Jesús Matés

849 total citations
19 papers, 361 citations indexed

About

Jesús Matés is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Jesús Matés has authored 19 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cardiology and Cardiovascular Medicine, 11 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Jesús Matés's work include Cardiac electrophysiology and arrhythmias (13 papers), Cardiovascular Effects of Exercise (8 papers) and Ion channel regulation and function (7 papers). Jesús Matés is often cited by papers focused on Cardiac electrophysiology and arrhythmias (13 papers), Cardiovascular Effects of Exercise (8 papers) and Ion channel regulation and function (7 papers). Jesús Matés collaborates with scholars based in Spain, Italy and United States. Jesús Matés's co-authors include Anna Iglesias, Ramón Brugada, Óscar Campuzano, Mónica Coll, Catarina Allegue, Josép Brugada, Bernat del Olmo, Carles Ferrer‐Costa, Georgia Sarquella‐Brugada and Ferran Picó and has published in prestigious journals such as PLoS ONE, The FASEB Journal and International Journal of Molecular Sciences.

In The Last Decade

Jesús Matés

19 papers receiving 354 citations

Peers

Jesús Matés

CCM

PMH

CMN

GENET

Catarina Allegue Spain

Bernat del Olmo Spain

Toshihiro Honda Japan

Mónica Coll Spain

Ferran Picó Spain

Lesley Turner Canada

Sung Yon Um United States

Hiroyasu Iwasa Japan

Jennifer D. Kunic United States

Horst Wedekind Germany

Catarina Allegue Spain

Jesús Matés

542 ×2.1

CCM

331 ×1.9

52 ×1.0

PMH

61 ×1.3

CMN

86 ×1.8

GENET

Citations per year, relative to Jesús Matés Jesús Matés (= 1×) peers Catarina Allegue

Countries citing papers authored by Jesús Matés

Since Specialization

Citations

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

Fields of papers citing papers by Jesús Matés

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jesús Matés

This figure shows the co-authorship network connecting the top 25 collaborators of Jesús Matés. A scholar is included among the top collaborators of Jesús Matés 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 Jesús Matés. Jesús Matés 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:

19 of 19 papers shown

Matés, Jesús, et al.. (2021). The Selectivity for Tumor Cells of Nuclear-Directed Cytotoxic RNases Is Mediated by the Nuclear/Cytoplasmic Distribution of p27KIP1. Molecules. 26(5). 1319–1319. 3 indexed citations

Pinsach‐Abuin, Mel·lina, Bernat del Olmo, Jesús Matés, et al.. (2021). Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants. Cell Reports Medicine. 2(4). 100250–100250. 4 indexed citations

Campuzano, Óscar, Georgia Sarquella‐Brugada, Anna Fernández-Falgueras, et al.. (2019). Genetic interpretation and clinical translation of minor genes related to Brugada syndrome. Human Mutation. 40(6). 749–764. 29 indexed citations

Campuzano, Óscar, Anna Fernández-Falgueras, Georgia Sarquella‐Brugada, et al.. (2019). Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants. Journal of Clinical Medicine. 8(7). 1035–1035. 26 indexed citations

Coll, Mónica, Carles Ferrer‐Costa, Sara Pich, et al.. (2018). Role of genetic and electrolyte abnormalities in prolonged QTc interval and sudden cardiac death in end-stage renal disease patients. PLoS ONE. 13(7). e0200756–e0200756. 10 indexed citations

Coll, Mónica, Pasquale Striano, Carles Ferrer‐Costa, et al.. (2017). Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP. PLoS ONE. 12(12). e0189618–e0189618. 34 indexed citations

Campuzano, Óscar, Ana María Cameán Fernández, Irene Mademont‐Soler, et al.. (2017). Sudden Arrhythmic Death During Exercise: A Post-Mortem Genetic Analysis. Sports Medicine. 47(10). 2101–2115. 13 indexed citations

Coll, Mónica, Alexandra Pérez‐Serra, Jesús Matés, et al.. (2017). Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death. Biology. 7(1). 3–3. 29 indexed citations

Campuzano, Óscar, Irene Mademont‐Soler, Mónica Coll, et al.. (2017). Genetic analysis in post-mortem samples with micro-ischemic alterations. Forensic Science International. 271. 120–125. 1 indexed citations

10.

Mademont‐Soler, Irene, Mel·lina Pinsach‐Abuin, Helena Riuró, et al.. (2016). Large Genomic Imbalances in Brugada Syndrome. PLoS ONE. 11(9). e0163514–e0163514. 16 indexed citations

11.

Campuzano, Óscar, Georgia Sarquella‐Brugada, Sergi César, et al.. (2016). A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia. Forensic Science International. 270. 173–177. 2 indexed citations

12.

Pinsach‐Abuin, Mel·lina, Jesús Matés, Bernat del Olmo, et al.. (2016). Regulome‐Seq: Searching for Single Nucleotide Variants (SNVs) Associated with Disease Beyond Protein‐Coding Regions. The FASEB Journal. 30(S1). 1 indexed citations

13.

Coll, Mónica, Catarina Allegue, Sara Partemi, et al.. (2015). Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing. International Journal of Legal Medicine. 130(2). 331–339. 47 indexed citations

14.

Allegue, Catarina, Mónica Coll, Jesús Matés, et al.. (2015). Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome. PLoS ONE. 10(7). e0133037–e0133037. 42 indexed citations

15.

Campuzano, Óscar, Irene Mademont‐Soler, Helena Riuró, et al.. (2015). Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death. International Journal of Molecular Sciences. 16(10). 25773–25787. 17 indexed citations

16.

Campuzano, Óscar, Catarina Allegue, Georgia Sarquella‐Brugada, et al.. (2014). The role of clinical, genetic and segregation evaluation in sudden infant death. Forensic Science International. 242. 9–15. 20 indexed citations

17.

Campuzano, Óscar, Georgia Sarquella‐Brugada, Irene Mademont‐Soler, et al.. (2014). Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology. PLoS ONE. 9(12). e114894–e114894. 24 indexed citations

18.

Campuzano, Óscar, Catarina Allegue, Mónica Coll, et al.. (2014). Post-mortem genetic analysis in juvenile cases of sudden cardiac death. Forensic Science International. 245. 30–37. 42 indexed citations

19.

Campuzano, Óscar, Catarina Allegue, Elisabet Selga, et al.. (2014). P335Sudden unexplained death in Catalonia: comprehensive genetic analysis in post-mortem samples. Cardiovascular Research. 103(suppl 1). S61.2–S61. 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.

Explore authors with similar magnitude of impact