Valeria Novelli

4.0k total citations
28 papers, 1.8k citations indexed

About

Valeria Novelli is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Physiology. According to data from OpenAlex, Valeria Novelli has authored 28 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Cardiology and Cardiovascular Medicine, 14 papers in Molecular Biology and 4 papers in Physiology. Recurrent topics in Valeria Novelli's work include Cardiac electrophysiology and arrhythmias (16 papers), Cardiovascular Effects of Exercise (11 papers) and Ion channel regulation and function (9 papers). Valeria Novelli is often cited by papers focused on Cardiac electrophysiology and arrhythmias (16 papers), Cardiovascular Effects of Exercise (11 papers) and Ion channel regulation and function (9 papers). Valeria Novelli collaborates with scholars based in Italy, United States and United Kingdom. Valeria Novelli's co-authors include Chiara Viviani Anselmi, Annibale Alessandro Puca, Carlo Napolitano, Roberta Roncarati, Silvia G. Priori, Alberto Malovini, Riccardo Bellazzi, Gianluigi Condorelli, Francesco Villa and Mirella Memmi and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and PLoS ONE.

In The Last Decade

Valeria Novelli

26 papers receiving 1.8k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Valeria Novelli Italy 17 1.2k 885 251 196 171 28 1.8k
Donna H. Korzick United States 22 407 0.4× 384 0.4× 13 0.1× 120 0.6× 279 1.6× 49 1.0k
Randi J. Parks United States 14 257 0.2× 706 0.8× 58 0.2× 49 0.3× 255 1.5× 18 1.1k
Tadaaki Iwasaki Japan 15 505 0.4× 652 0.7× 35 0.1× 93 0.5× 189 1.1× 69 1.4k
Scott K. Powers United States 16 261 0.2× 628 0.7× 16 0.1× 227 1.2× 476 2.8× 21 1.4k
Kim A. Sjøberg Denmark 22 133 0.1× 708 0.8× 27 0.1× 68 0.3× 971 5.7× 36 1.6k
Lucile Dollet Sweden 14 77 0.1× 568 0.6× 33 0.1× 84 0.4× 519 3.0× 16 1.0k
Y. Goto Japan 10 278 0.2× 859 1.0× 22 0.1× 64 0.3× 126 0.7× 23 1.2k
Mohammad Saifur Rohman Indonesia 13 239 0.2× 156 0.2× 36 0.1× 18 0.1× 160 0.9× 97 724
Ming-Hui Zou United States 11 158 0.1× 386 0.4× 23 0.1× 24 0.1× 160 0.9× 12 958
Christophe Graveleau United States 8 459 0.4× 489 0.6× 71 0.3× 27 0.1× 375 2.2× 8 1.0k

Countries citing papers authored by Valeria Novelli

Since Specialization
Citations

This map shows the geographic impact of Valeria 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 Valeria Novelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Valeria Novelli more than expected).

Fields of papers citing papers by Valeria Novelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Valeria 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 Valeria Novelli. The network helps show where Valeria Novelli may publish in the future.

