genetic counterpart. 2020 ·Clinical and Experimental Rheumatology ·Carlo Perricone, Paola Conigliaro, Cinzia Ciccacci, Elisa Marcucci, Giacomo Cafaro, Elena Bartoloni, Roberto Perricone, Giuseppe Novelli, Paola Borgiani, Roberto Gerli	7
14	SMA Human iPSC-Derived Motor Neurons Show Perturbed Differentiation and Reduced miR-335-5p Expression 2016 ·International Journal of Molecular Sciences ·Michela Murdocca, Silvia Anna Ciafrè, Paola Spitalieri, (unknown), Massimo Sanchez, Giuseppe Novelli, Federica Sangiuolo	18
15	Generation of Human Induced Pluripotent Stem Cells from Extraembryonic Tissues of Fetuses Affected by Monogenic Diseases 2015 ·Cellular Reprogramming ·Paola Spitalieri, (unknown), Annalisa Botta, Michela Murdocca, Maria Rosaria D’Apice, Augusto Orlandi, Emiliano Giardina, Massimo Santoro, Francesco Brancati, Giuseppe Novelli, Federica Sangiuolo	18
16	Identification of Multipotent Cytotrophoblast Cells from Human First Trimester Chorionic Villi 2009 ·Cloning and Stem Cells ·Paola Spitalieri, Giancarlo Cortese, Adalgisa Pietropolli, Antonio Filareto, Susanna Dolci, Francesca Gioia Klinger, Emiliano Giardina, Silvia Di Cesare, Laura Bernardini, Davide Lauro, Maria Lucia Scaldaferri, Gennaro Citro, Giuseppe Novelli, Massimo De Felici, Federica Sangiuolo	22
17	Screening of EDA1 Gene in X-Linked Anhidrotic Ectodermal Dysplasia Using DHPLC: Identification of 14 Novel Mutations in Italian Patients 2008 ·Genetic Testing ·Chiara Conte, Stefano Gambardella, (unknown), Fabrizio Rinaldi, Daniele Di Marino, Mattia Falconi, Placido Bramanti, Alessandro Desideri, Giuseppe Novelli	11
18	Risk Prediction for Clinical Phenotype in Myotonic Dystrophy Type 1: Data from 2,650 Patients 2007 ·Genetic Testing ·Leila Salehi, E. Bonifazi, Enrico Di Stasio, Massimo Gennarelli, Annalisa Botta, (unknown), (unknown), Roberto Massa, Giovanni Antonini, C. Angelini, Giuseppe Novelli	46
19	A Single Strand Conformation Polymorphism-Based Carrier Test for Spinal Muscular Atrophy 2001 ·Genetic Testing ·Sabrina Semprini, Alessandra Tacconelli, Francesca Capon, Francesco Brancati, Bruno Dallapiccola, Giuseppe Novelli	11
20	Identification of Three Novel Cystic Fibrosis Mutations in a Sample of Italian Cystic Fibrosis Patients 1993 ·Human Heredity ·(unknown), Giuseppe Novelli, Bernard Mercier, Federica Sangiuolo, (unknown), (unknown), (unknown)	16

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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