Raffaella Bloise

13.4k total citations · 5 hit papers
55 papers, 7.6k citations indexed

About

Raffaella Bloise is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Raffaella Bloise has authored 55 papers receiving a total of 7.6k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Cardiology and Cardiovascular Medicine, 35 papers in Molecular Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Raffaella Bloise's work include Cardiac electrophysiology and arrhythmias (48 papers), Ion channel regulation and function (34 papers) and Cardiac pacing and defibrillation studies (14 papers). Raffaella Bloise is often cited by papers focused on Cardiac electrophysiology and arrhythmias (48 papers), Ion channel regulation and function (34 papers) and Cardiac pacing and defibrillation studies (14 papers). Raffaella Bloise collaborates with scholars based in Italy, United States and Spain. Raffaella Bloise's co-authors include Silvia G. Priori, Carlo Napolitano, Peter J. Schwartz, Mirella Memmi, E Ronchetti, Jannì Nastoli, Gabriele Vignati, Maurizio Gasparini, Massimiliano Grillo and Vincenzo Sorrentino and has published in prestigious journals such as New England Journal of Medicine, Cell and JAMA.

In The Last Decade

Raffaella Bloise

52 papers receiving 7.4k citations

Hit Papers

CaV1.2 Calcium Channel Dysfunction Causes a Multisystem D... 2001 2026 2009 2017 2004 2001 2003 2002 2002 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism
    2004 1.1k citations Igor Splawski, Katherine W. Timothy et al. Cell profile →
  2. Mutations in the Cardiac Ryanodine Receptor Gene ( hRyR2 ) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia
    2001 980 citations Silvia G. Priori, Carlo Napolitano et al. Circulation profile →
  3. Risk Stratification in the Long-QT Syndrome
    2003 953 citations Silvia G. Priori, Peter J. Schwartz et al. profile →
  4. Clinical and Molecular Characterization of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
    2002 788 citations Silvia G. Priori, Carlo Napolitano et al. Circulation profile →
  5. Natural History of Brugada Syndrome
    2002 690 citations Silvia G. Priori, Carlo Napolitano et al. Circulation profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raffaella Bloise Italy 25 6.8k 4.9k 797 319 213 55 7.6k
Katherine W. Timothy United States 31 9.6k 1.4× 8.8k 1.8× 1.7k 2.1× 472 1.5× 261 1.2× 46 11.2k
Paul A. Brink South Africa 29 3.0k 0.4× 1.9k 0.4× 267 0.3× 152 0.5× 240 1.1× 76 3.7k
Alexey E. Lyashkov United States 27 1.3k 0.2× 1.3k 0.3× 388 0.5× 36 0.1× 95 0.4× 51 2.2k
Yoshihisa Naruse Japan 23 808 0.1× 618 0.1× 248 0.3× 127 0.4× 149 0.7× 108 2.0k
Hirotsugu Tsuchimochi Japan 27 765 0.1× 427 0.1× 157 0.2× 84 0.3× 312 1.5× 86 1.9k
John P. Konhilas United States 25 1.4k 0.2× 929 0.2× 127 0.2× 164 0.5× 154 0.7× 75 2.4k
Andrzej Chruscinski Canada 17 283 0.0× 1.1k 0.2× 687 0.9× 80 0.3× 199 0.9× 42 2.1k
John E. Linley United Kingdom 19 247 0.0× 1.1k 0.2× 584 0.7× 123 0.4× 148 0.7× 31 1.9k
Joseph R. Tobin United States 28 290 0.0× 504 0.1× 473 0.6× 86 0.3× 386 1.8× 66 2.1k
A. Rudehill Sweden 33 559 0.1× 828 0.2× 1.1k 1.3× 31 0.1× 504 2.4× 73 2.9k

