Lia Crotti

18.5k total citations · 2 hit papers
158 papers, 7.6k citations indexed

About

Lia Crotti is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lia Crotti has authored 158 papers receiving a total of 7.6k indexed citations (citations by other indexed papers that have themselves been cited), including 143 papers in Cardiology and Cardiovascular Medicine, 84 papers in Molecular Biology and 13 papers in Cellular and Molecular Neuroscience. Recurrent topics in Lia Crotti's work include Cardiac electrophysiology and arrhythmias (118 papers), Ion channel regulation and function (66 papers) and Cardiomyopathy and Myosin Studies (26 papers). Lia Crotti is often cited by papers focused on Cardiac electrophysiology and arrhythmias (118 papers), Ion channel regulation and function (66 papers) and Cardiomyopathy and Myosin Studies (26 papers). Lia Crotti collaborates with scholars based in Italy, United States and South Africa. Lia Crotti's co-authors include Peter J. Schwartz, Roberto Insolia, Alfred L. George, Carla Spazzolini, Matteo Pedrazzini, Federica Dagradi, Chiara Ferrandi, Michael J. Ackerman, Silvia G. Priori and Paul A. Brink and has published in prestigious journals such as New England Journal of Medicine, JAMA and Circulation.

In The Last Decade

Lia Crotti

153 papers receiving 7.5k 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.

Prevalence of the Congenital Long-QT Syndrome

2009 695 citations Peter J. Schwartz, Marco Stramba‐Badiale et al. Circulation profile →
Long-QT Syndrome

2012 431 citations Peter J. Schwartz, Lia Crotti et al. Circulation Arrhythmia and Electrophysiology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lia Crotti Italy	43	6.6k	4.7k	677	268	238	158	7.6k
Jonathan C. Makielski United States	47	5.6k 0.8×	5.8k 1.3×	1.5k 2.3×	354 1.3×	209 0.9×	120	7.7k
Raffaella Bloise Italy	25	6.8k 1.0×	4.9k 1.1×	797 1.2×	213 0.8×	86 0.4×	55	7.6k
Connie R. Bezzina Netherlands	50	7.3k 1.1×	6.1k 1.3×	1.1k 1.7×	264 1.0×	62 0.3×	180	8.8k
Harold A. Spurgeon United States	43	5.1k 0.8×	2.5k 0.5×	1.1k 1.6×	461 1.7×	75 0.3×	86	6.7k
J. David Port United States	33	2.3k 0.3×	2.7k 0.6×	573 0.8×	374 1.4×	48 0.2×	92	4.6k
Óscar Campuzano Spain	32	2.2k 0.3×	1.5k 0.3×	289 0.4×	111 0.4×	77 0.3×	147	3.1k
John P. Headrick Australia	41	1.6k 0.2×	1.6k 0.4×	386 0.6×	363 1.4×	128 0.5×	166	4.9k
Zeljko J. Bosnjak United States	42	1.6k 0.2×	2.1k 0.5×	757 1.1×	876 3.3×	152 0.6×	249	5.8k
Peter Dominiak Germany	32	2.2k 0.3×	1.1k 0.2×	528 0.8×	426 1.6×	635 2.7×	132	4.8k
Kathryn G. Lamping United States	33	1.5k 0.2×	1.1k 0.2×	495 0.7×	433 1.6×	79 0.3×	78	3.3k

Countries citing papers authored by Lia Crotti

Since Specialization

Citations

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

Fields of papers citing papers by Lia Crotti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lia Crotti

This figure shows the co-authorship network connecting the top 25 collaborators of Lia Crotti. A scholar is included among the top collaborators of Lia Crotti 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 Lia Crotti. Lia Crotti 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

Sarto, Patrizio, Lia Crotti, Federica Dagradi, et al.. (2025). TP-fusion at peak exercise: a novel marker for the recognition of unsuspected long QT syndrome patients. EP Europace. 27(7). 1 indexed citations

Schwartz, Peter J. & Lia Crotti. (2025). Long QT Syndrome. New England Journal of Medicine. 393(20). 2023–2034.

