Matteo Pedrazzini

3.6k total citations · 1 hit paper
27 papers, 1.8k citations indexed

About

Matteo Pedrazzini is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Matteo Pedrazzini has authored 27 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Cardiology and Cardiovascular Medicine, 17 papers in Molecular Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Matteo Pedrazzini's work include Cardiac electrophysiology and arrhythmias (23 papers), Ion channel regulation and function (13 papers) and Cardiac pacing and defibrillation studies (3 papers). Matteo Pedrazzini is often cited by papers focused on Cardiac electrophysiology and arrhythmias (23 papers), Ion channel regulation and function (13 papers) and Cardiac pacing and defibrillation studies (3 papers). Matteo Pedrazzini collaborates with scholars based in Italy, United States and South Africa. Matteo Pedrazzini's co-authors include Lia Crotti, Peter J. Schwartz, Roberto Insolia, Alfred L. George, Chiara Ferrandi, Torleiv O. Rognum, Marianne Arnestad, Åshild Vege, Carla Spazzolini and Dao Wen Wang and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and PLoS ONE.

In The Last Decade

Matteo Pedrazzini

27 papers receiving 1.7k 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 →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Matteo Pedrazzini Italy	13	1.6k	1.1k	176	150	73	27	1.8k
Roberto Insolia Italy	12	2.2k 1.4×	1.5k 1.4×	186 1.1×	212 1.4×	90 1.2×	26	2.4k
Carla M. Haglund United States	10	1.3k 0.8×	897 0.8×	34 0.2×	155 1.0×	69 0.9×	12	1.5k
J. C. Kentish United Kingdom	7	489 0.3×	368 0.3×	23 0.1×	88 0.6×	81 1.1×	9	772
Ramón Brugada Spain	12	539 0.3×	359 0.3×	10 0.1×	59 0.4×	29 0.4×	21	726
A Jervell Norway	7	1.2k 0.7×	869 0.8×	15 0.1×	97 0.6×	21 0.3×	10	1.3k
N. Wilson Canada	15	460 0.3×	158 0.1×	54 0.3×	77 0.5×	18 0.2×	41	784
Emmanuel Drouin France	13	536 0.3×	363 0.3×	84 0.5×	105 0.7×	10 0.1×	45	708
W T Woods United States	15	320 0.2×	165 0.2×	17 0.1×	83 0.6×	30 0.4×	30	697
Jørn Bathen Norway	11	683 0.4×	526 0.5×	6 0.0×	103 0.7×	18 0.2×	19	848
Natalia Kraeva Canada	17	333 0.2×	513 0.5×	4 0.0×	125 0.8×	21 0.3×	33	669

Countries citing papers authored by Matteo Pedrazzini

Since Specialization

Citations

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

Fields of papers citing papers by Matteo Pedrazzini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matteo Pedrazzini

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

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

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

Lavra, Luca, Fiorenza Magi, Alessandra Ulivieri, et al.. (2021). Generation and characterization of the human induced pluripotent stem cell (hiPSC) line NCUFi001-A from a patient carrying KCNQ1 G314S mutation. Stem Cell Research. 54. 102418–102418. 2 indexed citations

Schwartz, Peter J., Maria‐Christina Kotta, Matteo Pedrazzini, et al.. (2021). Mutation location and I Ks regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region. European Heart Journal. 42(46). 4743–4755. 26 indexed citations

Sala, Luca, Manuela Mura, Marcella Rocchetti, et al.. (2020). MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes. Cardiovascular Research. 117(3). 767–779. 32 indexed citations

Dagradi, Federica, Carla Spazzolini, Silvia Castelletti, et al.. (2020). Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome. Circulation. 142(25). 2405–2415. 32 indexed citations

Catarsi, Paolo, Vittorio Rosti, Giacomo Morreale, et al.. (2015). JAK2 Exon 14 Skipping in Patients with Primary Myelofibrosis: A Minor Splice Variant Modulated by the JAK2-V617F Allele Burden. PLoS ONE. 10(1). e0116636–e0116636. 6 indexed citations

Crotti, Lia, Carla Spazzolini, Alessandra Pia Porretta, et al.. (2012). Vagal Reflexes Following an Exercise Stress Test. Journal of the American College of Cardiology. 60(24). 2515–2524. 36 indexed citations

10.

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 →

11.

Crotti, Lia, Matteo Pedrazzini, Roberto Insolia, et al.. (2009). Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada Syndrome.. PubMed. 126(2). 339–339. 2 indexed citations

12.

Desai, Reshma R., Lia Crotti, Marianne Arnestad, et al.. (2008). Cardiac potassium channel dysfunction in sudden infant death syndrome. Journal of Molecular and Cellular Cardiology. 44(3). 571–581. 159 indexed citations

13.

Crotti, Lia, Marzena Anna Lewandowska, Peter J. Schwartz, et al.. (2008). A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome. Heart Rhythm. 6(2). 212–218. 29 indexed citations

14.

Wang, Dao Wen, Lia Crotti, Wataru Shimizu, et al.. (2008). Malignant Perinatal Variant of Long-QT Syndrome Caused by a Profoundly Dysfunctional Cardiac Sodium Channel. Circulation Arrhythmia and Electrophysiology. 1(5). 370–378. 34 indexed citations

15.

Crotti, Lia, Chiara Ferrandi, Roberto Insolia, et al.. (2007). Gene symbol: SCN5A.. PubMed. 120(6). 911–2. 1 indexed citations

16.

Crotti, Lia, Roberto Insolia, Matteo Pedrazzini, et al.. (2007). Gene symbol: KCNQ1.. PubMed. 120(6). 912–912. 2 indexed citations

17.

Arnestad, Marianne, Lia Crotti, Torleiv O. Rognum, et al.. (2007). Prevalence of Long-QT Syndrome Gene Variants in Sudden Infant Death Syndrome. Circulation. 115(3). 361–367. 364 indexed citations

18.

Crotti, Lia, Andrew L. Lundquist, Roberto Insolia, et al.. (2005). KCNH2 -K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome. Circulation. 112(9). 1251–1258. 167 indexed citations

19.

Ferrari, Gaetano Maria De, Lia Crotti, Andrew L. Lundquist, et al.. (2005). Long QT syndrome with cardiac arrest and transient short QT due to a novel KCNH2 mutation causing both loss and gain of function. Heart Rhythm. 2(5). S145–S145. 1 indexed citations

20.

Pedrazzini, Matteo, Oscar D. Bruno, & Eduardo G. Gros. (1983). Analysis of urinary steroid profiles of women with Cushing's syndrome by computerised gas chromatography-mass spectrometry.. PubMed. 33(3). 243–52. 1 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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