Matteo Vatta

4.6k total citations
60 papers, 2.4k citations indexed

About

Matteo Vatta is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Matteo Vatta has authored 60 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Cardiology and Cardiovascular Medicine, 40 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Matteo Vatta's work include Cardiomyopathy and Myosin Studies (33 papers), Cardiac electrophysiology and arrhythmias (30 papers) and Ion channel regulation and function (22 papers). Matteo Vatta is often cited by papers focused on Cardiomyopathy and Myosin Studies (33 papers), Cardiac electrophysiology and arrhythmias (30 papers) and Ion channel regulation and function (22 papers). Matteo Vatta collaborates with scholars based in United States, Italy and Japan. Matteo Vatta's co-authors include Jeffrey A. Towbin, Neil E. Bowles, Ramón Brugada, Pedro Brugada, Josép Brugada, Charles Antzelevitch, Robert Dumaine, Michael J. Ackerman, Vladislav V. Nesterenko and David J. Tester and has published in prestigious journals such as The Lancet, Circulation and Journal of Clinical Investigation.

In The Last Decade

Matteo Vatta

59 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matteo Vatta United States 23 2.0k 1.7k 210 169 153 60 2.4k
Matteo Vatta United States 21 2.0k 1.0× 1.4k 0.8× 150 0.7× 117 0.7× 137 0.9× 59 2.5k
Roger D. Bies United States 15 1.2k 0.6× 1.1k 0.7× 139 0.7× 127 0.8× 200 1.3× 19 2.0k
José R. Pinto United States 27 1.9k 0.9× 1.1k 0.7× 85 0.4× 106 0.6× 86 0.6× 96 2.3k
Jan W. Schrickel Germany 27 1.5k 0.8× 737 0.4× 134 0.6× 125 0.7× 151 1.0× 95 2.3k
Andreas Perrot Germany 35 2.1k 1.1× 1.8k 1.1× 123 0.6× 138 0.8× 162 1.1× 71 3.1k
Florence Kyndt France 19 2.3k 1.2× 1.9k 1.1× 234 1.1× 82 0.5× 147 1.0× 45 2.7k
Paul H. Goldspink United States 22 712 0.4× 705 0.4× 94 0.4× 132 0.8× 102 0.7× 51 1.3k
David Y. Barefield United States 20 811 0.4× 877 0.5× 72 0.3× 133 0.8× 86 0.6× 41 1.4k
Kathleen A. Quane Ireland 14 672 0.3× 999 0.6× 217 1.0× 51 0.3× 93 0.6× 18 1.2k
Teresa Bohlmeyer United States 16 1.0k 0.5× 1.1k 0.6× 87 0.4× 73 0.4× 156 1.0× 18 1.7k

Countries citing papers authored by Matteo Vatta

Since Specialization
Citations

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

Fields of papers citing papers by Matteo Vatta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matteo Vatta