Crotti, Lia, Federica Dagradi, J. Martijn Bos, et al.. (2024). Therapeutic Efficacy of Mexiletine for Long QT Syndrome Type 2: Evidence From Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes, Transgenic Rabbits, and Patients. Circulation. 150(7). 531–543. 16 indexed citations

Gauthey, Anaïs, Martin Manninger, Katarzyna Małaczyńska-Rajpold, et al.. (2024). Genetic testing for inherited arrhythmia syndromes and cardiomyopathies: results of the European Heart Rhythm Association survey. EP Europace. 26(9). 2 indexed citations

Dusi, Veronica, Federica Dagradi, Carla Spazzolini, et al.. (2024). Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation. European Heart Journal. 45(29). 2647–2656. 15 indexed citations

Shimamoto, Keiko, Federica Dagradi, Seiko Ohno, et al.. (2024). Clinical Features, Long-Term Prognosis, and Clinical Management of Genotype-Negative Long QT Syndrome Patients. JACC. Clinical electrophysiology. 10(12). 2584–2596. 6 indexed citations

Kotta, Maria‐Christina, Margherita Torchio, Pauline Bayliss, et al.. (2023). Cardiac Genetic Investigation of Sudden Infant and Early Childhood Death: A Study From Victims to Families. Journal of the American Heart Association. 12(17). e029100–e029100. 10 indexed citations

Girolami, Francesca, Alessia Gozzini, Alessia Tomberli, et al.. (2023). Genetic Testing and Counselling in Hypertrophic Cardiomyopathy: Frequently Asked Questions. Journal of Clinical Medicine. 12(7). 2489–2489. 5 indexed citations

Crotti, Lia, et al.. (2023). Current gaps in knowledge in inherited arrhythmia syndromes. Netherlands Heart Journal. 31(7-8). 272–281. 1 indexed citations

10.

Bernardini, Andrea, Lia Crotti, Iacopo Olivotto, & Franco Cecchi. (2023). Diagnostic and prognostic electrocardiographic features in patients with hypertrophic cardiomyopathy. European Heart Journal Supplements. 25(Supplement_C). C173–C178. 8 indexed citations

11.

Castelletti, Silvia, Belinda Gray, Cristina Basso, et al.. (2022). Indications and utility of cardiac genetic testing in athletes. European Journal of Preventive Cardiology. 29(12). 1582–1591. 18 indexed citations

12.

Sala, Luca, Manuela Mura, Alessandra Moretti, et al.. (2022). Use of hiPSC-Derived Cardiomyocytes to Rule Out Proarrhythmic Effects of Drugs: The Case of Hydroxychloroquine in COVID-19. Frontiers in Physiology. 12. 730127–730127. 6 indexed citations

13.

Asatryan, Babken, Yael Ben‐Haim, Stephan Dobner, et al.. (2021). Sex-Related Differences in Cardiac Channelopathies. Circulation. 143(7). 739–752. 23 indexed citations

14.

Ameri, Pietro, Gabriele G. Schiattarella, Lia Crotti, et al.. (2020). Novel Basic Science Insights to Improve the Management of Heart Failure: Review of the Working Group on Cellular and Molecular Biology of the Heart of the Italian Society of Cardiology. International Journal of Molecular Sciences. 21(4). 1192–1192. 8 indexed citations

15.

Crotti, Lia, et al.. (2013). Condizioni cliniche associate ad anomalie dell’intervallo QT: implicazioni cliniche. Giornale italiano di cardiologia. 14(1). 55–65. 3 indexed citations

16.

Hennessey, Jessica A., Cherisse A. Marcou, Chuan Wang, et al.. (2013). FGF12 is a candidate Brugada syndrome locus. Heart Rhythm. 10(12). 1886–1894. 72 indexed citations

17.

Ishikawa, Taisuke, Akinori Sato, Cherisse A. Marcou, et al.. (2012). A Novel Disease Gene for Brugada Syndrome. Circulation Arrhythmia and Electrophysiology. 5(6). 1098–1107. 80 indexed citations

18.

Schwartz, Peter J., Marco Stramba‐Badiale, Lia Crotti, et al.. (2009). Prevalence of the Congenital Long-QT Syndrome. Circulation. 120(18). 1761–1767. 695 indexed citations breakdown →

19.

Makita, Naomasa, Elijah R. Behr, Wataru Shimizu, et al.. (2008). The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome. Journal of Clinical Investigation. 118(6). 2219–29. 160 indexed citations

20.

Crotti, Lia, Carla Spazzolini, Peter J. Schwartz, et al.. (2007). The Common Long-QT Syndrome Mutation KCNQ1/A341V Causes Unusually Severe Clinical Manifestations in Patients With Different Ethnic Backgrounds. Circulation. 116(21). 2366–2375. 112 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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