Mirella Memmi

6.5k total citations · 3 hit papers
33 papers, 4.2k citations indexed

About

Mirella Memmi is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Mirella Memmi has authored 33 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Cardiology and Cardiovascular Medicine, 22 papers in Molecular Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Mirella Memmi's work include Cardiac electrophysiology and arrhythmias (26 papers), Ion channel regulation and function (20 papers) and Cardiovascular Effects of Exercise (9 papers). Mirella Memmi is often cited by papers focused on Cardiac electrophysiology and arrhythmias (26 papers), Ion channel regulation and function (20 papers) and Cardiovascular Effects of Exercise (9 papers). Mirella Memmi collaborates with scholars based in Italy, United States and Brazil. Mirella Memmi's co-authors include Silvia G. Priori, Carlo Napolitano, Raffaella Bloise, Gabriele Vignati, Vincenzo Sorrentino, Gian Antonio Danieli, Natascia Tiso, Barbara Colombi, Andrew R. Marks and Fabrizio Drago and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Circulation.

In The Last Decade

Mirella Memmi

31 papers receiving 4.1k citations

Hit Papers

align trajectories

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.

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 →
Clinical and Molecular Characterization of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

2002 788 citations Silvia G. Priori, Carlo Napolitano et al. Circulation profile →
FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

2003 561 citations Xander H.T. Wehrens, Stephan E. Lehnart et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mirella Memmi Italy	19	3.9k	3.1k	524	86	83	33	4.2k
Xianming Lin United States	27	1.3k 0.3×	1.4k 0.5×	258 0.5×	98 1.1×	60 0.7×	49	2.1k
Yuji Hisamatsu Japan	12	1.9k 0.5×	1.9k 0.6×	438 0.8×	102 1.2×	20 0.2×	18	2.4k
Marieke W. Veldkamp Netherlands	27	2.7k 0.7×	2.2k 0.7×	563 1.1×	93 1.1×	41 0.5×	47	3.0k
Nathalie Neyroud France	18	1.6k 0.4×	1.6k 0.5×	379 0.7×	21 0.2×	68 0.8×	34	1.9k
Alessandra Besana Italy	14	1.1k 0.3×	768 0.3×	165 0.3×	70 0.8×	36 0.4×	17	1.4k
Katharine M. Dibb United Kingdom	22	1.3k 0.3×	928 0.3×	319 0.6×	73 0.8×	18 0.2×	44	1.6k
Isabelle Baró France	32	1.9k 0.5×	2.2k 0.7×	619 1.2×	127 1.5×	58 0.7×	59	2.7k
Sami F. Noujaim United States	22	1.1k 0.3×	824 0.3×	222 0.4×	49 0.6×	56 0.7×	51	1.5k
Bettina Linck Germany	19	711 0.2×	869 0.3×	227 0.4×	55 0.6×	21 0.3×	31	1.2k
James A. Fraser United Kingdom	22	800 0.2×	867 0.3×	287 0.5×	32 0.4×	15 0.2×	51	1.2k

Countries citing papers authored by Mirella Memmi

Since Specialization

Citations

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

Fields of papers citing papers by Mirella Memmi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mirella Memmi

This figure shows the co-authorship network connecting the top 25 collaborators of Mirella Memmi. A scholar is included among the top collaborators of Mirella Memmi 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 Mirella Memmi. Mirella Memmi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

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, Andrea Mazzanti, et al.. (2024). Nonmodifiable Risk Factors Predict Outcomes in Brugada Syndrome. Journal of the American College of Cardiology. 84(21). 2087–2098. 4 indexed citations

3.

Catalano, Oronzo, Giulia Bendotti, Mirella Memmi, et al.. (2023). Evidence of Carotid Atherosclerosis Vulnerability Regression in Real Life From Magnetic Resonance Imaging: Results of the MAGNETIC Prospective Study. Journal of the American Heart Association. 12(2). e026469–e026469. 3 indexed citations

4.

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

5.

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

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.

Nicora, Giovanna, Ivan Limongelli, Patrick Gambelli, et al.. (2018). CardioVAI: An automatic implementation of ACMG-AMP variant interpretation guidelines in the diagnosis of cardiovascular diseases. Human Mutation. 39(12). 1835–1846. 29 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.

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

10.

Napolitano, Carlo, Raffaella Bloise, Mirella Memmi, & Silvia G. Priori. (2013). Clinical utility gene card for: Catecholaminergic polymorphic ventricular tachycardia (CPVT). European Journal of Human Genetics. 22(1). 152–152. 18 indexed citations

11.

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

12.

Liu, Nian, Barbara Colombi, Mirella Memmi, et al.. (2006). Arrhythmogenesis in Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation Research. 99(3). 292–298. 237 indexed citations

13.

Wehrens, Xander H.T., Stephan E. Lehnart, Fannie Huang, et al.. (2003). FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death. Cell. 113(7). 829–840. 561 indexed citations breakdown →

14.

Grant, Augustus O., Michael P. Carboni, Valentina Neplioueva, et al.. (2002). Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation. Journal of Clinical Investigation. 110(8). 1201–1209. 12 indexed citations

15.

Grant, Augustus O., Michael P. Carboni, Valentina Neplioueva, et al.. (2002). Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation. Journal of Clinical Investigation. 110(8). 1201–1209. 137 indexed citations

16.

Grant, Augustus O., Michael P. Carboni, Valentina Neplioueva, et al.. (2002). Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation. Journal of Clinical Investigation. 110(8). 1201–1209. 167 indexed citations

17.

Rivolta, Ilaria, Hugues Abriel, Michihiro Tateyama, et al.. (2001). Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes. Journal of Biological Chemistry. 276(33). 30623–30630. 166 indexed citations

18.

Priori, Silvia G., Carlo Napolitano, Natascia Tiso, et al.. (2001). Mutations in the Cardiac Ryanodine Receptor Gene ( hRyR2 ) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation. 103(2). 196–200. 980 indexed citations breakdown →

19.

Marks, Andrew R., et al.. (2001). Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia. Journal of Cellular Physiology. 190(1). 1–6. 150 indexed citations

20.

Rizzo, Vittoria, Mirella Memmi, Remigio Moratti, Gianvico Melzi d’Eril, & Emilio Perucca. (1996). Concentrations of l-dopa in plasma and plasma ultrafiltrates. Journal of Pharmaceutical and Biomedical Analysis. 14(8-10). 1043–1046. 11 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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