Co-authorship network of co-authors of Valeria Novelli

This figure shows the co-authorship network connecting the top 25 collaborators of Valeria Novelli. A scholar is included among the top collaborators of Valeria 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 Valeria Novelli. Valeria 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.
Novelli, Valeria, Francesco Canonico, Renzo Laborante, et al.. (2025). Unraveling the Genetic Heartbeat: Decoding Cardiac Involvement in Duchenne Muscular Dystrophy. Biomedicines. 13(1). 102–102. 2 indexed citations
2.
Scarà, Antonio, Luigi Sciarra, Elena Cavarretta, et al.. (2025). Brugada Syndrome in Sports Cardiology: An Expert Opinion Statement of the Italian Society of Sports Cardiology (SICSport). The American Journal of Cardiology. 244. 9–17.
3.
D’Amario, Domenico, Maria Lucia Narducci, Valeria Novelli, et al.. (2025). Arrhythmic Risk Stratification and Sudden Cardiac Death Prevention in Duchenne Muscular Dystrophy: A Critical Appraisal. Reviews in Cardiovascular Medicine. 26(3). 27089–27089. 1 indexed citations
4.
Chiesa, Mattia, Matteo Pedrazzini, Saima Mushtaq, et al.. (2022). Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients. Biomolecules. 12(8). 1043–1043. 7 indexed citations
5.
Novelli, Valeria, Mirella Memmi, Alberto Malovini, et al.. (2022). Role of CACNA1C in Brugada syndrome: Prevalence and phenotype of probands referred for genetic testing. Heart Rhythm. 19(5). 798–806. 11 indexed citations
6.
Narducci, Maria Lucia, Valeria Novelli, Antonio Bisignani, et al.. (2021). Diagnostic Workflow in Competitive Athletes with Ventricular Arrhythmias and Suspected Concealed Cardiomyopathies. Medicina. 57(2). 182–182.
7.
Walsh, Roddy, Arnon Adler, Ahmad S. Amin, et al.. (2021). Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death. European Heart Journal. 43(15). 1500–1510. 71 indexed citations
8.
Adler, Arnon, Valeria Novelli, Ahmad S. Amin, et al.. (2020). An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome. Circulation. 141(6). 418–428. 204 indexed citations
9.
Novelli, Valeria, Antonio Bisignani, Gemma Pelargonio, et al.. (2020). Clinical utility of genetic testing in the early diagnosis of Danon disease mimicking hypertrophic cardiomyopathy: a case report. BMC Cardiovascular Disorders. 20(1). 156–156. 2 indexed citations
10.
Hosseini, S. Mohsen, Raymond H. Kim, Sharmila Udupa, et al.. (2018). Reappraisal of Reported Genes for Sudden Arrhythmic Death. Circulation. 138(12). 1195–1205. 210 indexed citations
11.
Novelli, Valeria, Kabir Malkani, & Marina Cerrone. (2018). Pleiotropic Phenotypes Associated With PKP2 Variants. Frontiers in Cardiovascular Medicine. 5. 184–184. 24 indexed citations
12.
Palluzzi, Fernando, Raffaele Ferrari, Francesca Graziano, et al.. (2017). A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia. PLoS ONE. 12(10). e0185797–e0185797. 29 indexed citations
13.
Novelli, Valeria, Patrick Gambelli, Mirella Memmi, & Carlo Napolitano. (2016). Challenges in Molecular Diagnostics of Channelopathies in the Next-Generation Sequencing Era: Less Is More?. Frontiers in Cardiovascular Medicine. 3. 29–29. 3 indexed citations
14.
Mazzanti, Andrea, Kevin Ng, Alessandro Faragli, et al.. (2016). Arrhythmogenic Right Ventricular Cardiomyopathy. Journal of the American College of Cardiology. 68(23). 2540–2550. 103 indexed citations
15.
Cerrone, Marina, Xianming Lin, Mingliang Zhang, et al.. (2013). Missense Mutations in Plakophilin-2 Cause Sodium Current Deficit and Associate With a Brugada Syndrome Phenotype. Circulation. 129(10). 1092–1103. 233 indexed citations
16.
Mazzanti, Andrea, A. Kanthan, Nicola Monteforte, et al.. (2013). Novel Insight Into the Natural History of Short QT Syndrome. Journal of the American College of Cardiology. 63(13). 1300–1308. 141 indexed citations
17.
Cerrone, Marina, Xinchun Lin, Esperanza Agulló-Pascual, et al.. (2013). Missense Mutations in Plakophilin-2 Can Cause Brugada Syndrome Phenotype By Decreasing Sodium Current and Nav1.5 Membrane Localization. Heart Rhythm. 10(11). 1743–1743. 5 indexed citations
18.
Malovini, Alberto, Maddalena Illario, Guido Iaccarino, et al.. (2011). Association Study on Long-Living Individuals from Southern Italy Identifies rs10491334 in the CAMKIV Gene That Regulates Survival Proteins. Rejuvenation Research. 14(3). 283–291. 52 indexed citations
19.
Anselmi, Chiara Viviani, Alberto Malovini, Roberta Roncarati, et al.. (2009). Association of the FOXO3A Locus with Extreme Longevity in a Southern Italian Centenarian Study. Rejuvenation Research. 12(2). 95–104. 234 indexed citations
20.
Prattichizzo, Clelia, et al.. (2008). Mutational spectrum of the oral-facial-digital type I syndrome: a study on a large collection of patients. Human Mutation. 29(10). 1237–1246. 65 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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