This figure shows the co-authorship network connecting the top 25 collaborators of Matteo Vatta. A scholar is included among the top collaborators of Matteo Vatta 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 Vatta. Matteo Vatta 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.
Morales, Ana, Ren Sheng, Thomas E. Callis, et al.. (2023). Real-World Genetic Testing Utilization Among Patients With Cardiomyopathy. Circulation Genomic and Precision Medicine. 17(1). e004028–e004028. 2 indexed citations
2.
Parcha, Vibhu, et al.. (2023). De novo heterozygous pathogenic FBN1 variant in an autopsy case of multiple aneurysms and right renal artery dissection: a case report. Frontiers in Cardiovascular Medicine. 10. 1 indexed citations
3.
Helm, Benjamin M., et al.. (2023). Disruption of FBN1 by an Alu element insertion: A novel genetic cause of Marfan syndrome. European Journal of Medical Genetics. 66(7). 104775–104775.
4.
Morales, Ana, Susan Rojahn, John Garcia, et al.. (2021). Comprehensive Genetic Testing for Pediatric Hypertrophic Cardiomyopathy Reveals Clinical Management Opportunities and Syndromic Conditions. Pediatric Cardiology. 43(3). 616–623. 6 indexed citations
5.
Celestino-Soper, Patrícia B. S., Anisiia Doytchinova, William J. Groh, et al.. (2015). Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel. PLoS ONE. 10(12). e0143588–e0143588. 5 indexed citations
6.
Vatta, Matteo & Michael J. Ackerman. (2010). Genetics of Heart Failure and Sudden Death. Heart Failure Clinics. 6(4). 507–514. 2 indexed citations
7.
Ai, Tomohiko, Jeffrey A. Towbin, Ramón Brugada, et al.. (2009). A Nonsense SCN5A Mutation Associated with Brugada‐Type Electrocardiogram and Intraventricular Conduction Defects. Pacing and Clinical Electrophysiology. 32(9). 1231–1236. 6 indexed citations
8.
Wu, Jie, Wataru Shimizu, Wei‐Guang Ding, et al.. (2009). KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disorders. Heart Rhythm. 7(2). 199–205. 19 indexed citations
9.
Singh, Harinder R., Yang Zhao, Saad Siddiqui, et al.. (2009). A novel Alu‐mediated Xq28 microdeletion ablates TAZ and partially deletes DNL1L in a patient with Barth syndrome. American Journal of Medical Genetics Part A. 149A(5). 1082–1085. 13 indexed citations
10.
Wu, Geru, Tomohiko Ai, Jeffrey J. Kim, et al.. (2008). α-1-Syntrophin Mutation and the Long-QT Syndrome. Circulation Arrhythmia and Electrophysiology. 1(3). 193–201. 85 indexed citations
11.
Vatta, Matteo, Michael J. Ackerman, Bin Ye, et al.. (2006). Mutant Caveolin-3 Induces Persistent Late Sodium Current and Is Associated With Long-QT Syndrome. Circulation. 114(20). 2104–2112. 356 indexed citations
12.
Friedlander, Yechiel, Matteo Vatta, Nona Sotoodehnia, et al.. (2005). Possible Association of the Human KCNE1 (minK) Gene and QT Interval in Healthy Subjects: Evidence from Association and Linkage Analyses in Israeli Families. Annals of Human Genetics. 69(6). 645–656. 22 indexed citations
13.
Vatta, Matteo, Anthony Chang, & Colin J. McMahon. (2005). Altered expression of dystrophin within the thoracic aorta in coarctation. Cardiology in the Young. 15(1). 73–74. 2 indexed citations
14.
McMahon, Colin J., Matteo Vatta, Charles D. Fraser, Jeffrey A. Towbin, & Anthony Chang. (2004). Altered dystrophin expression in the right atrium of a patient after Fontan procedure with atrial flutter: Figure 1. Heart. 90(12). e65–e65. 4 indexed citations
15.
Hong, Kui, Matteo Vatta, Naravat Poungvarin, et al.. (2003). SUDS and Brugada Syndrome Linked by the Same SCN5A Mutation. Japanese Circulation Journal-english Edition. 67. 196. 2 indexed citations
16.
Tsubata, Shinichi, Karla R. Bowles, Matteo Vatta, et al.. (2000). Mutations in the human δ-sarcoglycan gene in familial and sporadic dilated cardiomyopathy. Journal of Clinical Investigation. 106(5). 655–662. 255 indexed citations
17.
Vatta, Matteo, Hua Li, & Jeffrey A. Towbin. (2000). Molecular biology of arrhythmic syndromes. Current Opinion in Cardiology. 15(1). 12–22. 23 indexed citations
18.
Vatta, Matteo, et al.. (1998). Genetic polymorphisms of the renin-angiotensin system in familial dilated cardiomyopathy. Journal of the American College of Cardiology. 31. 350–350. 2 indexed citations
19.
Milas̆in, Jelena, Francesco Muntoni, Giovanni Maria Severini, et al.. (1996). A Point Mutation in the 5' Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated Cardiomyopathy. Human Molecular Genetics. 5(1). 73–79. 125 indexed citations
20.
Mestroni, Luisa, Francesco Muntoni, Jelena Milas̆in, et al.. (1996). Familial dilated cardiomyopathy with subclinical skeletal muscle involvement. Circulation. 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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