Countries citing papers authored by Raffaella Bloise

Since Specialization
Citations

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

Fields of papers citing papers by Raffaella Bloise

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raffaella Bloise

This figure shows the co-authorship network connecting the top 25 collaborators of Raffaella Bloise. A scholar is included among the top collaborators of Raffaella Bloise 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 Raffaella Bloise. Raffaella Bloise 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.
Kukavica, Deni, Alessandro Trancuccio, Mirella Memmi, et al.. (2025). Prognostic relevance of baseline exercise stress test in RYR2-related CPVT. EP Europace. 27(2).
2.
Kukavica, Deni, Alessandro Trancuccio, Alessandro Esposito, et al.. (2023). Artificial intelligence-driven echocardiographic classification identifies Brugada Syndrome patients at higher arrhythmic risk. European Heart Journal. 44(Supplement_2). 1 indexed citations
3.
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
4.
Curcio, Antonio, Alberto Malovini, Andrea Mazzanti, et al.. (2021). Identification of a SCN5A founder mutation causing sudden death, Brugada syndrome, and conduction blocks in Southern Italy. Heart Rhythm. 18(10). 1698–1706. 1 indexed citations
5.
Drago, Fabrizio, Raffaella Bloise, Gabriele Bronzetti, et al.. (2020). Italian recommendations for the management of pediatric patients under twelve years of age with suspected or manifest Brugada syndrome. PubMed. 72(1). 1–13. 7 indexed citations
6.
Mazzanti, Andrea, Riccardo Maragna, Nicola Monteforte, et al.. (2018). Interplay Between Genetic Substrate, QTc Duration, and Arrhythmia Risk in Patients With Long QT Syndrome. Journal of the American College of Cardiology. 71(15). 1663–1671. 108 indexed citations
7.
Mazzanti, Andrea, Riccardo Maragna, Άννα Κωστοπούλου, et al.. (2017). Hydroquinidine Prevents Life-Threatening Arrhythmic Events in Patients With Short QT Syndrome. Journal of the American College of Cardiology. 70(24). 3010–3015. 52 indexed citations
8.
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
9.
Corona‐Rivera, Jorge Román, Raffaella Bloise, Silvia G. Priori, et al.. (2015). Unusual retrospective prenatal findings in a male newborn with Timothy syndrome type 1. European Journal of Medical Genetics. 58(6-7). 332–335. 11 indexed citations
10.
Pasquale, Elisa Di, Francesco Lodola, Michele Miragoli, et al.. (2013). CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia. Cell Death and Disease. 4(10). e843–e843. 94 indexed citations
11.
Silvester, Nicole, Raffaella Bloise, Mark C. Bagley, et al.. (2011). Ouabain is a Pharmacomimic of Mutant RyR2 Ca2+ Release Dysfunction but is not a Serum-Borne Trigger of CPVT. Biophysical Journal. 100(3). 412a–413a. 1 indexed citations
12.
Tomás, Marta, Carlo Napolitano, Raffaella Bloise, et al.. (2010). Polymorphisms in the NOS1APGene Modulate QT Interval Duration and Risk of Arrhythmias in the Long QT Syndrome. Journal of the American College of Cardiology. 55(24). 2745–2752. 118 indexed citations
13.
Losito, Luciana, Marta De Rinaldis, Silvia G. Priori, et al.. (2008). Charcot-Marie-Tooth type 1a in a child with Long QT syndrome. European Journal of Paediatric Neurology. 13(5). 459–462. 5 indexed citations
14.
15.
Bloise, Raffaella, Carlo Napolitano, Katherine W. Timothy, et al.. (2006). Abstract 2439: Clinical Profile and Risk of Sudden Death in Children with Timothy Syndrome. Circulation. 114. 1 indexed citations
16.
Napolitano, Carlo, Raffaella Bloise, & Silvia G. Priori. (2006). Long QT syndrome and short QT syndrome: how to make correct diagnosis and what about eligibility for sports activity. Journal of Cardiovascular Medicine. 7(4). 250–256. 27 indexed citations
17.
Napolitano, Carlo, Silvia G. Priori, Peter J. Schwartz, et al.. (2005). Genetic Testing in the Long QT Syndrome. JAMA. 294(23). 2975–2975. 344 indexed citations
18.
Splawski, Igor, Katherine W. Timothy, Niels Decher, et al.. (2004). CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism. Cell. 119(1). 19–31. 1112 indexed citations breakdown →
19.
Rosa, Gabriella De, Angelica Bibiana Delogu, Marco Piastra, et al.. (2004). Cathecolaminergic Polymorphic Ventricular Tachycardia. Pediatric Emergency Care. 20(3). 175–177. 20 indexed citations
20.
Gasparini, Maurizio, Silvia G. Priori, Massimo Mantica, et al.. (2002). Programmed Electrical Stimulation in Brugada Syndrome: How Reproducible Are the Results?. Journal of Cardiovascular Electrophysiology. 13(9). 880–887. 40 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Katherine W. Timothy Breakdown of academic impact, for papers by Paul A. Brink Breakdown of academic impact, for papers by Alexey E. Lyashkov Breakdown of academic impact, for papers by Yoshihisa Naruse Breakdown of academic impact, for papers by Hirotsugu Tsuchimochi Breakdown of academic impact, for papers by John P. Konhilas Breakdown of academic impact, for papers by Andrzej Chruscinski Breakdown of academic impact, for papers by John E. Linley Breakdown of academic impact, for papers by Joseph R. Tobin Breakdown of academic impact, for papers by A. Rudehill
Rankless by CCL
2026